化学学报 ›› 2003, Vol. 61 ›› Issue (8): 1319-1322. 上一篇    下一篇

研究论文

(Bu_4N)[Ni(dmit)_2]的一步合成及一种新晶相

方奇;夏光明;刘国群;许文   

  1. 山东大学
  • 发布日期:2003-08-15

One-step Synthesis of (Bu_4N)[Ni(dmit)_2] and Its New C2/c Crystalline Phase

Fang Qi;Xia Guangming;Liu Guoqun;Xu Wen   

  1. State Key Laboratory of Crstal Materials, Shandong University
  • Published:2003-08-15

用中心离子替代和空气自动氧化的方法由(Bu_4N)_2[Zn(dmit)_2]一步合成了 (Bu_4N)[Ni(dmit)_2],这种方法可推广到其它Z[M(dmit)_2]配合物和Z[M(dmit) _2]_2导电配合物的合成(Bu_4N)[Ni(dmit)_2]结晶过程中出现两个晶相,其中空间 群为C2/c的侧心单斜相为新晶相,X射线结构测定结果为:a=2.0191(2)nm, b=1. 3404(1) nm,β=105.55(1)~°,V=3165.5(6)nm~3, R=0.055, 晶体中的Ni(dmit) _2]-呈D_(2h)点群对称性,平面性接近完美,共轭性相当显著,相邻Ni(dmit)_2] -平面间的夹角为75.56(3)~°。

关键词: 镍络合物, 晶体结构, X射线衍射分析, 季胺

(Bu_4N)[Ni(dmit)2] was synthesized by substituting Zn2+ in (Bu_4N) _2[Zn(dmit)_2] with Ni2+ and by auto-oxidation in acetone solution. This simple method can be extended to synthesize other Z [ M ( dmit )2 ] type complexes and Z[M(dmit)2]2 type conductive complexes. Two crystalline phases of (Bu_4N) [Ni(dmit)_2] , namely triclinic P1-bar phase and monoclinic C2/c phase which has been proved new, were obtained. The crystalline data of the C2/c phase are: a =2.0191(2) nm, 6 = 1.3404(1) nm, c = 1.2141(1) nm, β= 105.554(8)°, F=3165.5(6) nm3, R =0.055, C2/c space group.

Key words: NICKEL COMPLEX, CRYSTAL STRUCTURE, XRD, QUATERNARY AMMONIUM COMPOUNDS

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