应用化学 ›› 1988, Vol. 0 ›› Issue (5): 30-33.

• 研究论文 • 上一篇    下一篇

氮磷配位的钛酸酯络合物的X射线光电子能谱研究

黄赛棠, 汤如溶, 李冰, 丁安林   

  1. 中国科学院上海有机化学研究所
  • 收稿日期:1987-07-16 修回日期:1988-03-31 出版日期:1988-10-10 发布日期:1988-10-10
  • 基金资助:
    国家自然科学基金

X-RAY PHOTOELECTRON SPECTROSCOPY STUDY OF N-OR P-COORDINATED TITANATE COMPLEXES

Huang Saitang, Tang Rurong, Li Bing, Ding Anling   

  1. Shanghai Institute of Organic Chemistry, Academia Sinica
  • Received:1987-07-16 Revised:1988-03-31 Published:1988-10-10 Online:1988-10-10

摘要: 制备了单烷基羧酸型和磺酸型钛酸酯氮配位与磷配位的配合物.用XPS法证明有N→Ti或P→Ti配位键生成,并从化学位移量推测了键的强度,磺酸型较羧酸型易配位,羟基取代胺的氮配体配位较容易发生;磷配位由于存在Ti→P的反馈作用,使化学位移不如氮配位明显.此外,异丙基钛酸酯与乙醇胺的反应物,证明分子内有N→Ti配位键生成.

关键词: 钛酸酯, 氮配位, 磷配位, 配合物, X 射线光电子能谱

Abstract: The N-or P-coordinated complexes of monoalkyl carboxyl and sulfonyl titanate were prepared.By means of XPS the N→Ti or P→Ti coordination bonds in these complexes were ascertained,and the relative bonding strength were estimated from the magnitude of the chemical shift data.The sulfonyl titanates are easier to be coordinated with N or P ligands, than the carboxyl titanates;and the hydroxysubstituted amines were coordinated easily with titanates;The chemical shifts of P-coordinated complexes were not pronounced as in the complexes with N-ligands.It may be caused by the"back donation"of Ti→P in these complexes. In addition,The intra-molecular N→Ti coordinate linkage has also been identified in the reaction products of isopropyl titanate and ethyl hydroxyl amines.

Key words: titanate, N-coordinate, P-coordinate, Complex, XPS