0000000000379903

AUTHOR

Nicolas Desbois

0000-0002-1156-4608

showing 74 related works from this author

Nonfullerene Polymer Solar Cells Reaching a 9.29% Efficiency Using a BODIPY-Thiophene Backboned Donor Material

2018

A conjugated polymer donor containing BODIPY-thiophene dyads in the backbone, P(BdP-EHT), combined with a low bandgap nonfullerene acceptor (SMDPP) consisting of carbazole and diketopyrrolopyrrole units linked with a tetracyanobutadiene acceptor π-linker, was used to design bulk heterojunction polymer solar cells. After the optimization of the donor to acceptor weight ratio and solvent vapor annealing of the P(BdP-EHT):SMDPP active layer, the resulting polymer solar cell showed an overall power conversion efficiency of 9.29%, which is significantly higher than that for the polymer solar cell based on PC71BM (7.41%) processed under identical conditions. This improved power conversion efficie…

Materials scienceOrganic solar cellOpen-circuit voltageCarbazoleEnergy conversion efficiencyEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryElectrochemistryChemical Engineering (miscellaneous)Electrical and Electronic Engineering0210 nano-technologyHOMO/LUMOShort circuitACS Applied Energy Materials
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The first example of cofacial bis(dipyrrins)

2016

International audience; Two series of cofacial bis(dipyrrins) were prepared and their photophysical properties as well as their bimolecular fluorescence quenching with C-60 were investigated. DFT and TDDFT computations were also performed as a modeling tool to address the nature of the fluorescence state and the possible inter-chromophore interactions. Clearly, there is no evidence for such interactions and the bimolecular quenching of fluorescence, in comparison with mono-dipyrrins, indicates that C-60-bis(dipyrrin) contacts occur from the outside of the "mouth" of the cofacial structure.

010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisTransition metalexcitation-energiesmolecular-orbital methodsorganometallic compoundsMaterials Chemistry[CHIM]Chemical Sciencessinglet energy transfersdensity-functional theoryvalence basis-setsGroup 2 organometallic chemistryQuenching (fluorescence)010405 organic chemistryChemistryGeneral ChemistryTime-dependent density functional theorytransition-metalsFluorescence0104 chemical scienceslight-harvesting systems2nd-row elementsDensity functional theoryextended basis-sets
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Surface Acoustic Wave Sensors for the Detection of Hazardous Compounds in Indoor Air

2017

Presented at the Eurosensors 2017 Conference, Paris, France, 3–6 September 2017.; International audience; In this work, the authors show the capabilities of Surface Acoustic Wave (SAW) devices coupled with various absorbents to probe the properties of gas sensitive materials for the manufacturing of hazardous gas sensors. The great capabilities of cobalt corroles for the trapping of carbon monoxide (CO) were exploited to produce selective sensors. These corroles were deposited on SAW delay lines surfaces and then exposed to carbon monoxide (CO) in standard conditions. Concentrations of a few hundreds of ppb were measured emphasizing the interest of such sensors for the detection of CO. Anot…

Materials scienceSAWIndoor airchemistry.chemical_elementlcsh:ANanotechnologyTrapping010402 general chemistry01 natural sciencescarbon monoxidechemistry.chemical_compoundHazardous wastePorositySurface acoustic wave[CHIM.MATE]Chemical Sciences/Material chemistry06 humanities and the artsNano-porous films060202 literary studies0104 chemical sciencescobalt corroleschemistry[ CHIM.MATE ] Chemical Sciences/Material chemistry0602 languages and literatureformaldehydeSurface acoustic wave sensorlcsh:General WorksCobaltLove wavesCarbon monoxideProceedings of Eurosensors 2017, Paris, France, 3–6 September 2017
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Easy access to heterobimetallic complexes for medical imaging applications via microwave-enhanced cycloaddition

2015

The Cu(I)-catalysed Huisgen cycloaddition, known as “click” reaction, has been applied to the synthesis of a range of triazole-linked porphyrin/corrole to DOTA/NOTA derivatives. Microwave irradiation significantly accelerates the reaction. The synthesis of heterobimetallic complexes was easily achieved in up to 60% isolated yield. Heterobimetallic complexes were easily prepared as potential MRI/PET (SPECT) bimodal contrast agents incorporating one metal (Mn, Gd) for the enhancement of contrast for MRI applications and one “cold” metal (Cu, Ga, In) for future radionuclear imaging applications. Preliminary relaxivity measurements showed that the reported complexes are promising contrast agent…

NOTAmicrowavePhotochemistryFull Research Paperlcsh:QD241-441Metalchemistry.chemical_compoundlcsh:Organic chemistrycorroleDOTACorrolelcsh:ScienceOrganic ChemistryPorphyrinCombinatorial chemistryCycloadditionChemistryDOTAchemistryYield (chemistry)visual_artclick chemistryClick chemistryvisual_art.visual_art_mediumlcsh:QporphyrinMicrowaveBeilstein Journal of Organic Chemistry
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Two-Photon Absorption Properties and Structures of BODIPY and Its Dyad, Triad and Tetrad.

2018

A series consisting of a dyad, a triad and a tetrad containing either two, three and four BODIPY units, respectively, has been synthesized and fully characterized and compared to two mono-BODIPY analogs (used as references). The one- and two-photon photophysical properties have been measured and the X-ray structures of four of the BODIPY derivatives have been determined. In the 700-900 nm range, the two-photon absorption (TPA) cross sections range from 30 GM to 160 GM for these compounds.

010405 organic chemistryChemistryTriad (anatomy)General Chemistry010402 general chemistry01 natural sciencesTwo-photon absorption0104 chemical scienceschemistry.chemical_compoundCrystallographymedicine.anatomical_structuremedicineBODIPYAbsorption (chemistry)TetradChemPlusChem
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Random Structural Modification of a Low-Band-Gap BODIPY-Based Polymer

2017

International audience; A BODIPY thiophene polymer modified by extending conjugation of the BODIPY chromophore is reported. This modification induces tunability of energy levels and therefore absorption wavelengths in order to target lower energies.

Materials scienceBand gapthin-film transistors02 engineering and technology010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural scienceschemistry.chemical_compoundmolecular-orbital methodsorganometallic compounds[CHIM]Chemical SciencesPhysical and Theoretical Chemistrydensity-functional theoryAbsorption (electromagnetic radiation)valence basis-setsdistyryl-boradiazaindaceneschemistry.chemical_classificationPolymer modifiedfield-effect transistorspi-conjugated copolymers[CHIM.MATE]Chemical Sciences/Material chemistryPolymerChromophore021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWavelengthsolar-cellsGeneral Energychemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryextended basis-setsBODIPY0210 nano-technologyThe Journal of Physical Chemistry C
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Antipoxvirus Activity Evaluation of Optimized Corroles Based on Development of Autofluorescent ANCHOR Myxoma Virus

2021

International audience; A series of 43 antiviral corrole-based molecules have been tested on myxoma virus (Lausanne-like T1MYXV strain). An autofluorescent MYXV, with an ANCHOR cassette, has been used for the studies. A(2)B-fluorocorroles display various toxicities, from 40 being very toxic (CC50 = 1.7 mu M) to nontoxic 38 (CC50 > 50 mu M), whereas A(3)-fluorocorroles, with one to three fluorine atoms, are not toxic (with the exception of corroles 9, 10, and 22). In vitro, these compounds show a good selectivity index when used alone. Corrole 35 seems to be the most promising compound, which displays a high selectivity index with the lowest IC50. Interestingly, this "Hit" corrole is easy to…

0301 basic medicinePorphyrins[SDV]Life Sciences [q-bio]030106 microbiologyresistant strainMyxoma virusAntiviral Agents03 medical and health scienceschemistry.chemical_compoundmyxoma viruscorroleIn vivoAnimalsCorroleIC50Strain (chemistry)biologybiology.organism_classificationantiviralAcute toxicityIn vitro3. Good healthdsDNA virus030104 developmental biologyInfectious DiseaseschemistryBiochemistrypoxvirusRabbitsSelectivity
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Synthesis, Electrochemistry, and Photophysics of Aza-BODIPY Porphyrin Dyes

