Intramolecular cation-pi interactions control the conformation of nonrestricted (phenylalkyl)pyridines

Isabella Richter; Jusaku Minari; Philip Axe; John P Lowe; Tony D James; Kazuo Sakurai; Steven D Bull; John S Fossey

doi:10.1039/b716937j

Intramolecular cation-pi interactions control the conformation of nonrestricted (phenylalkyl)pyridines

Isabella Richter
, Jusaku Minari
, Philip Axe
, John P Lowe
, Tony D James
, Kazuo Sakurai
, Steven D Bull
, John S Fossey

Research output: Contribution to journal › Article › peer-review

36 Citations (Scopus)

Abstract

NOEsy and fluorescence spectroscopy reveal that conversion of conformationally flexible (phenylalkyl)pyridines into their corresponding N-methyl-pyridinium iodides results in intramolecular pi-stacking.

Original language	English
Pages (from-to)	1082-1084
Number of pages	3
Journal	Chemical Communications
Volume	n/a
Issue number	9
DOIs	https://doi.org/10.1039/b716937j
Publication status	Published - 1 Jan 2008

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@article{f803441eceb3410aaddfcdb15ce87e22,

title = "Intramolecular cation-pi interactions control the conformation of nonrestricted (phenylalkyl)pyridines",

abstract = "NOEsy and fluorescence spectroscopy reveal that conversion of conformationally flexible (phenylalkyl)pyridines into their corresponding N-methyl-pyridinium iodides results in intramolecular pi-stacking.",

author = "Isabella Richter and Jusaku Minari and Philip Axe and Lowe, \{John P\} and James, \{Tony D\} and Kazuo Sakurai and Bull, \{Steven D\} and Fossey, \{John S\}",

year = "2008",

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doi = "10.1039/b716937j",

language = "English",

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journal = "Chemical Communications",

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T1 - Intramolecular cation-pi interactions control the conformation of nonrestricted (phenylalkyl)pyridines

AU - Richter, Isabella

AU - Minari, Jusaku

AU - Axe, Philip

AU - Lowe, John P

AU - James, Tony D

AU - Sakurai, Kazuo

AU - Bull, Steven D

AU - Fossey, John S

PY - 2008/1/1

Y1 - 2008/1/1

N2 - NOEsy and fluorescence spectroscopy reveal that conversion of conformationally flexible (phenylalkyl)pyridines into their corresponding N-methyl-pyridinium iodides results in intramolecular pi-stacking.

AB - NOEsy and fluorescence spectroscopy reveal that conversion of conformationally flexible (phenylalkyl)pyridines into their corresponding N-methyl-pyridinium iodides results in intramolecular pi-stacking.

U2 - 10.1039/b716937j

DO - 10.1039/b716937j

M3 - Article

C2 - 18292897

SN - 1364-548X

VL - n/a

SP - 1082

EP - 1084

JO - Chemical Communications

JF - Chemical Communications

IS - 9

ER -

Intramolecular cation-pi interactions control the conformation of nonrestricted (phenylalkyl)pyridines

Abstract

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