A Heck-type coupling for the synthesis of novel bridged metallochlorin-fullerene C-60 dyads
Artikel i vetenskaplig tidskrift, 2006

A short and convenient synthesis of metallochlorin-C-60 dyads based on a Heck-type hetero coupling at the 3(2) position of a chlorin is described. p-Bromobenzaldehyde was treated with Zn-metalated 13(2)-demethoxycarbonylmethylpheophorbide a, using a palladium acetate/LiCl catalyst mixture under phase-transfer conditions in DMF at 70 degrees C. The resulting asymmetric olefin was obtained in a high trans/cis ratio. The desired trans isomer was separated and subsequently transformed into a donor-acceptor dyad by a 1,3-dipolar cycloaddition to C-60 in the presence of sarcosine in refluxing toluene. The resulting dyads are expected to undergo efficient photoinduced electron transfer and can potentially be utilized in solar energy conversion devices. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006).

Författare

M. Katterle

Universität Potsdam

A. R. Holzwarth

Max Planck-institutet

Aldo Jesorka

Chalmers, Kemi- och bioteknik, Fysikalisk kemi

European Journal of Organic Chemistry

1434-193X (ISSN)

414-422

Ämneskategorier

Kemi

DOI

10.1002/ejoc.200500494