Gas phase hydroformylation of propene catalyzed by a polymer bound rhodium(I) complex

The continuous gas phase hydroformylation of propene is catalyzed by a cationic rhodium carbonyl complex co-ordinatively bound to a copolymer of 2-vinylpyridine and methyl acrylate crosslinked with 5 mol% ethene diacrylate. The counter ion had a strong effect on both activity and deactivation. At 40...

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Bibliographic Details
Published inJournal of molecular catalysis Vol. 80; no. 3; pp. 365 - 375
Main Authors Heinrich, Bernd, Chen, Yuying, Hjortkjær, Jes
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 06.04.1993
Elsevier Sequoia
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Summary:The continuous gas phase hydroformylation of propene is catalyzed by a cationic rhodium carbonyl complex co-ordinatively bound to a copolymer of 2-vinylpyridine and methyl acrylate crosslinked with 5 mol% ethene diacrylate. The counter ion had a strong effect on both activity and deactivation. At 403 K and 1100 kPa total pressure (C 3:CO:H 2=2.4:2.2:1.0) the total initial rate was 8.5 × 10 −7 mol/(s gRh) with tetraphenylborate as counter ion. The regioselectivity was close to 1. The catalyst rapidly lost about 50% of its initial activity. Deactivation was accompanied by benzene formation, indicating a reaction of the tetraphenylborate counter ion with traces of water. As benzene formation diminished, deactivation slowed down. A catalyst with chloride as charge balancing ligand was less active and needed activation at higher temperatures than the tetraphenylborate complex. Only slow deactivation was observed with this catalyst.
ISSN:0304-5102
DOI:10.1016/0304-5102(93)85009-I