Synthesis of redox-active, intramolecular charge-transfer chromophores by the [2+2] cycloaddition of ethynylated 2H-Cyclohepta[b]furan-2-ones with tetracyanoethylene

Chemistry - A European Journal

Volumn 17, Issue 18, 2011, Pages 5116-5129

  Shoji, Taku ^a   Higashi, Junya ^b   Ito, Shunji ^c   Okujima, Tetsuo ^d   Yasunami, Masafumi ^e   Morita, Noboru ^b  

^a SHINSHU UNIVERSITY   (Japan)

^b TOHOKU UNIVERSITY   (Japan)

^c HIROSAKI UNIVERSITY   (Japan)

^d EHIME UNIVERSITY   (Japan)

^e NIHON UNIVERSITY   (Japan)

Author keywords

charge transfer; cycloaddition; donor acceptor systems; electrochemistry; heteroazulenes

Indexed keywords

[2 + 2] CYCLOADDITION; ACCEPTOR MOIETIES; ALKYNYLATIONS; COLOR CHANGES; CYCLOADDUCTS; DIFFERENTIAL PULSE VOLTAMMETRY; DONOR-ACCEPTOR SYSTEMS; ELECTROCHEMICAL REDUCTIONS; ETHYNYL; HETEROAZULENES; INTRAMOLECULAR CHARGE TRANSFERS; INTRAMOLECULAR CHARGE-TRANSFER INTERACTIONS; MULTI-STEP; REDOX BEHAVIOR; REDOX-ACTIVE; RING OPENING; TETRACYANOETHYLENE; THEORETICAL CALCULATIONS; UV/ VIS SPECTROSCOPY;

AROMATIC COMPOUNDS; BUTENES; CHARGE TRANSFER; CHROMOPHORES; CYCLOADDITION; ELECTROCHEMICAL PROPERTIES; ELECTROCHEMISTRY; ELECTROLYTIC REDUCTION; ION EXCHANGE; MASS TRANSFER; ORGANIC POLLUTANTS; SYNTHESIS (CHEMICAL);

CYCLIC VOLTAMMETRY;

EID: 79954593499     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003628     Document Type: Article

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