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 | |
| Publication status | Published - 2014 |
| Externally published | Yes |
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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: Contribution to journal › Article
}
TY - JOUR
T1 - 1
T2 - 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
PY - 2014
Y1 - 2014
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
UR - http://www.scopus.com/inward/record.url?scp=84919779894&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84919779894&partnerID=8YFLogxK
U2 - 10.1016/j.jfluchem.2014.09.025
DO - 10.1016/j.jfluchem.2014.09.025
M3 - Article
AN - SCOPUS:84919779894
VL - 168
SP - 193
EP - 197
JO - Journal of Fluorine Chemistry
JF - Journal of Fluorine Chemistry
SN - 0022-1139
ER -