(1,10-Phenanthroline)bis(piperidinecarbodithioato-S,S')cadmium(II), [Cd(pipdtc)(2)(1,10-phen)] (1) and (2,2'-bipyridine)bis(piperidinecarbodithioato-S,S')cadmium(II), [Cd(pipdtc)(2)(bipy)] (2) adducts were prepared and the crystal structures are reported. Cd-S and Cd-N distances and the angles subtended at cadmium are almost the same in both complexes but the Cd-S distances in the adducts are longer than those in Cd(pipdtc)2 (3) complexes due to the presence of an additional neutral ligand. Thioureide C-N distance in 1 and 2 are supported by vC-N bands observed at 1471 and 1470 cm(-1), respectively. S2p binding energies for the adducts show a significant reduction in value compared to the parent dithiocarbamate indicating the weakening of the Cd-S bond on adduct formation. The observed reduction in binding energy is due to the increased electron density on the metal in the adducts. The cyclic voltammetric study on the complexes also show an increase of electron density on cadmium in the adducts compared to Cd(pipdtc)(2). (c) 2008 Elsevier Ltd. All rights reserved.
(1,10-
邻菲罗啉)双(
哌啶羰基二
硫代酸-S,S')
镉(II),[Cd(pipdtc)2(1,10-phen)] (1) 和 (
2,2'-联吡啶)双(
哌啶羰基二
硫代酸-S,S')
镉(II),[Cd(pipdtc)2(bipy)] (2) 配合物被制备,其晶体结构如下。在两种配合物中,Cd-S 和 Cd-N 的距离以及在
镉原子处的夹角几乎相同,但由于存在额外的中性
配体,配合物中的 Cd-S 距离比 Cd(pipdtc)2 (3) 配合物中的更长。1 和 2 中的
硫脲 C-N 距离分别由在 1471 和 1470 cm⁻¹ 处观察到的 vC-N 带所支持。配合物的 S2p 结合能与母体二
硫代
碳酸盐相比有显著下降,表明在配合物形成过程中 Cd-S 键的减弱。结合能的降低是由于配合物中
金属上电子密度增加所致。对配合物的环伏安研究还表明,与 Cd(pipdtc)2 相比,配合物中
镉上的电子密度有所增加。© 2008 Elsevier Ltd. 保留所有权利。