首页> 外文期刊>Journal of the American Chemical Society >SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF THE FIRST ISOLATED HOMOLEPTIC ORGANOPLATINUM(IV) COMPOUND - [PT(C6CL5)(4)]
【24h】

SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF THE FIRST ISOLATED HOMOLEPTIC ORGANOPLATINUM(IV) COMPOUND - [PT(C6CL5)(4)]

机译:第一类分离的有机(IV)有机化合物-[PT(C6CL5)(4)]的合成与结构表征

获取原文
获取原文并翻译 | 示例
       

摘要

The neutral member of the triad [Pt(C6Cl5)(4)](n-) (n = 0, 1, or 2) has been synthesized and characterized. Treatment of [NBu(4)(n)][Pt-III(C6Cl5)(4)] (2) with an excess of chlorine in CCl4 in the presence of AlCl3 gives a high yield (80%) of orange [Pt-IV(C6Cl5)(4)] (3) which can also be generated by electrochemical oxidation of 2 in CH2Cl2 at 1.8 V. Complex 3 has been characterized by elemental analysis and spectroscopy (IR, mass, C-13 and Pt-195 NMR, and EXAFS) as well as by electrochemistry and an X-ray crystal structure determination of its toluene solvate. Cyclic voltammetry indicates that the oxidation of 2 to 3 is accompanied by a substantial structural change, a change confirmed by the EXAFS analyses which imply the symmetry of the [Pt(C6Cl5)(4)] moiety is lowered, with two o-chlorine atoms entering the platinum coordination sphere. The X-ray study showed that crystals of 3.C6H5CH3 are monoclinic, space group P2(1)/c, with a = 11.5972(18) Angstrom, b = 21.213(4) Angstrom, c = 16.838(3) Angstrom, beta = 102.04(2)degrees, V = 4051.22 Angstrom(3), and Z = 4. The structural study of 3 reveals the Pt center in a distorted octahedral environment; two of the C6Cl5 groups behave as conventional a-bonded ligands, while the other two act as chelating ligands bonded through the ipso-C atom and one of the ortho-C1 atoms. Crystals of 3 contain the enantiomeric couple (OC-6-32-A)- and (OC-6-32-C)-bis(pentachlorophenyl-kappa C)bis(pentachloro-kappa Cl-2-phenyl-kappa-C)platinum(IV). Complex 3 is diamagnetic and air- and moisture-stable but with limited thermal stability; at room temperature it eliminates C6Cl5-C6Cl5 even in the solid state. It undergoes conproportionation with [NBu(4)(n)](2)[Pt-II(C6Cl5)(4)] (1) yielding 2. [References: 61]
机译:三元组[Pt(C6Cl5)(4)](n-)(n = 0、1或2)的中性成员已合成并表征。在AlCl3存在下用过量的氯气在CCl4中处理[NBu(4)(n)] [Pt-III(C6Cl5)(4)](2)得到高产率(80%)的橙色[Pt- IV(C6Cl5)(4)](3),也可以通过在1.8 V下的CH2Cl2中2的电化学氧化来生成。络合物3已通过元素分析和光谱法(IR,质量,C-13和Pt-195 NMR)表征,以及EXAFS),并通过电化学和X射线晶体结构测定其甲苯溶剂化物。循环伏安法表明2至3的氧化伴随着实质性的结构变化,这一变化已通过EXAFS分析确认,这暗示了[Pt(C6Cl5)(4)]部分的对称性降低,带有两个邻氯原子进入白金协调领域。 X射线研究表明,3.C6H5CH3晶体为单斜晶,空间群P2(1)/ c,a = 11.5972(18)埃,b = 21.213(4)埃,c = 16.838(3)埃,beta = 102.04(2)度,V = 4051.22埃(3),Z =4。3的结构研究揭示了在扭曲的八面体环境中的Pt中心。两个C6Cl5基团的行为与常规的a键合配体相同,而另两个C6Cl5基团则是通过ipso-C原子和一个邻位C1原子键合的螯合配体。 3的晶体包含对映体对(OC-6-32-A)和(OC-6-32-C)-双(五氯苯基-κC)双(五氯-κCl-2-苯基-C-C)铂(IV)。配合物3是抗磁性的,对空气和水分稳定,但热稳定性有限。在室温下,即使在固态下也能消除C6Cl5-C6Cl5。它与[NBu(4)(n)](2)[Pt-II(C6Cl5)(4)](1)配比,生成2。[参考文献:61]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号