期刊文献+

四种新型柔性吡啶基配合物的合成、结构及配体构象与配合物结构的关系 被引量:4

Syntheses,Structures of Four New Complexes Constructed by Flexible Pyridine Ligand and the Relationship Between Conformations and Structures
下载PDF
导出
摘要 合成了柔性配体3-吡啶甲酸-1,2-乙二酯(3-pyridinecarboxylic acid 1,2-ethanediyl ester,pcaede),并将其分别与Co盐和Hg盐进行组装,得到4个新配合物[Co(pcaede)2Cl2.2CH3CN.H2O]n(1),[Co(pcae-de)2Cl2.H2O]n(2),[Hg(pcaede)I2]n(3)和[Hg(pcaede)Br2]n(4),对其进行了元素分析、红外光谱及X射线单晶结构分析.配合物1和2为含有孔道的一维链状结构,配合物3是1D内消旋螺旋链,配合物4则是锯齿形1D链状结构.研究结果显示,孔道中填充的溶剂分子和平衡阴离子对配合物的组装有显著的影响.此外对4个配合物中配体的构象进行了理论计算. Four new complexes [Co(pcaede)2Cl2 2CH3CN H2O]n(1),[Co(pcaede)2Cl2·H2O]n(2),[Hg(pcaede)I2]n(3) and [Hg(pcaede)Br2]n(4) were prepared with a flexible ligand 3-pyridinecarboxylic acid 1,2-ethanediyl ester(pcaede) and Co/Hg salts.They were characterized by elemental analysis,IR and X-ray single-crystal diffraction.Complexes 1 and 2 both have an one-dimensional(1D) chain sturcture with channels.Complex 3 processes a 1D meso-helix sturcture,and complex 4 exhibits a 1D infinite zig-zag chain structrue.The results demonstrated that the solvent molecules filled in channels and counteranions have a significant impact on the assembly of the complexes.Moreover,theoretical calculations were carried about the conformation of the ligand in four complexes.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2010年第5期867-873,共7页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20971065) 国家“九七三”计划项目(批准号:2007CB925103,2010CB923303)资助
关键词 晶体结构 柔性配体 构象 理论计算 Crystal structure Flexible ligand Conformation Theoretical calculation
  • 相关文献

参考文献24

  • 1ChenB. L., Wang L. B., XiaoY. Q., etal.. Angew. Chem. Int. Ed.[J], 2009, 48(3): 500-503.
  • 2Allendorf M. D., Bauer C. A., Bhakta R. K., etal.. Chem. Soc. Rev. [J], 2009, 38(5): 1330-1352.
  • 3ShaJ. Q., PengJ., ZhangY., etal.. Cryst. Growth Des.[J], 2009, 9(4):1708-1715.
  • 4Carson C. G. , Hardcastle K. , Schwartz J. , et al.. Eur. J. Inorg. Chem. [J], 2009, 16:2338-2343.
  • 5Tang J. K., Costa J. S., GolobicA., et al.. Inorg. Chem.[J], 2009, 48(12):5473-5479.
  • 6WaltonK. S., SnurrR. Q.. J. Am. Chem. Soc.[J],2007, 129(27):8552-8556.
  • 7Morris R. E. , Wheatley P. S.. Angew. Chem. Int. Ed. [J] , 2008, 47(27) : 4966-4981.
  • 8Monge A. , Snejko N. , Puebla E. G. , et al.. Chem. Commun. [J] , 2005, 10:1291-1293.
  • 9PoornacharyS. K., ChowP. S., TanR. B. H.. Cryst. Growth Des.[J], 2008, 8(1):179-185.
  • 10Navarro J. A. R. , Barea E. , Dieguez A. R. , et al.. J. Am. Chem. Soc. [J] , 2008, 130(12) : 3978-3984.

二级参考文献24

  • 1Robin A. Y. , Fromm K. M.. Coord. Chem. Rev. [J] , 2006, 250:2127--2157.
  • 2Kitagawa S. , Uemura K.. Chem. Soc. Rev. [ J] , 2005, 34 : 109--119.
  • 3Erxleben A.. Coord. Chem. Rev. [J], 2003, 246:203--228.
  • 4Yaghi O. M. , O'Heeffe M. , Oekwig N. W. , et al.. Nature[J] , 2003, 423:705-714.
  • 5Foguet-Albiol D. , Brien T. O. A. , Wernsdorfer W. , et al.. Angew. Chem. Int. Ed. Engl. [J], 2005, 44(6) : 897-901.
  • 6Lin W. B. , Evans O. R. , Yee G. T.. J. Solid State Chem. [J], 2000, 152(1) : 152-158.
  • 7Fujiya M., Kwon Y. J., Washizu S., et al.. J. Am. Chem Soc. [J], 1994, 116(3) : 1151-1152.
  • 8Hoskins B. F., Robson R., Slizys D. A.. Angew. Chem. Int. Ed. Engl. [J], 1997, 36(21): 2336-2338.
  • 9Zhu H. F. , Zhao W. , Okamura T. , et al.. New J. Chem. [J] , 2004, 28(8) : 1010-1018.
  • 10Noro S., Kitaura R., Kondo M., et al..J. Am. Chem. Soc. [J], 2002, 124(11) : 2568--2583.

共引文献4

同被引文献38

引证文献4

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部