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

I Richter; J Minari; P Axe; J P Lowe; T D James; K Sakurai; S D Bull; J S Fossey

doi:10.1039/b716937j

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

I Richter, J Minari, P Axe, J P Lowe, T D James, K Sakurai, S D Bull, J S Fossey

Department of Chemistry

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
Issue number	9
DOIs	https://doi.org/10.1039/b716937j
Publication status	Published - 2008

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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 = "I Richter and J Minari and P Axe and Lowe, {J P} and James, {T D} and K Sakurai and Bull, {S D} and Fossey, {J S}",

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

AU - Richter, I

AU - Minari, J

AU - Axe, P

AU - Lowe, J P

AU - James, T D

AU - Sakurai, K

AU - Bull, S D

AU - Fossey, J S

N1 - ID number: ISI:000253492500011

PY - 2008

Y1 - 2008

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.

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U2 - 10.1039/b716937j

DO - 10.1039/b716937j

M3 - Article

SP - 1082

EP - 1084

JO - Chemical communications (Cambridge, England)

JF - Chemical communications (Cambridge, England)

SN - 1359-7345

IS - 9

ER -