TY - JOUR
T1 - Quantifying electronic similarities between NHC–gold(i) complexes and their isolobal imidazolium precursors
AU - Azofra, Luis Miguel
AU - Veenboer, Richard M. P.
AU - Falivene, Laura
AU - Vummaleti, Sai V. C.
AU - poater, albert
AU - Nolan, Steven P.
AU - Cavallo, Luigi
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: L. M. A. is an ULPGC Postdoc Fellow, and thanks Universidad de Las Palmas de Gran Canaria (ULPGC). L. F., S. V. C. V., S. P. N. and L. C. acknowledge King Abdullah University of Science and Technology (KAUST) for support. R. M. P. V. and S. P. N. thank the European Research Council (ERC). A. P. is a Serra Húnter Fellow, and thanks the MICINN for the project PGC2018-097722-B-I00. We also thank the KAUST Supercomputing Laboratory, housing the supercomputer Shaheen II, for providing computational resources.
PY - 2019
Y1 - 2019
N2 - A series of NHC–gold(I) (NHC = N-heterocyclic carbene) complexes has been studied by DFT calculations, enabling comparison of electronic and NMR behaviour with related protonated and free NHC molecules. Based on calculations, the NMR resonances of the carbenic C2 carbon atom in [Au(NHC)(Cl)] and [NHC(H)][Cl] exhibit increased shielding when compared to the free N-heterocyclic carbenes by an average of 46.6 ± 2.2 and 73.7 ± 4.3 ppm, respectively. A similar trend is observed when analysing the paramagnetic term of the magnetic shielding tensor. Although gold(I) and proton are considered isolobal fragments, imidazolium compounds lack π-backdonation due to the energetic unavailability of d-orbitals in H+. We propose that NHC–gold(I) complexes exhibit important π-backdonation irrespective of the relative amount of σ-donation between the NHC and gold(I)–X (X = anionic ligand) moieties in Au–NHC complexes. Interestingly, a correlation exists between the calculated shielding for gold (197Au) and the π-donation and π-backdonation contributions. We describe that this correlation also exists when analysing the σ-backdonation term, a property generally ignored yet representing a significant energetic contribution to the stability of the C2–Au bond.
AB - A series of NHC–gold(I) (NHC = N-heterocyclic carbene) complexes has been studied by DFT calculations, enabling comparison of electronic and NMR behaviour with related protonated and free NHC molecules. Based on calculations, the NMR resonances of the carbenic C2 carbon atom in [Au(NHC)(Cl)] and [NHC(H)][Cl] exhibit increased shielding when compared to the free N-heterocyclic carbenes by an average of 46.6 ± 2.2 and 73.7 ± 4.3 ppm, respectively. A similar trend is observed when analysing the paramagnetic term of the magnetic shielding tensor. Although gold(I) and proton are considered isolobal fragments, imidazolium compounds lack π-backdonation due to the energetic unavailability of d-orbitals in H+. We propose that NHC–gold(I) complexes exhibit important π-backdonation irrespective of the relative amount of σ-donation between the NHC and gold(I)–X (X = anionic ligand) moieties in Au–NHC complexes. Interestingly, a correlation exists between the calculated shielding for gold (197Au) and the π-donation and π-backdonation contributions. We describe that this correlation also exists when analysing the σ-backdonation term, a property generally ignored yet representing a significant energetic contribution to the stability of the C2–Au bond.
UR - http://hdl.handle.net/10754/656011
UR - http://xlink.rsc.org/?DOI=C9CP02844G
UR - http://www.scopus.com/inward/record.url?scp=85069454587&partnerID=8YFLogxK
U2 - 10.1039/c9cp02844g
DO - 10.1039/c9cp02844g
M3 - Article
C2 - 31268443
SN - 1463-9076
VL - 21
SP - 15615
EP - 15622
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 28
ER -