氢甲酰化
铑
催化作用
化学
醛
离子液体
多金属氧酸盐
磷化氢
苯乙烯
配体(生物化学)
无机化学
有机化学
共聚物
生物化学
受体
聚合物
作者
Xinjia Wei,Yongjun Jiang,Yuan Ma,Jian Fang,Qingpo Peng,Wen Xu,Huiying Liao,Fengxue Zhang,Sheng Dai,Zhenshan Hou
标识
DOI:10.1002/chem.202200374
摘要
Abstract We have developed a Keggin polyoxometalate (POM)‐based ionic‐liquid (IL)‐immobilizing rhodium single‐atom Rh catalyst (MTOA) 5 [SiW 11 O 39 Rh] (MOTA=methyltrioctylammonium cation) that can afford exceptionally high catalytic activity for the hydroformylation of alkenes to produce aldehydes at an ultralow loading of Rh (ca. 3 ppm). For styrene hydroformylation, both the conversion and the yield of the aldehyde can reach almost 99 %, and a TOF as high as 9000 h −1 was obtained without using any phosphine ligand in the reaction process. Further characterization by FTIR, ICP and ESI‐MS analysis revealed that the single Rh atom was incorporated in the lacunary POM anions. In particular, the bulky IL cation can play an additional role in stabilizing Rh species and thus prevent aggregation and leaching of Rh species. The IL catalyst was miscible with n ‐hexane at temperatures; this contributed to exceptionally high activity for hydroformylation even at ultra‐low loading of IL catalyst.
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