Abstract
Mixed ligand complexes of Pd(II) and Cd(II) with
N
-picolyl-amine dithiocarbamate (PAC-dtc) as primary ligand and tertiary phosphine ligand as secondary ligands have been synthesized and characterized via elemental analysis, molar conductance, NMR (
1
H and
31
P), and IR techniques. The PAC-dtc ligand displayed in a monodentate fashion via sulfur atom whereas diphosphine ligands coordinated as a bidentate mode to afford a square planner around the Pd(II) ion or tetrahedral around the Cd(II) ion. Except for complexes [Cd(PAC-dtc)
2
(dppe)] and [Cd(PAC-dtc)
2
(PPh
3
)
2
], the prepared complexes showed significant antimicrobial activity when evaluated against Staphylococcus aureus, Pseudomonas aeruginosa, Candida albicans and Aspergillus niger. Moreover, DFT calculations were performed to investigate three complexes {[Pd(PAC-dtc)
2
(dppe)](1), [Cd(PAC-dtc)
2
(dppe)](2), [Cd(PAC-dtc)
2
(PPh
3
)
2
](7)}, and their quantum parameters were evaluated using the Gaussian 09 program at the B3LYP/Lanl2dz theoretical level. The optimized structures of the three complexes were square planar and tetrahedral geometry. The calculated bond lengths and bond angles showed a slightly distorted tetrahedral geometry for [Cd(PAC-dtc)
2
(dppe)](2) compared to [Cd(PAC-dtc)
2
(PPh
3
)
2
](7) due to the ring constrain in the dppe ligand. Moreover, the [Pd(PAC-dtc)
2
(dppe)](1) complex showed higher stability compared to
Cd(2)
and
Cd(7)
complexes which can be attributed to the higher back-donation of Pd(1) complex.