Search results for "Conjugated system"

showing 10 items of 225 documents

Effect of free rotation in polypyridinic ligands of Ru(ii) complexes applied in light-emitting electrochemical cells

2013

In the present work we report the synthesis and the electrochemical, photoluminescent and electroluminescent properties of two new Ru(II) complexes described by the general formula [Ru(phen)2X](2+), where phen is 1,10-phenanthroline. The X ligand consists of a 2,2'-bipyridine (bpy) unit substituted with two phenyl rings connected to the bpy core through a saturated (Lhydro = 4,4'-diphenylethyl-2,2'-bipyridine) or a conjugated (LH = 4,4'-bis(α-styrene)-2,2'-bipyridine) carbon-carbon bridge. The photoluminescent spectra indicate that, both in solution and solid state, the complex bearing the aliphatic substitution bridges exhibits a higher quantum yield and a longer excited state lifetime tha…

Inorganic ChemistryCrystallographyPhotoluminescenceChemistryStereochemistryLigandExcited stateQuantum yieldLight emissionConjugated systemElectroluminescenceElectrochemistryDalton Transactions
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Physicochemical Characterization of σ-Bonded Aryl Iron(III) Porphycenes. X-ray Structures of (EtioPc)Fe(3,5-C6F2H3) and (EtioPc)In(C6H5), Where EtioP…

1998

A series of iron(III) σ-bonded porphycenes are characterized by their electrochemical and spectroscopic properties. The investigated compounds are represented as (EtioPc)Fe(R), where EtioPc = the dianion of 2,7,12,17-tetraethyl-3,6,13,16-tetramethylporphycene and R = C6H5, 3,5-C6F2H3, 3,4,5-C6F3H2 or 2,3,5,6-C6F4H. Each compound is characterized as to its ESR, NMR, and UV−visible properties which are compared to corresponding compounds in an analogous series of (OEP)Fe(R) and (OETPP)Fe(R) derivatives where OEP and OETPP are the dianions of octaethyl- and octaethyltetraphenylporphyrin, respectively. The (EtioPc)Fe(R) complexes contain either high- or low-spin Fe(III), depending on the specif…

Inorganic Chemistrychemistry.chemical_compoundCrystallographychemistryLigandArylInorganic chemistryX-rayCrystal structurePhysical and Theoretical ChemistryConjugated systemElectrochemistryCharacterization (materials science)Inorganic Chemistry
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Conformational Analysis of beta-Lactam-Containing Ferrocene Peptides

2009

The homochiral 3-amino-1-(4-methoxyphenyl)-4-phenyl-beta-lactam (≡ Alm) was conjugated with Boc-Ala giving Ala-Alm (9) after Boc-deprotection (Boc = tert-butoxycarbonyl, Ala = alanine). Coupling of FcCOOH (1) and Boc-Fca (10) with “ dipeptide” 9 resulted in the formation of FcCO-Ala-Alm (12) and the trisamide Boc-Fca-Ala-Alm (13), respectively (Fc = ferrocenyl, Fca = 1’ -aminoferrocene-1-carboxylic acid). The reactions were accomplished by the HOBt/EDC procedure and the products were obtained in good yields (HOBt = 1-hydroxybenzotriazole, EDC = N-(3-dimethylaminopropyl)-N’ -ethylcarbodiimide hydrochloride). Symmetrically 1, 1’ -disubstituted “ tetrapeptide” Fn(CO-Ala-Alm)2 (14) was prepared…

Inorganic Chemistryconformation analysis ; density functional calculations ; hydrogen bonds ; metallocenes ; molecular modelingchemistry.chemical_compoundDipeptidechemistryMolecular modelTetrapeptideFerroceneHydrogen bondStereochemistryIntramolecular forceLactamConjugated system
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Conjugated linolenic acid (CLna), conjugated linoleic acid (CLA), and other biohydrogenation intermediates in plasma and milk fat of cows fed raw or …

2007

International audience; Thirty lactating dairy cows were used in a 333 Latin-square design to investigate the effects of a raw or extruded blend of linseed and wheat bran (70:30) on plasma and milk fatty-acids (FA). Linseed diets, containing 16.6% linseed blend on a dry-matter basis, decreased milk yield and protein percentage. They decreased the proportions of FA with less than 18 carbons in plasma and milk and resulted in cis -9, cis -12, cis -15 18:3 proportions that were more than three and four times higher in plasma and milk, respectively, whereas cis -9, cis -12 18:2 proportions were decreased by 10–15%. The cis -9, trans -11, cis -15 18:3 isomer of conjugated linolenic acid was not …

MILK FATTY ACIDLinolenic acidConjugated linoleic acidEXTRUSIONConjugated systemSF1-110003 medical and health scienceschemistry.chemical_compoundMilk yieldBiologie animalePlasma lipidsLINSEEDACIDE LINOLEIQUE[SDV.SA.SPA] Life Sciences [q-bio]/Agricultural sciences/Animal production studiesFood science030304 developmental biologyCONJUGATED LINOLENIC ACIDMilk fatty acidConjugated linolenic acid0303 health sciencesBranExtrusionLinseed0402 animal and dairy sciencefood and beverages04 agricultural and veterinary sciencesCONJUGATED LINOLEIC ACID040201 dairy & animal scienceAnimal culturechemistryMilk fat[SDV.SA.SPA]Life Sciences [q-bio]/Agricultural sciences/Animal production studiesAlimentation et NutritionAnimal Science and ZoologyConjugated linoleic acid
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Nanoaggregates Based on New Poly-Hydroxyethyl-Aspartamide Copolymers for Oral Insulin Absorption

