Aromaticity on the fly: Cyclic transition state stabilization at finite temperature

Tamás Rozgonyi, Albert Bartók-Pártay, András Stirling

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Abstract

We study the transition state of pericyclic reactions at elevated temperature with unbiased ab initio molecular dynamics. We find that the transition state of the intramolecular rearrangements for barbaralane and bullvalene remains aromatic at high temperature despite the significant thermal atomic motions. Structural, magnetic, and electronic properties of the dynamical transition state show the concertedness and aromatic character. Free-energy calculations also support the validity of the transition state theory for the present rearrangement reactions. The calculations demonstrate that cyclic delocalization represents a strong force to synchronize the thermal atomic motions even at high temperatures.

Original languageEnglish
Pages (from-to)1207-1211
Number of pages5
JournalJournal of Physical Chemistry A
Volume114
Issue number2
DOIs
Publication statusPublished - Jan 21 2010

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ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

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