Synthesis and characterization of a sterically encumbered homoleptic tetraalkyliron(III) ferrate complex

被引:3
作者
Sears, Jeffrey D. [1 ]
Munoz, Salvador B., III [1 ]
Cuenca, Maria Camila Aguilera [1 ]
Brennessel, William W. [1 ]
Neidig, Michael L. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14267 USA
基金
美国国家卫生研究院;
关键词
Iron-alkyl complexes; X-ray crystallography; OFT calculations; Mossbauer spectroscopy; EPR spectroscopy; DENSITY-FUNCTIONAL THEORY; MAGNETIC CIRCULAR-DICHROISM; CROSS-COUPLING REACTIONS; ZETA VALENCE QUALITY; ELECTRONIC-STRUCTURE; BASIS-SETS; IRON; REACTIVITY; INTERMEDIATE; ELUCIDATION;
D O I
10.1016/j.poly.2018.10.041
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Homoleptic iron-alkyl complexes have been implicated as key intermediates in iron-catalyzed cross coupling with simple iron salts. Tetraalkyliron(II1) ferrate species have been shown to be accessible with either methyl or benzyl ligands, where the former complex is S = 3/2 and distorted square planar while the latter is a S= 5/2 distorted tetrahedral species. In the current study, a new tetraalkyliron(III) complex is synthesized containing modified methylene substituents that incorporate large trimethylsilyl (TMS) groups to further probe steric and electronic ligand effects in tetraalkyliron(III) complexes by increasing the electron-donating ability of the ligand while retaining steric bulk. Detailed structural and DFT studies provide insight into electronic structure and bonding of the four-coordinate trimethylsilylmethyl iron(III) complex compared to the previously reported analogs containing methyl and benzyl ligands. (C) 2018 Elsevier Ltd. All rights reserved.
引用
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页码:91 / 96
页数:6
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