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In Search of the Weak, Six‐Membered Intramolecular Hydrogen Bond in the Solution and Solid States of Guanidinobenzimidazole
Author(s) -
Chen Jing,
Willis Peter G.,
Parkin Sean,
Cammers Arthur
Publication year - 2005
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200400448
Subject(s) - intramolecular force , chemistry , hydrogen bond , low barrier hydrogen bond , hydrogen , imidazole , intramolecular reaction , crystallography , stereochemistry , computational chemistry , molecule , organic chemistry
The chemical literature presents evidence for the nonexistence of the intramolecular hydrogen bond in neutral 2‐guanidinobenzimidazole, a result that defies chemical intuition. In the current study, analyses of substituted 2‐guanidinobenzimidazoles by dynamic 1 H NMR, IR, and X‐ray diffraction unveiled the contribution of the intramolecular hydrogen bond to the overall structure and conformational equilibria. The presence of the intramolecular hydrogen bond in this work and its absence in previous studies of the unsubstituted parent compound is reconciled by the fact that intramolecular hydrogen bonds between the imidazole moieties and guanidino NH 2 protons were weak. The intramolecular hydrogen bonds were more apparent in derivatives with guanidino NHR. The behavior of the latter indicated competition between and coexistence of inter‐ and intramolecular hydrogen bonding. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)