High-Frequency C-13 and Si-29 NMR Chemical Shifts in Diamagnetic Low-Valence Compounds of TI-I and Pb-II: Decisive Role of Relativistic Effects

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Publikace nespadá pod Fakultu sportovních studií, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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VÍCHA Jan MAREK Radek STRAKA Michal

Rok publikování 2016
Druh Článek v odborném periodiku
Časopis / Zdroj Inorganic Chemistry
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www DOI: 10.1021/acs.inorgchem.5b02689
Doi http://dx.doi.org/10.1021/acs.inorgchem.5b02689
Obor Anorganická chemie
Klíčová slova Density-Functional Theory; Relativistic effects; Spin-orbit coupling; Magnetic coupling;
Přiložené soubory
Popis The C-13 and Si-29 NMR signals of ligand atoms directly bonded to TII or Pb-II heavy-element centers are predicted to resonate at very high frequencies, up to 400 ppm for C-13 and over 1000 ppm for Si-29, outside the typical experimental NMR chemical-shift ranges for a given type of nuclei. The large C-13 and Si-29 NMR chemical shifts are ascribed to sizable relativistic spin-orbit effects, which can amount to more than 200 ppm for C-13 and more than 1000 ppm for Si-29, values unexpected for diamagnetic compounds of the main group elements. The origin of the vast spin-orbit contributions to the C-13 and Si-29 NMR shifts is traced to the highly efficient 6p -> 6p* metal-based orbital magnetic couplings and related to the 6p orbital-based bonding together with the low-energy gaps between the occupied and virtual orbital subspaces in the subvalent TII and Pb-II compounds. New NMR spectral regions for these compounds are suggested based on the fully relativistic density functional theory calculations in the Dirac-Coulomb framework carefully calibrated on the experimentally known NMR data for TII and Pb-II complexes.
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