The Lewis Base Stabilized Parent Arsanylborane H 2 AsBH 2 ⋅NMe 3 | Zendy

Marquardt Christian | Zendy; Adolf Ariane | Zendy; Stauber Andreas | Zendy; Bodensteiner Michael | Zendy; Virovets Alexander V. | Zendy; Timoshkin Alexey Y. | Zendy; Scheer Manfred | Zendy

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The Lewis Base Stabilized Parent Arsanylborane H 2 AsBH 2 ⋅NMe 3

Author(s) -

Marquardt Christian,

Adolf Ariane,

Stauber Andreas,

Bodensteiner Michael,

Virovets Alexander V.,

Timoshkin Alexey Y.,

Scheer Manfred

Publication year - 2013

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.201302110

Subject(s) - reactivity (psychology) , monomer , lewis acids and bases , yield (engineering) , base (topology) , computer science , service (business) , chemistry , database , organic chemistry , mathematics , materials science , business , catalysis , medicine , mathematical analysis , alternative medicine , pathology , marketing , polymer , metallurgy

Exclusively hydrogen‐substituted arsanylboranes : The synthesis of the unprecedented Lewis base stabilized monomeric parent compound of the arsanylborane H 2 AsBH 2 ⋅ NMe 3 was achieved in a one‐pot reaction in high yield and purity. The analogous phosphanylborane was synthesized in a similar manner. A series of different reactions was performed on H 2 AsBH 2 ⋅ NMe 3 to show its broad reactivity pattern.

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