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Magnetic Shielding, Aromaticity, Antiaromaticity and Bonding in the Low-Lying Electronic States of S N. | LitMetric

AI Article Synopsis

Article Abstract

Aromaticity, antiaromaticity and chemical bonding in the ground (S ), first singlet excited (S ) and lowest triplet (T ) electronic states of disulfur dinitride, S N , were investigated by analysing the isotropic magnetic shielding, σ (r), in the space surrounding the molecule for each electronic state. The σ (r) values were calculated by state-optimized CASSCF/cc-pVTZ wave functions with 22 electrons in 16 orbitals constructed from gauge-including atomic orbitals (GIAOs). The S and T electronic states were confirmed as 1 A and 1 B , respectively, through linear response CC3/aug-cc-pVTZ calculations of the vertical excitation energies for eight singlet (S -S ) and eight triplet (T -T ) electronic states. The aromaticities of S , S and T were also assessed using additional magnetic criteria including nucleus-independent chemical shifts (NICS) and magnetic susceptibilities calculated at several levels of theory, the highest of which were CCSDT-GIAO/cc-pVTZ for S and CASSCF(22,16)-GIAO/aug-cc-pVQZ for S and T . The results strongly suggest that: 1) the S electronic ground state of S N is aromatic but less so than the electronic ground state of benzene; 2) S is profoundly antiaromatic, to an extent that removes any bonding interactions that would keep the atoms together; and 3) T is also antiaromatic, but its antiaromaticity is more moderate and similar to that observed in the electronic ground state of square cyclobutadiene. S N is the first example of an inorganic ring for which theory predicts substantial changes in aromaticity upon vertical transition from the ground state to the first singlet excited or lowest triplet electronic states.

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http://dx.doi.org/10.1002/chem.201804292DOI Listing

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