Mimics of Pincer Ligands: An Accessible Phosphine-Free N‑(Pyrimidin-2-yl)-1,2-azole-3-carboxamide Framework for Binuclear Pd(II) Complexes and High-Turnover Catalysis in Water

We report for the first time cyclic phosphine-free “head to tail” N,N,N pincer-like (pincer complexes mimicking) N-(pyrimidin-2-yl)-1,2-azole-3-carboxamide Pd­(II) complexes with deprotonated amide groups as high-turnover catalysts (TON up to 106, TOF up to 1.2 × 107 h–1) for cross-coupling reaction...

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Bibliographic Details
Published in:Inorganic chemistry 2020-08, Vol.59 (15), p.10384-10388
Main Authors: Kletskov, Alexey V, Bumagin, Nikolay A, Petkevich, Sergey K, Dikusar, Evgenij A, Lyakhov, Alexander S, Ivashkevich, Ludmila S, Kolesnik, Iryna A, Potkin, Vladimir I
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Language:English
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Summary:We report for the first time cyclic phosphine-free “head to tail” N,N,N pincer-like (pincer complexes mimicking) N-(pyrimidin-2-yl)-1,2-azole-3-carboxamide Pd­(II) complexes with deprotonated amide groups as high-turnover catalysts (TON up to 106, TOF up to 1.2 × 107 h–1) for cross-coupling reactions on the background of up to quantitative yields under Green Chemistry conditions. The potency of the described catalyst family representatives was demonstrated in Suzuki–Miyaura, Mizoroki–Heck, and Sonogashira reactions on industrially practical examples. Corresponding ligands could be synthesized based on readily available reagents through simple chemical transformations. Within the complex structures, a highly unusual 1,3,5,7-tetraza-2,6-dipalladocane frame could be observed.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.0c01035