2016

International audience; The synthesis of dyad and triad aza-BODIPY-porphyrin systems in two steps starting from an aryl-substituted aza-BODIPY chromophore is described. The properties of the resulting aza-BODIPY-porphyrin conjugates have been extensively investigated by means of electrochemistry, spectroelectrochemistry, and absorption/emission spectroscopy. Fluorescence measurements have revealed a dramatic loss of luminescence intensity, mainly due to competitive energy transfer and photoinduced electron transfer involving charge separation followed by recombination.

resonance energy-transferporphyrinoidstetraarylazadipyrromethenes010402 general chemistryPhotochemistryElectrochemistry01 natural sciences7. Clean energy[ CHIM ] Chemical SciencesCatalysisFluorescence spectroscopyPhotoinduced electron transfersinglet oxygentransfersphotoinduced electron-transferphotoinduced electron transferchemistry.chemical_compoundgeneration[CHIM]Chemical Scienceselectrogenerated chemiluminescencespectroscopic propertiespolyadsAbsorption (electromagnetic radiation)aza-BODIPYs010405 organic chemistryfullereneOrganic ChemistryGeneral ChemistryChromophorefluorescence spectroscopyPorphyrinFluorescence0104 chemical sciences3. Good healthchemistryelectrochemistryderivativesLuminescence
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Electrochemical and Spectroelectrochemical Properties of Free-Base Pyridyl- and N -Alkyl-4-Pyridylporphyrins in Nonaqueous Media

2015

International audience; Twelve structurally related pyridyl and meso-N-methylpyridylporphyrin derivatives are investigated electrochemically in different nonaqueous media. The UV/Vis spectrum of each newly investigated porphyrin was measured before and after electro-reduction and, based on this data, the site of electron transfer is proposed. An interaction occurs between the meso-pyridyl or meso-N-alkyl-4-pyridyl substituents and the porphyrin p-ring system, the magnitude of which depends upon the number of linked pyridyl or N-alkyl-4-pyridyl groups in the compound, the solvent, the supporting electrolyte, and/or other anions added to the solution.

bindingSupporting electrolyteInorganic chemistrycationic porphyrinreductiondnanElectrochemistryporphyrinsdimethylformamide[ CHIM ] Chemical SciencesCatalysischemistry.chemical_compoundElectron transferPolymer chemistry[CHIM]Chemical SciencesAlkylchemistry.chemical_classificationnonaqueous mediacomplex-formationChemistryn-dimethylformamidespectral characterizationaggregationFree basespectroelectrochemistryPorphyrinSolventinteracting centerspotentialselectrochemistry
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cis-Dichloroplatinum(II) complexes tethered to dibenzo[c,h][1,6]naphthyridin-6-ones: Synthesis and cytotoxicity in human cancer cell lines in vitro

2013

A novel family of cisplatin-type complexes tethered to dibenzo[c,h][1,6]naphthyridin-6-one topoisomerase inhibitor via a polymethylene chain and their nonplatinated counterparts were prepared. Their potential cytotoxicity was assessed in three human colorectal cancer cell lines HCT 116, SW480 and HT-29 and compared to the reference molecules cisplatin and oxaliplatin. Platinated compounds were poorly active whilst nonplatinated dibenzo[c,h][1,6]naphthyridin-6-one moieties exhibited higher cytotoxic properties than cisplatin and oxaliplatin whatever the length of the polymethylene chain; molecules containing the tri- and hexamethylene chain length were the most cytotoxic.

Organoplatinum Compoundsmedicine.drug_classStereochemistryAntineoplastic AgentsStructure-Activity RelationshipCell Line TumorDrug DiscoverymedicineHumansCytotoxic T cellMoleculeNaphthyridinesCytotoxicityCell ProliferationPharmacologyCisplatinDose-Response Relationship DrugMolecular StructureChemistryOrganic ChemistryGeneral MedicineHCT116 CellsIn vitroOxaliplatinCell cultureDrug Screening Assays AntitumorHT29 CellsTopoisomerase inhibitormedicine.drugEuropean Journal of Medicinal Chemistry
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Synthesis, Characterization, and Electrochemistry of Open-Chain Pentapyrroles and Sapphyrins with Highly Electron-Withdrawing meso -Tetraaryl Substit…

2017

International audience; A series of open-chain pentapyrroles and sapphyrins with highly electron-withdrawing substituents (i.e., CN, CF3 , or CO2 Me) on the meso-phenyl rings was synthesized and characterized as to the spectral properties, protonation reactions, and electrochemistry in non-aqueous media. The investigated compounds are represented as (Ar)4 PPyH3 and (Ar)4 SapH3 where PPy and Sap correspond to the tri-anion of the open-chain pentapyrrole and sapphyrin, respectively, and Ar=p-CNPh, p-CF3 Ph, or p-CO2 MePh. UV/Vis and 1 H NMR spectroscopy as well as mass spectrometry data are given for the confirmation of the structures for the newly synthesized compounds. An X-ray structure fo…

Absorption spectroscopyprotonationInorganic chemistryporphyrinoidsProtonationpentapyrroles010402 general chemistry01 natural sciencesRedox[ CHIM ] Chemical SciencesCatalysischemistry.chemical_compound[SPI]Engineering Sciences [physics]PyridinePolymer chemistryTrifluoroacetic acid[CHIM]Chemical SciencesEquilibrium constantsapphyrins010405 organic chemistryOrganic ChemistryGeneral Chemistry0104 chemical scienceschemistryelectrochemistryProton NMRCyclic voltammetry
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Porous materials applied to biomarker sensing in exhaled breath for monitoring and detecting non-invasive pathologies

2020

International audience; Overview of the use of porous materials for gas sensing to analyze the exhaled breath of patients for disease identification.The quantification of specific gases among thousand of VOCs (Volatile Organic Compounds) present in the human breath at the ppm/ppb level can be used to evidence the presence of diseases in the human body. The detection of these biomarkers in human exhaled breath through a noninvasive approach is an important field of research which is still attracting important attention to this day. A portable device working at room temperature and usable directly on exhaled breath samples is still a challenge requiring a sensing material with high performanc…

Materials scienceCrystalline materialsNon invasiveNanotechnology[CHIM.MATE]Chemical Sciences/Material chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyHighly selective01 natural sciences0104 chemical sciencesInorganic Chemistry[CHIM.POLY]Chemical Sciences/PolymersBreath TestsExhalationLimit of DetectionHighly porousHumans[CHIM.COOR]Chemical Sciences/Coordination chemistry[SDV.IB]Life Sciences [q-bio]/Bioengineering0210 nano-technologyPorous mediumPorosityBiomarkersDalton Transactions
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Cobalt Corroles with Bis‐Ammonia or Mono‐DMSO Axial Ligands. Electrochemical, Spectroscopic Characterizations and Ligand Binding Properties

2018

International audience; Four bis-ammonia ligated cobalt corroles and four mono-DMSO ligated cobalt corroles with different mesoaryl substituents on the macrocycle (A 2 Band A 3-corroles) were synthesized and investigated as to their electrochemical and spec-troscopic properties under different solution conditions. The complexation energies of the investigated cobalt corroles were theoretically calculated to illustrate the propensity of the cobalt center for pentacoordination or hexa-coordination with various axial ligands (DMSO, CO, py and NH 3). The structure of one hexacoordinate bis-NH 3 cobalt corrole complex was also determined by X-ray diffraction.

chemistry.chemical_classification010405 organic chemistrychemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryAmmoniachemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryPolymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltEuropean Journal of Inorganic Chemistry
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A bacteriochlorin-diketopyrrolopyrrole triad as a donor for solution-processed bulk heterojunction organic solar cells

