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Reactivity study of Lewis superacidic carborane-based analogue of 9-bromo-9-borafluorene towards Lewis bases.
Xiang, Libo; Matler, Alexander; Tan, Leibo; Ye, Qing.
Affiliation
  • Xiang L; Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. qing.ye@uni-wuerzburg.de.
  • Matler A; Institute for Sustainable Chemistry& Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.
  • Tan L; Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. qing.ye@uni-wuerzburg.de.
  • Ye Q; Institute for Sustainable Chemistry& Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany.
Dalton Trans ; 53(28): 11655-11658, 2024 Jul 16.
Article in En | MEDLINE | ID: mdl-38946218
ABSTRACT
In this contribution, we present the reactions of the o-carborane-based analogue of 9-bromo-9-borafluorene, a Lewis superacid, with diverse Lewis bases. A range of acid-base adducts, along with an intramolecular C-H activation product, were generated. All new compounds have been fully characterized.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: Germany