Facile alternative route to cis-[PtCl2(PTA)2] and [PtCl(PTA)3]Cl (PTA=1,3,5-triaza-7-phosphaadamantane)

被引:5
|
作者
Demakova, Marina Ya. [1 ]
Luzyanin, Konstantin V. [1 ]
Starova, Galina L. [1 ]
Kukushkin, Vadim Yu. [1 ,2 ]
机构
[1] St Petersburg State Univ, Inst Chem, St Petersburg 198504, Russia
[2] Russian Acad Sci, Inst Macromol Cpds, St Petersburg 199004, Russia
关键词
Platinum(II) complexes; 1,3,5-Triaza-7-phosphaadamantane; Ligand substitution; 1,3,5-TRIAZA-7-PHOSPHAADAMANTANE PTA COMPLEXES; INTRAMOLECULAR HYDROAMINATION; ANTIPROLIFERATIVE ACTIVITY; COORDINATION CHEMISTRY; MOLECULAR-STRUCTURE; SPECTRAL PROPERTIES; AQUEOUS-SOLUTION; METAL-COMPLEXES; WATER; DERIVATIVES;
D O I
10.1016/j.inoche.2014.10.002
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of trans-[PtCl2(Me2SO)(2)] with 2 equivs of 1,3,5-triaza-7-phosphaadamantane (PTA) in MeNO2 at RT furnished cis-[PtCl2(PTA)(2)] (1) in 87% isolated yield. Corresponding reaction of K-2[PtCl4] with 1 equiv, of PTA in aqueous EtOH at RT led to [PtCl(PTA)(3)]Cl (2) in 84% isolated yield. Complexes 1 and 2 were characterized by elemental analyses (C, H, N), HR-ESI+/--MS, IR, H-1 and P-31{H-1} NMR spectroscopic techniques, and by single-crystal X-ray diffraction for 1. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 18
页数:2
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