Diruthenium tetracarbonyl sawhorse complexes bearing N-heterocylic carbene and phosphine ligands: Synthesis, structural characterization, and catalytic activity

被引:5
|
作者
Rohrabaugh, Thomas N., Jr. [1 ]
Doverspike, Joshua C. [1 ]
Geib, Steven J. [2 ]
Sawyer, Evan D. [1 ]
Stibbard, Mitchell R. [1 ]
Malosh, Thomas J. [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Johnstown, PA 15904 USA
[2] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
Ruthenium; Dinuclear complexes; Catalysis; Carbene ligands; Phosphine ligands; Carboxylato bridges; RUTHENIUM CARBONYL CARBOXYLATES; LOW-PRESSURE HYDROFORMYLATION; X-RAY-STRUCTURE; BINUCLEAR RUTHENIUM(I); DIMETHYL OXALATE; ETHYLENE-GLYCOL; HYDROGEN-BOND; DERIVATIVES; REDUCTION; CHEMISTRY;
D O I
10.1016/j.jorganchem.2015.11.006
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A number of dinuclear ruthenium(I) sawhorse complexes substituted with an N-heterocyclic carbene or various phosphine ligands have been prepared and characterized by FT-IR, NMR, and elemental analysis. Treatment of [Ru-2(mu-O2CCH3)(2)(CO)(4)](n) with 2-electron donating ligands (L) yields the dimeric derivatives Ru-2(m-O2CCH3)(2)(CO)(4)L-2, where L = IMes [1,3-bis(2,4,6-trimethylphenyl) imidazol-2-ylidene] (1), P(o-CH3C6H4)(3) (2), P(C6F5)(3) (3), P(c-C6H11)(3) (4), and P(C6H5)(3) (5). The syntheses of 1-3 are reported herein; the syntheses of 4 and 5 have been previously reported. The crystal structures of 1-3 have been determined by single crystal X-ray diffraction. Factors influencing the structures of 1-5 are discussed and compared to DFT calculated geometries. An initial assay of the catalytic activities of 1-5, employing the isomerization of 1-hexene, has been performed. (C) 2015 Elsevier B.V. All rights reserved.
引用
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页码:1 / 8
页数:8
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