Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/348889
Type: Artigo
Title: Exploring the coordination chemistry of isomerizable terpyridine derivatives for successful analyses of cis and trans isomers by travelling wave ion mobility mass spectrometry
Author: Santos, Jonnatan J.
Toma, Sergio H.
Lalli, Priscila M.
Riccio, Maria F.
Eberlin, Marcos N.
Toma, Henrique E.
Araki, Koiti
Abstract: The photochemical cis–trans isomerization of the 4-{4-[2-(pyridin-4-yl)ethenyl]phenyl}-2,2′:6′,2′′-terpyridine ligand (vpytpy) was investigated by UV-vis, NMR and TWIM-MS. Ion mobility mass spectrometry was performed pursuing the quantification of the isomeric composition during photolysis, however an in-source trans-to-cis isomerization process was observed. In order to overcome this inherent phenomenon, the isomerization of the vpytpy species was suppressed by complexation, reacting with iron(II) ions, and forming the [Fe(vpytpy)2]2+ complex. The strategy of “freezing” the cis–trans isomerizable ligand at a given geometric conformation was effective, preventing further isomerization, thus allowing the distinction of each one of the isomers in the photolysed mixture. In addition, the experimental drift times were related to the calculated surface areas of the three possible cis–cis, cis–trans and trans–trans iron(II) complex isomers. The stabilization of the ligand in a given conformation also allows us to obtain the cis–cis and cis–trans complexes exhibiting the ligand in the metastable cis-conformation, as well as in the thermodynamically stable trans-conformation
Subject: Espectrometria de massa
Country: Reino Unido
Editor: Royal Society of Chemistry
Rights: Fechado
Identifier DOI: 10.1039/c2an35320b
Address: https://pubs.rsc.org/en/content/articlelanding/2012/AN/c2an35320b
Date Issue: 2012
Appears in Collections:IQ - Artigos e Outros Documentos

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