Search results for "Complexes"

showing 10 items of 875 documents

NHC-Based Iron Sensitizers for DSSCs

2018

International audience; Nanostructured dye-sensitized solar cells (DSSCs) are promising photovoltaic devices because of their low cost and transparency. Ruthenium polypyridine complexes have long been considered as lead sensitizers for DSSCs, allowing them to reach up to 11% conversion efficiency. However, ruthenium suffers from serious drawbacks potentially limiting its widespread applicability, mainly related to its potential toxicity and scarcity. This has motivated continuous research efforts to develop valuable alternatives from cheap earth-abundant metals, and among them, iron is particularly attractive. Making iron complexes applicable in DSSCs is highly challenging due to an ultrafa…

NHC ligands[CHIM.ORGA]Chemical Sciences/Organic chemistry[CHIM.COOR] Chemical Sciences/Coordination chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistrylcsh:QD146-197[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryiron complexes[CHIM] Chemical Scienceslcsh:Inorganic chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryexcited statesCèl·lules fotoelèctriquesphotophysicsFerro
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Recent Advances of Spin Crossover Research

2004

Thermal spin transition (spin crossover), one of the most fascinating dynamic electronic structure phenomena occurring in coordination compounds of third row transition metal ions, mostly of iron(II), iron(III) and cobalt(II) with critical ligand field strengths competing with the spin pairing energy, has attracted increasing attention by many research groups. One of the reasons is the promising potential for practical applications. In this chapter we intend to cover essential recent work, primarily accomplished within the European research network on "Thermal and Optical Switching of Molecular Spin States (TOSS)". New spin crossover compounds and their thermal spin transition behaviour, al…

NUCLEAR INELASTIC-SCATTERINGLigand field theorySpin statescooperativitySpin transitionElectronic structurephysical propertiespressurespin crossoverSpin crossoverINTRAMOLECULAR MAGNETIC INTERACTIONlight effectsIRON(II) COMPLEXESSpin-½TRANSITION MOLECULAR MATERIALSLONG-RANGE INTERACTIONCondensed matter physicsChemistrySpin engineeringISING-LIKE SYSTEMSPairingPHOTOINDUCED PHASE-TRANSITIONSTATE TRAPPING LIESSTCondensed Matter::Strongly Correlated ElectronsX-RAY-STRUCTURELIGHT-INDUCED BISTABILITY
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Hydrolysis of Monomethyl-, Dimethyl-, and Trimethyltin(IV) Cations in Fairly Concentrated Aqueous Solutions at I = 1 mol L-1 (NaNO3) and T = 298.15 K…

2011

The hydrolysis of methyltin(IV) cations at fairly high concentrations was investigated to evaluate the formation of polynuclear species in aqueous solution. The hydrolysis of monomethyltin(IV), dimethyltin(IV), and trimethyltin(IV) was studied by potentiometry at T = 298.15 K and at I = 1 mol L-1 in NaNO3 aqueous solutions. The results obtained gave evidence for the formation of the following polynuclear species, in addition to the mononuclear species already reported, which were also considered in the models proposed for the three systems investigated: [(CH3)Sn(OH)3]0, [(CH3)Sn(OH)4]-, [((CH3)Sn)2(OH)4]2+, [((CH3)Sn)2(OH)5]+, [((CH3)Sn)2(OH)7]-, [((CH3)Sn)3(OH)5]4+, [((CH3)Sn)3(OH)7]2þ, [(…

NUCLEAR-MAGNETIC-RESONANCE; HYDROXO COMPLEXES; IONIC-STRENGTH DEPENDENCE; SN-119 NMR-SPECTROSCOPYAqueous solutionChemistryStereochemistryHYDROXO COMPLEXESGeneral Chemical EngineeringGeneral ChemistryMedicinal chemistrySN-119 NMR-SPECTROSCOPYHydrolysisIONIC-STRENGTH DEPENDENCEMolespeciation organotin hydrolysis polynuclear speciesSettore CHIM/01 - Chimica AnaliticaNUCLEAR-MAGNETIC-RESONANCE
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Polynitrile anions as ligands: From magnetic polymeric architectures to spin crossover materials

2010

International audience; The use of polynitrile anions as ligands (L) either alone or in combination with neutral co-ligands (L′) is a very promising and appealing strategy to get molecular architectures with different topologies and dimensionalities thanks to their ability to coordinate and bridge metal ions in many different ways. The presence of several potentially coordinating nitrile groups (or even other donor groups as –OH, –SH or –NH2), their rigidity and their electronic delocalization allow the synthesis of original magnetic high dimensional coordination polymers with transition metals ions. Furthermore, these ligands have shown coordinating and bridging capabilities in novel discr…

