4.6 Article

Relativistic Spin-Orbit Electronegativity and the Chemical Bond Between a Heavy Atom and a Light Atom

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 28, Issue 24, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202200277

Keywords

bond distances; bond theory; electron charge density; quantum chemistry; spin-orbit coupling

Funding

  1. Czech Science Foundation [21-06991S]
  2. MEYS CR from the Large Infrastructures for Research, Experimental Development and Innovations project e-Infrastructure [CZ-LM2018140]
  3. Slovak Grant Agency VEGA [2/0135/21, APVV-19-0516]
  4. Slovak Grant Agency APVV [2/0135/21, APVV-19-0516]

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Relativistic effects can change the chemical bonds and spectroscopic properties of heavy-element compounds. This work introduces the concept of spin-orbit electronegativity for heavy atoms and explains the effects using spin-orbit electron deformation density. The change in electronegativity induced by spin-orbit coupling is quantified for a series of hydrides, and the trends across the periodic table are demonstrated and explained.
Relativistic effects are known to alter the chemical bonds and spectroscopic properties of heavy-element compounds. In this work, we introduce the concept of spin-orbit (SO) electronegativity of a heavy atom, as reflected by an SO-induced change in the interatomic distance between the heavy atom (HA) and a neighboring light atom (LA). We provide a transparent interpretation of these SO effects by using the concept of spin-orbit electron deformation density (SO-EDD). Spin-orbit coupling at the HA induces rearrangement of the electron density for the scalar-relativistically optimized geometry that, in turn, exerts a new force on the LA. The resulting expansion or contraction of the HA-LA bond depends on the nature and electron configuration of the HA. In addition, we quantify the change in atomic electronegativity induced by SO coupling for a series of hydrides, thereby complementing the SO-EDD picture. The trends in the SO-induced electronegativity and the HA-LA bond length across the periodic table of elements are demonstrated and interpreted, and also linked, intuitively, with the SO-induced NMR shielding at the LA.

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