Synthesis of diamido N-heterocyclic imines (DAC = NH) via staudinger or reductive N-N bond cleavage approach

TitleSynthesis of diamido N-heterocyclic imines (DAC = NH) via staudinger or reductive N-N bond cleavage approach
Publication TypeJournal Article
Year of Publication2025
AuthorsBalayan, K, Sharma, H, Vanka, K, Gonnade, RG, Sen, SS
JournalOrganometallics
Volume44
Issue11
Pagination1129-1133
Date PublishedMAY
Type of ArticleArticle
ISSN0276-7333
Abstract

This report communicates the first examples of N-heterocyclic imines based on electrophilic diamido carbenes (DACs). While 2 is prepared by classical Staudinger synthesis, 4 is obtained via an unusual reductive N-N bond cleavage of an azine by HCl. The exocyclic C=N bond lengths in 2 and 4 are substantially shorter than those based on N-heterocyclic carbenes and cyclic (alkyl)(amino)carbene reflecting the electrophilic character of DACs.

DOI10.1021/acs.organomet.5c00120
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

2.7

Divison category: 
Catalysis and Inorganic Chemistry
Physical and Materials Chemistry
Database: 
Web of Science (WoS)

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