期刊文献+

钴配合物[Co(C_4H_3N_2CoO_2)_2(H_2O)_4]的制备、晶体结构与性质表征 被引量:1

Synthesis,Structure and Characterization of [Co(C_4H_3N_2CoO_2)_2(H_2O)_4]
下载PDF
导出
摘要 制备了一个新的钴的[Co(C4H3N2CoO2)2(H2O)4](C4H4N2CoO2=4,6-二羟基嘧啶),通过X-射线衍射、热重分析和荧光光谱对配合物的结构和性质进行了测试和表征.晶体结构分析表明,该晶体属于单斜晶系,空间群C2/c,晶胞参数:a=13.528(3),b=7.2240(13),c=13.001(2);α=90°,β=109.448(2)°,γ=90°;V=1198.0(4)3,μ=1.485mm-1,Dc=1.958 Mg/m3,F(000)=724,R=0.0302,wR=0.0894(I>2σ(I)).在配合物的结构单元中,Co原子与两个4,6-二羟基嘧啶和四个水分子配位,形成略有畸变的拉伸八面体配合物.配合物的结构单元[Co(C4H3N2CoO2)2(H2O)4]之间进一步通过分子间氢键和π-π堆积作用相互交叉连接在一起形成三维超分子化合物. A new coordination compound [Co(C4H3N2CoO2)2(H2O)4](C4H3N2CoO2= 4,6-dihydroxypyrimidine) has been synthesized,characterized by elemental analysis,infrared spectra,Thermogravimetric analysis,fluorescence spectra,X-ray and diffraction method.Crystal structure data show that the crystal belongs to the monoclinic,space group C2/c,with a = 13.528(3)A,b= 7.2240(13) A,c= 13.001(2)A,α= 90°,β= 109.448(2)°,γ= 90°,V= 1198.0(4)A3,μ= 1.485mm-1,Dc = 1.958 Mg/m^3,F(000) = 724,R= 0.0302,wR = 0.0894(I 2σ(I)) for 3242 observed reflections,with I 2σ(I).In the complex,Co(II) atom is six-coordinated by two N atoms from two 4,6-dihydroxypyrimidine ligands and four O atoms from four water molecules.A three-dimensional supramolecular structure is formed through hydrogen-bonding and π-π packing interactions.
出处 《洛阳师范学院学报》 2010年第2期49-52,共4页 Journal of Luoyang Normal University
关键词 钴配合物 4 6-二羟基嘧啶 晶体结构 荧光光谱 cobalt complex 4 6-dihydroxypyrimidine crystal structure fluorescence spectra
  • 相关文献

参考文献10

二级参考文献60

共引文献22

同被引文献19

  • 1袁霞,罗和安,李芳.分子筛负载席夫碱钴配合物的制备及其催化氧气氧化环己烷(英文)[J].分子催化,2007,21(1):26-31. 被引量:9
  • 2BATTEN S R, ROBSON R. Interpenetrating nets: or- dered,periodic entanglement[ J]. Angew. Chem. Int. Ed. , 1998,37(11) :1 461-1 494.
  • 3LEININGER S, OLENYUK B, STANG P J. Self-assembly of discrete cyclic nanostructures mediated by transition metals [ J ]. Chem. Rev. , 2000,100 ( 3 ) : 853-907.
  • 4ROWSELL J L C, YAGHI 0 M. Strategies for hydrogen storage in metal-organic frameworks [ J ]. Angew. Chem. Int. Ed. ,2005,44(30) :4 670-4 679.
  • 5SAUVAGE J P. Transition metal-containing rotaxanes and catenanes in motion:toward molecular machines and mo- tors[ J]. Acc. Chem. Res. , 1998,31 (10) :611-619.
  • 6SEO J S,WHANG D, LEE H, et al. A homochiral metal- organic porous material for enantioselective separation and catalysis [ J ]. Nature,2000,404 ( 6 781 ) : 982-986.
  • 7EVANS 0 R, LIN Wen-bin. Crystal engineering of NLO materials based on metal-organic coordination networks [ J]. Acc. Chem. Res. ,2002,35(7) :511-522.
  • 8YAGHI O M ,O'KEEFFE M ,OCKWIG N W,et al. Global change : dishing the dirt on coral reefs [ J ]. Nature, 2003, 423:705-714.
  • 9ROWSELL J L C, YAGHI 0 M. Metal-organic frame- works : a new class of porous materials [ J ]. Microporous Mesoporous Mater. , 2004,73 : 3-14.
  • 10XIAO Dong-rong, WANG En-bo, AN Hai-yan, et al. Syn- theses and structures of three unprecedented metal-cipro- floxacin complexes with helical character [ J ]. Cryst. Growth Des. ,2007,7(3) :506-512.

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