期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 127, 期 12, 页码 4423-4432出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja044154g
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Addressed herein is the 20+ year-old question of whether the true benzene and cyclohexene hydrogenation catalysts derived from the organometallic precursor [Rh(eta(5)-C5Me5)Cl-2](2), 1, are homogeneous or heterogeneous. The methodology employed is that developed earlier (Lin, Y.; Finke, R. G. Inorg Chem. 1994, 33, 4891, A More General Approach to Distinguishing Homogeneous from Heterogeneous Catalysis...). The kinetic evidence especially, but also the metal product (nanoclusters plus bulk metal), Hg(0) poisoning and other experiments, provide compelling evidence that Rh(0) nanoclusters are the true benzene hydrogenation heterogeneous catalyst derived from [Rh(eta 5-C5Me5)Cl-2](2), 1, at the required more vigorous conditions of 50-100 degrees C and 50 atm H-2. However, the same methods reveal that the cyclohexene hydrogenation catalyst derived from 1 at the milder conditions of 22 degrees C and 3.7 atm H-2 is a nonnanocluster, homogeneous catalyst, most likely the previously identified complex, [Rh(eta(5)-C5Me5)(H)(2)(solvent)] (Gill, D. S.; White, C.; Maitlis, P. M J. C. S. Dalton Trans. 1978, 617). In short, the present results solve the two-decade-old problem of identifying the true benzene and cyclohexene hydrogenation catalysts derived from [Rh(eta(5)-C5Me5)Cl-2](2). Perhaps most significant is the demonstration that the methodology employed has the ability to identify both heterogeneous and homogeneous catalysts from the same catalyst precursor.
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