Search results for "HOT"

showing 10 items of 14851 documents

Electrochemical meso-functionalization of magnesium(II) porphine

2010

International audience; Regioselective meso-functionalization of the totally unsubstituted magnesium(II) porphine was performed by controlled potential electrolysis with pyridine and triphenylphosphine as nucleophiles leading to the original pyridinium and phosphonium substituted derivatives, respectively. The crystallographic structure of the latter is described as the only meso-phosphonium porphyrin reported to date.

010405 organic chemistryMagnesiumMetals and AlloysRegioselectivitychemistry.chemical_elementGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesPorphyrinCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundNucleophilechemistryPolymer chemistryPyridineMaterials ChemistryCeramics and Composites[CHIM.COOR]Chemical Sciences/Coordination chemistryPhosphoniumPyridiniumTriphenylphosphine
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Influence of Substituent and Benzoannulation on Photophysical Properties of 1-Benzoylmethyleneisoquinoline Difluoroborates

2015

A series of 1-benzoylmethyleneisoquinoline difluoroborates were synthesized, and their photophysical properties were determined. The effect of the substituent and benzoannulation on their properties was investigated to make a comparison with recently published results focused on related quinolines. The photophysical properties of isoquinoline derivatives differ from those of quinolines, and the most pronounced differences are found for the fluorescence quantum yields. Both experimental and theoretical approaches were used to explain the observed photophysical properties.

010405 organic chemistryOrganic ChemistrySubstituent010402 general chemistryPhotochemistry01 natural sciencesFluorescence0104 chemical scienceschemistry.chemical_compoundchemistryIsoquinolineta116photophysical propertiesJournal of Organic Chemistry
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Cobaltocenium substituents as electron acceptors in photosynthetic model dyads

2017

Abstract Cobaltocenium carboxylic acid hexafluorophosphate has been attached to a zinc(II) meso-tetraphenyl porphyrin chromophore via an amide linkage. Optical and electrochemical studies reveal that the metallocene and the porphyrin interact only negligibly in the ground state of the dyad. Photoinduced charge-shift from the zinc porphyrin to the cobaltocenium substituent to give the zinc porphyrin radical cation and the cobaltocene occurs upon exciting the porphyrin with light. Steady state emission, time-resolved fluorescence and transient absorption pump–probe spectroscopy in addition to density functional theory calculations suggest that the charge shift to the cobaltocenium substituent…

010405 organic chemistryOrganic ChemistrySubstituentChromophore010402 general chemistryPhotochemistry01 natural sciencesBiochemistryPorphyrinPhotoinduced electron transfer0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryExcited stateHexafluorophosphateCobaltoceneMaterials ChemistryPhysical and Theoretical ChemistryTriplet stateJournal of Organometallic Chemistry
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Kinetic and Electrochemical Studies of the Oxidative Addition of Demanding Organic Halides to Pd(0): the Efficiency of Polyphosphane Ligands in Low P…

2013

International audience; Oxidative addition (OA) of organic halides to palladium(0) species is a fundamental reaction step which initiates the C–C bond formation catalytic processes typical of Pd(0)/Pd(II) chemistry. The use of structurally congested polyphosphane ligands in palladium-catalyzed C–C bond formation has generated very high turnover numbers (TONs) in topical reactions such as Heck, Suzuki, Sonogashira couplings, and direct sp2C–H functionalization. Herein, the OA of aryl bromides to Pd(0) complexes stabilized by ferrocenylpolyphosphane ligands L1 (tetraphosphane), L2 (triphosphane), and L3 (diphosphane) is considered. The investigation of kinetic constants for the addition of Ph…

010405 organic chemistryReaction stepInorganic chemistrychemistry.chemical_elementHalide[CHIM.CATA]Chemical Sciences/CatalysisBond formation010402 general chemistryPhotochemistryKinetic energyElectrochemistry01 natural sciencesOxidative addition0104 chemical sciencesCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/CatalysischemistryPhysical and Theoretical ChemistryPalladium
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Effect of Iodination on the Photophysics of the Laser Borane anti-B18H22: Generation of Efficient Photosensitizers of Oxygen

2019

Treatment of the laser borane anti-B18H22 (compound 1) with iodine in ethanol gives the monoiodinated derivative 7-I-anti-B18H21 (compound 2) in 67% yield, or, by reaction with iodine or ICl in the presence of AlCl3 in dichloromethane, the diiodinated derivative 4,4'-I2-anti-B18H20 (compound 3) in 85% yield. On excitation with 360 nm light, both compounds 2 and 3 give strong green phosphorescent emissions (λmax = 525 nm, ΦL = 0.41 and λmax = 545 nm, ΦL = 0.71 respectively) that are quenched by dioxygen to produce O2(1Δg) singlet oxygen with quantum yields of ΦΔ = 0.52 and 0.36 respectively. Similarly strong emissions can be stimulated via the nonlinear process of two-photon absorption when …

010405 organic chemistrySinglet oxygenNuclear magnetic resonance spectroscopyBorane010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryYield (chemistry)Physical and Theoretical ChemistrySpectroscopyPhosphorescenceDerivative (chemistry)DichloromethaneInorganic Chemistry
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Photo-Chromium: Sensitizer for Visible-Light-Induced Oxidative C−H Bond Functionalization-Electron or Energy Transfer?

