TY - JOUR
T1 - Mononuclear, dinuclear and 1-D polymeric complexes of Cd(II) of a pyridyl pyrazole ligand
T2 - Syntheses, crystal structures and photoluminescence studies
AU - Das, Kinsuk
AU - Konar, Saugata
AU - Jana, Atanu
AU - Barik, Anil Kumar
AU - Roy, Sangita
AU - Kar, Susanta Kumar
PY - 2013/3/27
Y1 - 2013/3/27
N2 - The syntheses, crystal structures and photoluminescence properties of four new Cd(II) complexes are reported using strongly coordinating ligand 3,5-dimethyl-1-(2′-pyridyl) pyrazole (L) in presence of anionic ancillary bridging ligands as nitrite, chloride and dicyanamide. Among the complexes two (1 and 2) are monomeric, 3 is μ2-chloro bridged dimer and the last one (4) is a mixed alternate chloro-end to end (EE) dicyanamide bridged 1D polymer. All the four complexes have been X-ray crystallographically characterized. The ligand L behaves as a potent bidentate neutral N, N donor. Geometrical diversity of Cd(II) complexes is due to no loss or gain of crystal field stability with the variation of geometry. Consequently the stability of a structure depends on steric requirements. The ligand L shows considerable fluorescence and all four complexes in methanol exhibit interesting photoluminescence properties with different emission intensities. The band maxima and fluorescence efficiency (in methanol) are found to be dependent on the coordination chromophore and structural rigidity induced by the incorporated Cd(II) ion. Among the synthesized complexes 1 exhibits the highest fluorescence intensity in methanol.
AB - The syntheses, crystal structures and photoluminescence properties of four new Cd(II) complexes are reported using strongly coordinating ligand 3,5-dimethyl-1-(2′-pyridyl) pyrazole (L) in presence of anionic ancillary bridging ligands as nitrite, chloride and dicyanamide. Among the complexes two (1 and 2) are monomeric, 3 is μ2-chloro bridged dimer and the last one (4) is a mixed alternate chloro-end to end (EE) dicyanamide bridged 1D polymer. All the four complexes have been X-ray crystallographically characterized. The ligand L behaves as a potent bidentate neutral N, N donor. Geometrical diversity of Cd(II) complexes is due to no loss or gain of crystal field stability with the variation of geometry. Consequently the stability of a structure depends on steric requirements. The ligand L shows considerable fluorescence and all four complexes in methanol exhibit interesting photoluminescence properties with different emission intensities. The band maxima and fluorescence efficiency (in methanol) are found to be dependent on the coordination chromophore and structural rigidity induced by the incorporated Cd(II) ion. Among the synthesized complexes 1 exhibits the highest fluorescence intensity in methanol.
KW - Cadmium (II) complexes
KW - Photoluminescence
KW - Pyridyl-pyrazole ligand
KW - X-ray crystal structure
UR - http://www.scopus.com/inward/record.url?scp=84871975864&partnerID=8YFLogxK
U2 - 10.1016/j.molstruc.2012.11.036
DO - 10.1016/j.molstruc.2012.11.036
M3 - Article
AN - SCOPUS:84871975864
SN - 0022-2860
VL - 1036
SP - 392
EP - 401
JO - Journal of Molecular Structure
JF - Journal of Molecular Structure
ER -