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Reactivity of a Dihydrodiborene with CO: Coordination, Insertion, Cleavage and Spontaneous Cyclic Alkyne Formation

Please always quote using this URN: urn:nbn:de:bvb:20-opus-153318
  • Under a CO atmosphere the dihydrodiborene [(cAAC)HB=BH(cAAC)] underwent coordination of CO concomitant with reversible hydrogen migration from boron to the carbene carbon atom, as well as reversible CO insertion into the B=B bond. Heating of the CO-adduct resulted in two unusual cAAC ring-expansion products, one presenting a B=C bond to a six-membered 1,2-azaborinane-3-ylidene, the other an unprecedented nine-membered cyclic alkyne resulting from reductive cleavage of CO and spontaneous C≡C triple bond formation.

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Metadaten
Author: Merle Arrowsmith, Julian Böhnke, Holger BraunschweigORCiD, Mehmet Ali Celik
URN:urn:nbn:de:bvb:20-opus-153318
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:2017
Source:Angewandte Chemie Intnational Edition 10.1002/anie.201707907
DOI:https://doi.org/10.1002/anie.201707907
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 546 Anorganische Chemie
Tag:CO activation; cyclic (alkyl)(amino)carbene; diborene; insertion; ring expansion
Release Date:2017/10/02
EU-Project number / Contract (GA) number:669054
OpenAIRE:OpenAIRE
Note:
This is the pre-peer reviewed version of the following article: Arrowsmith, M., Böhnke, J., Braunschweig, H. and Celik, M., Reactivity of a Dihydrodiborene with CO: Coordination, Insertion, Cleavage and Spontaneous Cyclic Alkyne Formation. Angew. Chem. Int. Ed. 2017, 129,14475 –14480. Accepted Author Manuscript. doi:10.1002/anie.201707907. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Licence (German):License LogoDeutsches Urheberrecht