Article ID Journal Published Year Pages File Type
1340346 Polyhedron 2008 8 Pages PDF
Abstract

Access to 1,3-dineopentyl-benzimidazol-2-ylidene (1) by deprotonation of various benzimidazolium salts was studied. [Ag(1)Cl] was prepared from the corresponding benzimidazolium chloride. X-ray crystal structure analyses of benzo-, naphtho- and quinoxalino-anellated imidazolium salts displayed neither significant changes nor systematic trends of bond lengths and angles within the five-membered ring. Consistently downfield shifts of the 13C1H(2) nuclei reflect the influence of electron-withdrawing anellation.

Graphical abstractAccess to 1,3-dineopentyl-benzimidazol-2-ylidene (1) by deprotonation of various benzimidazolium salts was studied. [Ag(1)Cl] was prepared from the corresponding benzimidazolium chloride. X-ray crystal structure analyses of benzo-, naphtho- and quinoxalino-anellated imidazolium salts are presented. Downfield shifts of the 13C1H(2) nuclei reflect the influence of electron-withdrawing anellation.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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