Synthesis and Characterization of Cerium and Yttrium Alkoxide Complexes Supported by Ferrocene-Based Chelating Ligands

被引：83

作者：

Broderick, Erin M. ^{[1
]}

Thuy-Boun, Peter S. ^{[1
]}

Guo, Neng ^{[2
]}

Vogel, Carola S. ^{[3
]}

Sutter, Joerg ^{[3
]}

Miller, Jeffrey T. ^{[2
]}

Meyer, Karsten ^{[3
]}

Diaconescu, Paula L. ^{[1
]}

机构：

[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA

[2] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA

[3] Univ Erlangen Nurnberg, Dept Chem & Pharm, D-91058 Erlangen, Germany

来源：

INORGANIC CHEMISTRY | 2011年 / 50卷 / 07期

关键词：

TRANSITION-METAL-COMPLEXES; X-RAY CRYSTAL; COORDINATION CHEMISTRY; NICKEL(III) COMPLEXES; RUTHENIUM COMPLEXES; MOLECULAR-STRUCTURE; STAUDINGER REACTION; OXIDATION; CATALYSTS; POLYMERIZATION;

D O I：

10.1021/ic102076g

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Two series of Schiff base metal complexes were investigated, where each series was supported by an ancillary ligand incorporating a ferrocene backbone and different N=X functionalities. One ligand is based on an imine, while the other is based on an iminophosphorane group. Cerium(IV), cerium(III), and yttrium(III) alkoxide complexes supported by the two ligands were synthesized. All metal complexes were characterized by cyclic voltammetry. Additionally, NMR, Mossbauer, X-ray absorption near-edge structure (XANES), and absorption spectroscopies were used. The experimental data indicate that iron remains in the +2 oxidation state and that cerium(IV) does not engage in a redox behavior with the ancillary ligand.

引用

页码：2870 / 2877

页数：8

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