One-pot synthesis of functionalized, highly substituted porphodimethenes

Treatment of nickel(II)complexes of 2,3,7,8,12,13,17,18-octaethylporphyrin with a combination of organolithium and alkyl iodide reagents gives conveni ent access to di-, tri-and tetra-meso-substituted porphodimethenes with dif ferent substituent patterns in a one-pot synthesis. The substituents can po ssess a variety of functional groups like -I, COOEt and CN. The reaction is stereospecific and gives the target compounds in good yields (50-80%). 5,1 5-Diarylporphyrins react: in a different manner. Upon treatment with n-buty llithium followed by addition of alkyl iodides with small residues (e.g. et hyl, cyanomethyl) they undergo a trialkylation yielding e.g. (5-butyl-5,5 ' ,15-triethyl-10,20-diphenylporphyrinato)nickel(II). Highly substituted por phodimethenes can also be prepared in one step and good yield (similar to 6 0%) using di-meso-2,3,7,8, 12,13,17,18-octa-beta -substituted porphyrins, L iR and DDQ in good yield (similar to 60%). The conformations of the synthes ized porphodimethenes were investigated via two dimensional NMR, NOE and X- ray crystallographic experiments. (C) 2001 Published by Elsevier Science Lt d.