Synthesis and Characterization of Ferrocene-Chelating Heteroscorpionate Complexes of Nickel(11) and Zinc(II)

被引:22
作者
Abubekerov, Mark [1 ]
Diaconescu, Paula L. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
RING-OPENING POLYMERIZATION; REDOX CONTROL; TRIS(1-PYRAZOLYL)BORATE LIGANDS; STRUCTURAL-CHARACTERIZATION; CHEMISTRY; CATALYST; POLY(PYRAZOLYL)BORATE; HYDROTHIOLATION; DERIVATIVES; REACTIVITY;
D O I
10.1021/ic502691b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The first example of a ferrocene-chelating heteroscorpionate, [Li(THF)(2)][fc(PPh2)(BH[(3,5-Me)(2)pz](2))] ((fc(P,B))Li(THF)(2), fc = 1,1'-ferrocenediyl) is described. Starting from a previously reported compound, fcBr(PPh2), a series of ferrocene derivatives, fc(PPh2)(B[OMe](2)), [Li(OEt2)][fc(PPh2)(BH3)], [Li(THF)(2)][fc(PPh2)(BH[(3,5-Me)(2)pz](2))] (pz = pyrazole), was isolated and characterized. Compound (fc(P,B))Li(THF)(2) allowed the synthesis of the corresponding nickel and zinc complexes, (fc(P,B))NiCl, (fc(P,B))NiMe, (fcP,B)ZnCl, and (fcP,B)ZnMe. All compounds were characterized by NMR spectroscopy, while the zinc and nickel complexes were also characterized by X-ray crystallography. The redox behavior of (fc(P,B))NiCl, (fc(P,B))NiMe, (fc(P,B))ZnCl, and (fc(P,B))ZnMe was studied by cyclic voltammetry and supported by density functional theory calculations.
引用
收藏
页码:1778 / 1784
页数:7
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