Energy of Formation of an Acyclic N-Methyltrifluoromethanesulfonamide Dimer View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-02

AUTHORS

N. N. Chipanina, L. V. Sherstyannikova, I. V. Sterkhova, V. K. Turchaninov, B. A. Shainyan

ABSTRACT

The energy of formation of an open-chain N-methyltrifluoromethanesulfonamide dimer stabilized by the N-H⋯O=S hydrogen bond is 20.1 kJ mol−1 (CH2Cl2). This value exceeds by ∼12 kJ mol−1 the energy of formation of cyclic secondary methanesulfonamide self-associates per hydrogen bond.

PAGES

268-271

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11176-005-0211-4

DOI

http://dx.doi.org/10.1007/s11176-005-0211-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000850442


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