Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities

We report here the synthesis, characterization and behavior of a series of Pt(II) cyclometalated rollover complexes with two substituted bipyridines, 6-ethyl-2,2′-bipyridine (bpy<sup>6Et</sup>) and 6-methoxy-2,2′-bipyridine (bpy<sup>6OMe</sup>), in comparison with previously...

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Main Authors: Antonio Zucca, Luca Maidich, Maria I. Pilo, Sara Pischedda, Mondina Sedda, Sergio Stoccoro
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Applied Sciences
Subjects:
Online Access:https://www.mdpi.com/2076-3417/10/19/6665
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author Antonio Zucca
Luca Maidich
Maria I. Pilo
Sara Pischedda
Mondina Sedda
Sergio Stoccoro
author_facet Antonio Zucca
Luca Maidich
Maria I. Pilo
Sara Pischedda
Mondina Sedda
Sergio Stoccoro
author_sort Antonio Zucca
collection DOAJ
description We report here the synthesis, characterization and behavior of a series of Pt(II) cyclometalated rollover complexes with two substituted bipyridines, 6-ethyl-2,2′-bipyridine (bpy<sup>6Et</sup>) and 6-methoxy-2,2′-bipyridine (bpy<sup>6OMe</sup>), in comparison with previously studied 2,2′-bipyridine complexes. The two ligands have similar steric hindrance but different electronic properties. As a result, the reactivity of the two series of complexes follows very different routes. In particular, the new complexes behave differently towards protonation reactions, differences given by substituents and ancillary ligands, added to the presence of several nucleophilic centers. Reaction of complex [Pt(bpy<sup>6OMe</sup>-H)(PPh<sub>3</sub>)Me)] with [H<sub>3</sub>O⋅18-crown-6][BF<sub>4</sub>] results in a retro-rollover reaction whose final product is the cationic adduct [Pt(bpy<sup>6OMe</sup>)(PPh<sub>3</sub>)Me)]<sup>+</sup>. Surprisingly, only the isomer with the <i>cis</i>-PPh<sub>3</sub>-OMe geometry is formed; in spite of an expected instability due to steric hindrance, Density-Functional theory (DFT) calculations showed that this isomer is the most stable. This result shows that the cone angle is far from being a real “solid cone” and should lead to a different interpretation of well-known concepts concerning steric bulk of ligands, such as cone angle. Proton affinity values of ligands, neutral complexes and their protonated counterparts were analyzed by means of DFT calculations, allowing a comparison of their properties.
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spelling doaj.art-6ea03eab3c504c4d9c5945cb4c00fddb2023-11-20T14:52:15ZengMDPI AGApplied Sciences2076-34172020-09-011019666510.3390/app10196665Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple PersonalitiesAntonio Zucca0Luca Maidich1Maria I. Pilo2Sara Pischedda3Mondina Sedda4Sergio Stoccoro5Dipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyDipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyDipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyDipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyDipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyDipartimento di Chimica e Farmacia, Università degli Studi di Sassari, via Vienna 2, 07100 Sassari, ItalyWe report here the synthesis, characterization and behavior of a series of Pt(II) cyclometalated rollover complexes with two substituted bipyridines, 6-ethyl-2,2′-bipyridine (bpy<sup>6Et</sup>) and 6-methoxy-2,2′-bipyridine (bpy<sup>6OMe</sup>), in comparison with previously studied 2,2′-bipyridine complexes. The two ligands have similar steric hindrance but different electronic properties. As a result, the reactivity of the two series of complexes follows very different routes. In particular, the new complexes behave differently towards protonation reactions, differences given by substituents and ancillary ligands, added to the presence of several nucleophilic centers. Reaction of complex [Pt(bpy<sup>6OMe</sup>-H)(PPh<sub>3</sub>)Me)] with [H<sub>3</sub>O⋅18-crown-6][BF<sub>4</sub>] results in a retro-rollover reaction whose final product is the cationic adduct [Pt(bpy<sup>6OMe</sup>)(PPh<sub>3</sub>)Me)]<sup>+</sup>. Surprisingly, only the isomer with the <i>cis</i>-PPh<sub>3</sub>-OMe geometry is formed; in spite of an expected instability due to steric hindrance, Density-Functional theory (DFT) calculations showed that this isomer is the most stable. This result shows that the cone angle is far from being a real “solid cone” and should lead to a different interpretation of well-known concepts concerning steric bulk of ligands, such as cone angle. Proton affinity values of ligands, neutral complexes and their protonated counterparts were analyzed by means of DFT calculations, allowing a comparison of their properties.https://www.mdpi.com/2076-3417/10/19/6665cyclometalated compoundsrollover cyclometalationbipyridines
spellingShingle Antonio Zucca
Luca Maidich
Maria I. Pilo
Sara Pischedda
Mondina Sedda
Sergio Stoccoro
Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
Applied Sciences
cyclometalated compounds
rollover cyclometalation
bipyridines
title Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
title_full Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
title_fullStr Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
title_full_unstemmed Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
title_short Pt(II) Derivatives with Rollover-Coordinated 6-substituted 2,2′-bipyridines: Ligands with Multiple Personalities
title_sort pt ii derivatives with rollover coordinated 6 substituted 2 2 bipyridines ligands with multiple personalities
topic cyclometalated compounds
rollover cyclometalation
bipyridines
url https://www.mdpi.com/2076-3417/10/19/6665
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