| Literature DB >> 11672072 |
David A. Shultz1, Kevin P. Gwaltney, Hyoyoung Lee.
Abstract
The syntheses and fluid-solution EPR spectra of nitroxide-substituted porphyrins 1-3 are described. The phenylnitroxide is attached to the meso-position of three porphyrins: (a) directly through a single bond (1); (b) through an ethenyl group (2); and (c) through an ethynyl group (3). The spin distribution in each of the three radicals is discussed and compared to model compounds 4-9. It is suggested that delocalization increases in the order 2, 1, 3.Entities:
Year: 1998 PMID: 11672072 DOI: 10.1021/jo971736q
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354