The influence of relativistic effects on nuclear magnetic resonance spin-spin coupling constant polarizabilities of H2O2, H2S2, H2Se2 and H2Te2

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Gabriel I. Pagola, Martin A. B. Larsen, Marta B. Ferraro, Stephan P. A. Sauer

Relativistic and non-relativistic calculations have been performed on hydrogen peroxide, dihydrogen disulfide, dihydrogen diselenide and dihydrogen ditelluride, H2X2 (X = O, S, Se, Te), in order to investigate the consequences of relativistic effects on their structures as well as their nuclear magnetic resonance (NMR) spin-spin coupling constants and spin-spin coupling constant polarizabilites. The study has been performed using both one-component non-relativistic and four-component relativistic calculations at the density functional theory (DFT) level with the B3LYP exchange-correlation functional. The calculation of nuclear spin-spin coupling constant polarizabilities has been performed by evaluating the components of the third order tensor, nuclear spin-spin coupling polarizability, using quadratic response theory. From this the pseudoscalar associated with this tensor has also been calculated. The results show that relativistic corrections become very important for H2Se2 and H2Te2 and hint that a new chiral discrimination technique via NMR spectroscopy might be possible for molecules containing elements like Se or Te.
Original languageEnglish
JournalJournal of Computational Chemistry
Volume39
Issue number31
Pages (from-to)2589-2600
Number of pages12
ISSN0192-8651
DOIs
Publication statusPublished - 2018

    Research areas

  • The Faculty of Science - NMR, Relativistic Effects, density functional theory (DFT), Spin-spin coupling constant, chirality

ID: 202747827