Catalyst‐Free Diborylation and Silaboration of Azoarenes: A Simple Photoinduced Approach

Abstract The diborylation of the N=N double bond of azoarenes has been achieved using a commercially available diboron reagent, B 2 cat 2 [bis(catecholato)diboron]. By utilizing the photo‐switchable nature of azoarenes under blue‐LED light irradiation, an uncatalyzed diborylation and silaboration yielded a broad range of functionalized hydrazine derivatives. The mechanistic origin validates the importance of cis configuration, which is corroborated by theoretical calculations.

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Publication Details

Journal
Angewandte Chemie
Published
2024-10-13
DOI
https://doi.org/10.1002/ange.202415913
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalyst‐Free Diborylation and Silaboration of Azoarenes: A Simple Photoinduced Approach

K. Geetharani, Reetu Rani Mondal, Apurba Kumar Pal
Angewandte Chemie
Organoboron and organosilicon chemistry
article

Catalyst‐Free Diborylation and Silaboration of Azoarenes: A Simple Photoinduced Approach

K. Geetharani, Reetu Rani Mondal, Apurba Kumar Pal
article en

Abstract

Abstract The diborylation of the N=N double bond of azoarenes has been achieved using a commercially available diboron reagent, B 2 cat 2 [bis(catecholato)diboron]. By utilizing the photo‐switchable nature of azoarenes under blue‐LED light irradiation, an uncatalyzed diborylation and silaboration yielded a broad range of functionalized hydrazine derivatives. The mechanistic origin validates the importance of cis configuration, which is corroborated by theoretical calculations.

Angewandte ChemieVol. 137(3)
Indian Institute of Science Bangalore (IN)
Indian Institute of Science, Ministry of Education, India, Science and Engineering Research Board
Openalex Percentile: Top 87%
Organoboron and organosilicon chemistry
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