首页> 外文学位 >Late transition metal coordination chemistry and reactivity of bis(diphenylphosphino)alkylamine ligands.
【24h】

Late transition metal coordination chemistry and reactivity of bis(diphenylphosphino)alkylamine ligands.

机译:双(二苯基膦基)烷基胺配体的后期过渡金属配位化学和反应性。

获取原文
获取原文并翻译 | 示例

摘要

The chemistry, spectroscopic and structural properties of a variety of Pd(I), Pd(II), Pt(II), Ag(I) and Fe(0) complexes of the bis(diphenylphosphino)alkylamine (dppaa: R = H; dppa or Me; dppma) ligands were investigated. This examination is part of a comparative study with the related bis(diphenylphosphino)methane (dppm) complexes of the same metals.;A series of monomeric chelated complexes of the Pt group metals were prepared in an effort to probe the geometry of the dppaa ligands chelated onto metals. The single crystal x-ray structures of Pd(;The monomeric Pd complexes serve as starting materials used to synthesize the Pd(I) dimeric complex (Pd;The solid and solution state behaviour of dimeric Ag(I) dppaa complexes of a variety of stoichiometries provides some insight into the effect of changing the amine alkyl group. The two nmr active isotopes of silver provide extra information with which to probe the solution state behaviour of these complexes through ;The deviation from expected behaviour in the iron carbonyl chemistry of the dppa ligand led to an investigation of an interesting tris-chelate complex of Fe(III). The crystal structure of this complex, Fe ((OP(Ph)
机译:双(二苯基膦基)烷基胺的各种Pd(I),Pd(II),Pt(II),Ag(I)和Fe(0)配合物的化学,光谱和结构性质(dppaa:R = H;研究了dppa或Me; dppma)配体。这项检查是对相同金属的相关双(二苯基膦基)甲烷(dppm)配合物进行比较研究的一部分。;制备了一系列Pt类金属的单体螯合配合物,以探索dppaa配体的几何形状螯合到金属上。 Pd(;)单体Pd配合物的单晶X射线结构用作合成Pd(I)二聚体配合物(Pd;各种Ag(I)dppaa二聚体Ag(I)dppaa配合物的固相和溶液状态行为的起始材料化学计量学为改变胺烷基的作用提供了一些见识,银的两个nmr活性同位素提供了额外的信息,可通过这些信息通过以下方式探查这些配合物的溶液状态行为; dppa羰基铁化学反应中预期行为的偏离配体导致了对有趣的三价铁螯合物的研究(Fe((OP(Ph)

著录项

  • 作者

    Frankel, Daniel Carl.;

  • 作者单位

    University of Toronto (Canada).;

  • 授予单位 University of Toronto (Canada).;
  • 学科 Inorganic chemistry.
  • 学位 Ph.D.
  • 年度 1993
  • 页码 168 p.
  • 总页数 168
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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