NitrileMetal ions in aqueous solutionMetal(II) complexesInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCoordination complexInorganic ChemistryDelocalized electronchemistry.chemical_compoundTransition metalSpin crossoverMagnetic propertiesMagnetic transitionMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrychemistry.chemical_classificationThermochromismThermochromism010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryPolymer0104 chemical sciencesCoordination polymersCrystallographyPolynitrilechemistryStructural transitionNitrile ligandCyano ligand
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Pt(II) nitrile complexes: New insights on old complexes from a combined experimental and theoretical study

2017

Abstract The spectroscopic characterization of cis - and trans -[PtCl 2 (NCR) 2 ] (R = CH 3 , Ph, CH 2 Ph) was reported in solid state and solution phase. Moreover, the X-ray structures of cis -[PtCl 2 (NCCH 3 ) 2 ], cis - and trans -[PtCl 2 (NCPh) 2 ] were redetermined at low temperature. FT-IR and NMR showed a blue-shift and a slight shielding of the νCN and δ ( 13 C CN ) values, respectively, in a counterintuitive way with respect to the well known improved reactivity towards nucleophiles of nitriles ligands coordinated to platinum(II), when compared to their free forms. These spectroscopic behaviors were also confirmed by theoretical experiments at DFT level. Moreover, DFT approach show…

NitrileStereochemistrySolid-statechemistry.chemical_elementTheoretical calculations010402 general chemistry01 natural sciencesMedicinal chemistryCP MAS NMR studyInorganic Chemistrychemistry.chemical_compoundNucleophilePlatinum nitrile complexesMaterials ChemistryOrbital controlReactivity (chemistry)Platinum nitrile complexePhysical and Theoretical Chemistry010405 organic chemistrySolution phase0104 chemical sciencesBenzonitrilechemistrySettore CHIM/03 - Chimica Generale E InorganicaCP MAS NMR study; Platinum nitrile complexes; Spectroscopic characterization; Theoretical calculationsSpectroscopic characterizationPlatinum
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Half-sandwich Mo(III) complexes with asymmetric diazadiene ligands

2006

The asymmetric 1,4-diazadiene ligands R ∗ N CHCH NR ∗ [R ∗  = ( S )-CH(CH 3 )Ph], R 2 ∗ dad , and 2,2′-bis(4-ethyloxazoline), as-ox, have been used to generate half-sandwich Mo III derivatives by addition to Cp 2 Mo 2 Cl 4 . Ligand R 2 ∗ dad affords a mononuclear, paramagnetic 17-electron product, CpMoCl 2 ( R 2 ∗ dad ) , whereas as-ox leads to the isolation of a dinuclear compound where only one molecule of ligand has been added per two Mo atoms, Cp 2 Mo 2 Cl 4 (as-ox). In the presence of free as-ox, this compound coexists with the paramagnetic mononuclear complex in solution. Both products are capable of controlling the radical polymerization of styrene under typical atom transfer radical…

Nitroxide mediated radical polymerizationRadical polymerizationHalf-sandwich complexesDiazadiene010402 general chemistry01 natural sciencesMedicinal chemistryStyreneInorganic Chemistrychemistry.chemical_compoundTacticityPolymer chemistryMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPolystyreneAtom transfer radical polymerizationMolybdenum010405 organic chemistryLigandAtom-transfer radical-polymerization[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolystyreneInorganica Chimica Acta
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Tetrathiafulvalene-Polychlorotriphenylmethyl Dyads: Influence of Bridge and Open-Shell Characteristics on Linear and Nonlinear Optical Properties

2017

Three conjugated donor-π-acceptor radical systems (1 a–1 c) were prepared by bridging a tetrathiafulvalene (TTF) electron-donor unit to a polychlorotriphenylmethyl (PTM) electron-acceptor radical through vinylene units of different lengths. The dependence of the intramolecular charge transfer on the length of the conjugated bridge has been analyzed by different electrochemical and spectroscopic techniques. Linear optical properties and the second-order nonlinear optical (NLO) response of these derivatives have been computed by comparing systems 1 a–1 c with the non-radical analogues (2 a–2 c). Interestingly, an enhanced NLO response is predicted for dyads 1 a–1 c with PTM in the radical for…

Nonlinear opticsRadicalConjugated system010402 general chemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundDonor–acceptor complexesOpen shellchemistry.chemical_classification010405 organic chemistryOrganic ChemistryNonlinear opticsGeneral ChemistryElectron acceptorAcceptor3. Good health0104 chemical sciencesCrystallographychemistryIntramolecular forceTetrathiafulvaleneIntramolecular charge transferPTM radicalsTetrathiafulvaleneChemistry - A European Journal
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Deregulation of the EGFR/PI3K/PTEN/Akt/mTORC1 pathway in breast cancer: possibilities for therapeutic intervention

