Cationic Chains of Parent Arsanylboranes and Substituted Phosphanylboranes

Marquardt, Christian and Balazs, Gabor and Baumann, Josef and Virovets, Alexander V. and Scheer, Manfred (2017) Cationic Chains of Parent Arsanylboranes and Substituted Phosphanylboranes. CHEMISTRY-A EUROPEAN JOURNAL, 23 (47). pp. 11423-11429. ISSN 0947-6539, 1521-3765

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Abstract

The substituted monomeric phosphanylboranes Ph2P-BH2 center dot NMe3 (1) and tBuHP-BH2 center dot NMe3 (2) have been used for the synthesis of cationic chain compounds built up by R2P-BH2 units. With a simple synthesis route, the highly stable cations [Me3N center dot H2B-PR1R2-BH2 center dot NMe3](+) (1a, 2a) and [Me3N center dot H2B-PR1R2-BH2-PR1R2 center dot BH2 center dot NMe3]+(1b, 2b) (R 1 = R-2= Ph; R-1= H, R-2= tBu) are obtained as iodide (I-) salts. The reaction of H2As-BH2 center dot NMe3 (3) with IBH2 center dot SMe2 leads to [Me3N center dot H2B-AsH2-BH2-AsH2-BH2 center dot NMe3][ I] (3a), the longest so far known arsanylborane chain. Compound 3a reacts with acetonitrile through a formal hydroarsination reaction to form [cyclo-{As(BH2 center dot NMe3)(CMe= NH)(2)(BH2)}][I] (4). The reported synthetic strategy has proved to be a powerful tool for the formation of small, cationic oligomeric units. All products were comprehensively characterized by X-ray structure analysis, NMR, IR spectroscopy, and mass spectrometry in cooperation with DFT calculations.

Item Type: Article
Uncontrolled Keywords: CONVENIENT ROUTE; PHOSPHORUS; CHEMISTRY; DERIVATIVES; COMPLEXES; DICATIONS; BORANE; SALTS; PHOSPHANES; BONDS; arsenic; boron; cationic chains; phosphorus; pnictogenylboranes
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 13:16
Last Modified: 11 Feb 2019 14:32
URI: https://pred.uni-regensburg.de/id/eprint/1370

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