Solid-Phase Cyclopalladation of Bis(thioamide) Pincer Ligands Based on m-Phenylenediamine

In recent years, the trend towards developing more efficient and green approaches to the synthesis of chemical compounds has engulfed new areas of chemistry, including organometallic synthesis. In this work, the peculiarities of direct cyclopalladation of m-phenylenediamine-based bis(thioamide) ligands are studied both in solution and in the absence of a solvent in order to estimate the possibility of obtaining target Pd(II) pincer complexes using a more ecologically friendly methodology.

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Publication Details

Journal
Russian Journal of Coordination Chemistry
Published
2025-03-01
DOI
https://doi.org/10.1134/s1070328424601535
Primary Topic
Synthesis and Catalytic Reactions
Type
article
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article

Solid-Phase Cyclopalladation of Bis(thioamide) Pincer Ligands Based on m-Phenylenediamine

Diana V. Aleksanyan, Yulia Vladimirovna Nelyubina, Zinaida S. Klemenkova, V. A. Kozlov
Russian Journal of Coordination Chemistry
Synthesis and Catalytic Reactions
article

Solid-Phase Cyclopalladation of Bis(thioamide) Pincer Ligands Based on m-Phenylenediamine

Diana V. Aleksanyan, Yulia Vladimirovna Nelyubina, Zinaida S. Klemenkova, V. A. Kozlov
article en

Abstract

In recent years, the trend towards developing more efficient and green approaches to the synthesis of chemical compounds has engulfed new areas of chemistry, including organometallic synthesis. In this work, the peculiarities of direct cyclopalladation of m-phenylenediamine-based bis(thioamide) ligands are studied both in solution and in the absence of a solvent in order to estimate the possibility of obtaining target Pd(II) pincer complexes using a more ecologically friendly methodology.

Russian Journal of Coordination ChemistryVol. 51(3)
A. N. Nesmeyanov Institute of Organoelement Compounds (RU), Institute of Problems of Chemical Physics (RU)
Clean water and sanitation
Openalex Percentile: Top 90%
Synthesis and Catalytic Reactions
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