2014

// Nicole M. Davis 1 , Melissa Sokolosky 1 , Kristin Stadelman 1 , Stephen L. Abrams 1 , Massimo Libra 2 , Saverio Candido 2 , Ferdinando Nicoletti 2 , Jerry Polesel 3 , Roberta Maestro 4 , Antonino D’Assoro 5 , Lyudmyla Drobot 6 , Dariusz Rakus 7 , Agnieszka Gizak 7 , Piotr Laidler 8 , Joanna Dulinska-Litewka 8 , Joerg Basecke 9 , Sanja Mijatovic 10 , Danijela Maksimovic-Ivanic 10 , Giuseppe Montalto 11,12 , Melchiorre Cervello 12 , Timothy L. Fitzgerald 13 , Zoya N. Demidenko 14 , Alberto M. Martelli 15 , Lucio Cocco 15 , Linda S. Steelman 1 and James A. McCubrey 1 1 Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University Greenville, NC 27858 USA 2 …

Oncologymedicine.medical_specialtytherapy resistanceClass I Phosphatidylinositol 3-Kinasesmedicine.medical_treatmentBreast NeoplasmsReviewBiologyMechanistic Target of Rapamycin Complex 1PI3KMetastasisTargeted therapyPhosphatidylinositol 3-KinasesBreast cancerTARGETED THERAPYInternal medicinemedicinePTENHumansTargeted Therapy Therapy Resistance Mutations PI3K mTOR rapamycinskin and connective tissue diseasesProtein kinase BneoplasmsPI3K/AKT/mTOR pathwayRoswell Park Cancer InstituterapamycinTOR Serine-Threonine KinasesMTORPTEN PhosphohydrolaseCancerTargeted TherapyTherapy Resistancemedicine.diseaseTargeted Therapy; Therapy Resistance; Mutations; PI3K; mTOR; rapamycin3. Good healthErbB ReceptorsGene Expression Regulation NeoplasticOncologyMultiprotein ComplexesCancer researchbiology.proteinFemaleReceptor Epidermal Growth FactormutationRAPAMYCINProto-Oncogene Proteins c-aktMutationsSignal Transduction
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Optical Fibre NO2 Sensor Based on Lutetium Bisphthalocyanine in a Mesoporous Silica Matrix

2018

International audience; In this article, we describe a NO2 sensor consisting of a coating based on lutetium bisphthalocyanine (LuPc2) in mesoporous silica. The sensor exploits the absorption spectrum change of this material which strongly and reversibly decreases in contact with NO2. NO2 is measured by following the amplitude change in the reflected spectrum of the coating deposited on the tip of a silica fibre. As diffusion of NO2 in LuPc2 is slow, the response time could be slow. To reduce it, the active molecules are dispersed in a mesoporous silica matrix deposited by a sol-gel process (Evaporation Induced Self Assembly) avoiding the formation of large crystals. Doing so, the response i…

Optical fiberMaterials scienceAbsorption spectroscopynitrogen dioxideairchemistry.chemical_element02 engineering and technologyengineering.materialphthalocyanineslcsh:Chemical technology010402 general chemistry01 natural sciencesBiochemistrylangmuir-blodgett-filmsArticleAnalytical Chemistrylaw.inventionoptical fibre sensors; sol-gel; nitrogen dioxide; lutetium bisphthalocyanineCoatinglawsol-gel[CHIM]Chemical Scienceslcsh:TP1-1185Electrical and Electronic EngineeringThin filmInstrumentationSol-gelcomplexeshybridMesoporous silicaoptical fibre sensorsrespiratory system021001 nanoscience & nanotechnologyEvaporation (deposition)Atomic and Molecular Physics and OpticsLutetium0104 chemical sciencesselective detectionozonechemistryChemical engineering13. Climate actionthin-filmsengineeringlutetium bisphthalocyanine0210 nano-technologySensors; Volume 18; Issue 3; Pages: 740
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Phosphorescent hybrid organic-inorganic light-emitting diodes.

2010

Organic electronicsMaterials scienceLuminescencebusiness.industryMechanical EngineeringCarbonatesCesiumIridiumlaw.inventionSolid-state lightingMechanics of MaterialslawCoordination ComplexesOrganic inorganicPhosphorescent organic light-emitting diodeOptoelectronicsGeneral Materials SciencePolyvinylsZinc OxidePhosphorescenceLuminescencebusinessElectrodesLight-emitting diodeAdvanced materials (Deerfield Beach, Fla.)
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