Abstract (EN):
Neutral and cationic pyrrolidine-fused chlorins and isobacteriochlorins derived from mesotetrakis(pentafluorophenyl)porphyrin undergo cycloreversion reactions in the gas phase, either when desorbed from a liquid matrix by ion bombardment or when electrosprayed. Cycloreversion occurs through loss of either neutral or charged moieties, with and without hydrogen and methyl radical migration, and both as high- and low-energy collision processes. For the doubly charged isobacteriochlorin, one-electron reduction with methyl loss occurs under ion bombardment and electrospray, through hypervalent pyrrolidinium radical formation. Copyright (C) 2004 John Wiley Sons, Ltd.
Language:
English
Type (Professor's evaluation):
Scientific
No. of pages:
11