Search results for "donor-acceptor system"

showing 4 items of 4 documents

Selective Stepwise Suzuki Cross-Coupling Reaction for the Modelling of Photosynthetic Donor−Acceptor Systems

2009

A Suzuki reaction performed as a selective stepwise substitution of two boryl groups on a diarylporphyrin precursor is reported for straightforward construction of a porphyrin trimer, modeling photosynthetic donor-acceptor systems.

[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic ChemistryTrimer010402 general chemistryPhotosynthesisPhotochemistry01 natural sciencesBiochemistryPorphyrinCoupling reaction0104 chemical scienceschemistry.chemical_compounddonor-acceptor systemchemistrySuzuki reaction[ CHIM.ORGA ] Chemical Sciences/Organic chemistryface to faceSuzuki couplingPhysical and Theoretical ChemistryDonor acceptorporphyrinComputingMilieux_MISCELLANEOUSOrganic Letters
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Low‐Valent Germanylidene Anions: Efficient Single‐Site Nucleophiles for Activation of Small Molecules

2021

Abstract Rare mononuclear and helical chain low‐valent germanylidene anions supported by cyclic (alkyl)(amino)carbene and hypermetallyl ligands were synthesised by stepwise reduction from corresponding germylene precursors via stable and isolable germanium radicals. The electronic structures of the anions can be described with ylidene and ylidone resonance forms with the Ge−C π‐electrons capable of binding even weak electrophiles. The germanylidene anions reacted with CO2 to give μ‐CO2‐κC:κO complexes, a rare coordination mode for low‐valent germanium and inaccessible for the related neutral germylones. These results implicate low‐valent germanylidene anions as efficient single‐site nucleop…

small molecule activationkemialliset yhdisteetdonor-acceptor systemsRadical010402 general chemistry01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundsub-valent compoundsNucleophilemain group elementsAlkylchemistry.chemical_classificationkemialliset reaktiot010405 organic chemistryChemistryCommunicationOrganic ChemistrymolekyylitGeneral ChemistryResonance (chemistry)Small moleculeCommunications0104 chemical sciences3. Good healthgermaniumaktivointiMain group elementElectrophileCarbenevalenssi (kemia)Chemistry – A European Journal
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A Straightforward Electroactive π-Extended Tetrathiafulvalene (exTTF) Building Block

2012

The synthesis and X-ray structure of a new and readily available exTTF derivative (6) bearing a methyltriphenylphosphonium bromide moiety as a new building block for the construction of electroactive molecules is reported. The phosphonium salt 6, which was prepared in one step from 2-hydroxymethyl-exTTF as a stable yellow solid in 84 % yield, efficiently undergoes Wittig olefination reactions with a variety of aldehydes to predominantly form the E isomer. Electronic spectra and cyclic voltammetry of the novel compounds reveal the electronic communication between the electroactive units.

ConjugationOlefinationOrganic ChemistryPhosphonium saltPi interactionSettore CHIM/06 - Chimica OrganicaPhotochemistryFused-ring systemCombinatorial chemistryMaterialchemistry.chemical_compoundchemistryBromideWittig reactionMoietyPi interactionPhysical and Theoretical ChemistryCyclic voltammetryDonor-acceptor systemTetrathiafulvaleneDerivative (chemistry)European Journal of Organic Chemistry
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Solvatochromic behaviour of new donor–acceptor oligothiophenes

2021

Oligothiophene derivatives play a central role in the formulation of materials used in devices in the field of organic electronics. In this work, we report the results of the study of UV-vis absorption and fluorescence spectra, in several solvents, of a series of oligothiophenes recently synthesized in our laboratory. The studied oligothiophenes present different structures due to several factors: the donor– acceptor (D–A) or acceptor–donor–acceptor (A–D–A) architecture, the number of thiophene rings in the backbone (ranging from three to eight), the number and position of solubilizing octyl chains in the backbone, and the type of acceptor moieties (from Knoevenagel condensation either with…

oligothiophenessolvatochromism02 engineering and technology010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundMaterials ChemistryThiopheneOrganic electronicsanodic dimerizationSolvatochromismSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyAcceptor0104 chemical scienceschemistryoligothiophenes; solvatochromism; anodic dimerizationKnoevenagel condensationAbsorption (chemistry)0210 nano-technologyDonor acceptorOligothiophenes fluorescence donor-acceptor systemsNew Journal of Chemistry
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