Reversible Formation of a Cerium-Bound Terminal Hydride: Ce(C5Me4SiMe3)2(H)(thf)

被引：12
作者：
Summerscales, Owen T. [1 ]
Batista, Enrique R. [2 ]
Scott, Brian L. [3 ]
Wilkerson, Marianne P. [1 ]
Sutton, Andrew D. [1 ]
机构：
[1] Los Alamos Natl Lab, Div Chem, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USA
[3] Los Alamos Natl Lab, Mat & Phys Applicat Div, Los Alamos, NM 87545 USA
来源：
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY | 2016年 / 28期
关键词：
Hydrides; C-H activation; Lanthanides; Cerium; C-H ACTIVATION; FLUORINE EXCHANGE; CRYSTAL-STRUCTURE; BOND METATHESIS; COMPLEXES; HYDROGEN; DERIVATIVES; LANTHANIDE; CHEMISTRY; ELEMENTS;
D O I：
10.1002/ejic.201600737
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
The use of the bulky cyclopentadienyl ligand Cp' (Cp' = C5Me4SiMe3) to stabilize cerium hydrides has resulted in the preparation of two novel tuck-in complexes with C-H activated SiMe3 groups. Subsequent reaction of these with H-2 in thf gives a lanthanide terminal hydride species Ce(Cp')(2)(H)(thf) which reversibly regenerates the tuck-in complex under sustained vacuum. This compound is only the second structurally characterized terminal cerium hydride. This new hydride is a catalyst in H/D exchange reactions between with both sp(3)-CH and sp(2)-CH bonds, and for the hydrogenation of unsaturated alkene bonds.
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页码：4551 / 4556
页数：6
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