Selective Dimerization of Lewis-Acid/Base-Stabilized Phosphanylalanes

Bodensteiner, Michael and Timoshkin, Alexey Y. and Peresypkina, Eugenia V. and Vogel, Ulf and Scheer, Manfred (2013) Selective Dimerization of Lewis-Acid/Base-Stabilized Phosphanylalanes. CHEMISTRY-A EUROPEAN JOURNAL, 19 (3). pp. 957-963. ISSN 0947-6539,

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Abstract

The reaction of [{(CO)5W}PRH2] (R=H, Ph) with H3Al.NR3 (R=Et, Me) leads to the formation of four-membered heterocyclic compounds [({(CO)5W}P(H)AlH. NEt3)2] and [({(CO)5W}PhPAlH. NMe3)2]. Upon dissolving the solid compounds, fast equilibria between the isomers are observed on the NMR timescale. Further insight into the stability and reactivity of the isomers was gained by applying theoretical methods. DFT calculations predict that hydrogen elimination in the case of [({(CO)5W}PhPAlH.NMe3)2] may be reversible.

Item Type: Article
Uncontrolled Keywords: FREE HYDROGEN ACTIVATION; PHOSPHORUS-BORON BONDS; AMMONIA-BORANE; HYDROLYTIC DEHYDROGENATION; ALUMINUM-PHOSPHORUS; CATALYZED FORMATION; CONJUGATE BASE; REACTIVITY; STORAGE; ROUTE; aluminum; density functional calculations; dimerization; isomerization; phosphorus
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie
Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Manfred Scheer
Depositing User: Dr. Gernot Deinzer
Date Deposited: 29 Apr 2020 09:27
Last Modified: 29 Apr 2020 09:27
URI: https://pred.uni-regensburg.de/id/eprint/17509

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