2019

We have designed an A–π–D–π–A small-molecule triad consisting of a bacteriochlorin (BC) donor central core linked with two diketopyrrolopyrrole (DPP) acceptors via ethynyl bridges (BC-DPP-1). BC-DPP-1 has a narrow optical bandgap of 1.38 eV with highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of −4.93 eV and −3.40 eV, respectively, and it was used as an electron donor along with [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as an acceptor for solution-processed small-molecule organic solar cells. After optimizing the weight ratio between BC-DPP-1 and PC71BM and pyridine as a solvent additive and subsequent solvent vapor annealing using THF, an …

Materials scienceOrganic solar cellBand gapPhotovoltaic systemEnergy conversion efficiencyAnalytical chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical sciencesMaterials Chemistry0210 nano-technologyTernary operationHOMO/LUMOJournal of Materials Chemistry C
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Synthesis, electrochemistry, protonation and X-ray analysis of meso-aryl substituted open-chain pentapyrroles

2019

Five meso-tetraaryl open-chain pentapyrroles were synthesized and characterized as to their electrochemistry and protonation reactions in nonaqueous media. The investigated compounds are represented as (Ar)4PPyH3 where Ar [Formula: see text],[Formula: see text]-F2Ph, [Formula: see text]-BrPh, Ph, [Formula: see text],[Formula: see text],[Formula: see text]-(OMe)3Ph or [Formula: see text]-MePh and were characterized by UV-vis and 1H NMR spectroscopy, mass spectrometry and electrochemistry. Cyclic voltammetry was used to measure redox potentials, while protonation involving the conversion of (Ar)4PPyH3 to [(Ar)4PPyH5][Formula: see text] was monitored by UV-vis absorption spectroscopy. Equilib…

chemistry.chemical_compoundchemistryChain (algebraic topology)ArylProtonationGeneral ChemistryX ray analysisElectrochemistryMedicinal chemistryJournal of Porphyrins and Phthalocyanines
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Non-linear optical, electrochemical and spectroelectrochemical properties of amphiphilic inner salt porphyrinic systems

2016

Three zwitterionic meso-substituted A3B- and AB2C-porphyrins containing one sulfonato alkylpyridinium substituent and three or two alkoxy-substituted phenyl groups were synthesized in good yield and fully characterized as to their physicochemical properties by a variety of techniques. This new series of inner salt donor-acceptor meso-substituted porphyrin derivatives were prepared for possible application as amphiphilic probes for membrane insertion in the area of combined second-harmonic and two-photon fluorescence cellular microscopy. To this end, the linear and nonlinear optical properties of the compounds were characterized, together with their electrochemical and spectroelectrochemica…

designInorganic chemistrySubstituentamphiphilic inner salt02 engineering and technology010402 general chemistryElectrochemistryPhotochemistry[ CHIM ] Chemical Scienceselectron-accepting moieties01 natural sciencesnon-linear optical propertychemistry.chemical_compoundAmphiphilechromophores[CHIM]Chemical SciencesMoleculeChemistryfrequency dispersionSecond-harmonic generationspectroelectrochemistrydipolar complexesGeneral Chemistry021001 nanoscience & nanotechnologyPorphyrinFluorescence0104 chemical sciences2nd-harmonic generationelectrochemistrymicroscopycharge-transferfluorescenceAbsorption (chemistry)hyper-rayleigh scattering0210 nano-technologyJournal of Porphyrins and Phthalocyanines
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Covalent Organic Frameworks for the detection of CO

2021

International audience; Every year in the world, carbon monoxide (CO) is responsible for thousands of intoxications and hundreds of deaths. The detection (CO) at few ppm levels is thus a critical point for the control of the air quality. Corrole belongs to the family of porphyrinoids which is largely used for sensing applications [1]. We have shown that cobalt metallocorroles are able to bind carbon monoxide in the axial position with a high affinity even in the presence of nitrogen and dioxygen, the two main components of the atmosphere [2]. We have recently prepared sensing devices for low CO detection level (sub-ppm) using cobalt corroles deposited as films on a Surface Acoustic Wave dev…

inorganic chemicals[SPI.OTHER]Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/Other
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Tuning the Electrochemistry of Free-Base Porphyrins in Acidic Nonaqueous Media: Influence of Solvent, Supporting Electrolyte, and Ring Substituents

2016

International audience; A detailed study of reduction potentials, electroreduction mechanisms and acid-base chemistry was carried out on two series of free-base porphyrins in nonaqueous media. The first series is represented by four-pyrrole substituted tetraphenylporphyrin (TPP) derivatives, two of which are planar and two of which are nonplanar in their non-protonated form. The second comprises porphyrins with 0-4 meso-phenyl groups on the macrocycle. Equilibrium constants for conversion of each neutral porphyrin to its diprotic [H4P] 2+ form were determined and the electrochemistry was then elucidated as a function of: (i) type of nonaqueous solvent, (ii) anion of supporting electrolyte, …

free-base porphyrinsSupporting electrolyteprotonationInorganic chemistry010402 general chemistryElectrochemistry[ CHIM ] Chemical Sciences01 natural sciencesCatalysistetraphenylporphyrin monoacidschemistry.chemical_compoundconformational-analysismetal derivativesTetraphenylporphyrin[CHIM]Chemical SciencesReactivity (chemistry)tetraarylporphyrinsEquilibrium constantcomplexes010405 organic chemistryFree basecrystal-structurespectroelectrochemistryanionDiprotic acidPorphyrin0104 chemical sciencessupporting electrolytechemistryelectrochemistryexpanded porphyrindiacids[CHIM.OTHE]Chemical Sciences/Otherabsorption
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Design of Porphyrin-dota-Like Scaffolds as All-in-One Multimodal Heterometallic Complexes for Medical Imaging

2013

A series of four multimodal ligands incorporating one porphyrin moiety and one or more dota-like macrocycles all-in-one in the same molecular architecture have been synthesized and full characterized. The corresponding gadolinium(III) complexes were also synthesized and heterometallic complexes incorporating both gadolinium(III) and copper(II) ions were prepared as potential MRI/PET multimodal contrast agents. One ligand (L4) includes an amine moiety that can be activated for easy conversion into an isothiocyanate group for further anchoring to a biological vector. Preliminary relaxivity, cytotoxicity, and MRI studies showed that the complexes developed in this work are very promising medic…

StereochemistryLigandGadoliniumOrganic Chemistrychemistry.chemical_elementMri studiesCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryIsothiocyanateDOTAMoietyAmine gas treatingPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Polymer solar cell based on ternary active layer consists of medium bandgap polymer and two non-fullerene acceptors

2020

Abstract An efficient PSCs consisting of a ternary active layer containing a medium bandgap conjugated polymer P and two well-known non-fullerene acceptors i.e. ITIC-m and Y6 was fabricated. An overall Power Conversion Efficiency (PCE) of about 15.13% was achieved, with the optimized ternary active layer consisting of 20 wt% of ITIC-m in acceptors i.e. P:ITIC-m:Y6 (1:0.3:1.2). This value is higher than that for the binary counter parts i.e. 12.10% and 13.16% for P:ITIC-m (1:1.5 w:w) and P:Y6 (1:1.5 w:w). The higher short circuit current density of the ternary active layer PSCs is related to the broader absorption spectra as compared to the binary active layer analogs. The open circuit volta…

Materials scienceRenewable Energy Sustainability and the EnvironmentBand gapOpen-circuit voltage020209 energyAnalytical chemistry02 engineering and technology021001 nanoscience & nanotechnologyAcceptorPolymer solar cellActive layer0202 electrical engineering electronic engineering information engineeringGeneral Materials Science0210 nano-technologyTernary operationShort circuitHOMO/LUMOSolar Energy
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Inside Cover: Synthesis and Characterization of Carbazole-Linked Porphyrin Tweezers (Chem. Eur. J. 34/2015)

2015

ChemistryCarbazoleOrganic ChemistrySonogashira couplingGeneral ChemistryElectrochemistryPhotochemistryPorphyrinCatalysisCharacterization (materials science)chemistry.chemical_compoundTweezersCover (algebra)Glaser couplingChemistry - A European Journal
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Synthesis and Antiviral Activity Evaluation of Nitroporphyrins and Nitrocorroles as Potential Agents against Human Cytomegalovirus Infection.

