Symmetrical and unsymmetrical thiophosphoryl-thiocarbamate pincer ligands: cyclopalladation in solution and under solvent-free conditions

The modern concept of green chemistry calls for the development of more environmentally benign synthetic protocols and a reduction in the use of auxiliary substances, including solvents. In this work the effect of a thiophosphoryl pendant arm on the cyclopalladation features of both symmetrical and unsymmetrical thiocarbamate pincer ligands was explored. The ligands were 1,3-bis(carbamoyloxy)-5-(diphenylthiophosphoryl)- or 1-carbamoyloxy-3-(diphenylthiophosphoryl)benzenes, the palladium source was (PhCN)<sub>2</sub>PdCl<sub>2</sub>.

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Publication Details

Journal
Mendeleev Communications
Published
2025-01-01
DOI
https://doi.org/10.71267/mencom.7705
Citations
1
Primary Topic
Organometallic Complex Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94

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article

Symmetrical and unsymmetrical thiophosphoryl-thiocarbamate pincer ligands: cyclopalladation in solution and under solvent-free conditions

Diana V. Aleksanyan, Kozlov Va, Aleksander M. Shakhov, Yulia Vladimirovna Nelyubina et al.
1 citations
Mendeleev Communications
Organometallic Complex Synthesis and Catalysis
0.94
article

Symmetrical and unsymmetrical thiophosphoryl-thiocarbamate pincer ligands: cyclopalladation in solution and under solvent-free conditions

Diana V. Aleksanyan, Kozlov Va, Aleksander M. Shakhov, Yulia Vladimirovna Nelyubina, Zinaida S. Klemenkova, С. Е. Соловьева
article en
1 citations

Abstract

The modern concept of green chemistry calls for the development of more environmentally benign synthetic protocols and a reduction in the use of auxiliary substances, including solvents. In this work the effect of a thiophosphoryl pendant arm on the cyclopalladation features of both symmetrical and unsymmetrical thiocarbamate pincer ligands was explored. The ligands were 1,3-bis(carbamoyloxy)-5-(diphenylthiophosphoryl)- or 1-carbamoyloxy-3-(diphenylthiophosphoryl)benzenes, the palladium source was (PhCN)<sub>2</sub>PdCl<sub>2</sub>.

Mendeleev CommunicationsVol. 35(4)
Semenov Institute of Chemical Physics (RU), A. N. Nesmeyanov Institute of Organoelement Compounds (RU), N.D. Zelinsky Institute of Organic Chemistry (RU), Institute of Problems of Chemical Physics (RU)
Ministry of Education and Science of the Russian Federation, Russian Science Foundation
Openalex Percentile: Top 26%
Organometallic Complex Synthesis and Catalysis
0.94
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