期刊
CHEMCATCHEM
卷 10, 期 22, 页码 5306-5313出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201801551
关键词
pillararenes; aqueous biphasic catalysis; hydroformylation; molecular recognition; inclusion complexes
资金
- Chevreul Institute [FR 2638]
- Ministere de l'Enseignement Superieur et de la Recherche
- Region Nord - Pas de Calais
- FEDER
Aqueous biphasic catalysis continues to attract strong interest, especially when very hydrophobic substrates are concerned. Indeed, their insolubility in water strongly limit their transformation by water-soluble organometallic catalysts. To improve contacts between the substrate-containing organic phase and the catalyst-containing phase, one of the best solutions consists in using interfacial additives capable of supramolecularly recognize the substrate and/or the catalyst. In the present study, modified pillar5arenes are considered as interfacial additives and their performance is assessed in Rh-catalyzed hydroformylation of long alkyl-chain alkenes (higher olefins). Pillar5arenes substituted by carboxylate functions and methyl groups P5 A-(Me)(10-x)-(CH2COOMe)(x) are compared to pillar5arenes substituted by polyethylene glycol (PEG) chains (P5 A-(Me)(5)-(PEG)(5) and P5 A-(PEG)(10)). Utilization of P5 A-(Me)(10-x)-(CH2COOMe)(x) leads to high conversion and regioselectivity (linear/branched aldehyde ratio) in Rh-catalyzed hydroformylation of 1-decene and 1-hexadecene. Compared with other interfacial additives such as modified cyclodextrins, the studied pillar5arenes show lower chemo-selectivity, similar catalytic activity and higher regioselectivity.
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