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Construction of Linear and Branched Tetraboranes via 1,1- and 1,2-Diboration of Diborenes

Please always quote using this URN: urn:nbn:de:bvb:20-opus-178276
  • Sterically unencumbered diborenes based on a benzylphosphine chelate undergo diboration reactions with bis(catecholato)diboron in the absence of a catalyst to yield tetraboranes. The symmetrical diborenes studied undergo 1,2- diborations, whereas an unsymmetrical derivative was found to yield a triborylborane-phosphine adduct as the result of a formal 1,1-diboration. A related borylborylene compound also underwent a 1,2-diboration to produce a borylene-borane adduct.

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Metadaten
Author: Tom Stennett, Rüdiger Bertermann, Holger BraunschweigORCiD
URN:urn:nbn:de:bvb:20-opus-178276
Document Type:Preprint
Faculties:Fakultät für Chemie und Pharmazie / Institut für Anorganische Chemie
Language:English
Parent Title (English):Angewandte Chemie, International Edition
Year of Completion:2018
Source:Angewandte Chemie International Edition 2018, 57, 15896-15901 https://doi.org/10.1002/anie.201809976
DOI:https://doi.org/10.1002/anie.201809976
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 546 Anorganische Chemie
Tag:boron; chain structures; diboration; isomers; low-valent compounds
Release Date:2019/03/19
EU-Project number / Contract (GA) number:669054
OpenAIRE:OpenAIRE
Note:
This is the pre-peer reviewed version of the following article: T. E. Stennett, R. Bertermann, H. Braunschweig, Angew. Chem. Int. Ed. 2018, 57, 15896., which has been published in final form at https://doi.org/10.1002/anie.201809976. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Licence (German):License LogoDeutsches Urheberrecht