1-(1H-Benzimidazol-1-ylmeth-yl)-3-[2-(di-isopropyl-amino)eth-yl] -1H-benzimid-azolium bromide 0.25-hydrate
Document Type
Article
Publication Date
4-15-2009
Abstract
The title N-heterocyclic carbene derivative, C23H 30N5+·Br-·0.25H2O, was synthesized using microwave heating and was characterized by 1H and 13C NMR spectroscopy and a single-crystal X-ray diffraction study. The structure of the title compound are stabilized by a network of intra- and inter-molecular C - H?Br hydrogen-bonding inter-actions. The crystal structure is further stabilized by ?-? stacking inter-actions between benzene and imidazole fragment rings of parallel benzo[d]imidazole rings, with a separation of 3.486 (3) Å between the centroids of the benzene and imidazole rings. There is also an inter-molecular C - H?? inter-action in the crystal structure. The C - N bond lengths for the central benzimidazole ring are shorter than the average single C - N bond, thus showing varying degrees of double-bond character and indicating partial electron delocalization within the C - N - C - N - C fragment. The isopropyl group is disordered over two sites with occupancies of 0.792 (10) and 0.208 (10). © 2009.
Recommended Citation
Arslan, Hakan; VanDerveer, Don; Demir, Serpil; Zdemir, Smail; and Cetinkaya, Bekir, "1-(1H-Benzimidazol-1-ylmeth-yl)-3-[2-(di-isopropyl-amino)eth-yl] -1H-benzimid-azolium bromide 0.25-hydrate" (2009). College of Health, Science, and Technology. 26.
https://digitalcommons.uncfsu.edu/college_health_science_technology/26