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作 者:薛照明 张宣军 田玉鹏 吴杰颖 蒋民华 Fun Hoong Kun
机构地区:[1]Department of Chemistry, Anhui University, Hefei 230039, China [2]Department of Chemistry, Anhui University, Hefei 230039, China, State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China,State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, China [3]State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China [4]X-ray Crystallography Laboratory, School of Physics, Universiti Sains Malaysia 11800, Penang, Malaysia
出 处:《Chinese Journal of Structural Chemistry》2003年第3期265-269,共5页结构化学(英文)
基 金:Supported by a grant for the State Key Program of China (G1998061402); the National Natural Science Foundation of China (29871001, 20071001, and 50272001)
摘 要:The nickel(Ⅱ) complex with the new ligand of S-benzyl-b-N-[10-ethyl- phenothiazine-3-methylene]dithiocarbazate(HL) crystallizes in the triclinic system, space group P?with a = 7.516(1), b = 11.322(1), c = 13.366(1) , a = 84.818(1), b = 81.688(1), g = 76.037(1), V = 1090.26(3) 3, Z = 1, Dc = 1.413 g/cm3, F(000) = 482, m(MoKa) = 0.774 mm-1 (l = 0.7103 ?, R = 0.0573 and wR = 0.1375 for 3357 observed reflections with I ≥ 2s(I). The HL has lost a proton from its tautomeric thiol form and acts as a single negatively charged bidentate ligand coordinating to the nickel ion via the mercapto sulfur and b-nitrogen atoms. The geometry around Ni(Ⅱ) is almost square-planar with two equivalent NiN and NiS bonds. The nonlinear absorption of HL and NiL2 solutions (in DMF) was measured by open-aperture Z-scan technique at the wavelength of 532 nm.
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