Activation of CO2 by a Heterobimetallic Zr/Co Complex

被引：158

作者：

Krogman, Jeremy P. ^{[1
]}

Foxman, Bruce M. ^{[1
]}

Thomas, Christine M. ^{[1
]}

机构：

[1] Brandeis Univ, Dept Chem, Waltham, MA 02454 USA

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2011年 / 133卷 / 37期

关键词：

CARBON-DIOXIDE; TRAPPING REACTIONS; METAL; REDUCTION; GENERATION; ZIRCONIUM; OXO; REACTIVITY; BONDS; ZR;

D O I：

10.1021/ja2071847

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

At room temperature, the early/late heterobimetallic complex Co((i)Pr(2)PNMes)(3)Zr(THF). has been shown to oxidatively add CO2, generating (OC)Co((i)Pr(2)PNMes)(2) (mu-O)Zr((i)Pr(2)PNMes). This compound can be further reduced under varying conditions to generate either the Zr oxoanion (THF)(3)Na-O-Zr(MesNP(i)Pr(2))(3)Co(CO) or the Zr carbonate complex (THF)(4)Na-2(CO3)-Zr(MesNP(i)Pr(2))(3) Co (CO). Additionally, reactivity of the CO2-derived product has been observed with PhSiH3 to generate the Co-hydride/Zr-siloxide product (OC)(H)Co((i)Pr(2)PNMes)(3)ZrOSiH2Ph.

引用

页码：14582 / 14585

页数：4

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