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- W4317568944 abstract "A series of three closely related unsymmetrical pincer ligands featuring thione sulfur donors have been derived from m-thiophosphorylated phenyl isothiocyanate to probe the effect of a spectator heteroatom in the flanking ring on their direct cyclopalladation. The reaction efficiency is shown to drastically increase on passing from a thionated thiazolidinone derivative to its oxazolidinone analog, and further to an imidazolidinone ligand. The investigations by IR and NMR spectroscopy as well as X-ray diffraction confirmed the realization of S,C,S'-type pincer coordination but did not reveal considerable differences in the molecular structures of the Pd(II) complexes obtained; however, the results of DFT calculations provided some valuable insights into the peculiarities of their formation. In addition, the possibility of solid-phase synthesis of the target pincer complexes upon thermally induced CH activation has been demonstrated. This methodology does not afford a significant yield enhancement over the conventional solution-based technique but appears to be highly advantageous in terms of the absence of a solvent at the synthesis step and reaction time." @default.
- W4317568944 created "2023-01-21" @default.
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- W4317568944 date "2023-03-01" @default.
- W4317568944 modified "2023-10-16" @default.
- W4317568944 title "Experimental and computational insights into the direct cyclopalladation of different unsymmetrical, yet closely related pincer ligands with thione sulfur donors" @default.
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- W4317568944 doi "https://doi.org/10.1016/j.poly.2023.116303" @default.
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