期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 689, 期 4, 页码 766-769出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2003.12.008
关键词
phosphine-phosphonite; ferrocene; rhodium; dinuclear; hydroformylation; enantiopure complex
We previously reported the easy access to mixed ferrocenediyl ligands bearing phosphine and phosphonite moieties. Using this strategy, a new enantiopure phosphine-menthylphosphonite ferrocenediyl has been synthesised. This mixed ligand leads to original unsymmetrical dinuclear rhodium coordination-complexes. One example of this new class of quasi-close bridging A frame dinuclear rhodium complexes, fully characterised by multinuclear H-1, C-13, P-31 and Rh-103 NMR and optical rotation measurements, is presented. Preliminary tests have shown an activity improvement in the hydroformylation of oct-1-ene using the phosphine-menthylphosphonite ferrocenediyl auxiliary compared to known phosphine-phosphonite ligands. (C) 2003 Elsevier B.V. All rights reserved.
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