Synthesis and properties of guanidine-pyridine hybridligands and structural characterisation of their mono- and bis(chelated) cobalt complexes

The synthesis of four guanidine-pyridine hybridligands and their spectroscopic features in MeCN are described. In order to demonstrate their coordinating properties, the corresponding cobalt(II)chloride complexes have been prepared and completely characterised by means of X-ray structure analysis, UV/Vis spectroscopy and mass spectrometry. The neutral complexes {1,1,3,3-tetramethyl-2-(quinolin-8-yl)guanidine}cobalt(II)-dichloride [Co(TMGqu)Cl2] and {N-(1,3-dimethylimidazolidin-2-yliden)pyridin-8-amine}cobalt(II)-dichloride [Co(DMEGpy)Cl2] exhibit a tetrahedral coordination of the cobalt atom, whereas in bis[chlorobis{N-(1,3-dimethylimidazolidin-2-yliden)quinolin-8-amine}cobalt(II)]tetrachlorocobaltate [Co(DMEGqu)2Cl]2[CoCl4] and chlorobis{1,1,3,3-tetramethyl-2-((pyridin-2-yl)methyl)guanidine}cobalt(II)chloride [Co(TMGpy)2Cl]Cl, the cobalt atom is coordinated in a trigonal pyramidal environment. These trigonal pyramidal complex cations represent the first bis(chelated) guanidine cobalt complexes in which the pyridine donor resides on the apical position and the guanidine donor forms with the chlorine atom the base of the pyramid. Besides the structural characterisation, the quenching effect of the cobalt(II) ion (d7) on the ligand fluorescence has been studied.

The synthesis of four guanidine-pyridine hybridligands and their spectroscopic features in MeCN are described. Their cobalt complexes show interesting structural features: the neutral complexes [Co(TMGqu)Cl2] and [Co(DMEGpy)Cl2] exhibit a tetrahedral coordination, whereas in [Co(DMEGqu)2Cl]2[CoCl4] and [Co(TMGpy)2Cl]Cl, the cobalt atom is coordinated in a trigonal pyramidal environment. These complex cations represent the first bis(chelated) guanidine cobalt complexes. Additionally, the quenching effect of the cobalt(II) ion (d7) on the ligand fluorescence has been studied.Figure optionsDownload as PowerPoint slide