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Volumn 5, Issue 9, 1999, Pages 2518-2530

A new class of giant tetrads for studying aspects of long-range intramolecular electron transfer processes: Synthesis and computational studies

Author keywords

Computational chemistry; Cycloadditions; Electron transfer; Multichromophores; Stereochemistry

Indexed keywords

1,4 NAPHTHOQUINONE DERIVATIVE; ALKADIENE; BIPYRIDINE DERIVATIVE; HYDROQUINONE DERIVATIVE; NAPHTHALENE DERIVATIVE; NORBORNANE DERIVATIVE; PARAQUAT; PORPHYRIN DERIVATIVE; PYRROLE DERIVATIVE; SOLVENT;

EID: 0032841220     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3765(19990903)5:9<2518::AID-CHEM2518>3.0.CO;2-1     Document Type: Article
Times cited : (26)

References (85)
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    • note
    • See footnotes on the first page of this article for details of how to obtain the supporting information (10 pages).
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    • note
    • The precise origin of the stabilising interaction between the porphyrin and bpy groups is unknown, although it is clearly not caused by dispersive forces. Presumably, the stabilisation involves multipole -multipole and multipole-induced-multipole interactions which we simply call electrostatic interactions.
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    • note
    • The dielectric constants of chloroform, acetone and acetonitrile are 4.8, 21 and 37.5, respectively.
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    • note
    • 1H NMR study of solvent effects on chemical shifts in these molecules.
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    • note
    • -1 is still significant;
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    • [1d]
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.