N-Alkylcorroles

Author:

Pizzoli Francesco1,Nardis Sara1,Fata Alessia1,Marsotto Martina1,Petrella Greta1,Fronczek Frank R.2,Smith Kevin M.2,Paolesse Roberto1

Affiliation:

1. Department of Chemical Science and Technologies, University of Rome Tor Vergata, via della Ricerca Scientifica 1, 00133 Rome, Italy

2. Department of Chemistry, Louisiana State University, Baton Rouge, LA, 70803, USA

Abstract

A series of inner core [Formula: see text]-alkylcorroles were synthesized and characterized. The introduction of both linear and branched alkyl groups was achieved, demonstrating the quite large scope of the reaction. Polyalkylation results in the formation of the [Formula: see text]-21,[Formula: see text]-22 regioisomer, although the introduction of the second alkyl group is less facile than previously observed in the case of the methyl substituent. Complete functionalization of the inner core nitrogens has been investigated, but only the N,N,N-trimethyl derivatives were obtained. The characterization of these species demonstrated a different arrangement of the methyl groups to the macrocyclic plane, which is peculiar when compared with the conformation of the analogous porphyrin derivatives. These [Formula: see text]-alkylcorroles should prove to be of potential interest as ligands for various metal ions.

Funder

Rome Technopole

Publisher

World Scientific Pub Co Pte Ltd

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