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机构地区:[1]Department of Chemistry, Northwest Normal University, Lanzhou, 730070
出 处:《Chinese Journal of Polymer Science》1992年第1期89-93,共5页高分子科学(英文版)
基 金:The project is supported by National Natural Science Foundation of China
摘 要:The polymer-supported cluster FeCo3 (CO)_(12) (μ3-AuPph_2 CH_2) (4) has been synthesized through reaction of CH_2 ph_2 PAuCl with the cluster anion FeCo_3 (CO)_(12)^-. They are characterized through IR spectra, electronic spectra and XPS, with homogenous analog FeCo_3 (CO)_(12) (μ3-AuPph_3) (3) as reference compound. The cluster (3) and the polymer-supported cluster (4) are good catalysts for hydroformylation of olefins. They have better activity and selectivity than the cluster (1) and (2).The supported cluster (4) is more stable and has catalytic activity at higher temperature than its homogeneous analog (3). From the metal core level binding energies in XPS and λ_(max) in electronic spectra, it is found that the metal-metal bonds in (4) are reinforced bypolymer supporter. The cluster (3) and (4) can be reused , and possibly do not fragment to one metal species in the course of catalytic reaction.The polymer-supported cluster FeCo3 (CO)_(12) (μ3-AuPph_2 CH_2) (4) has been synthesized through reaction of CH_2 ph_2 PAuCl with the cluster anion FeCo_3 (CO)_(12)^-. They are characterized through IR spectra, electronic spectra and XPS, with homogenous analog FeCo_3 (CO)_(12) (μ3-AuPph_3) (3) as reference compound. The cluster (3) and the polymer-supported cluster (4) are good catalysts for hydroformylation of olefins. They have better activity and selectivity than the cluster (1) and (2).The supported cluster (4) is more stable and has catalytic activity at higher temperature than its homogeneous analog (3). From the metal core level binding energies in XPS and λ_(max) in electronic spectra, it is found that the metal-metal bonds in (4) are reinforced bypolymer supporter. The cluster (3) and (4) can be reused , and possibly do not fragment to one metal species in the course of catalytic reaction.
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