Fluorination Effects in XPhos Gold(I) Fluorothiolates

Abstract

Gold phosphine derivatives such as thiolates have been recently proposed as catalysts or catalyst precursors. The relevance of the supramolecular environment on the fine-tuning of the catalytical activity on these compounds incentivizes the use of tools that are convenient to characterize in detail the non-covalent landscape of the systems. Herein, we show the molecular and supramolecular diversity caused by the changes in the fluorination pattern in a family of new XPhos goldfluorothiolate derivatives. Furthermore, we studied the supramolecular interactions around the Au centers using quantum chemical topology tools, in particular the quantum theory of atoms in molecules (QTAIM) and the non-covalent interaction index. Our results give detailed insights into the fluorination effects on the strength of intramolecular and intermolecular interactions in these systems. We have also used QTAIM delocalization indexes to define a novel hapticity indicator. Finally, we assessed the trans influence of the fluorothiolates on the phosphine in terms of the change in the δ 31P-NMR. These results show the feasibility of the use of fluorination in the modulation of the electronic properties of Buchwald phosphine gold(I) compounds, and thereby its potential catalytic activity.

Structural Diversity and Argentophilic Interactions in Small Phosphine Silver(I) Thiolate Clusters

“…Hence, we calculated the electron density distribution of the molecular units using DFT. This approach has proven useful in detailed analyses of the bonding scenario of metal complexes [53–58] . The QTAIM descriptors we used herein to characterize covalent and non‐covalent interactions are based on the electron density and energy densities at the bond critical points (bcp).…”