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

doi:10.1016/j.jfluchem.2014.09.025

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: Contribution to journal › Article › peer-review

4 Citations (Scopus)

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.

Original language	English
Pages (from-to)	193-197
Number of pages	5
Journal	Journal of Fluorine Chemistry
Volume	168
DOIs	https://doi.org/10.1016/j.jfluchem.2014.09.025
Publication status	Published - 2014 Dec
Externally published	Yes

Keywords

Cocrystal
Computational study
Molecular recognitions

ASJC Scopus subject areas

Biochemistry
Environmental Chemistry
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1016/j.jfluchem.2014.09.025

Cite this

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

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.",

keywords = "Cocrystal, Computational study, Molecular recognitions",

author = "Akiko Hori and Haruhi Takeda and Premkumar, {J. Richard} and Sastry, {G. Narahari}",

note = "Funding Information: A.H thank Prof. Hidetaka Yuge and Mr. Yuuki Akimoto of Kitasato University for valuable discussion and helpful supports. G.N.S and J.R.P thank CSIR , New Delhi for 12 th five year project INTELCOAT ( CSC-0114 ) and DST , New Delhi for funding the project ( SR/S1/PC-58/2009 ). Publisher Copyright: {\textcopyright} 2014 Elsevier B.V. All rights reserved.",

year = "2014",

month = dec,

doi = "10.1016/j.jfluchem.2014.09.025",

language = "English",

volume = "168",

pages = "193--197",

journal = "Journal of Fluorine Chemistry",

issn = "0022-1139",

publisher = "Elsevier BV",

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TY - JOUR

T1 - 1:1 and 2:1 cocrystallizations of alkoxy-substituted naphthalene derivatives with octafluoronaphthalene through arene-perfluoroarene interactions

AU - Hori, Akiko

AU - Takeda, Haruhi

AU - Premkumar, J. Richard

AU - Sastry, G. Narahari

N1 - Funding Information: A.H thank Prof. Hidetaka Yuge and Mr. Yuuki Akimoto of Kitasato University for valuable discussion and helpful supports. G.N.S and J.R.P thank CSIR , New Delhi for 12 th five year project INTELCOAT ( CSC-0114 ) and DST , New Delhi for funding the project ( SR/S1/PC-58/2009 ). Publisher Copyright: © 2014 Elsevier B.V. All rights reserved.

PY - 2014/12

Y1 - 2014/12

N2 - 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.

AB - 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.

KW - Cocrystal

KW - Computational study

KW - Molecular recognitions

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U2 - 10.1016/j.jfluchem.2014.09.025

DO - 10.1016/j.jfluchem.2014.09.025

M3 - Article

AN - SCOPUS:84919779894

SN - 0022-1139

VL - 168

SP - 193

EP - 197

JO - Journal of Fluorine Chemistry

JF - Journal of Fluorine Chemistry

ER -

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

Abstract

Keywords

ASJC Scopus subject areas

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