2015

Different nitroporphyrinoid derivatives were synthesized and studied as potential agents against human Cytomegalovirus. Interestingly, two nitrocorroles display strong activity against human Cytomegalovirus with IC 50 < 0.5 μM. These compounds also possess antiproliferative activities without detected in vivo toxicity. Therefore, nitrocorroles appear for the first time as potential active compounds that can be applied in human health.

Human cytomegalovirusHuman healthInfectious DiseasesChemistrymedicineIn vivo toxicitymedicine.diseaseVirologyACS infectious diseases
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Synthetic strategy for preparation of a folate corrole DOTA heterobimetallic Cu–Gd complex as a potential bimodal contrast agent in medical imaging

2015

Abstract An efficient sequential route to synthesize heterobimetallic complexes is reported herein. A folate, Cu corrole, Gd DOTA complex that addresses the requirements of a potential contrast agent (CA) for bimodal imaging (e.g., MRI/PET) is reported. The over-expression of the folate receptor in a variety of malignant tumors, along with its limited expression in healthy tissues, makes this an attractive tumor-specific molecular target. Synthesis of a bimetallic ligand potentially targeting the folate receptor, was easily achieved in only a few steps. Interestingly, preliminary studies showed that the relaxivity of the folic heterobimetallic derivative was higher in comparison to a clinic…

StereochemistryGadoliniumMRI contrast agentOrganic Chemistrychemistry.chemical_elementLigand (biochemistry)BiochemistryCombinatorial chemistryImaging agentchemistry.chemical_compoundchemistryIn vivoFolate receptorDrug DiscoveryDOTACorroleTetrahedron Letters
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Porphyrins and BODIPY as Building Blocks for Efficient Donor Materials in Bulk Heterojunction Solar Cells

2017

International audience; Advances in the synthesis and application of highly efficient polymers and small molecules over the last two decades have enabled the rapid advancement in the development of organic solar cells and photovoltaic technology as a promising alternative to conventional solar cells, based on silicon and other inorganic semiconducting materials. Among the different types of organic semiconducting materials, porphyrins and BODIPY-based small molecules and conjugated polymers attract high interest as efficient semiconducting organic materials for dye sensitized solar cells and bulk heterojunction organic solar cells. The highest power conversion efficiency exceeding 9% has be…

Materials scienceOrganic solar cellEnergy Engineering and Power Technologypower-conversion efficiency02 engineering and technologydonor materials010402 general chemistryporphyrins7. Clean energy01 natural sciencesPolymer solar cellbulk heterojunction solar cellsphotoinduced electron-transferchemistry.chemical_compoundBODIPYElectrical and Electronic Engineeringsmall-moleculelow-bandgap polymerbusiness.industryfield-effect transistors[CHIM.MATE]Chemical Sciences/Material chemistryHybrid solar cellpi-conjugated copolymersd-a021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsphotovoltaic propertieschemistryopen-circuit voltage[ CHIM.MATE ] Chemical Sciences/Material chemistryOptoelectronicsorganic photovoltaicsBODIPY0210 nano-technologybusiness
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Photovoltaic Properties of a Porphyrin-Containing Polymer as Donor in Bulk Heterojunction Solar Cells With Low Energy Loss

2017

chemistry.chemical_classificationMaterials sciencebusiness.industryPhotovoltaic systemEnergy conversion efficiencyEnergy Engineering and Power Technology02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPorphyrinAtomic and Molecular Physics and OpticsPolymer solar cell0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry.chemical_compoundLow energychemistryOptoelectronicsElectrical and Electronic Engineering0210 nano-technologybusinessSolar RRL
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BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

2018

Two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized. In BD-pPor and BD-tPor, porphyrins are linked to the central BODIPY by phenyl and thiophene bridges, respectively. The optical and electrochemical properties were systematically investigated in order to employ them as donors along with PC71BM as an acceptor for solution processed bulk heterojunction organic solar cells. After the optimization of the active layer, the organic solar cells based on BD-pPor and BD-tPor exhibit overall power conversion efficiencies of 6.67% and 8.98% with an energy loss of 0.63 eV and 0.50 eV. Th…

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesPolymer solar cellchemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiopheneGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the Environment[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall moleculeAcceptorPorphyrin0104 chemical scienceschemistryBODIPY0210 nano-technology
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Synthesis of Polyfused Heterocycle Derivatives Containing the Dipyridoimidazole Core by Friedländer’s Reaction: Access to Analogs of Ellipticine

2005

Reaction of 3-amino-2-formylimidazo[l,2-a]pyridine with various aldehydes and ketones by Friedlander's methodology afforded an entry to dipyridoimidazole, tri(tetra)azacyclopenta[b]fluorene, tri(tetra)azabenzo[b]-fluorene and triazaindeno[2,1-b]phenanthrene derivatives. Intercalation with a synthetic oligodeoxynucleotide was examined.

StereochemistryIntercalation (chemistry)[CHIM.THER]Chemical Sciences/Medicinal ChemistryFluorene010402 general chemistry01 natural sciencesAnalytical ChemistryEllipticinechemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSPharmacologybiology[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryPhenanthrenebiology.organism_classification0104 chemical scienceschemistryTetra[ CHIM.RADIO ] Chemical Sciences/Radiochemistry[CHIM.RADIO]Chemical Sciences/RadiochemistryHETEROCYCLES
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Tetracationic and Tetraanionic Manganese Porphyrins: Electrochemical and Spectroelectrochemical Characterization

2017

International audience; The electrochemistry and spectroelectrochemistry of four tetrapositively charged and two tetranegatively charged porphyrins were characterized in two nonaqueous solvents (dimethyl sulfoxide and N,N-dimethylformamide) containing 0.1 M tetra-n-butylammonium perchlorate. The tetrapositively charged compounds are represented by the tetrapyridylporphyrins [TRPyPM]4+(X-)4, where R is a methyl or [2-[2-(2-methoxy)ethoxy]ethoxy]ethyl group, M = MnIIII, MnIIICl, CuII, or PdII, and X = I- or Cl-. The tetranegatively charged porphyrins are represented by the tetrasulfonato derivatives [TPPSMn(OAc)]4-(NH4+)4 and [TArPSMn(OAc)]4-(NH4+)4, where Ar = 4-O-[2-[2-(2-methoxy)ethoxy]eth…

010405 organic chemistryDimethyl sulfoxidechemistry.chemical_element[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundPerchloratechemistry13. Climate actionAlkoxy groupPyridiniumEthyl groupPhysical and Theoretical Chemistry
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Protonation and Electrochemical Properties of Pyridyl- and Sulfonatophenyl-Substituted Porphyrins in Nonaqueous Media

2017

International audience; The protonation and electrochemical properties of positively charged and negatively charged porphyrins are reported in up to five different nonaqueous solvents. The positively charged porphyrins are represented by mono- and di-pyridyl derivatives having the formula Pyx(PhMe)4-xPM, where P=the dianion of the porphyrin macrocycle, PhMe is a meso-tolyl group, Py a meso-pyridyl group, x=1 or 2, and M=H2, NiII, CuII, ZnII, or CoII. The negatively charged porphyrins are comprised of meso-tetrasulfonato derivatives having the formula [(R)4(TPPS)H2]4−(X+)4, where [(TPPS)H2]4− represents the porphyrin with four SO3− groups on the meso-phenyl substituents of the macrocycle, R=…

010405 organic chemistryChemistryProtonation010402 general chemistryPhotochemistryElectrochemistry[ CHIM ] Chemical Sciences01 natural sciencesMedicinal chemistryPorphyrinRedoxCatalysis0104 chemical sciencesSolventchemistry.chemical_compoundPEG ratioElectrochemistryTrifluoroacetic acid[CHIM]Chemical SciencesTitrationChemElectroChem
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Electrochemistry of Bis(pyridine)cobalt (Nitrophenyl)corroles in Nonaqueous Media

