0000000000013569

AUTHOR

Andrei S. Batsanov

showing 4 related works from this author

Experimental and theoretical studies into the structural perturbations between neutral, oxidised and reduced forms of 1,4-dithiinoquinoxaline derivat…

2000

The syntheses and electrochemistry of thieno[3',4'r5,6][1,4]dithiino[2,3-b]quinoxaline (9), 2,3-bis(methylsulfanyl)[1,4]dithiino[2,3-b]quinoxaline (16) and 2,3-ethylenedisulfanyl[1,4]dithiino[2,3-b]quinoxaline (17) are reported, together with the X-ray crystal structures of 9, 16 and the charge-transfer complex 9.TCNQ. In the thieno derivative 9, the molecular structure undergoes a significant change from a boat conformer to a planar system, upon oxidation with TCNQ. Theoretical calculations show that oxidation leads to planarisation of the molecular structure due to the aromatisation of the dithiine moiety. The study of the oxidised/reduced species helps to rationalise the electrochemical …

NitrileChemistryStereochemistryGeneral ChemistryCrystal structureCharge-transfer complexElectrochemistrychemistry.chemical_compoundCrystallographyQuinoxalineMaterials ChemistryMoietyMoleculeConformational isomerismJournal of Materials Chemistry
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Donor-π-Acceptor Species Derived from Functionalised 1,3-Dithiol-2-ylidene Anthracene Donor Units Exhibiting Photoinduced Electron Transfer Propertie…

1998

Steric interactions between the anthraquinoid core and the 1,3-dithiole and dicyanomethylene groups play a key role in determining the physical properties of system 1. The intramolecular charge transfer properties of this donor–π-acceptor species have been explored and cyclic voltammetric data, X-ray crystal structures and ab initio calculations are also reported.

Steric effectsOrganic ChemistryDithiolGeneral ChemistryCrystal structurePhotochemistryAcceptorCatalysisPhotoinduced electron transferchemistry.chemical_compoundCrystallographyElectron transferchemistryAb initio quantum chemistry methodsIntramolecular forceChemistry - A European Journal
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Sulfur, tin and gold derivatives of 1-(2'-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2'-pyridyl, X = SH, SnMe3 or AuPPh3).

2004

Reaction of the lithium salt of 1-(2'-pyridyl)-ortho-carborane, Li[1-R-1,2-C(2)B(10)H(10)](R = 2'-NC(5)H(4)), with sulfur, followed by hydrolysis, gave the mercapto-o-carborane, 1-R-2-SH-1,2-C(2)B(10)H(10) which forms chiral crystals containing helical chains of molecules linked by intermolecular S-H...N hydrogen bonds. The cage C(1)-C(2) and exo C(2)-S bond lengths (1.730(3) and 1.775(2)[Angstrom], respectively) are indicative of exo S=C pi bonding. The tin derivative 1-R-2-SnMe(3)-1,2-C(2)B(10)H(10), prepared from Li[1-R-1,2-C(2)B(10)H(10)] and Me(3)SnCl, crystallises with no significant intermolecular interactions. The pyridyl group lies in the C(1)-C(2)-Sn plane, oriented to minimise th…

010405 organic chemistryChemistryHydrogen bondStereochemistryIntermolecular forcechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryBond lengthCrystallographyTrigonal bipyramidal molecular geometryCarboraneMoleculeTinDalton transactions (Cambridge, England : 2003)
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The Interplay of Inverted Redox Potentials and Aromaticity in the Oxidized States of New π-Electron Donors: 9-(1,3-Dithiol-2-ylidene)fluorene and 9-(…

2006

Derivatives of 9-(1,3-dithiol-2-ylidene)fluorene (9) and 9-(1,3-dithiol-2-ylidene)thioxanthene (10) have been synthesised using Horner-Wadsworth-Emmons reactions of (1,3-dithiol-2-yl)phosphonate reagents with fluorenone and thioxanthen-9-one. X-ray crystallography, solution electrochemistry, optical spectroscopy, spectroelectrochemistry and simultaneous electrochemistry and electron paramagnetic resonance (SEEPR), combined with theoretical calculations performed at the B3P86/6-31G** level, elucidate the interplay of the electronic and structural properties in these molecules. These compounds are strong two-electron donors, and the oxidation potentials depend on the electronic structure of t…

Organic ChemistryThioxantheneDithiolAromaticitySulfoxideGeneral ChemistryFluorenePhotochemistryCatalysisDicationchemistry.chemical_compoundchemistryFluorenoneRadical ionChemistry - A European Journal
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