Actinide Complexes Possessing Six-Membered N-Heterocyclic Iminato Moieties: Synthesis and Reactivity

被引:35
作者
Ghatak, Tapas [1 ]
Fridman, Natalia [1 ]
Eisen, Moris S. [1 ]
机构
[1] Technion Israel Inst Technol, Schulich Fac Chem, IL-32000 Haifa, Israel
基金
以色列科学基金会;
关键词
RING-OPENING POLYMERIZATION; HYDROGEN-DEUTERIUM EXCHANGE; INTERMOLECULAR HYDROAMINATION; ORGANOACTINIDE COMPLEXES; TERMINAL ALKYNES; CARBON-MONOXIDE; CATALYSTS; MECHANISM; ORGANOTHORIUM; DIMERIZATION;
D O I
10.1021/acs.organomet.7b00037
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel class of ligand systems possessing a six-membered N-heterocyclic iminato [perimidin-2-iminato ((PrN)-N-R, where R = isopropyl, cycloheptyl)] moiety is introduced. The complexation of these ligands with early actinides (An = Th and U) results in powerful catalysts [((PrN)-N-R)An(N{SiMe3)(2)}(3)] (3-6) for exigent insertion of alcohols into carbodiimides to produce the corresponding isoureas in short reaction times with excellent yields. Experimental, thermodynamic, and kinetic data as well as the results of stoichiometric reactions provide cumulative evidence that supports a plausible mechanism for the reaction.
引用
收藏
页码:1296 / 1302
页数:7
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