Synthesis of mesoionic carbene-triazole-based Pd(ii) complex: promoting C–H activation toward N-aryl carbazoles

Abstract

Here, we report a triazolylidene-based mesoionic carbene (MIC) Pd(II) complex as an efficient catalyst for the synthesis of N-aryl carbazoles via an intermolecular C–H amination reaction. The developed system shows high catalytic activity without phosphorus-based additives and delivers diverse carbazole derivatives in good to excellent yields. Further, these N-aryl carbazoles can be post-functionalized at the C1 selective position, including nitration with AgNO3 (4a) and chalcogenation with disulfides and diselenides (5a). The molecular structure of the Pd–MIC complex was confirmed by X-ray crystallography. Further, several control experiments were performed to support the proposed plausible catalytic pathway.

Graphical abstract: Synthesis of mesoionic carbene-triazole-based Pd(ii) complex: promoting C–H activation toward N-aryl carbazoles

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Article information

Article type
Paper
Submitted
06 Mar 2026
Accepted
18 May 2026
First published
19 May 2026

Org. Biomol. Chem., 2026, Advance Article

Synthesis of mesoionic carbene-triazole-based Pd(II) complex: promoting C–H activation toward N-aryl carbazoles

P. S. Gahlaut, B. Shekhawat, P. Lama and B. Jana, Org. Biomol. Chem., 2026, Advance Article , DOI: 10.1039/D6OB00378H

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