Chelating N,N′-(bis(pyridin-2-yl)alkylidene)propane-1,3-diamine pseudohalide copper(II) and cadmium(II) coordination compounds: Synthesis, structure and luminescence properties of [M(bpap)(X)]ClO4 and [M(bpap)(X)2] [M=Cu, Cd; , NCS−]

Synthesis and characterization of nickel(II) and copper(II) complexes with tetradentate Schiff base ligands

“…The similar pattern of cyclic voltammogram of 1 and 2 indicates the similarity of their structures. The results of cyclic voltammetry also closely resemble that of the similar reported compounds, which serve as further evidences for similar structural and electronic properties [43].…”

Polymeric topologies in cadmium(II) dithiophosphate adducts of the isomeric n-pyridinealdazines, n = 2, 3 and 4

“…While 1-D, 2-D and 3-D arrays of cadmium complexes attract attention in terms of their possible applications in chemical luminescence [1][2][3][4][5], the focus of our studies has been upon the delineation of the factors that control supramolecular aggregation in these and related systems. An emerging theme from our work indicates that steric control, exerted by (i) ligand-bound R groups, (ii) metalbound organic substituents, (iii) where applicable, restricted coordination ability of diimine bases, and (iv) some combination of (i)-(iii) above, can be exploited to generate specific aggregation patterns [6][7][8].…”

Synthesis, structure and spectral characterisation of a hydrogen-bonded polymeric manganese(III) Schiff base complex

“…Schiff bases always have proven themselves as useful chelators because of their preparational accessibilities, structural varieties and varied denticities [3]. So, transition metal Schiff base complexes still have been the most well-known resources in the scope of heterogeneous catalysis, molecular electronics, single molecule based magnetism and, above all, photochemistry [4][5][6][7].…”