1: 1 and 2:1 cocrystallizations of alkoxy-substituted naphthalene derivatives with octafluoronaphthalene through arene-perfluoroarene interactions

Akiko Hori, Haruhi Takeda, J. Richard Premkumar, G. Narahari Sastry

Research output: Research - peer-reviewArticle

  • 1 Citations

Abstract

Naphthalene derivatives with laterally orientated short side chains readily form cocrystals with octafluoronaphthalene in which the position and the length of the lateral chain can control the 1:1 and 2:1 cocrystallization stoichiometries and overlapped areas of the π-planes, showing that the systematic substitution patterns in the chains of molecules can be exploited to rationally designed cocrystals.

LanguageEnglish
Pages193-197
Number of pages5
JournalJournal of Fluorine Chemistry
Volume168
DOIs
StatePublished - 2014
Externally publishedYes

Fingerprint

Stoichiometry
Substitution reactions
Derivatives
Molecules
octafluoronaphthalene
alkoxyl radical
naphthalene
interactions
stoichiometry
substitution
substitutes
molecules

Keywords

  • Cocrystal
  • Computational study
  • Molecular recognitions

ASJC Scopus subject areas

  • Biochemistry
  • Inorganic Chemistry
  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Environmental Chemistry

Cite this

1 : 1 and 2:1 cocrystallizations of alkoxy-substituted naphthalene derivatives with octafluoronaphthalene through arene-perfluoroarene interactions. / Hori, Akiko; Takeda, Haruhi; Premkumar, J. Richard; Sastry, G. Narahari.

In: Journal of Fluorine Chemistry, Vol. 168, 2014, p. 193-197.

Research output: Research - peer-reviewArticle

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