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Volumn 20, Issue 7, 2014, Pages 1909-1917

Protonation of pyridyl-substituted TTF derivatives: Substituent effects in solution and in the proton-electron correlated charge-transfer complexes

Author keywords

hydrogen bonds; nitrogen heterocycles; proton electron systems; substituent effects; tetrathiafulvalene

Indexed keywords

CHARGE TRANSFER; COMPLEXATION; CRYSTAL STRUCTURE; DIMERS; ELECTRONIC STRUCTURE; ELECTRONS; PROTONATION; QUANTUM CHEMISTRY;

EID: 84895064163     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201302614     Document Type: Article
Times cited : (17)

References (53)
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    • The localization of the H-bonded proton at the red-colored donor molecule side is also supported by the larger CNï£ ¿C bond angle in the pyridine ring of the red-colored donor (120.6°) compared to that of the blue-colored one (116.9°), because a pyridine CNC bond angle generally becomes larger by protonation. For example, see:, T. Steiner, Angew. Chem. 2002, 114, 50-80
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.