首页 | 本学科首页   官方微博 | 高级检索  
     

Structural diversity and reactivity of d^10 metal- (4-pyridylthio)acetate system
引用本文:ZHANG YueHua,WANG Jing,ZHENG LingLing,HU Sheng,LIN ZhuoJia,TONG MingLiang. Structural diversity and reactivity of d^10 metal- (4-pyridylthio)acetate system[J]. 科学通报(英文版), 2009, 54(23): 4277-4284. DOI: 10.1007/s11434-009-0673-6
作者姓名:ZHANG YueHua  WANG Jing  ZHENG LingLing  HU Sheng  LIN ZhuoJia  TONG MingLiang
作者单位:Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, State Key Laboratory of Optoelectronic Materialsand Technologies, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
基金项目:Supported by the National Natural Science Foundation of China (Grant No. 20525102), Specialized Research Foundation for the Doctoral Program of Higher Education (Grant No. 20060558081), “Hundred Talents” Foundation of Sun Yat-Sen University, Doctoral Foudation of Ministry of Education of China for New Scholar (Grant No. 200805581015), and Natural Science Foundation of Guangdong Province (Grant No. 8451027501001515)
摘    要:The hydrothermal synthesis and crystal structures of four coordination polymers, namely, 2D [Zn(μ3-ta)(pytaH)]n (1), 2D [Zn(μ3-pyta)Cl]n (2), 1D [Cd(μ-pyta)2(H2O)]n (3), and 3D [Cd(μ3-pyta)(μ-Cl)]n (4) (pyta = (4-pyridylthio)acetate, ta = thioglycolate), are reported. They are based on (4-pyridylthio)acetate and its derived ligand. The ta^2- ligand present in 1 was generated from an in situ C(sp^2)-S bond cleavage of the pyta ligand. In these compounds, versatile intermolecular interactions, such as close S…S interactions and strong (O-H…O/N/S) or weak (C-H…O/S, C-H…Cl) hydrogen bonding interactions, play an important role in the formation of three-dimensional supramolecular networks in the solid state.

关 键 词:晶体结构  醋酸  多样性  氢键相互作用  反应  金属  系统  水热合成
收稿时间:2009-03-03
修稿时间:2009-08-26

Structural diversity and reactivity of d10 metal-(4-pyridylthio)acetate system
YueHua Zhang,Jing Wang,LingLing Zheng,Sheng Hu,ZhuoJia Lin,MingLiang Tong. Structural diversity and reactivity of d10 metal-(4-pyridylthio)acetate system[J]. Chinese science bulletin, 2009, 54(23): 4277-4284. DOI: 10.1007/s11434-009-0673-6
Authors:YueHua Zhang  Jing Wang  LingLing Zheng  Sheng Hu  ZhuoJia Lin  MingLiang Tong
Affiliation:Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, State Key Laboratory of Optoelectronic Materials and Technologies, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
Abstract:The hydrothermal synthesis and crystal structures of four coordination polymers, namely, 2D [Zn(μ3-ta)(pytaH)] n (1), 2D [Zn(μ3-pyta)Cl] n (2), 1D [Cd(μ-pyta)2(H2O)] n (3), and 3D [Cd(μ3-pyta)(μ-Cl)] n (4) (pyta = (4-pyridylthio)acetate, ta = thioglycolate), are reported. They are based on (4-pyridylthio)acetate and its derived ligand. The ta2− ligand present in 1 was generated from an in situ C(sp2)-S bond cleavage of the pyta ligand. In these compounds, versatile intermolecular interactions, such as close S…S interactions and strong (O-H…O/N/S) or weak (C-H…O/S, C-H…Cl) hydrogen bonding interactions, play an important role in the formation of three-dimensional supramolecular networks in the solid state.
Keywords:cadmium(II)   zinc(II)   coordination polymer   hydrothermal reaction   in situ S-C(sp2) cleavage
本文献已被 维普 SpringerLink 等数据库收录!
点击此处可从《科学通报(英文版)》浏览原始摘要信息
点击此处可从《科学通报(英文版)》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号