Is the Inversion of Phosphorus Trihalides (PF 3 , PCl 3 , PBr 3 , and PI 3 ) a Diradical Process?

Zoltan Varga, Pragya Verma, Donald G Truhlar

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Abstract

This work explores possible reaction paths for the inversion of a series of trigonal pyramidal phosphorus trihalides, PF 3 , PCl 3 , PBr 3 , and PI 3 , and it especially addresses the question of whether and when the bonding of the lowest-energy species along the inversion paths should be described as a hyper-open-shell diradical. The various paths for inversion are calculated using a single-reference method within the framework of Kohn-Sham density functional theory and also with multireference wave function methods. Our calculated results using both kinds of methods show that, for all the halogens studied (F, Cl, Br, and I), the lowest-energy singlet path for the inversion occurs by the formation of a C 2v transition structure rather than a D 3h transition structure. This geometrical preference agrees with what has been inferred previously based on closed-shell singlet calculations. But in the present study, we examined not only closed-shell singlet transition states but also open-shell singlet states and triplet states for calculating stationary points and inversion paths, and for some of the phosphorus trihalides, we found that paths involving open-shell configurations are lower in energy than those restricted to closed-shell configurations. We analyzed the changes along the paths in terms of hybridization and orientation of the frontier orbitals and in terms of locally avoided crossings, and the extent of the diradical character was quantified by calculating the effective number of unpaired electrons. Even for the singlet inversion path that goes via a D 3h structure, the barrier for PF 3 , PCl 3 , and PBr 3 is higher for a closed-shell singlet spin state than for the open-shell singlet configuration. Furthermore, the energy of the triplet D 3h structure is below even that of the open-shell D 3h singlet for PCl 3 , PBr 3 , and PI 3 . This necessitates rethinking the role of open-shell states in nominally closed-shell processes.

Original languageEnglish (US)
Pages (from-to)301-312
Number of pages12
JournalJournal of Physical Chemistry A
Volume123
Issue number1
DOIs
StatePublished - Oct 1 2019

Bibliographical note

Funding Information:
This research was supported by the Nanoporous Materials Genome Center supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences under Award DE-FG02-17ER16362.

Publisher Copyright:
© 2018 American Chemical Society.

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