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混合配体配合物[Pd(bpy)(L-asp)]·3。5H_2O的晶体结构及其稳定性研究
引用本文:高恩君,张丹,刘祁涛.混合配体配合物[Pd(bpy)(L-asp)]·3。5H_2O的晶体结构及其稳定性研究[J].化学学报,2003,61(11):1834-1838.
作者姓名:高恩君  张丹  刘祁涛
作者单位:1. 沈阳化工学院配位化学研究室,沈阳,110142;东北师范大学化学学院,长春,130024
2. 沈阳化工学院配位化学研究室,沈阳,110142
3. 辽宁大学化学科学与工程学院,沈阳,110036;东北师范大学化学学院,长春,130024
基金项目:辽宁省自然科学基金(No.20022018)和沈阳化工学院拔尖人才基金资助项目.
摘    要:合成了混合配体配合物单晶Pd(bpy)(L-asp)·]3.5H_2O(bpy=2,2'-联吡啶, L-asp~2=L-天冬氨酸根)。用红外光谱和元素分析对配合物的成键及组成进行了表 征。用X射线单晶衍射仪(CCD)测定配合物的结构,晶体属四方晶系,为P4(1) 2(1)2空间群。配合物为平面四边形结构,分子内存在氢键作用,其晶胞靠氢键 和芳环堆砌等弱相互作用力形成。用电位滴定法测定了配合物稳定常数lgKPd~ (2+)+bpy+L-asp~2<->Pd(bpy)(L-asp)]、表征常数△lgKPd(bpy)~(2+)Pd(L-asp) <->Pd(bpy)(L-asp)+Pd~(2+)]和lgXPd(bpy)_2~(2+)+Pd(L-asp)_2~(2-)<->2Pd (bpy)(L-asp)],各常数均大于相应的统计期望值,从分子内d-pπ电子效应和电性 中和角度对配合物额外稳定性进行了讨论。

关 键 词:联吡啶  P  天冬氨酸  钯化合物  元素分析  红外分光光度法  X射线衍射分析  晶体结构
修稿时间:2003年4月10日

Studies on the Crystal Structure and Stability in Solution of Mixed Ligand Complex of Palladium (II) with 2,2'-Bipyridine and L-Aspartic Acid
GAO,En Jun,a,c ZHANG,Dan a LIU,Qi Tao b,c.Studies on the Crystal Structure and Stability in Solution of Mixed Ligand Complex of Palladium (II) with 2,2''-Bipyridine and L-Aspartic Acid[J].Acta Chimica Sinica,2003,61(11):1834-1838.
Authors:GAO  En Jun  a  c ZHANG  Dan a LIU  Qi Tao b  c
Institution:Coordination Chemistry Section, Shenyang Institute of Chemical Technology;College of Chemistry, Northeast Normal University
Abstract:The mixed ligand complex Pd(bpy)(Z,-asp)*3.5H2O (bpy = 2,2'- bipyridine, L-asp= L-aspaitic acid) (1) has been synthesized and characterized by IR spectra, elemental analysis and electroconductivity. The molecular structure and the packing of 1 have been determined by single crystal X-ray structure analysis. The results show that the Pd( II ) in 1 has a square planar coordination geometry and the molecules of 1 are assembled via hydrogen bond and intermolecular aromatic ring stacking. The crystal of 1 belongs to tetragonal, space group P4(l)2(l)2, a - h - 1.5979(3) nm, c = 1.3749(5) ran, Z = %, V- 3.5105(15) ran3. The stability of the mixed ligand complex was determined by the pH potentiometric titration technique in water at 37 °C and 0.10 ionic strength (NaCl). The results show that the complex is quite stable, The higher scale values of relative stability AlgX and lgZ demonstrate that the complex possesses enhanced stability. The reasons that lead to these results were discussed in terms of 7r-electron back donation and electroneutralization.
Keywords:BIPYRIDINE P  ASPARTIC ACID  PALLADIUM COMPOUNDS  ELEMENTAL ANALYSIS  IR  XRD  CRYSTAL STRUCTURE
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