2018

International audience; A series of bis(pyridine)cobalt corroles with one or three nitrophenyl groups on the meso positions of the corrole macrocycle were synthesized and characterized as to their electrochemical and spectroscopic properties in dichloromethane, benzonitrile, and pyridine. The potentials for each electrode reaction were measured by cyclic voltammetry and the electron-transfer mechanisms evaluated by analysis of the electrochemical data combined with UV-visible spectra of the neutral, electroreduced, and electroxidized forms of the corroles. The proposed electronic configurations of the initial compounds and the prevailing redox reactions involving the electroactive central c…

[SPI.OTHER]Engineering Sciences [physics]/Otherelectronic-structuremanganese corroleschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistryConjugated system010402 general chemistryElectrochemistry01 natural sciencesInorganic Chemistryporphyrin-corrole dyadschemistry.chemical_compoundcopper corroleswater-oxidationPyridinePolymer chemistryacid-media[CHIM]Chemical Sciencesaryl-substituted corrolesredox potentialsPhysical and Theoretical ChemistryCorrole010405 organic chemistry0104 chemical sciencesSolventBenzonitrilechemistrystructural-characterizationefficient synthesisCyclic voltammetryCobaltInorganic Chemistry
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Recent developments in dipyrrin based metal complexes: Self-assembled nanoarchitectures and materials applications

2020

While dipyrrin-boron complexes (BODIPYs) and their derivatives have attracted much attention, dipyrrin-based metal complexes recently appeared as a novel luminescent material. So far, dipyrrin-metal complexes have been regarded as non-luminescent or weakly luminescent. Interestingly, introduction of steric hindrance at the meso-position and the development of heteroleptic complexes with proper frontier orbital ordering are two recent strategies that have been developed to improve their luminescent ability. Compared with BODIPYs, one of the distinctive advantages of dipyrrin-metal complexes is that they can form a series of self-assembled supramolecules and polymer assemblies via facile coo…

MetalChemistryvisual_artLuminescent materialvisual_art.visual_art_mediumNanotechnologyGeneral ChemistrySelf assembledJournal of Porphyrins and Phthalocyanines
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Cyclotriveratrylene-Containing Porphyrins

2016

International audience; The C-3-symmetric cyclotriveratrylene (CTV) was covalently bonded via click chemistry to 1, 2, 3, and 6 zinc(II) porphyrin units to various host for C-60. The binding constants, Ka, were measured from the quenching of the porphyrin fluorescence by C-60. These constants vary between 400 and 4000 M-1 and are considered weak. Computer modeling demonstrated that the zinc(II) porphyrin units, [Zn], exhibit a strong tendency to occupy the CTV cavity, hence blocking the access for C-60 to land on this site. Instead, the pincer of the type [Zn]-[Zn] and in one case [Zn]-CTV, were found to be the most probable geometry to promote host-guest associations in these systems.

cagesStereochemistrychemistry.chemical_elementCyclotriveratryleneZinc010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessupramolecular chemistrydendrimersInorganic Chemistrychemistry.chemical_compoundc-60[CHIM]Chemical SciencesmoleculesctvPhysical and Theoretical Chemistryinclusion complexesQuenching (fluorescence)010405 organic chemistryfullereneFluorescencePorphyrin0104 chemical sciencesPincer movementCrystallographychemistryCovalent bondClick chemistryderivativeshosts
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Synthesis and characterization of zinc carboxy–porphyrin complexes for dye sensitized solar cells

2018

Two zinc porphyrins, 2 and 8, have been synthesized. Porphyrin 8 displays better electronic communication between the dye and the TiO2 electrode. Photophysical measurements and electrochemistry experiments suggest that both porphyrins are very promising sensitizers for dye-sensitized solar cells (DSSCs). It was found that their molecular orbital energy levels favor electron injection and dye regeneration in DSSCs. Solar cells sensitized by 2 and 8 were fabricated, and it was found that they show power conversion efficiencies (PCEs) of 5.27% and 7.13%, respectively. Photovoltaic measurements (J–V curves) together with the incident photon-to-electron conversion efficiency spectra of the two c…

Energy conversion efficiencyPhotovoltaic systemchemistry.chemical_element02 engineering and technologyGeneral ChemistryZinc010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistryPhotochemistry01 natural sciencesPorphyrinElectron transport chainCatalysis0104 chemical sciencesDye-sensitized solar cellchemistry.chemical_compoundchemistryElectrodeMaterials Chemistry0210 nano-technologyNew Journal of Chemistry
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SAW based CO2 sensor: influence of functionalizing MOF crystal size on the sensor's selectivity

2021

International audience; The potential impact of indoor air quality on human health has become an increasingly important topic of public health and, thus, has stimulated an interest in hazardous compounds survey such as carbon dioxide. To address this issue, we started the development of a Surface Acoustic Wave device functionalized with metal-organic framework for the selective detection of carbon dioxide. Here, we propose preliminary results on the influence of the size of the metal-organic framework crystals on the sensor’s selectivity and on its evolution with the ageing of the sensor

[SPI.OTHER]Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/Other
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Synthesis of flexible nanotweezers with various metals and their application in carbon nanotube extraction

2018

Bisporphyrin-based flexible nanotweezers with various metals were synthesized and applied to the extraction of single-walled carbon nanotubes. Homo- and hetero-metallic bisporphyrins containing Co2+ were found to afford higher SWNT-extraction ability, while no or a little amount of SWNTs were extracted by bisporphyrins with other metals.

ChemistryExtraction (chemistry)02 engineering and technologyGeneral ChemistryCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical scienceslaw.inventionChemical engineeringlawMaterials Chemistry0210 nano-technologyNew Journal of Chemistry
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Electrochemistry of Mono- and Bis-CN Ligated Cobalt Corroles

2021

International audience; The electrochemical properties of numerous transition metal corroles have been examined under a variety of<br&gtsolution condition with special emphasis being placed on the innocent or non-innocent nature of the corrole<br&gtmacrocycle. This property, as well as the half-wave potentials and sites of electron transfers, are known to be<br&gtstrongly influenced by the type of central metal ion and degree of axial coordination, namely 4, 5 or 6-coordinate.<br&gtThe redox potentials of metallocorroles are also dependent upon the solvent and inductive, resonance or steric<br&gteffects dictated by peripheral substituents at the meso or β-pyrrole positions of the corrole li…

[SPI.OTHER]Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/Other
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Porphyrin Antenna-Enriched BODIPY–Thiophene Copolymer for Efficient Solar Cells

2018

International audience; Low bandgap A−π–D copolymer, P(BdP-DEHT), consisting of alternating BOronDIPYrromethene (BODIPY) and thiophene units bridged by ethynyl linkers, and its porphyrin-enriched analogue, P(BdP/Por-DEHT), were prepared, and their optical and electrochemical properties were studied. P(BdP-DEHT) exhibits strong absorption in the 500–800 nm range with an optical bandgap of 1.74 eV. On the basis of cyclic voltammetry, the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels are evaluated to be −5.40 and −3.66 eV, respectively. After the anchoring of zinc(II) porphyrin on the BODIPY unit, P(BdP/Por-DEHT) displays broadened absor…

Materials scienceBand gap02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyPolymer solar cellporphyrin substitutionDichlorobenzenechemistry.chemical_compoundThiopheneGeneral Materials ScienceHOMO/LUMOsolvent vapor annealing[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencespower conversion efficiencyCrystallographyApiD copolymerchemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryBODIPYCyclic voltammetry0210 nano-technologypolymer solar cells
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Functionnalized Surface Acoustic Wave Sensors for the Detection of Hazardous Gases

2018

International audience; In this work, we show the capabilities of Surface Acoustic Wave (SAW) devices to probe the properties of gas sensitive materials for the manufacturing of hazardous gas sensors. The great capabilities of cobalt corroles for the trapping of carbon monoxide (CO) were exploited to produce selective sensors. These corroles were deposited on SAW delay lines surfaces and then exposed to carbon monoxide (CO) in standard conditions. Concentrations of a few hundreds of ppb were measured emphasizing the interest of such sensors for the detection of CO. Another type of sensitive layers exhibiting specific porosity adapted to the trapping of formaldehyde (CH$_2$O) were deposited …

[SPI.OTHER]Engineering Sciences [physics]/OtherMaterials science[SPI.OTHER] Engineering Sciences [physics]/Other010405 organic chemistryDetection thresholdbusiness.industrySurface acoustic wavechemistry.chemical_element[CHIM.MATE]Chemical Sciences/Material chemistryTrapping010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryHazardous wasteOptoelectronicsSurface acoustic wave sensorPorositybusinessCobaltCarbon monoxide
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Mono-DMSO ligated cobalt nitrophenylcorroles: electrochemical and spectral characterization

2018

Four mono-DMSO ligated cobalt corroles with one or three meso-nitrophenyl substituents on the macrocycle were synthesized and investigated as to their electrochemical and spectroscopic properties in CH2Cl2 and DMSO. Comparisons are made between redox reactions of the five-coordinate DMSO adducts in the current study and earlier examined five- and six-coordinate cobalt corroles with pyridine axial ligands which were characterized in a variety of nonaqueous electrochemical solvents. The binding of carbon monoxide (CO) is also investigated.

