Search results for "PHOTOCHEMISTRY"

showing 10 items of 2034 documents

Rational synthetic design of well-defined Pt(bisethynyl)/Zn(porphyrin) oligomers for potential applications in photonics

2011

Well-defined oligomers of 1, 2, 3 and 4 units built upon the very soluble bis-1,15-(1,4-ethynylbenzene)-3,7,13,17-tetramethyl-2,8,12,18-tetrakis(n-hexyl) zinc(II) porphyrin ligand and the trans-bis(tri-n-butylphosphine)platinum(II) linker, with acetylene or trimethylsilane as end groups, has been prepared in the presence of a dichloromethane/diethylamine mixture (1 : 1 v/v) and CuX (X = Cl, I) at room temperature, analogue to a Sonogashira coupling. The new monodisperse organometallic oligomers were characterized by 1H, 31P NMR, UV-visible spectroscopies and MALDI-TOF mass spectrometry. The methyl groups placed at the 3,7,13,17-positions induces the locking of the C6H4 fragment in a perpend…

DiethylamineDimerSonogashira couplingTrimethylsilaneGeneral ChemistryChromophorePhotochemistryPorphyrinCatalysischemistry.chemical_compoundMonomerchemistryTetramerMaterials ChemistryNew Journal of Chemistry
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Keggin heteropolyacid H3PW12O40 supported on different oxides for catalytic and catalytic photo-assisted propene hydration

2013

Catalytic and catalytic photo-assisted hydration of propene to form 2-propanol in gas–solid regime at atmospheric pressure and 85 1C were carried out by using a heteropolyacid (POM) supported on different oxides. Binary materials were prepared by impregnation of H3PW12O40 on different commercial and home prepared supports (TiO2, SiO2, WO3, ZrO2, ZnO, Al2O3). Some of the composites were active both for catalytic and catalytic photo-assisted reactions. The Keggin type POM was completely and partially degraded, when supported on ZnO and Al2O3, respectively, and these binary solids always resulted as inactive for both catalytic and catalytic photo-assisted reactions. The supported Keggin POM sp…

DiffractionDiffuse reflectance infrared fourier transformAtmospheric pressureSurface PropertiesScanning electron microscopeWaterGeneral Physics and AstronomyOxidesAlkenesPhotochemical ProcessesPhotochemistryCatalysisTungstenCatalysisPropenechemistry.chemical_compoundchemistryPressureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesense organsIrradiationKeggin heteropolyacid catalytic propene hydration photo-assisted propene hydrationParticle SizePhysical and Theoretical ChemistryFourier transform infrared spectroscopyPhysical Chemistry Chemical Physics
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Photoluminescence in Carborane–Stilbene Triads : A Structural, Spectroscopic, and Computational Study

2016

A set of triads in which o- and m-carborane clusters are bonded to two stilbene units through Ccluster -CH2 bonds was synthesized, and their structures were confirmed by X-ray diffraction. A study on the influence of the o- and m- isomers on the absorption and photoluminescence properties of the stilbene units in solution revealed no charge-transfer contributions in the lowest excited state, as confirmed by (TD)DFT calculations. The presence of one or two B-I groups in m-carborane derivatives does not affect the emission properties of the stilbenes in solution, probably due to the rather large distance between the iodo substituents and the fluorophore. Nevertheless, a significant redshift o…

DiffractionFluorophorePhotoluminescencecarboranesalkenes010405 organic chemistryOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryExcited statedensity functional calculationsluminescenceCarboraneAbsorption (chemistry)Thin filmLuminescenceta116photophysicsChemistry: A European Journal
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Coupling of Benzynezirconocene with 1,4-Diphenyl-1,3-butadiyne

2000

The thermolysis of diphenylzirconocene in the presence of 1,4-diphenyl-1,3-butadiyne to yield the seven-membered zirconacyclocumulene 1 via the intermediacy of benzynezirconocene is described. This complex has been characterized by an X-ray diffraction study. Additionally, better knowledge of the bonding of the cumulene moiety was achieved by DFT calculations. Cleavage of the Zr−C bonds of 1 with methanol provided the corresponding butatriene 2.

DiffractionOrganic ChemistryThermal decompositionCumulenePhotochemistryCleavage (embryo)Inorganic ChemistryCoupling (electronics)chemistry.chemical_compoundchemistryYield (chemistry)MoietyMethanolPhysical and Theoretical ChemistryOrganometallics
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Electron paramagnetic resonance, ENDOR and TRIPLE resonance study of some 9,10-anthraquinone radicals in solution

1992

EPR, ENDOR and TRIPLE resonance spectra were recorded for 1,8-dihydroxy-3-methyl-9,10-anthraquinone and 9,10-anthraquinone-2-carboxylic acid anion radicals and the 9,10-anthraquinol-2-carboxylic acid cation radical. EPR spectra were recorded for the 5,8-dideuterio-1,4-dideuterioxy-9,10-anthraquinone anion radical, the 6,7-dideuterio-1,4-dideuterioxy-9,10-anthraquinone anion radical and the 1,4-dihydroxy-9,10-anthraquinol cation radical. The coupling contants of the 1,4-dihydroxy-9,10-anthraquinone anion radical were assigned by deuteriation.

