doi:10.1021/acs.organomet.2c00156engValentine, A. J.Taylor, L. J.Geer, A. M.Huke, C. D.Wood, K. E.Tovey, W.Lewis, W.Argent, S. P.Teale, A. M.McMaster, J.Kays, D. L.Structural and electronic studies of substituted m-terphenyl group 12 complexesART-2022-129684The effects of para-substitution on the structural and electronic properties of four series of two-coordinate m-terphenyl Group 12 complexes (R-Ar#)2M (M = Zn, Cd, Hg; R = t-Bu 1-3, SiMe3 4-6, Cl 7-9, CF3 10-12, where R-Ar# = 2, 6-{2, 6-Xyl}2-4-R-C6H2 and 2, 6-Xyl = 2, 6-Me2C6H3) have been investigated. X-ray crystallography shows little structural variation across the series, with no significant change in the C-M-C bond distances and angles. However, considerable electronic differences are revealed by heteronuclear nuclear magnetic resonance (NMR) spectroscopy; a linear correlation is observed between the 113Cd, 199Hg, and 1H (2, 6-Xyl methyl protons) NMR chemical shifts of the para-substituted complexes and the Hammett constants for the R-substituents. Specifically, an upfield shift in the NMR signal is observed with increasingly electron-withdrawing R-substituents. Density functional theory (DFT) calculations are employed to attempt to rationalize these trends. © 2022 The Authors. Published by American Chemical Society.2022http://zaguan.unizar.es/record/11873810.1021/acs.organomet.2c00156http://zaguan.unizar.es/record/118738oai:zaguan.unizar.es:118738Organometallics 41, 11 (2022), 1426–1433byhttp://creativecommons.org/licenses/by/3.0/es/info:eu-repo/semantics/openAccess