Targeting π-conjugated multiple donor-acceptor motifs exemplified by tetrathiafulvalene-linked quinoxalines and tetrabenz[bc,ef,hi,uv]ovalenes: Synthesis, spectroscopic, electrochemical, and theoretical characterization

Chemistry - An Asian Journal

Volumn 6, Issue 12, 2011, Pages 3312-3321

  Jia, Hong Peng ^a   Ding, Jie ^b   Ran, Ying Fen ^a   Liu, Shi Xia ^a   Blum, Carmen ^a   Petkova, Irina ^b   Hauser, Andreas ^b   Decurtins, Silvio ^a  

^a UNIVERSITY OF BERN   (Switzerland)

^b UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

charge transfer; donor acceptor systems; nanographene; redox chemistry; tetrathiafulvalene

Indexed keywords

ABSORBANCES; CHARGE TRANSFER STATE; DIAMINE MOIETIES; DONOR-ACCEPTOR SYSTEM; DONOR-ACCEPTORS; FUNCTIONALIZED; GOOD YIELD; H NMR SPECTRA; HIGH PURITY; INTRAMOLECULAR CHARGE TRANSFERS; NANOGRAPHENE; OXIDATION STATE; QUINOXALINES; RADICAL CATIONS; REDOX CHEMISTRY; REDOX-ACTIVE; ROOM TEMPERATURE; SCHIFF-BASE; STABILIZING EFFECTS; STOKES SHIFT; SYNTHETIC APPROACH; SYNTHETIC STRATEGIES; TETRATHIAFULVALENE DERIVATIVES; TETRATHIAFULVALENES; WIDE SPECTRAL RANGE;

DICHLOROMETHANE; ELECTROCHEMICAL OXIDATION; FUNCTIONAL MATERIALS; HYDROCARBONS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYCYCLIC AROMATIC HYDROCARBONS;

CHARGE TRANSFER;

EID: 82455210263     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201100515     Document Type: Article

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