Hydridothiazole Rhodium Complexes as a Result of C-H Bond Activation in Iminothiazoles Chelating Ligands
Jehan Al-hamidi1, Abdulhamid Alsaygh2, Ibrahim Al-Najjar2, *
Identifiers and Pagination:Year: 2014
First Page: 27
Last Page: 32
Publisher Id: CHEM-1-27
Article History:Received Date: 27/5/2014
Revision Received Date: 30/10/2014
Acceptance Date: 18/11/2014
Electronic publication date: 31/12/2014
Collection year: 2014
open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
A series of 20 Schiff base ligands derived from 2-aminothiazole and its derivatives and aryl aldehydes with either [RhCl(PPh3)3] or [Rh(µ-Cl)(COD)]2 in the presence of 4 equivalents of PPh3 lead to an Rh(III) cyclometallated complex and the imine ligand (C-H) bond has been added to the metal (C-M-H). The complexes were investigated by using I.R., 1H, 13C and 31P NMR Spectroscopic techniques. The signal of the (C-H) ligand was observed as trans to the nitrogen atom in the complex which is a donor ligand.
Total synthesis of hydridothiazole rhodium complexes possessing rhodium hydride signal at δ (-14.60 to-15.04) ppm, trans to N-donor ligand and iminoyl carbon (7C=N) signal in Rh (III) observed at δ (220.1-237.6)ppm, lower field and suggestive of carbine like properties.