010405 organic chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesAdductchemistry.chemical_compoundchemistryPyridinePolymer chemistryMaterials ChemistryCobaltCarbon monoxideNew Journal of Chemistry
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Synthesis and Characterization of Carbazole-Linked Porphyrin Tweezers

2015

Herein the synthesis, spectroscopic characterization, two-photon absorption and electrochemical properties of 3,6-disubstituted carbazole tweezers is reported. A dimer resulting from a Glaser homocoupling was isolated during a Sonogashira coupling reaction between a diethynyl-carbazole spacer and a 5-bromo-triarylporphyrin and the properties of this original compound were compared with the 3,6-disubstituted carbazole bisporphyrin tweezers. The dyads reported herein present a two-photon absorption maximum at 920 nm with two-photon absorption cross-section in the 1200 GM range. Despite a strong linear absorption in the Soret region and moderate fluorescence quantum yield, they both lead to a …

CarbazoleDimerOrganic ChemistrySonogashira couplingQuantum yieldGeneral ChemistryPhotochemistryPorphyrinCatalysischemistry.chemical_compoundchemistryTweezersGlaser couplingAbsorption (electromagnetic radiation)Chemistry - A European Journal
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Disclosing the actual efficiency of G-quadruplex-DNA–disrupting small molecules

2020

AbstractThe quest for small molecules that avidly bind to G-quadruplex-DNA (G4-DNA, or G4), so called G4-ligands, has invigorated the G4 research field from its very inception. Massive efforts have been invested to i- screen or design G4-ligands, ii- evaluate their G4-interacting properties in vitro through a series of now widely accepted and routinely implemented assays, and iii- use them as unique chemical biology tools to interrogate cellular networks that might involve G4s. In sharp contrast, only uncoordinated efforts at developing small molecules aimed at destabilizing G4s have been invested to date, even though it is now recognized that such molecular tools would have tremendous appl…

0303 health sciencesComputer scienceChemical biology[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology[CHIM.THER]Chemical Sciences/Medicinal ChemistryComputational biology010402 general chemistryG-quadruplex01 natural sciencesSmall moleculeIn vitro0104 chemical sciences03 medical and health scienceschemistry.chemical_compoundchemistryDNA030304 developmental biology
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DNA structure-specific sensitization of a metalloporphyrin leads to an efficient in vitro quadruplex detection molecular tool

2016

International audience; The search for convenient molecular probes for detecting DNA and RNA quadruplexes in vitro is marked by a rapid pace of progress, spurred on by the multiple roles these higher-order nucleic acid structures play in many genetic dysregulations. Here, we contribute to this search, reporting on a palladated porphyrin named Pd.TEGPy: its efficiency as quadruplex-selective fluorescent dye relies on a structural design that endows it with attractive supramolecular and electronic properties and makes it an efficient turn-on, quadruplex-selective fluorescent stain thanks to a DNA-mediated sensitization mechanism that ensures a high level of specificity.

0301 basic medicineSupramolecular chemistryNanotechnology[ CHIM ] Chemical SciencesCatalysis03 medical and health scienceschemistry.chemical_compoundenergy-transferMaterials Chemistrymedicine[CHIM]Chemical Sciencesheterocyclic compoundsrnaSensitizationComputingMilieux_MISCELLANEOUSvisualizationligandsaggregationselectivityRNAGeneral ChemistryFluorescencePorphyrindye-complexes030104 developmental biologymedicine.anatomical_structurechemistryBiophysicsNucleic acidcellsrecognitionMolecular probeporphyrinDNA
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Porous Organic Polymers (POPs) based on cobalt corroles for the detection of carbon monoxide

2021

International audience; Detection of carbon monoxide (CO) at few ppm levels is a critical point for quality control of domestic and<br&gtindustrial environment. CO is responsible for thousands of intoxications and hundreds of deaths per year in the<br&gtworld. Moreover, CO is a residual gas found in the industrial dihydrogen used for Proton Exchange Membrane<br&gtfuel cell, and deactivates the fuel cell prematurely. Corroles have been largely used in sensing applications.[1]<br&gtCobalt corroles display high binding affinity for carbon monoxide even in the presence of nitrogen and<br&gtdioxygen.[2] The affinity of the Co(III) metallocorroles for CO is directly correlated with the Lewis acid…

[SPI.OTHER]Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/Other
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Ligand Noninnocence in Cobalt Dipyrrin–Bisphenols: Spectroscopic, Electrochemical, and Theoretical Insights Indicating an Emerging Analogy with Corro…

2019

Three cobalt dipyrrin-bisphenol (DPPCo) complexes with different meso-aryl groups (pentafluorophenyl, phenyl, and mesityl) were synthesized and characterized based on their electrochemistry and spectroscopic properties in nonaqueous media. Each DPPCo undergoes multiple oxidations and reductions with the potentials, reversibility, and number of processes depending on the specific solution conditions, the specific macrocyclic substituents, and the type and number of axially coordinated ligands on the central cobalt ion. Theoretical calculations of the compounds with different coordination numbers are given in the current study in order to elucidate the cobalt-ion oxidation state and the innoc…

010405 organic chemistryLigandCoordination numberchemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistryMetalchemistryOxidation statelawComputational chemistryvisual_artvisual_art.visual_art_mediumMacrocyclic ligandPhysical and Theoretical ChemistryElectron paramagnetic resonanceCobaltInorganic Chemistry
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A3- and A2B-fluorocorroles: synthesis, X-ray characterization and antiviral activity evaluation against human cytomegalovirus infection

2020

Twenty-nine fluorinated corroles were prepared, spectroscopically characterized, and studied for their antiviral activity against human cytomegalovirus infection. Six corroles were also fully characterized by X-ray crystallography giving insights on their geometrical features. The halogenated corroles reported herein exhibit significantly improved antiviral activity over their non-halogenated counterparts and over nitro-corrole analogs previously reported. Full activity of thirteen A3-corroles is achieved with four fluorine atoms present on the meso-phenyl ring reaching a selectivity index above 300. The maximum activity is achieved for A2B-corroles with selectivity indexes above 400. We th…

PharmacologyHuman cytomegalovirus0303 health sciences010405 organic chemistryChemistryStereochemistryOrganic ChemistryX-rayPharmaceutical Sciencechemistry.chemical_elementmedicine.diseaseRing (chemistry)01 natural sciencesBiochemistry0104 chemical sciencesCharacterization (materials science)03 medical and health sciencesDrug DiscoverymedicineFluorineMolecular MedicineMoleculeSelectivity030304 developmental biologyRSC Medicinal Chemistry
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Porphyrin-Based Design of Bioinspired Multitarget Quadruplex Ligands

2014

Secondary nucleic acid structures, such as DNA and RNA quadruplexes, are potential targets for cancer therapies. Ligands that interact with these targets could thus find application as anticancer agents. Synthetic G-quartets have recently found numerous applications, including use as bioinspired G-quadruplex ligands. Herein, the design, synthesis and preliminary biophysical evaluation of a new prototype multitarget G-quadruplex ligand, (PNA)PorphySQ, are reported, where peptidic nucleic acid guanine ((PNA)G) was incorporated in the porphyrin-templated synthetic G-quartet (PorphySQ). Using fluorescence resonance energy transfer (FRET)-melting experiments, PorphySQ was shown to possess enhanc…

