Study of a bifuran vs. bithiophene unit for the rational design of π-conjugated systems. What have we learned?

Chemical Communications

Volumn 49, Issue 56, 2013, Pages 6256-6258

  Gidron, Ori ^a   Varsano, Neta ^a   Shimon, Linda J W ^a   Leitus, Gregory ^a   Bendikov, Michael ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

FURAN DERIVATIVE; THIOPHENE DERIVATIVE; BIFURAN; BITHIOPHENE; UNCLASSIFIED DRUG;

CHEMICAL STRUCTURE; CHEMISTRY; ARTICLE; CONJUGATION; CONTROLLED STUDY; FLUORESCENCE; ISOMER; MOLECULAR STABILITY; SOLUBILITY; PHOTOLUMINESCENCE; QUANTUM YIELD; SOLID STATE; STILLE REACTION;

FURANS; MOLECULAR STRUCTURE; THIOPHENES;

EID: 84880874427     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc41795f     Document Type: Article

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