ESI‐MS/MS of expanded porphyrins: a look into their structure and aromaticity. (25th April 2016)

• Record Type: Journal Article
• Authors: Ramos, Catarina IV; Figueira, Flávio; Polêto, Marcelo D; Amado, Francisco ML; Verli, Hugo; Tomé, João PC; Neves, M Graça PMS
• Is Part Of: Journal of mass spectrometry. Volume 51:Number 5(2016)
• Page Start: 342
• Page End: 349
• Publication Date: 2016-04-25
• Subjects: protonated expanded porphyrins -- electrospray mass spectrometry -- gas‐phase -- structure/aromaticity -- Hückel systems -- Möbius systems; Mass spectrometry -- Periodicals; 543.65
• DOI: 10.1002/jms.3760
• Languages: English
• ISSNs: 1076-5174

Abstract

Abstract : Electrospray mass spectrometry/mass spectrometry was used to investigate the gas‐phase properties of protonated expanded porphyrins, in order to correlate those with their structure and conformation. We have selected five expanded meso ‐pentafluorophenyl porphyrins, respectively, a pair of oxidized/reduced fused pentaphyrins (22 and 24 π electrons), a pair of oxidized/reduced regular hexaphyrins (26 and 28 π electrons) and a regular doubly N‐ fused hexaphyrin (28 π electrons). The gas‐phase behavior of the protonated species of oxidized and reduced expanded porphyrins is different. The oxidized species (aromatic Hückel systems) fragment more extensively, mainly by the loss of two HF molecules. The reduced species (Möbius aromatic or Möbius‐like aromatic systems) fragment less than their oxidized counterparts because of their increased flexibility. The protonated regular doubly fused hexaphyrin (non‐aromatic Hückel system) shows the least fragmentation even at higher collision energies. In general, cyclization through losses of HF molecules decreases from the aromatic Hückel systems to Möbius aromatic or Möbius‐like aromatic systems to non‐aromatic Hückel systems and is related to an increase in conformational distortion. Copyright © 2016 John Wiley & Sons, Ltd.