2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate

Although in the title salt, C10H9N2+·CF3SO3−, the C—C and C—N bond lengths within the aromatic rings are normal, there is a considerable difference in the C—N—C angles at the protonated and unprotonated N atoms, viz. 123.42 (10) and 117.10 (11)°, respectively. Bifurcated N—H...X (X = N or O) hydroge...

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Main Authors: Ryosuke Abe, Tsugiko Takase, Dai Oyama
Format: Article
Language:English
Published: International Union of Crystallography 2017-05-01
Series:IUCrData
Subjects:
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2414314617006897
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author Ryosuke Abe
Tsugiko Takase
Dai Oyama
author_facet Ryosuke Abe
Tsugiko Takase
Dai Oyama
author_sort Ryosuke Abe
collection DOAJ
description Although in the title salt, C10H9N2+·CF3SO3−, the C—C and C—N bond lengths within the aromatic rings are normal, there is a considerable difference in the C—N—C angles at the protonated and unprotonated N atoms, viz. 123.42 (10) and 117.10 (11)°, respectively. Bifurcated N—H...X (X = N or O) hydrogen bonds form within the cation and between cation and anion. As a result, the cation exists in a cis conformation in the solid state. An obvious π–π contact is also present between the non-protonated pyridyl rings of neighbouring cations.
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spelling doaj.art-12acdef521ce4ede8f7087936780941c2022-12-21T17:12:56ZengInternational Union of CrystallographyIUCrData2414-31462017-05-0125x17068910.1107/S2414314617006897wm40472-(Pyridin-2-yl)pyridinium trifluoromethanesulfonateRyosuke Abe0Tsugiko Takase1Dai Oyama2Graduate School of Science and Engineering, Fukushima University, 1 Kanayagawa, Fukushima 960-1296, JapanInstitute of Environmental Radioactivity, Fukushima University, 1 Kanayagawa, Fukushima 960-1296, JapanDepartment of Industrial Systems Engineering, Cluster of Science and Engineering, Fukushima University, 1 Kanayagawa, Fukushima 960-1296, JapanAlthough in the title salt, C10H9N2+·CF3SO3−, the C—C and C—N bond lengths within the aromatic rings are normal, there is a considerable difference in the C—N—C angles at the protonated and unprotonated N atoms, viz. 123.42 (10) and 117.10 (11)°, respectively. Bifurcated N—H...X (X = N or O) hydrogen bonds form within the cation and between cation and anion. As a result, the cation exists in a cis conformation in the solid state. An obvious π–π contact is also present between the non-protonated pyridyl rings of neighbouring cations.http://scripts.iucr.org/cgi-bin/paper?S2414314617006897crystal structurebipyridinium ionhydrogen bondingtrifluoromethanesulfonate
spellingShingle Ryosuke Abe
Tsugiko Takase
Dai Oyama
2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
IUCrData
crystal structure
bipyridinium ion
hydrogen bonding
trifluoromethanesulfonate
title 2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
title_full 2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
title_fullStr 2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
title_full_unstemmed 2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
title_short 2-(Pyridin-2-yl)pyridinium trifluoromethanesulfonate
title_sort 2 pyridin 2 yl pyridinium trifluoromethanesulfonate
topic crystal structure
bipyridinium ion
hydrogen bonding
trifluoromethanesulfonate
url http://scripts.iucr.org/cgi-bin/paper?S2414314617006897
work_keys_str_mv AT ryosukeabe 2pyridin2ylpyridiniumtrifluoromethanesulfonate
AT tsugikotakase 2pyridin2ylpyridiniumtrifluoromethanesulfonate
AT daioyama 2pyridin2ylpyridiniumtrifluoromethanesulfonate