2017

The chromium(III) sensitizer [Cr(ddpd)2]3+ - based on an earth-abundant metal center - possesses a unique excited state potential energy landscape (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine). The very large energy gap between the redox active and substitutionally labile 4T2 state and the long-lived low-energy 2E spin-flip state enables a selective, efficient sensitization of triplet dioxygen to give singlet dioxygen. Ultrafast intersystem crossing after the Franck Condon point from the 4T2 to the 2E excited state within 3.5 ps precludes intermolecular electron transfer pathways from the ultrashort-lived excited 4T2 state. This specific excited state reactivity enables a …

010405 organic chemistrySinglet oxygenOrganic ChemistryIntermolecular forcechemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundChromiumElectron transferIntersystem crossingchemistryExcited stateSinglet fissionReactivity (chemistry)Physical and Theoretical ChemistryChemPhotoChem
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Co–Co and Co–Fe cyano-bridged pentanuclear clusters based on a methylpyrazinyl-diamine tetradentate ligand: spin crossover and metal substitution eff…

2017

A pentanuclear [CoII3CoIII2] cluster complex has been developed by a solvothermal synthesis. Its highly stable metal-mixed Fe–Co derivatives display robust spin crossover (T1/2 = 268 K) controlled by the degree of substitution.

010405 organic chemistrySolvothermal synthesisSubstitution (logic)General Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical sciencesMetalCrystallographychemistry.chemical_compoundDegree of substitutionchemistrySpin crossovervisual_artDiaminevisual_art.visual_art_mediumCluster (physics)General Materials ScienceTetradentate ligandCrystEngComm
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Electrochemical and spectroelectrochemical studies of β-phosphorylated Zn porphyrins

2013

The electrochemical and spectroelectrochemical properties of two β-phosphorylated Zn porphyrins, [2-diethoxyphosphoryl-5,10,15,20-tetraphenylporphyrinato]zinc (1) and [2-diisopropoxyphosphoryl-5,10,15,20-tetraphenylporphyrinato]zinc (2), are reported in CH 2 Cl 2 and PhCN containing tetrabutylammonium perchlorate (TBAP) or tetrabutylammonium hexafluorophosphate (TBAPF6) as supporting electrolyte. Under certain solution conditions, three one-electron reductions are observed, with the last process being attributed to the product of a chemical reaction following formation of the porphyrin dianion. Two or three oxidations are observed for the same compounds, again depending upon the solution c…

010405 organic chemistrySupporting electrolyteDimerSubstituentchemistry.chemical_elementGeneral ChemistryZinc010402 general chemistryPhotochemistry01 natural sciencesPorphyrinRedox0104 chemical scienceschemistry.chemical_compoundRadical ionchemistryPolymer chemistryTetrabutylammonium hexafluorophosphate[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSJournal of Porphyrins and Phthalocyanines
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Long-range electronic connection in picket-fence like ferrocene–porphyrin derivatives

2012

The effects of a direct connection between ferrocene and porphyrin units have been thoroughly investigated by electrochemical and spectroscopic methods. These data not only reveal that substitution of the porphyrin macrocycle by one, two, three or four ferrocenyl groups strongly affects the electronic properties of the porphyrin and ferrocenyl moieties, they also clearly demonstrate that the metallocene centres are "connected" through the porphyrin-based electronic network. The dynamic properties of selected ferrocene-porphyrin conjugates have been investigated by VT NMR and metadynamic calculations. 1,3-Dithiolanyl protecting groups have been introduced on the upper rings of the ferrocene …

010405 organic chemistrySupramolecular chemistryCrystal structure010402 general chemistryPhotochemistryElectrochemistry01 natural sciencesPorphyrin0104 chemical sciencesDithiolaneInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryFerrocene[CHIM]Chemical SciencesMetalloceneComputingMilieux_MISCELLANEOUS
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Bowl-shape electron donors with absorptions in the visible range of the solar spectrum and their supramolecular assemblies with C 60

2012

We describe the synthesis, electronic, optical and photophysical properties of a family of three electron-donor bowl-shaped organic molecules that absorb light in the whole range of the visible spectrum (up to 800 nm in one case), and associate C60 in solution with binding constants in the range of 104–102 M−1 as measured from both UV-vis and fluorescence titrations in several solvents. These molecules are π-extended derivatives of tetrathiafulvalene, based on a truxene core to which two or three units of dithiole are covalently attached. The inclusion of the bulky dithiole groups is responsible for their bowl-shape geometry, which allows them to associate with C60, and their electron-donor…

010405 organic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundchemistryIntramolecular forceUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)TetrathiafulvaleneVisible spectrum
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