DiketoneChemistryRadicalGeneral ChemistryPhotochemistryResonance (chemistry)Anthraquinonelaw.inventionQuinoneIonchemistry.chemical_compoundlawGeneral Materials ScienceElectron paramagnetic resonanceHyperfine structureMagnetic Resonance in Chemistry
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Room temperature crystal structure of the fast switching M159T mutant of the fluorescent protein dronpa

2015

The fluorescent protein Dronpa undergoes reversible photoswitching reactions between the bright ‘on’ and dark ‘off’ states via photoisomerisation and proton transfer reactions. We report the room temperature crystal structure of the fast switching Met159Thr mutant of Dronpa at 2.0 A resolution in the bright on state. Structural differences with the wild type include shifted backbone positions of strand β8 containing Thr159 as well as an altered A-C dimer interface involving strands β7, β8, β10, and β11. The Met159Thr mutation increases the cavity volume for the p-hydroxybenzylidene-imidazolinone chromophore as a result of both the side chain difference and the backbone positional difference…

DimerMutantWild typeCrystal structureChromophorePhotochemistryBiochemistrychemistry.chemical_compoundDronpaMolecular dynamicsCrystallographychemistryStructural BiologySide chainMolecular BiologyProteins: Structure, Function, and Bioinformatics
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Electro- and Photo-driven Reduction of CO 2 by a trans -(Cl)-[Os(diimine)(CO) 2 Cl 2 ] Precursor Catalyst: Influence of the Diimine Substituent and A…

2016

A series of [OsII(NN)(CO)2Cl2] complexes where NN is a 2,2′-bipyridine ligand substituted in the 4,4′ positions by H (C1), CH3 (C2), C(CH3)3 (C3), or C(O)OCH(CH3)2 (C4) has been studied as catalysts for the reduction of CO2. Electrocatalysis shows that the selectivity of the reaction can be switched toward the production of CO or HCOO− with an electron-donating (C2, C3) or -withdrawing (C4) substituent, respectively. The electrocatalytic process is a result of the formation of an Os0-bonded polymer, which was characterized by electrochemistry, UV/Visible and EPR spectroscopies. Photolysis of the complexes under CO2 in DMF+TEOA produces CO as a major product with a remarkably stable turnover…

DimerSubstituent010402 general chemistryPhotochemistryElectrocatalyst01 natural sciencesCatalysisCatalysisphotoinduced electron transferInorganic Chemistrychemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryelectrocatalysisPhysical and Theoretical Chemistryta116DiimineComputingMilieux_MISCELLANEOUS010405 organic chemistryChemistryLigandOrganic Chemistryosmium0104 chemical sciencesCO2 reductionPhotocatalysisSelectivityphotocatalysis
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Control over the oxidative reactivity of metalloporphyrins. Efficient electrosynthesis of meso,meso-linked zinc porphyrin dimer.

2011

The electrochemical oxidation of zinc(II) 5,15-p-ditolyl-10-phenylporphyrin at its first oxidation potential leads to the formation of the corresponding meso-meso porphyrin dimer as the main product. The number of electrons abstracted, the addition of the hindered base 2,6-lutidine as well as operating in DMF, instead of a CH(2)Cl(2)/CH(3)CN mixture are the key parameters to obtain high yields of the desired coupling product. Indeed, when the electrolyses are carried out in the CH(2)Cl(2)/CH(3)CN mixture, the unexpected zinc(II) 5-chloro-10,20-p-ditolyl-15-phenyl porphyrin is produced as a by-product, the chlorine atom originating from the CH(2)Cl(2) solvent. The monomer and the dimer are c…

Dimerchemistry.chemical_elementZincElectrosynthesisElectrochemistryPhotochemistryPorphyrinInorganic ChemistrySolventchemistry.chemical_compoundMonomerchemistryPolymer chemistryReactivity (chemistry)Dalton transactions (Cambridge, England : 2003)
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Study of Reactivity in the 1,3-Dipolar Cycloaddition Reactions Leading to New Triazolopyrrolopyrazine Ring Systems

2010

The influence of the structural symmetry of the 2-pi double-reactive-sites component in the 1,3-dipolar cycloaddition reactions, involving nitrilimines as dipoles, was investigated. the experimental data showed that the loss of the symmetry leads to the formation of the monocycloadduct in good yields.

Dipole13-Dipolar Cycloaddition Reactions Triazolopyrrolopyrazine Ring SystemsChemistryOrganic Chemistry13-Dipolar cycloadditionStructural symmetryReactivity (chemistry)Ring (chemistry)PhotochemistrySettore CHIM/08 - Chimica FarmaceuticaSymmetry (physics)CycloadditionSynlett
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Spectral and electrooptical absorption and emission studies on internally hydrogen bonded benzoxazole `double' derivatives: 2,5-bis(benzoxazolyl)hydr…

1999

Abstract Ground and excited state dipole moments and polarizabilities of 2,5-bis(benzoxazolyl)hydroquinone (BBHQ) and 3,6-bis(benzoxazolyl)pyrocatechol (BBPC) are determined by means of electrooptical absorption and emission measurements. BBHQ is found to exhibit a small, while BBPC a large increase of the static polarizability in the Franck–Condon (FC) excited singlet state. The change of the dipole moments upon excitation to the FC state is zero within experimental error. However, both molecules show dipole moments in the fluorescent states of their phototautomers, of about 5 D, the major component being parallel to the long molecular axis. The experimental and theoretical results strongl…

DipoleProtonPolarizabilityChemistryExcited stateRelaxation (NMR)General Physics and AstronomyMoleculePhysical and Theoretical ChemistryPhotochemistryFluorescenceTautomerChemical Physics
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