氢甲酰化
合成气
钴
催化作用
化学
羰基化
区域选择性
一氧化碳
有机化学
无机化学
铑
作者
Baoxin Zhang,Christoph Kubis,Robert Franke
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-09-08
卷期号:377 (6611): 1223-1227
被引量:38
标识
DOI:10.1126/science.abm4465
摘要
Hydroformylation with unmodified cobalt carbonyl catalyst plays a crucial role in industrial production of surfactants and plasticizers. However, syngas pressures of 100 to 400 bar with reaction temperatures of 100° to 250°C are typically applied. We report here that unmodified cobalt carbonyl is a stable hydroformylation catalyst at 140°C under 30 bar of syngas. The activity was comparable to that of recently reported bisphosphine-coordinated cobalt(II) catalysts, which we could not reproduce under the reported conditions. Kinetic and in situ infrared spectroscopic studies confirmed the stability of the unmodified cobalt tetracarbonyl hydride [HCo(CO) 4 ]. Branched internal olefins were converted to aldehydes with high regioselectivity under low syngas pressures without phosphorus ligands. Bisphosphines had a small promotional effect on the catalyst at phosphorus-to-cobalt loading ratios below 0.6.
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