Regiodivergent metal-catalyzed B(4)- and C(1)-selenylation of -carboranes

Regiodivergent transition metal-catalyzed B(4)- and C(1)-selenylation reactions of o -carboranes have been demonstrated. Namely, Ru( ii )-catalysis selectively generated B(4)-selenylated o -carboranes from the reaction of o -carborane acids with arylselenyl bromides with the release of carbon dioxid...

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Published inChemical science (Cambridge) Vol. 14; no. 3; pp. 643 - 649
Main Authors Lee, Kyungsup, Harper, Jordan L, Kim, Tae Hyeon, Chan Noh, Hee, Kim, Dongwook, Ha-Yeon Cheong, Paul, Lee, Phil Ho
Format Journal Article
Published 18.01.2023
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Summary:Regiodivergent transition metal-catalyzed B(4)- and C(1)-selenylation reactions of o -carboranes have been demonstrated. Namely, Ru( ii )-catalysis selectively generated B(4)-selenylated o -carboranes from the reaction of o -carborane acids with arylselenyl bromides with the release of carbon dioxide. In contrast, Pd( ii ) catalysis provided exclusively C(1)-selenylated o -carboranes from the decarboxylative reaction of o -carborane acids with diaryl diselenides. In contrast to previous milestones in this area, these reactions demonstrate broad substrate scope with excellent yields. Combination of these methods leads to the formation of B(4)-C(1)-diselenylated o -carboranes. DFT studies revealed the mechanism of the Ru-process, with initial selenylation of the carborane cluster discovered to be essential for an energetically reasonable decarboxylation. This results in selenylation on the B(4) position prior to the decarboxylation event at C(1). This contrasted with the Pd-process in which the ready decarboxylation at C(1) leads to selenylation at C(1). Regiodivergent transition metal-catalyzed B(4)- and C(1)-selenylation reactions of o -carboranes have been demonstrated.
Bibliography:https://doi.org/10.1039/d2sc05590b
Electronic supplementary information (ESI) available. See DOI
ISSN:2041-6520
2041-6539
DOI:10.1039/d2sc05590b