Electrospray ionization study of tricarbonyl fac-[Re(CO) 3 (PO)(X)]-type complexes: influence of ancillary co-ligands in the release of carbon monoxide.

Autor: Tisato F; CNR - ICMATE, Corso Stati Uniti 4, 35127, Padova, Italy.; School of Science and Technology, Chemistry Division, CNR - ICCOM - URT Camerino, via S. Agostino n.1, I-62032, Camerino, Italy., Porchia M; CNR - ICMATE, Corso Stati Uniti 4, 35127, Padova, Italy., Shegani A; INRaSTES, NCSR 'Demokritos', 15310 Ag. Paraskevi Attikis, Athens, Greece., Maina T; INRaSTES, NCSR 'Demokritos', 15310 Ag. Paraskevi Attikis, Athens, Greece., Papadopoulos MS; INRaSTES, NCSR 'Demokritos', 15310 Ag. Paraskevi Attikis, Athens, Greece., Seraglia R; CNR - ICMATE, Corso Stati Uniti 4, 35127, Padova, Italy., Traldi P; IRPCDS, Corso Stati Uniti 4, 35127, Padova, Italy.
Jazyk: angličtina
Zdroj: Rapid communications in mass spectrometry : RCM [Rapid Commun Mass Spectrom] 2018 Aug 15; Vol. 32 (15), pp. 1199-1206.
DOI: 10.1002/rcm.8162
Abstrakt: Rationale: fac-[Re(CO) 3 (PO)(X)]-type complexes (PO = chelated bidentate tertiary phosphine (1-), X = various neutral, mono-dentate ligands) represent a class of compounds that meets the synthetic criteria for the preparation of potential carbon monoxide (CO) release molecules (CORMs) for medicinal application. The aim of our investigation was to achieve qualitative information whether the nature of the ancillary X ligand might influence the release of CO.
Methods: The release of CO has been investigated by means of product ion spectrometry of electrospray ionization (ESI)-generated [M + H] + species, produced by multiple collisional experiments, using an ion trap mass spectrometer.
Results: Tandem mass spectrometry applied to the protonated species [Re(CO) 3 (PO)(X) + H] + of seven complexes (those including X = OH 2 (1), isonitrile (2, 3), imidazole (4), pyridine (5) and phosphine (6, 7)) shows initial loss of coordinated water (1) or pyridine (5), whereas the majority of investigated entries display initial, sequential release of CO groups. The energetics of CO release have been investigated by breakdown curves for selected collisionally activated decomposition processes involving CO, and compared with those involving X groups.
Conclusions: The nature of the co-ligand X drives the primary loss in the MS n processes of [Re(CO) 3 (PO)(X) + H] + compounds. When X = solvent, the energetics of these decompositions follow the trend H 2 O < MeOH < CO. In each case, loss of CO is a favored fragmentation route with associated energies following the trend: N-py ≤ P-phosphine < C-isonitrile. Overall, MS n pathways indicate that [Re(PO)] (Re with chelated PO phosphine) constitutes the residual moiety. This behavior indicates that the presence of a functionalized phosphine is essential for a sequential, controlled release of CO.
(Copyright © 2018 John Wiley & Sons, Ltd.)
Databáze: MEDLINE
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