Tris(pyrazolyl)methane ligands: The neutral analogs of tris(pyrazolyl)borate ligands

被引:131
作者
Reger, DL [1 ]
机构
[1] Univ S Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
tris(pyrazolyl)methane ligands; tris(pyrazolyl)borate ligands; cationic metal complexes; copper(I); silver(I); cadmium(II); lead(II); thallium(I); stereochemically inactive lone pair; Cd-113; NMR;
D O I
10.1080/02603599908020413
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Despite the widespread use of tris(pyrazolyl)borate ligands, their isoelectronic, neutral analogs, tris(pyrazolyl)methane Ligands, have not been extensively studied. By use of appropriate starting materials, such as [Cu(NCMe)(4)]PF6 or [Cd-2(thf)(5)](BF4)(4), stable cationic complexes of the ligands HC(3,5-Me(2)pz)(3), HC(3-Phpz)(3) and HC(3-Bu(t)pz)(3) can be prepared with the metals copper(I), silver(I), cadmium(ll), lead(II) and thallium(I). In many cases isoelectronic groups of complexes, such as [HB(3,5-Me(2)pz)(3)](2)Cd, {[HC(3,5-Me(2)pz)(3)]Cd[HB(3,5-Me(2)pz)(3)]}(+), and {[HC(3,5-Me(2)pz)(3)](2)Cd}(2+), have been prepared and shown to have very similar structures. The Cd-113 NMR chemical shifts of the three complexes are also very similar. The isoelectronic complexes {[HC(pz)(3)](2)Pb}(2+) and [HB(pz)(3)](2)Pb have similar distorted six-coordinate structures. The isoelectronic pair {[HC(3,5-Me(2)pz)(3)](2)Pb}(2+) and [HB(3,5-Me(2)pz)(3)](2)Pb have very similar octahedral structures in which the lone pair on the lead(ll) is stereochemically inactive. Thus, for most cases the tris(pyrazolyl)methane and tris(pyrazolyl)borate ligands bond to these metals in a similar fashion.
引用
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页码:1 / 28
页数:28
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