Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity

A series of dibromo-N-acyclic (NAC) carbene complexes of platinum(II) were synthesized, starting from <i>trans-</i>[Pt(μ-Br)Br(PPh<sub>3</sub>)]<sub>2</sub> and according to a protocol previously optimized for the preparation of analogous chlorinated compounds. In...

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Main Authors: Anna Farasat, Francesca Nerli, Luca Labella, Marco Taddei, Simona Samaritani
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Inorganics
Subjects:
Online Access:https://www.mdpi.com/2304-6740/11/4/137
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author Anna Farasat
Francesca Nerli
Luca Labella
Marco Taddei
Simona Samaritani
author_facet Anna Farasat
Francesca Nerli
Luca Labella
Marco Taddei
Simona Samaritani
author_sort Anna Farasat
collection DOAJ
description A series of dibromo-N-acyclic (NAC) carbene complexes of platinum(II) were synthesized, starting from <i>trans-</i>[Pt(μ-Br)Br(PPh<sub>3</sub>)]<sub>2</sub> and according to a protocol previously optimized for the preparation of analogous chlorinated compounds. In the first step of the synthesis, the ring opening of the dinuclear precursor was carried out using suitable isonitrile ligands, while the following step consisted of the addition of <i>N</i>,<i>N</i>-diethylamine to the products obtained in the first step. The two reactions were separately investigated, and attention was given to the differences between brominated and chlorinated systems.
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spelling doaj.art-62ae03d1ade94ed681760290c416a68c2023-11-17T19:45:07ZengMDPI AGInorganics2304-67402023-03-0111413710.3390/inorganics11040137Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and ReactivityAnna Farasat0Francesca Nerli1Luca Labella2Marco Taddei3Simona Samaritani4Department of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, ItalyDepartment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, ItalyDepartment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, ItalyDepartment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, ItalyDepartment of Chemistry and Industrial Chemistry, University of Pisa, Via Giuseppe Moruzzi 13, 56124 Pisa, ItalyA series of dibromo-N-acyclic (NAC) carbene complexes of platinum(II) were synthesized, starting from <i>trans-</i>[Pt(μ-Br)Br(PPh<sub>3</sub>)]<sub>2</sub> and according to a protocol previously optimized for the preparation of analogous chlorinated compounds. In the first step of the synthesis, the ring opening of the dinuclear precursor was carried out using suitable isonitrile ligands, while the following step consisted of the addition of <i>N</i>,<i>N</i>-diethylamine to the products obtained in the first step. The two reactions were separately investigated, and attention was given to the differences between brominated and chlorinated systems.https://www.mdpi.com/2304-6740/11/4/137platinum(II) bromocomplexesisocyanide ligandscarbene ligandstriphenylphosphine
spellingShingle Anna Farasat
Francesca Nerli
Luca Labella
Marco Taddei
Simona Samaritani
Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
Inorganics
platinum(II) bromocomplexes
isocyanide ligands
carbene ligands
triphenylphosphine
title Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
title_full Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
title_fullStr Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
title_full_unstemmed Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
title_short Dibromo–Isonitrile and N-acyclic Carbene Complexes of Platinum(II): Synthesis and Reactivity
title_sort dibromo isonitrile and n acyclic carbene complexes of platinum ii synthesis and reactivity
topic platinum(II) bromocomplexes
isocyanide ligands
carbene ligands
triphenylphosphine
url https://www.mdpi.com/2304-6740/11/4/137
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