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金属桥联双二茂铁配合物的结构与三阶非线性光学性质研究
引用本文:田玉鹏,卢忠林,游效曾,罗保生,谌了容.金属桥联双二茂铁配合物的结构与三阶非线性光学性质研究[J].化学学报,1999,57(10):1068-1074.
作者姓名:田玉鹏  卢忠林  游效曾  罗保生  谌了容
作者单位:1. 安徽大学化学系,合肥,230039
2. 中山大学化学系,广州,510275
3. 南京大学配位化学国家重点实验室,南京,210093
4. 武汉大学分析测试中心,武汉,430072
基金项目:国家自然科学基金(29871001),安徽省自然科学基金资助项目
摘    要:三种金属桥联双二茂铁的三核配合物的合成、结构、电化学及三阶非线性光学性质,通过四圆X射线衍射测定,确定了铜配合物的晶体结构。铜配合物为高度畸变的平面四边形构型。双二茂铁处于顺式结构,这种结构由茂环间的π-π相互作用而变得稳定。研究表明,它们的结构、电化学性质及三阶非线性光学性质三者有密切的内在联系。平面型金属配合物桥联双二茂铁体系中电子离域程度高,在电化学上表现为两步连续单电子氧化过程,其三阶非线性光学效应较强,变形四面体型铜配合物桥联双二茂铁只有一个氧化还原过程,其三阶效应也较低。

关 键 词:二茂铁  非线性光学  晶体结构  铜络合物
修稿时间:1998年10月6日

Structure and third-order optical property: Studies on metal bridged biferrocene complexes
TIAN Yu-Peng,LU Zhong-lin,YOU Xiao-Zeng,LUO Bao-Sheng,CHEN Liao-rong.Structure and third-order optical property: Studies on metal bridged biferrocene complexes[J].Acta Chimica Sinica,1999,57(10):1068-1074.
Authors:TIAN Yu-Peng  LU Zhong-lin  YOU Xiao-Zeng  LUO Bao-Sheng  CHEN Liao-rong
Institution:Anhui Univ, Dept Chem.Hefei(230090);Zhongshan Univ., Dept Chem. Guangzhou(510275);Nanjing Univ, Coordinat Chem State Key Lab.Nanjing (210008)$DWuhan Univ., Center of Anal Measur.Wuhan(430072)
Abstract:A series of metal bridged biferrocene trinuclear complexes derived from Schiff base ligand, S-benzyl-N-(ferrocenyl-1-methylmethylidene) dithio carbazate (here after abbreviated as HL) have been synthesized and spectroscopically characterized. Single crystal structure analysis for the nickel complex, NiL~2, palladium complex, PdL~2 and copper complex, CuL~2 revealed that the Schiff base ligand acted as a singly negtively charged bidentate and coordinated to the metal atom via the mercapto sulphur and β-nitrogen atoms. The coordination geometry of nickel atom and the palladium atom is close to square planar configuration forming an extensive electron delocalization system. The two ligands coordinated to the metal atom in a novel cis- configuration with the two ferrocene moieties on the same side. Detailed structure analysis show that the novel cis-configuration is stabilized by the intramolecular π-π stack interaction between the two acetylcyclopantadienyl rings. The coordination geometry of copper atom in CuL~2 is closed to tetrahedral configuration of the Ni (II) and Pd(II) moieties can effectively transmit the redox effects of the ferrocene moieties, while the tetrahedral configuration of Cu(II) complex cannot. The results also show that the complexes NiL~2, PdL~2 exhibit higher third-order nonlinear response.
Keywords:bridge ferrocene metal complexes  crystal structure  electrochemistry  third - order nonlinear optical property  
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