A Convenient Route to Mixed Pnictogenylboranes

Hegen, Oliver and Marquardt, Christian and Timoshkin, Alexey Y. and Scheer, Manfred (2017) A Convenient Route to Mixed Pnictogenylboranes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 56 (41). pp. 12783-12787. ISSN 1433-7851, 1521-3773

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Abstract

We report on the synthesis and characterization of mixed pnictogenylboranes. The substitution of the Lewis base SMe2 in (OC)(5)W-PH2BH2-SMe2 (2) by different pnictogenylboranes ER2BH2-LB (E=P, As, Sb) leads to the Lewis acid/base stabilized butane analogue (OC)(5)W-PH2BH2ER2BH2-LB (3a,b: E=P; R=H, SiMe3; LB=NMe3; 4a,b: E=As; R=H, SiMe3; LB=NMe3; 5: E=Sb; R=SiMe3; LB=NHCMe). All of these compounds were characterized by single-crystal X-ray structure analysis, mass spectrometry, NMR, and IR spectroscopy. In addition, the very unstable phosphanylborane chain PH2BH2PH2BH2-NMe3 (1) was synthesized. DFT calculations provide insight into the thermodynamics of these reactions.

Item Type: Article
Uncontrolled Keywords: MOLECULAR-WEIGHT POLYAMINOBORANES; PHOSPHINE-BORANE ADDUCTS; POLYSILANE HIGH POLYMERS; AMINE-BORANES; CATALYZED DEHYDROPOLYMERIZATION; AMINOBORANE COMPLEXES; INORGANIC POLYMERS; HYDROGEN-STORAGE; CONJUGATE BASE; DEHYDROGENATION; antimony; arsenic; boron; molecular chains; phosphorus
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Manfred Scheer
Depositing User: Dr. Gernot Deinzer
Date Deposited: 14 Dec 2018 13:19
Last Modified: 11 Feb 2019 15:21
URI: https://pred.uni-regensburg.de/id/eprint/2029

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