Access to Unsupported Iminobismuthane and Tetraazabismole Species Enabled by a Rigid and Bulky Organobismuthinidene

ABSTRACT Herein, we report the reactivity of a monocoordinate bismuthinidene ( 1 ) with various organic azides. The reaction of 1 with p ‐toluenesulfonyl azide resulted in the formation of an unprecedented, unsupported iminobismuthane ( 2 ), which features the shortest reported Bi–N distance of 2.041(3) Å in an iminobismuthane. Conversely, the reaction of 1 with 4‐azidobiphenyl resulted in the first example of a species containing a tetraazabismole (BiN 4 ) heterocycle ( 3 ). We also highlight that 1 demonstrates catalytic activity, enabling the reduction of a selection of organic azides.

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Publication Details

Journal
Angewandte Chemie
Published
2026-09-18
DOI
https://doi.org/10.1002/ange.2998568
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
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Access to Unsupported Iminobismuthane and Tetraazabismole Species Enabled by a Rigid and Bulky Organobismuthinidene

Maurice van Gastel, Kristian L. Mears, Serena DeBeer, Josep Cornellà et al.
Angewandte Chemie
Synthesis and characterization of novel inorganic/organometallic compounds
article

Access to Unsupported Iminobismuthane and Tetraazabismole Species Enabled by a Rigid and Bulky Organobismuthinidene

Maurice van Gastel, Kristian L. Mears, Serena DeBeer, Josep Cornellà, Gabriele Deplano, Khai‐Nghi Truong, Davide Spinnato, Markus Leutzsch, Marcel Potocnik, Nils Nöthling
article en

Abstract

ABSTRACT Herein, we report the reactivity of a monocoordinate bismuthinidene ( 1 ) with various organic azides. The reaction of 1 with p ‐toluenesulfonyl azide resulted in the formation of an unprecedented, unsupported iminobismuthane ( 2 ), which features the shortest reported Bi–N distance of 2.041(3) Å in an iminobismuthane. Conversely, the reaction of 1 with 4‐azidobiphenyl resulted in the first example of a species containing a tetraazabismole (BiN 4 ) heterocycle ( 3 ). We also highlight that 1 demonstrates catalytic activity, enabling the reduction of a selection of organic azides.

Angewandte Chemie
Max-Planck-Institut für Kohlenforschung (DE), Toray International Europe (Germany) (DE), Max Planck Institute for Chemical Energy Conversion (DE)
Life below water
Openalex Percentile: Top 25%
Synthesis and characterization of novel inorganic/organometallic compounds
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Access to Unsupported Iminobismuthane and Tetraazabismole Species Enabled by a Rigid and Bulky Organobismuthinidene — Maurice van Gastel, Kristian L. Mears, et al. · Angewandte Chemie (2026) | TGRS Research Map | TGRS