| Literature DB >> 29306273 |
Hannes C Gottschalk1, Anja Poblotzki1, Martin A Suhm1, Muneerah M Al-Mogren2, Jens Antony3, Alexander A Auer4, Leonardo Baptista5, David M Benoit6, Giovanni Bistoni4, Fabian Bohle3, Rahma Dahmani7, Dzmitry Firaha8, Stefan Grimme3, Andreas Hansen3, Michael E Harding9, Majdi Hochlaf7, Christof Holzer10, Georg Jansen11, Wim Klopper10, Wassja A Kopp8, Leif C Kröger8, Kai Leonhard8, Halima Mouhib7, Frank Neese4, Max N Pereira5, Inga S Ulusoy12, Axel Wuttke1, Ricardo A Mata1.
Abstract
Herein we present the results of a blind challenge to quantum chemical methods in the calculation of dimerization preferences in the low temperature gas phase. The target of study was the first step of the microsolvation of furan, 2-methylfuran and 2,5-dimethylfuran with methanol. The dimers were investigated through IR spectroscopy of a supersonic jet expansion. From the measured bands, it was possible to identify a persistent hydrogen bonding OH-O motif in the predominant species. From the presence of another band, which can be attributed to an OH-π interaction, we were able to assert that the energy gap between the two types of dimers should be less than or close to 1 kJ/mol across the series. These values served as a first evaluation ruler for the 12 entries featured in the challenge. A tentative stricter evaluation of the challenge results is also carried out, combining theoretical and experimental results in order to define a smaller error bar. The process was carried out in a double-blind fashion, with both theory and experimental groups unaware of the results on the other side, with the exception of the 2,5-dimethylfuran system which was featured in an earlier publication.Entities:
Year: 2018 PMID: 29306273 DOI: 10.1063/1.5009011
Source DB: PubMed Journal: J Chem Phys ISSN: 0021-9606 Impact factor: 3.488