Author:
Ames James R.,Houghtaling Melissa A.,Terrian Deborah L.,Mitchell Timothy P.
Abstract
Preparation of bisannulated salts of 2,2′-biimidazole, 2-(2′-imidazolyl)benzimidazole, 2,2′-bibenzimidazole, and annulated salts of 1,1′-dimethyl-2,2′-biimidazole, 1,1′-dimethyl-2-(2′-imidazolyl)benzimidazole, and 1,1′-dimethyl-2,2′-bibenzimidazole is accomplished by direct alkylation of the parent azaheterocycle with excess 1,n-dihaloalkane. Discussions of the product conformations use electronic absorption spectra and NMR. The redox potentials of these salts are measured in DMF and CH3CN, and become increasingly more negative and less reversible as the systems become less planar. Keywords: electrochemistry, bridged azabiaryl salts.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
51 articles.
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