Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1334592 | Polyhedron | 2013 | 11 Pages |
Abstract
[RaaiRâ², RaaiRâ²H+]3 [Bi3I12]3â are obtained by refluxing BiI3 and RaaiRâ² (1-alkyl-2-(arylazo)imidazoles) in a 2-methoxyethanol-methanol mixture. The X-ray structure determination of [MeaaiMe, MeaaiMeH+]3 [Bi3I12]3â (MeaaiMe = 1-methyl-2-(p-tolylazo)imidazole) has shown that the iodide bridged bismuthate(III) ([Bi3I12]3â) is intercalated in the channels formed by MeaaiMe-MeaaiMeH+. UV light irradiation in DMF solution of the compounds shows E-to-Z (trans-to-cis) isomerisation of the arylazoimidazole about the -NN- group. The reverse transformation, Z-to-E, is very slow with light irradiation, while it is induced by a thermal process. The quantum yield (ÏEâZ) of the E-to-Z isomerisation is dependent on the molar mass and rotor volume of the compounds. The activation energy (Ea) of the Z-to-E isomerisation is calculated by a controlled temperature experiment. DFT computations were performed to explain the spectra and the photochromism.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Debashis Mallick, Kamal Krishna Sarker, Rajat Saha, Tapan Kumar Mondal, Chittaranjan Sinha,