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trans-Selective Insertional Dihydroboration of a cis-Diborene: Synthesis of Linear sp\(^3\)-sp\(^2\)-sp\(^3\)-Triboranes and Subsequent Cationization

Please always quote using this URN: urn:nbn:de:bvb:20-opus-208090
  • The reaction of aryl‐ and amino(dihydro)boranes with dibora[2]ferrocenophane 1 leads to the formation 1,3‐trans ‐dihydrotriboranes by formal hydrogenation and insertion of a borylene unit into the B=B bond. The aryltriborane derivatives undergo reversible photoisomerization to the cis ‐1,2‐μ‐H‐3‐hydrotriboranes, while hydride abstraction affords cationic triboranes, which represent the first doubly base‐stabilized B3H4\(^+\) analogues.

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Metadaten
Author: Uwe Schmidt, Luis Werner, Merle Arrowsmith, Andrea Deissenberger, Alexander Hermann, Alexander Hofmann, Stefan Ullrich, James D. Mattock, Alfredo Vargas, Holger BraunschweigORCiD
URN:urn:nbn:de:bvb:20-opus-208090
Document Type:Journal article
Faculties:Fakultät für Chemie und Pharmazie / Institut für Anorganische Chemie
Language:English
Parent Title (English):Angewandte Chemie International Edition
Year of Completion:2020
Volume:59
Issue:1
Pagenumber:325-329
Source:Angewandte Chemie International Edition 2020, 59(1), 325–329. DOI: 10.1002/anie.201911645
DOI:https://doi.org/10.1002/anie.201911645
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 546 Anorganische Chemie
Tag:diborenes
cations; hydroboration; photoisomerization; triboranes
Release Date:2020/09/21
EU-Project number / Contract (GA) number:669054
OpenAIRE:OpenAIRE
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International