Synthesis, Structure, and Reactivity of RuII Complexes with Trimethylsilylethinylamidinate Ligands

被引:17
作者
Seidel, Wolfram W. [1 ]
Dachtler, Woldemar [1 ]
Pape, Tania [2 ]
机构
[1] Univ Rostock, Inst Chem, D-18059 Rostock, Germany
[2] Univ Munster, Inst Anorgan & Analyt Chem, D-48149 Munster, Germany
来源
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE | 2012年 / 638卷 / 01期
关键词
N-ligands; Metathesis; Chelates; Substituent effects; X-ray diffraction; CYCLOPENTADIENYL-RUTHENIUM; INSERTION; CARBODIIMIDES; BOND; CS2; ACETYLENEDITHIOLATE; STABILIZATION; CHEMISTRY; ALKYNES; LI;
D O I
10.1002/zaac.201100431
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The mononuclear amidinate complexes [(?6-cymene)-RuCl(1a)] (2) and [(?6-C6H6)RuCl(1b)] (3), with the trimethylsilyl-ethinylamidinate ligands [Me3SiC=CC(N-c-C6H11)2] (1a) and[Me3SiC=CC(N-i-C3H7)2] (1b) were synthesized in high yields by salt metathesis. In addition, the related phosphane complexes[(?5-C5H5)Ru(PPh3)(1b)] (4a) [(?5-C5Me5)Ru(PPh3)(1b)] (4b), and [(?6-C6H6)Ru(PPh3)(1b)](BF4) (5-BF4) were prepared by ligand exchange reactions. Investigations on the removal of the trimethyl-silyl group using [Bu4N]F resulted in the isolation of [(?6-C6H6)Ru(PPh3){(N-i-C3H7)2CC=CH}](BF4) (6-BF4) bearing a terminal alkynyl hydrogen atom, while 2 and 3 revealed to yield intricate reaction mixtures. Compounds 1a/b to 6-BF4 were characterized by multinuclear NMR (1H, 13C, 31P) and IR spectroscopy and elemental analyses, including X-ray diffraction analysis of 1b, 2, and 3.
引用
收藏
页码:116 / 121
页数:6
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