2013

The aim of this work was to produce copolymers with an appropriate hydrophilic/hydrophobic balance able to form nanoaggregates with protein molecules and to be used as ideal materials in the field of oral peptide/protein delivery. New anionic polymers obtained by the conjugation of carboxy-bearing ligands, like succinic anhydride and/or cysteine, to hydrophobized α,β-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) copolymers have been synthesized and characterized. Starting copolymer was synthesized by the partial derivatization of hydroxyl groups on the PHEA backbone with butylamine (C4) (obtaining the PHEA-C4 copolymer, bearing a butyl moiety). The consecutive reaction of PHEA-C4 with succin…

Malemedicine.medical_treatmentAdministration OralPharmaceutical SciencenanoaggregateConjugated systemIntestinal absorptionDosage formpolyhydroxyethylaspartamidechemistry.chemical_compoundMaterials TestingDrug DiscoveryPolymer chemistryCopolymermedicineAnimalsInsulinNanotechnologyMoietyRats WistarDrug CarriersProtein StabilityChemistryInsulinSuccinic anhydrideprotein oral deliveryRatsIntestinal AbsorptionDrug deliverydrug deliveryNanoparticlesMolecular MedicinePeptides
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Enhanced electronic communication through a conjugated bridge in a porphyrin-fullerene donor-acceptor couple

2021

A ZnP-2EDOTV-C60 triad, with enhanced electronic communication between terminus donor and acceptor moieties, was synthesized and studied both experimentally and theoretically. Electrochemical measurements and density functional theory calculations support that the first oxidation takes place on the 3,4-ethylenedioxythiophenevinylene (2EDOTV) bridge followed by the oxidation of the ZnP moiety at slightly higher energies. The electronic communication between the terminal electron-donor ZnP and the electron-acceptor C60 units is enhanced by the conjugated EDOTV-based spacer leading to photoinduced electron transfer over the distance >2 nm in the picosecond time domain. The involvement of the s…

Materials science010405 organic chemistry116 Chemical sciencesGeneral ChemistryConjugated system010402 general chemistryPhotochemistry01 natural sciencesPorphyrinAcceptorPhotoinduced electron transfer0104 chemical scienceschemistry.chemical_compoundElectron transferchemistryPhotoinduced charge separationMaterials ChemistryMoietyDensity functional theory
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On-Surface Synthesis of Antiaromatic and Open-Shell Indeno[2,1- b ]fluorene Polymers and Their Lateral Fusion into Porous Ribbons

2019

Polycyclic hydrocarbons have received great attention due to their potential role in organic electronics and, for open-shell systems with unpaired electron densities, in spintronics and da-ta storage. However, the intrinsic instability of polyradical hydrocarbons severely limits de-tailed investigations of their electronic structure. Here, we report the on-surface synthesis of conjugated polymers consisting of indeno[2,1-b]fluorene units, which are antiaromatic and open-shell biradicaloids. The observed reaction products, which also include a non-benzenoid porous ribbon arising from lateral fusion of unprotected indeno[2,1-b]fluorene chains, have been characterized via low temperature scann…

Materials science530 PhysicsBand gapFOS: Physical sciencesConjugated systemFluorene010402 general chemistry01 natural sciencesBiochemistryCatalysislaw.inventionchemistry.chemical_compoundColloid and Surface Chemistrylaw540 ChemistryOrganic electronicsCondensed Matter - Materials ScienceSpintronicsMaterials Science (cond-mat.mtrl-sci)General Chemistry0104 chemical sciencesUnpaired electronchemistryChemical physicsScanning tunneling microscopeAntiaromaticityJournal of the American Chemical Society
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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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Soluble IF-ReS2 nanoparticles by surface functionalization with terpyridine ligands.

2010

A major drawback in the application of layered chalcogenide nanoparticles/tubes is their inertness to chemical and biological modification and functionalization. Their potential use in composite materials might be greatly enhanced by improving the chalcogenide/matrix interface bonding. A novel modification strategy for layered chalcogenide nanoparticles based on the chalcophilic affinity of metals and the chelating terpyridine is reported. The terpyridine anchor group can be conjugated to fluorescent tags or hydrophilic/hydrophobic groups that confer solubility in various solvents to the otherwise insoluble chalcogenide nanoparticles. The functionalized particles are characterized using TEM…

Materials scienceChalcogenideInorganic chemistryNanoparticleInfrared spectroscopySurfaces and InterfacesConjugated systemCondensed Matter Physicschemistry.chemical_compoundchemistryChemical engineeringElectrochemistrySurface modificationGeneral Materials ScienceSolubilityTerpyridineHigh-resolution transmission electron microscopySpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Polymerizable Well-Defined Oligo(thiophene amide)s and their ROMP Block Copolymers

2009

We report the synthesis of conjugated thiophene amide oligomers that constitute a new class of chromophores with potential for optoelectronic applications. The synthesis of defined norbornene-substituted oligothiophene amides using conventional coupling chemistry is described. Their electronic properties depend on the degree of oligomerization as UV/Vis and fluorescence spectroscopy demonstrate. A significant red shift in the spectra upon an increase in the oligomer length evidences conjugation of the thiophene rings via the amide linkages. ROMP of the norbornene-substituted oligomers gives homopolymers and block-copolymers with a solubilizing second block. The amphiphilic character of the …

Materials scienceCondensation polymerPolymers and PlasticsOrganic ChemistrySelf-condensationROMPConjugated systemOligomerchemistry.chemical_compoundchemistryAmidePolymer chemistryAmphiphileMaterials ChemistryThiopheneMacromolecular Rapid Communications
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