磷-31核磁共振自旋晶格弛豫时间作为负载型水相催化剂中吸附水的间接探针

Q4 Chemical Engineering 分子催化 Pub Date : 1994-11-27 DOI:10.1016/S0304-5102(94)87037-3
Barbara B. Bunn, Tamas Bartik , Berit Bartik , William R. Bebout, Thomas E. Glass, Brian E. Hanson
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引用次数: 11

摘要

由HRh (CO) (TPPTS)3和TPPTS (TPPTS =三磺化三苯基膦三钠盐)衍生的SAP氢甲酰化催化剂的磷-31自旋晶格弛豫时间T1's与负载水相的类液体性质一致。固相TPPTS的Ale T1为1150 s,而负载水相TPPTS的Ale T1为220 ~ 4.9 s。4.9 s的T1接近溶液中TPPTS的值,并且在H2O/P为24.9时观察到。在这个水含量水平上,先前报道的SAP催化剂对烯烃的氢甲酰化表现出最大的催化活性。
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Phosphorus-31 NMR spin lattice relaxation times as an indirect probe of adsorbed water in supported aqueous phase catalysts

Phosphorus-31 spin lattice relaxation times, T1's, for SAP hydroformylation catalysts derived from HRh (CO) (TPPTS)3 and TPPTS (TPPTS = trisulfonated triphenyl phosphine trisodium salt) are consistent with a liquid-like character for the supported aqueous phase. Ale T1 for solid TPPTS is 1150 s while for TPPTS in a supported aqueous phase T1 varies from 220 to 4.9 s. A T1 of 4.9 s is close to the value obtained for TPPTS in solution and is observed at a H2O/P ratio of 24.9. At this level of water content previously reported SAP catalysts have shown maximum catalytic activity for the hydroformylation of olefins.

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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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