Facile Reduction of a Uranyl(VI) β-ketoiminate Complex to U(IV) Upon Oxo Silylation

被引：56

作者：

Brown, Jessie L. ^{[1
]}

Mokhtarzadeh, Charles C. ^{[1
]}

Lever, Jeremie M. ^{[1
]}

Wu, Guang ^{[1
]}

Hayton, Trevor W. ^{[1
]}

机构：

[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA

来源：

INORGANIC CHEMISTRY | 2011年 / 50卷 / 11期

关键词：

EQUATORIAL COORDINATION; PENTAVALENT URANIUM; TERTIARY PHOSPHINE; CRYSTAL-STRUCTURES; SOLID-STATE; LIGANDS; ADDUCTS; CHEMISTRY; DICATION; BOND;

D O I：

10.1021/ic200387n

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Reaction of the uranyl beta-ketoiminate complex UO(2)((tBu)acnac)(2) (1) ((tBu)acnac = (t)BuNC(Ph)CHC(Ph)O) with Me(3)SiI, in the presence of Ph(3)P, results in the reductive silylation of the uranyl moiety and formation of the U(V) bis-silyloxide complex [Ph(3)PI][U(OSiMe(3))(2)I(4)] (2). Subsequent reaction of 2 with Lewis bases, such as 2,2'-bipyridine (bipy), 1,10-phenanthroline (phen), and tetrahydrofuran (THF), results in a further reduction of the metal center and isolation of the U(IV) complexes U(OSiMe(3))(2)I(2)(bipy)(2) (3), U(OSiMe(3))(2)I(2)-(phen)(2) (4), and [U(OSiMe(3))(2)I(THF)(4)][I(3)] (5), respectively.

引用

页码：5105 / 5112

页数：8

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