Cyclometalated C^C* Platinum(IV) NHC Complexes

We present a previously unknown series of cyclometalated platinum(IV) NHC complexes, obtained by oxidative addition of iodine, iodomethane, and different benzyl bromides to platinum(II) complexes with cyclometalated C^C* dibenzofuran, dibenzothiophene, and phenylimidazole ligands together with an acetylacetonate ligand. All compounds were characterized by standard techniques (<sup>1</sup>H, <sup>13</sup>C, and <sup>195</sup>Pt NMR and elemental analysis), and for three complexes, solid-state structures could be obtained. DFT calculations (B3LYP(d3)/def2-TZVPP including dispersion interactions in dichloromethane and acetone) were performed to investigate the mechanism of the oxidation and explain the exclusive formation of the observed <i>trans</i> products.

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Publication Details

Journal
Inorganic Chemistry
Published
2024-09-09
DOI
https://doi.org/10.1021/acs.inorgchem.4c01608
Citations
2
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
0.50
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article

Cyclometalated C^C* Platinum(IV) NHC Complexes

Tim Riesebeck, Alexander Tronnier, Thomas Straßner
2 citations
Inorganic Chemistry
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
0.50
article

Cyclometalated C^C* Platinum(IV) NHC Complexes

Tim Riesebeck, Alexander Tronnier, Thomas Straßner
article en
2 citations

Abstract

We present a previously unknown series of cyclometalated platinum(IV) NHC complexes, obtained by oxidative addition of iodine, iodomethane, and different benzyl bromides to platinum(II) complexes with cyclometalated C^C* dibenzofuran, dibenzothiophene, and phenylimidazole ligands together with an acetylacetonate ligand. All compounds were characterized by standard techniques (<sup>1</sup>H, <sup>13</sup>C, and <sup>195</sup>Pt NMR and elemental analysis), and for three complexes, solid-state structures could be obtained. DFT calculations (B3LYP(d3)/def2-TZVPP including dispersion interactions in dichloromethane and acetone) were performed to investigate the mechanism of the oxidation and explain the exclusive formation of the observed <i>trans</i> products.

Inorganic ChemistryVol. 63(38)
Technische Universität Dresden (DE)
Openalex Percentile: Top 39%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
0.50
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