Unsymmetric pyrrole, thiophene, and furan-conjugated comonomers prepared using azomethine connections: Potential new monomers for alternating homocoupled products

Journal of Organic Chemistry

Volumn 73, Issue 10, 2008, Pages 3859-3866

  Dufresne, Stéphane ^a   Skene, W G ^a  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; EXCITED STATES; MONOMERS; OXIDATION; QUENCHING;

AZOMETHINE BONDS; COMONOMERS; FURAN HETEROCYCLES; PHOTOPHYSICAL INVESTIGATION;

AROMATIC COMPOUNDS;

AZOMETHINE YLIDE; FURAN; MONOMER; PYRROLE; THIOPHENE;

ARTICLE; CONJUGATION; CYCLIC POTENTIOMETRY; ELECTROCHEMISTRY; FLUORESCENCE SPECTROSCOPY; LIGHT EMITTING DIODE; MOLECULAR SENSOR; OXIDATION; POLYMERIZATION; QUANTUM YIELD; SYNTHESIS; TEMPERATURE DEPENDENCE; WITTIG REACTION; X RAY CRYSTALLOGRAPHY;

EID: 43449121554     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8002503     Document Type: Article

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