Tetravalent Cerium Alkyl and Benzyl Complexes

被引:4
|
作者
Tateyama, Haruko [1 ]
Boggiano, Andrew C. [1 ]
Liao, Can [2 ]
Otte, Kaitlyn S. [1 ]
Li, Xiaosong [2 ]
La Pierre, Henry S. [1 ,3 ,4 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[3] Georgia Inst Technol, Sch Mech Engn, Nucl & Radiol Engn & Med Phys Program, Atlanta, GA 30332 USA
[4] Pacific Northwest Natl Lab, Phys Sci Div, Richland, WA 99352 USA
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; NMR SHIFTS; LIGAND; COVALENCY; ZIRCONIUM; ACTIVATION; REACTIVITY; CATALYSTS; TITANIUM; BEHAVIOR;
D O I
10.1021/jacs.4c01964
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High-valent cerium complexes of alkyl and benzyl ligands are unprecedented due to the incompatibility of the typically highly oxidizing Ce4+ ion and the reducing alkyl or benzyl ligand. Herein we report the synthesis and isolation of the first tetravalent cerium alkyl and benzyl complexes supported by the tri-tert-butyl imidophosphorane ligand, [NP(Bu-t)(3)](1-). The Ce4+ monoiodide complex, [Ce4+I(NP(tert-butyl)(3))(3)] (1-CeI), serves as a precursor to the alkyl and benzyl complexes, [Ce4+(Npt)(NP(tert-butyl)(3))(3)] (2-CeNpt) (Npt = neopentyl, CH2C(CH3)(3)) and [Ce4+(Bn)(NP(tert-butyl)(3))(3)] (2-CeBn) (Bn = benzyl, CH2Ph). The bonding and structure of these complexes are characterized by single-crystal XRD, NMR and UV-vis-NIR spectroscopy, cyclic voltammetry, and DFT studies.
引用
收藏
页码:10268 / 10273
页数:6
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