Exploring the Coordination Properties of Phosphonium‐Functionalized N‐Heterocyclic Carbenes Towards Gold

Author:

De Marco Riccardo12,Giuso Valerio2,Achard Thierry2,Rancan Marzio3,Baron Marco1,Armelao Lidia14,Mauro Matteo2,Bellemin‐Laponnaz Stéphane2,Tubaro Cristina13ORCID

Affiliation:

1. Dipartimento di Scienze Chimiche Università degli Studi di Padova Via Marzolo 1 35131 Padova Italy

2. Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS) Université de Strasbourg – CNRS UMR7504 23 rue du Loess, BP43 67034 Strasbourg Cedex2 France

3. ICMATE National Research Council (CNR) Via Marzolo 1 35131 Padova Italy

4. Department of Chemical Sciences and Materials Technologies (DSCTM) National Research Council (CNR) Piazzale A. Moro 7 Roma 00185 Italy

Abstract

AbstractGold(I) complexes with N‐heterocyclic carbene ligands functionalized with a pendant phosphonium moiety were synthesized by simple procedures. In particular, the simple addition of LiBr salt in the reaction media allows the formation of the NHC gold(I) mononuclear complexes, whilst in the absence of excess bromide ions the deprotonation of the methylene group in alpha position to the phosphonium group occurs, allowing the isolation of the dinuclear complexes with two C,C‐bridging NHC‐phosphonium ylide ligands. The complexes were characterized in solution with NMR spectroscopy and ESI‐MS spectrometry, as well as in the solid state by means of single crystal X‐ray diffraction analysis. Mononuclear gold(III) species were also isolated by Br2 oxidative addition to the mononuclear gold(I) species and fully characterized. Preliminary results of the biological effects on MCF7 cancer cells are also reported.

Funder

Dipartimento di Scienze Chimiche, Università degli Studi di Padova

Publisher

Wiley

Subject

Inorganic Chemistry

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