Models MolecularPeptide Nucleic AcidsGuaninePorphyrinsStereochemistryGuanineLigands010402 general chemistryG-quadruplex01 natural sciencesBiochemistryStructure-Activity Relationship03 medical and health scienceschemistry.chemical_compoundDrug Discovery[CHIM]Chemical SciencesStructure–activity relationshipheterocyclic compoundsGeneral Pharmacology Toxicology and PharmaceuticsBinding siteComputingMilieux_MISCELLANEOUS030304 developmental biologyPharmacology0303 health sciencesBinding SitesChemistryLigandOrganic ChemistryDNA0104 chemical sciencesG-QuadruplexesFörster resonance energy transferNucleic acidNucleic Acid ConformationRNAMolecular MedicineDNAChemMedChem
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A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
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Influence of interfering gases on a carbon monoxide differential sensor based on SAW devices functionalized with cobalt and copper corroles

2021

International audience; <!--[if gte mso 9]&gt<xml&gt <w:WordDocument&gt <w:View&gtNormal</w:View&gt <w:Zoom&gt0</w:Zoom&gt <w:TrackMoves/&gt <w:TrackFormatting/&gt <w:HyphenationZone&gt21</w:HyphenationZone&gt <w:PunctuationKerning/&gt <w:ValidateAgainstSchemas/&gt <w:SaveIfXMLInvalid&gtfalse</w:SaveIfXMLInvalid&gt <w:IgnoreMixedContent&gtfalse</w:IgnoreMixedContent&gt <w:AlwaysShowPlaceholderText&gtfalse</w:AlwaysShowPlaceholderText&gt <w:DoNotPromoteQF/&gt <w:LidThemeOther&gtFR</w:LidThemeOther&gt <w:Compatibility&gt <w:BreakWrappedTables/&gt <w:SnapToGridInCell/&gt <w:WrapTextWithPunct/&gt <w:UseAsianBreakRules/&gt <w:DontGrowAutofit/&gt <w:SplitPgBreakAndParaMark/&gt <w:EnableOpenTypeKe…

[SPI.OTHER]Engineering Sciences [physics]/OtherMaterials sciencechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundIndoor air qualityMaterials ChemistryElectrical and Electronic EngineeringInstrumentationPotential impactbusiness.industry[SPI.OTHER] Engineering Sciences [physics]/OtherSurface acoustic waveMetals and AlloysHumidity021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopper0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryOptoelectronics0210 nano-technologybusinessCobaltSensitivity (electronics)Carbon monoxide
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Near-infrared emissive bacteriochlorin-diketopyrrolopyrrole triads: Synthesis and photophysical properties

2019

International audience; The synthesis of unprecedented energy transfer triads containing a near-infrared (NIR) emissive bacteriochlorin subunit and two diketopyrrolopyrrole (DPP) moieties linked to each other via ethynyl or zero-carbon spacers is presented. Their optical and fluorescence properties were determined in CHCl3 and toluene. These photophysical measurements highlight the ability of DPP scaffold to act as an effective energy donor, which once excited in the range 450-550 nm resulting nearly exclusively NIR emission of hydroporphyrin (ETE > 96%). Since DPP dyes are valuable structurally tunable fluorophores that may be used in the construction of high-performance multicomponent pho…

Energy-transfer triadMaterials science[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringEnergy transferNear-infrared spectroscopyRational design02 engineering and technologyChromophoreFluorophore010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences7. Clean energyFluorescence0104 chemical sciencesNearinfrared fluorescence HighlightsEffective energyExcited state0210 nano-technologyBacteriochlorinDiketopyrrolopyrrole
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Redox properties of nitrophenylporphyrins and electrosynthesis of nitrophenyl-linked Zn porphyrin dimers or arrays

2014

Five nitrophenylporphyrins were investigated as to their electrochemical properties in CH 2 Cl 2 containing 0.1 M TBAP. The investigated compounds are represented as ( NO 2 Ph )x Ph 4-x PorM , where Por represents the dianion of the porphyrin macrocycle, Ph is a phenyl group on meso-position of the macrocycle, NO 2 Ph is a meso-substituted nitrophenyl group, M = 2 H , Pd II or Zn II and x = 1 or 2. Each porphyrin undergoes an initial one electron reduction at E1/2 = -1.07 to -1.12 V where the added negative charge is almost totally localized on the meso-nitrophenyl group of the compound. This reversible reduction is then followed by one or more irreversible reductions of the nitrophenyl an…

chemistry.chemical_compoundchemistryOne-electron reductionPhenyl groupGeneral ChemistryConjugated systemElectrosynthesisPhotochemistryElectrochemistryPorphyrinMedicinal chemistryRedoxIonJournal of Porphyrins and Phthalocyanines
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Slow and Fast Singlet Energy Transfers in BODIPY-gallium(III)corrole Dyads Linked by Flexible Chains

2014

Red (no styryl), green (monostyryl), and blue (distyryl) BODIPY-gallium(III) (BODIPY = boron-dipyrromethene) corrole dyads have been prepared in high yields using click chemistry, and their photophysical properties are reported. An original and efficient control of the direction of the singlet energy transfers is reported, going either from BODIPY to the gallium-corrole units or from gallium-corroles to BODIPY, depending upon the nature of the substitution on BODIPY. In one case (green), both directions are possible. The mechanism for the energy transfers is interpreted by means of through-space Förster resonance energy transfer (FRET).

Inorganic Chemistrychemistry.chemical_compoundFörster resonance energy transferChemistryEnergy transferClick chemistrychemistry.chemical_elementSinglet statePhysical and Theoretical ChemistryBODIPYGalliumCorrolePhotochemistryInorganic Chemistry
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Gold dipyrrin-bisphenolates: A combined experimental and DFT study of metal-ligand interactions

2020

Given that noninnocent and metalloradical-type electronic structures are ubiquitous among dipyrrin-bisphenolate (DPP) complexes, we synthesized the gold(III) derivatives as potentially innocent paradigms against which the properties of other metallo-DPP derivatives can be evaluated. Electronic absorption spectra, electrochemical studies, a single-crystal X-ray structure, and DFT calculations all suggest that the ground states of the new complexes indeed correspond to an innocent AuIII–DPP3−, paralleling a similar description noted for Au corroles. Interestingly, while DFT calculations indicate purely ligand-centered oxidations, reduction of AuDPP is predicted to occur across both the metal …

MetalAbsorption spectroscopyComputational chemistryChemistryLigandGeneral Chemical Engineeringvisual_artChemical Sciencesvisual_art.visual_art_mediumGeneral ChemistryVDP::Matematikk og Naturvitenskap: 400ElectrochemistryVDP::Mathematics and natural science: 400
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A3- and A2B-nitrocorroles: synthesis and antiviral activity evaluation against human cytomegalovirus infection

2020

Human cytomegalovirus (hCMV) is responsible for several pathologies impacting immunocompromised patients and can trigger life-threatening infection. Several antivirals are available and are used in the clinic, but hCMV resistant strains have appeared and patients have encountered therapeutic failure. Hence, there is a constant need for new best in class or first in class antiviral molecules. We have previously shown that nitrocorroles could be used as a potent anti-hCMV agent without acute toxicity in mice. They therefore represent an excellent platform to perform structure–activity relationship (SAR) studies and to increase efficiency or reduce toxicity. We have generated original A2B- and…

PharmacologyHuman cytomegalovirus0303 health sciences010405 organic chemistrybusiness.industryOrganic ChemistryPharmaceutical Sciencemedicine.disease01 natural sciencesBiochemistryAcute toxicity0104 chemical sciences03 medical and health sciencesDrug DiscoveryToxicityCancer researchMolecular MedicineMedicineTherapeutic failurebusiness030304 developmental biologyRSC Medicinal Chemistry
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CCDC 1539258: Experimental Crystal Structure Determination

