Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6551
Title: Synthesis, X-ray structure analysis and density functional study of an unusual anhydrous 5,6-dimethylbenzo-1,3-imidazolium(H3) chloride
Authors: Tamasi, Gabriella 
Carpini, Alice
Valensin, Daniela 
Cini, Renzo
Issue Date: 2015
Project: None 
Journal: JOURNAL OF MOLECULAR STRUCTURE
Abstract: 
The heteroaromatic base 5,6-dimethylbenzo-1,3-imidazole (DMBI) proved to be a Brönsted base in an anhydrous ethanol solution, which contained fac,trans-[Ru(CO)3Cl2]2 at 55 C in air when the DMBI:Ru molar ratio was 2:1. The reaction produced colorless anhydrous single crystals of {(HDMBI)+Cl}, C9H11ClN2, which were collected and analyzed using X-ray diffraction (XRD) techniques. A network of N–HCl hydrogen bond type interactions linking the protonated hetero-aromatic base to the chloride anions (bridging bases) stabilizes the crystal and mimics the N–HCl interactions that play important roles in CCl channel biological systems. The shortest NCl contact distance and corresponding N–HCl angle are 3.073(3) Å and 173(3), respectively. The packing is also assisted by weaker C–HCl hydrogen bond-type interactions and an extensive network of pp stacking interactions involving HDMBI+ cations. Density functional calculations at the B3LYP/6-31G⁄⁄ and /6-311++G⁄⁄ levels for models of fragments of the crystal structure allowed for the evaluation of geometric parameters, hydrogen bond-type interaction formation energies, and infrared parameters for {(HDMBI)+Cl} and {(HDMBI)+Cl(HDMBI)+}.
Description: 
63587
URI: http://hdl.handle.net/20.500.12779/6551
ISSN: 0022-2860
DOI: 10.1016/j.molstruc.2014.09.054
Appears in Collections:Publications

Show full item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.