Synthesis and structural characterization of fluorenyltris(pyrazol-l-yl)borate ligands as new examples of cyclopentadienyl/scorpionate hybrid ligands

被引：14

作者：

Bieller, S ^{[1
]}

Bolte, M ^{[1
]}

Lerner, HW ^{[1
]}

Wagner, M ^{[1
]}

机构：

[1] Univ Frankfurt, Inst Anorgan Chem, D-60439 Frankfurt, Germany

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2005年 / 690卷 / 08期

关键词：

fluorenyl ligand; scorpionate ligand; zinc complex; X-ray crystallography;

D O I：

10.1016/j.jorganchem.2004.11.004

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Two fluorenyl/tris(pyrazol-1-yl)borate hybrid ligands, FlBpz(3)Li and FlB(pz(3-tBu))(3)Li, have been synthesized and structurally characterized by X-ray crystallography (Fl: 9-fluorenyl; pz: pyrazolyl). From the reaction of FIBpz(3)Li and ZnCl2 in THF, the dinuclear complex (THF)(3)Lipz(Fl)Bpz(2)ZnCl(2) was obtained in which a ZnCl2 moiety is chelated by two pyrazolyl ligands while the third pz ring coordinates to an Li(THF)3 fragment. Acetonitrile solutions of the compound gradually transform into the mononuclear species Fl(pz)Bpz(2)Znpz(2)B(pz)Fl featuring a distorted tetrahedral ZnN4 core. In all molecular structures of [FlBpz(3)](-) or [FlB(pz(3-tBu))(3)](-) complexes investigated so far, the hybrid ligands adopt very similar conformations with only two pyrazolyl rings bonded to the central metal, whereas the third pyrazolyl acts as dangling substituent. The fluorenyl substituent of FIBpz(3)Li may be deprotonated with KH in quantitative yield. (c) 2004 Elsevier B.V. All rights reserved.

引用

页码：1935 / 1946

页数：12

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