Protonation of metal-metal bonds in coordinatively unsaturated diruthenium cores

被引:8
|
作者
Mayer, Tobias [1 ]
Boettcher, Hans-Christian [1 ]
机构
[1] Univ Munich, Dept Chem, D-81377 Munich, Germany
关键词
Ruthenium; Carbonyl; Coordinative unsaturation; Phosphido-bridged; Crystal structure; RAY CRYSTAL-STRUCTURES; COMPLEXES;
D O I
10.1016/j.poly.2012.11.049
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The addition reaction of a proton towards the coordinatively unsaturated diruthenium complexes [Ru-2(CO)(4)(mu-H)(mu-(PBu2)-Bu-t)(mu-(PP)-P-boolean AND)] (Ru=Ru) ((PP)-P-boolean AND = Ph2PC(=CH2)PPh2, dppen, lb; (PP)-P-boolean AND = Ph2PN(H)PPh2, dppa, 1c; (PP)-P-boolean AND = Ph2PN(Ph)PPh2, dpppha, 1d) has been investigated. Thus the species 1b-d exhibit a high metal basicity and react with protons from tetrafluoroboric acid in dichloromethane to afford the corresponding oxidative addition products [Ru-2(CO)(4)(mu-H)(2)(mu-(PEu2)-Eu-t)(mu-(PP)-P-boolean AND)]BF4 (2b-d) in good yields. During these reactions a shortening of the metal-metal bond in each case was observed as confirmed by X-ray diffraction studies. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:507 / 511
页数:5
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