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Ligand Effects in Carbon−Boron Coupling Processes Mediated by σ‐BH Platinum Complexes
Author(s) -
Ríos Pablo,
FernándezdeCórdova Francisco José,
Borge Javier,
Curado Natalia,
Lledós Agustí,
Conejero Salvador
Publication year - 2021
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.202100428
Subject(s) - imes , chemistry , ligand (biochemistry) , platinum , boron , boranes , crystallography , carbene , stereochemistry , medicinal chemistry , photochemistry , computational chemistry , organic chemistry , catalysis , biochemistry , receptor
The reaction of tri‐coordinated boranes (derived from dioxaborolanes and diazaborolanes) with cyclometalated low‐electron count platinum complexes [Pt(NHC’)(NHC)][BAr F ] (NHC=I t Bu i Pr, IMes, IMes*) led, at low temperature, to the formation of the corresponding σ‐BH species. Some of these species have been characterized by X‐Ray diffraction methods showing a rare η 1 ‐coordination mode. These compounds are thermally unstable and undergo a carbon‐boron coupling process whose reversibility depends on the NHC ligand. DFT calculations indicate that the energy barriers required for C−B bond formation events (together with Pt−H bonds) are lower than the competitive reactions leading to C−H bond formation (and Pt−B bonds). However, the C−B coupling products appear to be formed under kinetic control with I t Bu i Pr ligands, whereas the relative low energy barrier leading to C−H bond formation is sufficiently low to form the thermodynamically more stable platinum boryl complexes at rt. The latter energy barrier is, nevertheless, too high for the systems bearing IMes and IMes* ligands.