Improving regioselectivity in the rhodium catalyzed hydroformylation of protoporphyrin-IX and chlorophyll a derivatives

• Type: Article in International Scientific Journal
• Date: 2005

Authors

Peixoto, AF (Author) FCUP; Pereira, MM (Author) Other; Sousa, AF (Author) Other; Pais, AAC (Author) Other; Neves, MGPMS (Author) Other; Silva, AMS (Author) Other; Cavaleiro, JAS (Author) Other

Journal

Title: Journal of Molecular Catalysis A: Chemical

Vol. 235

Pages: 185-193

ISSN: 1381-1169

Publisher: Elsevier B.V.

Indexing

ISI Web of Knowledge - 8 Citations

Scopus - 10 Citations

Other information

Authenticus ID: P-000-2N0

DOI: 10.1016/j.molcata.2005.04.008

Abstract (EN): An efficient and selective catalytic process to promote the hydroformylation of protoporphyrin-IX dimethyl ester, the respective nickel(R) and zinc(II) complexes and also of methyl pheophorbide a allomer is described. The effect of the central metal ion, pressure, temperature and phosphine ligand structure on the regioselectivity of the reactions is discussed and molecular PM3 calculations are presented in order to rationalize these effects. The hydroformylation reaction of protoporphyrin-IX dimethyl ester using triphenylphosphine (PPh3) as ligand, at 30 bar and 31 degrees C yielded 98% of branched aldehyde. However, using 9,9-dimethyl-4,6-bis(diphenylphosphino)xanthene (Xantphos), as ligand, at 20 bar and 80 degrees C, 74% of linear aldehyde was observed. The regioselectivity of the reaction is strongly dependent on the central metal ion. The zinc(II) complex of protoporphyrin-IX dimethyl ester favours the formation of the branched aldehyde (99%) independently of reaction conditions, while the regioselectivity with the nickel(11) complex showed a dependence both on pressure and temperature. The hydroformylation of methyl pheophorbide a allomer yields 98% of the branched aldehyde even at 20 bar and 80 degrees C reaction conditions.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9