2017

Related Article: Wenqian Shan, Nicolas Desbois, Virginie Blondeau-Patissier, Mario L. Naitana, Valentin Quesneau, Yoann Rousselin, Claude P. Gros, Zhongping Ou, Karl M. Kadish|2017|Chem.-Eur.J.|23|12833|doi:10.1002/chem.201701968

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters5101520-tetrakis(4-(trifluoromethyl)phenyl)pentapyrrin chloroform solvateExperimental 3D Coordinates
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CCDC 1578032: Experimental Crystal Structure Determination

2018

Related Article: Xiaoqin Jiang, Mario L. Naitana, Nicolas Desbois, Valentin Quesneau, Stéphane Brandès, Yoann Rousselin, Wenqian Shan, W. Ryan Osterloh, Virginie Blondeau-Patissier, Claude P. Gros, Karl M. Kadish|2018|Inorg.Chem.|57|1226|doi:10.1021/acs.inorgchem.7b02655

Space GroupCrystallographyCrystal System(10-(4-fluoro-3-nitrophenyl)-515-dimesitylcorrolato)-bis(pyridine)-cobalt(iii) cyclohexane tetrahydrofuran solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1910519: Experimental Crystal Structure Determination

2020

Related Article: Sandrine Kappler-Gratias, Léo Bucher, Nicolas Desbois, Yoann Rousselin, Kerstin Bystricky, Claude P. Gros, Franck Gallardo|2020|RSC Med. Chem.|11|783|doi:10.1039/D0MD00127A

Space GroupCrystallographyCrystal SystemCrystal Structure515-bis(2356-tetrafluorophenyl)-10-(2-fluoropyridin-4-yl)corrole methanol solvateCell ParametersExperimental 3D Coordinates
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CCDC 1964008: Experimental Crystal Structure Determination

2020

Related Article: Kolle E. Thomas, Nicolas Desbois, Jeanet Conradie, Simon J. Teat, Claude P. Gros, Abhik Ghosh|2020|RSC Advances|10|533|doi:10.1039/C9RA09228E

Space GroupCrystallographyCrystal SystemCrystal Structure(2-[5-({5-[2-oxidophenyl]-2H-pyrrol-2-ylidene}[4-(trifluoromethyl)phenyl]methyl)-1H-pyrrol-2-yl]phenolato)-gold(iii)Cell ParametersExperimental 3D Coordinates
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CCDC 1880078: Experimental Crystal Structure Determination

2019

Related Article: Wenqian Shan, Nicolas Desbois, Sandrine Pacquelet, Stéphane Brandès, Yoann Rousselin, Jeanet Conradie, Abhik Ghosh, Claude P. Gros, Karl M. Kadish|2019|Inorg.Chem.|58|7677|doi:10.1021/acs.inorgchem.8b03006

diammine-(2-(5-((5-(2-oxidophenyl)-2H-pyrrol-2-ylidene)(pentafluorophenyl)methyl)-1H-pyrrol-2-yl)phenolato)-cobalt(iii) chloroform solvate monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1812155: Experimental Crystal Structure Determination

2018

Related Article: Valentin Quesneau, Wenqian Shan, Nicolas Desbois, Stephane Brandes, Yoann Rousselin, Meddy Vanotti, Virginie Blondeau-Patissier, Mario Naitana, Paul Fleurat-Lessard, Eric Van Caemelbecke, Karl M. Kadish, Claude P. Gros|2018|Eur.J.Inorg.Chem.|2018|4265|doi:10.1002/ejic.201800897

Space GroupCrystallographyCrystal SystemCrystal Structurediammine-(51015-tris(26-dichlorophenyl)corrolato)-cobalt(iii) n-hexane solvateCell ParametersExperimental 3D Coordinates
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CCDC 1830060: Experimental Crystal Structure Determination

2019

Related Article: Jian Yang, Yoann Rousselin, Léo Bucher, Nicolas Desbois, Frédéric Bolze, Hai-Jun Xu, Claude P. Gros|2018|ChemPlusChem|83|838|doi:10.1002/cplu.201800361

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstetrakis(4-(28-diethyl-55-difluoro-1379-tetramethyl-5H-dipyrrolo[12-c:2'1'-f][132]diazaborinin-4-ium-5-id-10-yl)phenyl)methane unknown solvateExperimental 3D Coordinates
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CCDC 1554869: Experimental Crystal Structure Determination

2019

Related Article: Wenqian Shan, Valentin Quesneau, Nicolas Desbois, Virginie Blondeau-Patissier, Mario L. Naitana, Yoann Rousselin, Claude P. Gros, Zhongping Ou, Karl M. Kadish|2019|J.Porphyrins Phthalocyanines|23|213|doi:10.1142/S1088424619500214

25-bis((4-bromophenyl)(5-((4-bromophenyl)pyrrol-2-ylmethylidene)pyrrol-2-yl)methylene)pyrrole chloroform solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1830057: Experimental Crystal Structure Determination

2019

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4-(28-diethyl-55-difluoro-1379-tetramethyl-5H-4lambda55lambda5-dipyrrolo[12-c:2'1'-f][132]diazaborinin-10-yl)-NN-diphenylanilineSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 977462: Experimental Crystal Structure Determination

2015

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters5101520-tetrakis(3-(2-Azidoethoxy)propyl)porphyrinExperimental 3D Coordinates
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CCDC 1910517: Experimental Crystal Structure Determination

2020

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Space GroupCrystallography515-bis(4-(dimethylamino)-2356-tetrafluorophenyl)-10-(2356-tetrafluorophenyl)corrole ethanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1910516: Experimental Crystal Structure Determination

2020

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10-(pentafluorophenyl)-515-bis(2356-tetrafluorophenyl)corrole methanol solvateExperimental 3D Coordinates
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2019

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Space GroupCrystallography1010'-[5510101515-hexabutyl-12-(28-diethyl-55-difluoro-1379-tetramethyl-5H-6lambda55lambda5-dipyrrolo[12-c:2'1'-f][132]diazaborinin-10-yl)-1015-dihydro-5H-diindeno[12-a:1'2'-c]fluorene-27-diyl]bis(28-diethyl-55-difluoro-1379-tetramethyl-5H-4lambda55lambda5-dipyrrolo[12-c:2'1'-f][132]diazaborinine) chloroform ethanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1910518: Experimental Crystal Structure Determination

2020

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters10-(4-(dimethylamino)-2356-tetrafluorophenyl)-515-bis(2356-tetrafluorophenyl)corrole ethanol solvateExperimental 3D Coordinates
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CCDC 1910052: Experimental Crystal Structure Determination

2019

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717-dibromo-5-methoxy-221212-tetramethyl-231213-tetrahydroporphyrinSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1910515: Experimental Crystal Structure Determination

2020

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Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates515-bis(pentafluorophenyl)-10-(2356-tetrafluorophenyl)corrole ethanol solvate
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CCDC 977461: Experimental Crystal Structure Determination

2015

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CCDC 882546: Experimental Crystal Structure Determination

2013

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(mu~2~-515-bis(4-(((4710-tris(2-t-Butoxy-2-oxoethyl)-14710-tetraazacyclododecan-1-yl)acetyl)amino)phenyl)-1020-dimesitylporphyrin)-di-sodium dibromide chloroform solvateExperimental 3D Coordinates
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CCDC 1815709: Experimental Crystal Structure Determination

2018

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters515-dimesityl-10-(246-trimethoxyphenyl)corrole acetone solvateExperimental 3D Coordinates
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CCDC 1910514: Experimental Crystal Structure Determination

2020

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Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(51015-tris(2356-tetrafluorophenyl)corrolato)-ethanol-manganese ethanol solvateExperimental 3D Coordinates
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CCDC 1830058: Experimental Crystal Structure Determination

2019

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1010'-[oxybis(21-phenylene)]bis(28-diethyl-55-difluoro-1379-tetramethyl-5H-4lambda55lambda5-dipyrrolo[12-c:2'1'-f][132]diazaborinine)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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