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ESI-MS studies of mixed-ligand Fe(II) complexes containing 1,10-phenanthroline and 1,10-phenanthroline-5,6-dione as ligands

✍ Scribed by Renata Kobetić; Dubravka Gembarovski; Goran Baranović; Vesna Gabelica


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
241 KB
Volume
43
Category
Article
ISSN
1076-5174

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✦ Synopsis


Abstract

In order to monitor the progression of the synthesis and the separation of novel mixed‐ligand iron complexes containing 1,10‐phenanthroline, 1,10‐phenanthroline‐5,6‐dione, and NCS^−^ as ligands all products were mass analyzed by electrospray ionization ion trap MS/MS. The spectra of methanol (MeOH), acetonitrile (ACN), water, and ethanol (EtOH) solutions were collected and the results were compared. It was detected under applied electrospray ionization mass spectrometry (ESI‐MS) conditions that MeOH, water, and EtOH formed solvent clusters around the free or complexed 1,10‐phenanthroline‐5,6‐dione. Owing to the solvent‐ligand hydrogen‐bond formation, the solvent‐ligand clusters were formed in the polar protic solvents. The number of protic solvent molecules per complex ion in cluster depended on the number of 1,10‐phenanthroline‐5,6‐dione ligands in the complex ion. Unlike MeOH, EtOH, or water, ACN was not involved in the formation of the solvent clusters with the iron complexes containing 1,10‐phenanthroline‐5,6‐dione as ligand. We also showed that the NCS^−^ group under certain solvent conditions served as a bidentate ligand. Copyright © 2008 John Wiley & Sons, Ltd.


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## Abstract Two new complexes, [Ru(phen)~2~(ppd)]^2+^ (**1**) and [Ru(phen)(ppd)~2~]^2+^ (**2**) (ppd=pteridino[6,7‐__f__] [1,10]phenanthroline‐11,13(10__H__,12__H__)‐dione, phen=1,10‐phenanthroline) were synthesized and characterized by ES‐MS, ^1^H‐NMR spectroscopy, and elemental analysis. The int