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首页> 外文期刊>Advanced synthesis & catalysis >Synthetic Applications of Synergism using Catalytic Binuclear Elimination Reactions. Further Examples of Rhodium-Manganese and Rhodium-Rhenium-Catalyzed Hydroformylations
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Synthetic Applications of Synergism using Catalytic Binuclear Elimination Reactions. Further Examples of Rhodium-Manganese and Rhodium-Rhenium-Catalyzed Hydroformylations

机译:使用催化双核消除反应的协同作用的合成应用。铑锰和铑R催化的羰基化反应的其他例子

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摘要

Synergism has been previously observed in both rhodium-manganese- and rhodium-rhenium-catalyzed hydroformylation. Furthermore, detailed in situ spectroscopic investigations have conclusively shown that the phenomenological origin of this synergistic effect is catalytic binuclear elimination (J. Am. Chem. Soc. 2003, 125, 5540-5548; 2007, 129, 13327-13334). In the present contribution, further substrates are used in the hydroformylation reaction with both rhodium-manganese and rhodium-rhenium. In situ spectroscopic studies show that (i) significant rate enhancements occur in the mixed metal systems with the new substrates and (ii) the organo-metallics present in the active systems, and their con-centration profiles are consistent with those present in the previously studied catalytic binuclear elimination reactions (CBER). It is therefore concluded that catalytic binuclear elimination is a rather general mechanism in mixed metal hydroformylations and is rather independent of the substrates used. Further discussion is given to mechanistic aspects, synthetic efficiency, and the possibility that such synergistic effects might be useful to other classes of organic syntheses.
机译:先前已经在铑-锰-和铑-催化的加氢甲酰化中观察到协同作用。此外,详细的原位光谱研究最终表明,这种协同作用的现象学起源是催化双核消除(J. Am。Chem。Soc。2003,125,5540-5548; 2007,129,13327-13334)。在本发明中,另外的底物与铑锰和铑hydro一起用于加氢甲酰化反应中。原位光谱研究表明:(i)具有新底物的混合金属系统发生了显着的速率提高;(ii)活性系统中存在的有机金属,其浓度分布与以前的浓度分布一致研究了催化双核消除反应(CBER)。因此得出的结论是,催化双核消除是混合金属加氢甲酰化中相当普遍的机制,并且与所用的底物无关。进一步讨论了机械方面,合成效率以及这种协同效应可能对其他类别的有机合成有用的可能性。

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