Formation of Cationic Peptide Radicals by Gas-Phase Redox Reactions with Trivalent Chromium, Manganese, Iron, and Cobalt Complexes

• Published in: Journal of the American Chemical Society 2005-04, Vol.127 (16), p.6109-6115
• Main Authors: Barlow, Christopher K, McFadyen, W. David, O'Hair, Richard A. J
• Format: Article
• Language: English
• Subjects: Cations; Chemistry; Chromium - chemistry; Cobalt - chemistry; Ethylenediamines - chemistry; Exact sciences and technology; Free Radicals - chemistry; Gases; Iron - chemistry; Mass spectrometry; Metals, Heavy - chemistry; Oligopeptides - chemistry; Organic chemistry; Organometallic Compounds - chemistry; Oxidation-Reduction; Reactivity and mechanisms
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja043088f

The collision-induced dissociation (CID) of a series of gas-phase complexes [MIII(salen)(P)]+ [where M = Cr, Mn, Fe, and Co; P = hexapeptides YGGFLR, WGGFLR, and GGGFLR; and salen = N,N‘-ethylenebis(salicylideneaminato)] has been examined with respect to the ability of the complexes to form the corresponding cationic peptide radical ions, P+•, by homolytic cleavage of the metal peptide bond. This is the first example of the use of gas-phase ternary metal peptide complexes to produce the corresponding cationic peptide radical for a metal other than copper(II). The fragmentation reactions competing with radical formation are highly dependent on the metal ion used. In addition, examination of modified complexes in which the periphery of the salen was substituted allowed evaluation of electronic effects on the CID process, presumably without significant change in the geometry surrounding the metal. This substitution demonstrates that the ligand can be used to tune the dissociation chemistry to favor radical formation and suppress unwanted further fragmentation of the peptide radical that is typically observed immediately following its dissociation from the complex.