Exploring the Influence of (n-1)d Subvalence Correlation and of Spin-Orbit Coupling on Chalcogen Bonding
Nisha Mehta, Jan M.L. Martin

TL;DR
This study uses computational methods to analyze how subvalence (n-1)d correlation and spin-orbit coupling influence chalcogen bonding, revealing their significant and sometimes opposing effects on interaction energies and stability.
Contribution
It provides a detailed computational analysis of the roles of (n-1)d subvalence correlation and spin-orbit coupling in chalcogen bonding, highlighting their relative importance and effects.
Findings
(n-1)d correlation decreases interaction energies in chalcogen bonds.
Spin-orbit coupling effects are comparable to (n-1)d correlation for Te complexes.
SOC2 stabilizes monomers more than dimers, reducing binding.
Abstract
This article presents a comprehensive computational investigation into chalcogen bonding interactions, focusing specifically on elucidating the role of subvalence (n1)d and (n1)sp correlation. The incorporation of inner-shell (n1)d correlation leads to a decrease in interaction energies for chalcogen-bonded systems (at least those studied herein), contradicting the observations regarding halogen bonding documented by Kesharwani et al. in \textit{J. Phys. Chem. A}, \textbf{2018}, 122 (8), 2184-2197. The significance of (n1)sp subvalence correlation appears to be lower by an order of magnitude. Notably, among the various components of interaction energies computed at the PNO-LCCSD(T) or DF-CCSD levels, we identify the PNO-LMP2 or DF-MP2 component of the (n1)d correlation as predominant. Furthermore, we delve into the impact of second-order spin-orbit coupling (SOC2) on…
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