Literature DB >> 29676906

Relativistic Spin-Orbit Heavy Atom on the Light Atom NMR Chemical Shifts: General Trends Across the Periodic Table Explained.

Jan Vícha1, Stanislav Komorovsky2, Michal Repisky3, Radek Marek4, Michal Straka5.   

Abstract

The importance of relativistic effects on the NMR parameters in heavy-atom (HA) compounds, particularly the SO-HALA (Spin-Orbit Heavy Atom on the Light Atom) effect on NMR chemical shifts, has been known for about 40 years. Yet, a general correlation between the electronic structure and SO-HALA effect has been missing. By analyzing 1H NMR chemical shifts of the sixth-period hydrides (Cs-At), we discovered general electronic-structure principles and mechanisms that dictate the size and sign of the SO-HALA NMR chemical shifts. In brief, partially occupied HA valence shells induce relativistic shielding at the light atom (LA) nuclei, while empty HA valence shells induce relativistic deshielding. In particular, the LA nucleus is relativistically shielded in 5d2-5d8 and 6p4 HA hydrides and deshielded in 4f0, 5d0, 6s0, and 6p0 HA hydrides. This general and intuitive concept explains periodic trends in the 1H NMR chemical shifts along the sixth-period hydrides (Cs-At) studied in this work. We present substantial evidence that the introduced principles have a general validity across the periodic table and can be extended to nonhydride LAs. The decades-old question of why compounds with occupied frontier π molecular orbitals (MOs) cause SO-HALA shielding at the LA nuclei, while the frontier σ MOs cause deshielding is answered. We further derive connection between the SO-HALA NMR chemical shifts and Spin-Orbit-induced Electron Deformation Density (SO-EDD), a property that can be obtained easily from differential electron densities and can be represented graphically. SO-EDD provides an intuitive understanding of the SO-HALA effect in terms of the depletion/concentration of the electron density at LA nuclei caused by spin-orbit coupling due to HA in the presence of a magnetic field. Using an analogy between the SO-EDD concept and arguments from classic NMR theory, the complex question of the SO-HALA NMR chemical shifts becomes easily understandable for a wide chemical audience.

Entities:  

Year:  2018        PMID: 29676906     DOI: 10.1021/acs.jctc.8b00144

Source DB:  PubMed          Journal:  J Chem Theory Comput        ISSN: 1549-9618            Impact factor:   6.006


  5 in total

1.  Expanding the hydride chemistry: antiperovskites A3MO4H (A = Rb, Cs; M = Mo, W) introducing the transition oxometalate hydrides.

Authors:  Alexander Mutschke; Annika Schulz; Marko Bertmer; Clemens Ritter; Antti J Karttunen; Gregor Kieslich; Nathalie Kunkel
Journal:  Chem Sci       Date:  2022-05-25       Impact factor: 9.969

2.  Quantum chemical calculations of 31P NMR chemical shifts of P-donor ligands in platinum(II) complexes.

Authors:  Martin Sojka; Marek Nečas; Jaromir Toušek
Journal:  J Mol Model       Date:  2019-10-28       Impact factor: 1.810

3.  1H NMR is not a proof of hydrogen bonds in transition metal complexes.

Authors:  J Vícha; C Foroutan-Nejad; M Straka
Journal:  Nat Commun       Date:  2019-04-09       Impact factor: 14.919

4.  Low-Valent Group 14 Phosphinidenide Complexes [({SIDipp}P)2 M] Exhibit P-M pπ-pπ Interaction (M=Ge, Sn, Pb).

Authors:  Markus Balmer; Yannick J Franzke; Florian Weigend; Carsten von Hänisch
Journal:  Chemistry       Date:  2019-12-03       Impact factor: 5.236

5.  First-Principles Calculation of 1H NMR Chemical Shifts of Complex Metal Polyhydrides: The Essential Inclusion of Relativity and Dynamics.

Authors:  Abril C Castro; David Balcells; Michal Repisky; Trygve Helgaker; Michele Cascella
Journal:  Inorg Chem       Date:  2020-11-23       Impact factor: 5.165

  5 in total

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