Slow nitrogen lnversion-N-O rotation in 2-alkoxy-1,1,3,3-tetramethylisoindolines

W. Ken Busfield; Ian D. Jenkins; San H. Thang; Graeme Moad; Ezio Rizzardo; David H. Solomon

doi:10.1039/C39850001249

Slow nitrogen lnversion-N-O rotation in 2-alkoxy-1,1,3,3-tetramethylisoindolines

W. Ken Busfield, Ian D. Jenkins, San H. Thang, Graeme Moad, Ezio Rizzardo, David H. Solomon

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

17 Citations (Scopus)

Abstract

2-Alkoxy-1,1,3,3-tetramethylisoindolines appear to undergo a coupled N-inversion-N-O-bond-rotation with free energies of activation of approximately 55-75 kJ mol^-1.

Original language	English
Pages (from-to)	1249-1250
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	18
DOIs	https://doi.org/10.1039/C39850001249
Publication status	Published - 1 Jan 1985

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10.1039/C39850001249

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Cite this

@article{e9bb12e8c142401cb6b45cd88c8ffdcb,

title = "Slow nitrogen lnversion-N-O rotation in 2-alkoxy-1,1,3,3-tetramethylisoindolines",

abstract = "2-Alkoxy-1,1,3,3-tetramethylisoindolines appear to undergo a coupled N-inversion-N-O-bond-rotation with free energies of activation of approximately 55-75 kJ mol-1.",

author = "Busfield, {W. Ken} and Jenkins, {Ian D.} and Thang, {San H.} and Graeme Moad and Ezio Rizzardo and Solomon, {David H.}",

year = "1985",

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doi = "10.1039/C39850001249",

language = "English",

pages = "1249--1250",

journal = "Journal of the Chemical Society, Chemical Communications",

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publisher = "The Royal Society of Chemistry",

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T1 - Slow nitrogen lnversion-N-O rotation in 2-alkoxy-1,1,3,3-tetramethylisoindolines

AU - Busfield, W. Ken

AU - Jenkins, Ian D.

AU - Thang, San H.

AU - Moad, Graeme

AU - Rizzardo, Ezio

AU - Solomon, David H.

PY - 1985/1/1

Y1 - 1985/1/1

N2 - 2-Alkoxy-1,1,3,3-tetramethylisoindolines appear to undergo a coupled N-inversion-N-O-bond-rotation with free energies of activation of approximately 55-75 kJ mol-1.

AB - 2-Alkoxy-1,1,3,3-tetramethylisoindolines appear to undergo a coupled N-inversion-N-O-bond-rotation with free energies of activation of approximately 55-75 kJ mol-1.

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U2 - 10.1039/C39850001249

DO - 10.1039/C39850001249

M3 - Article

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EP - 1250

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

SN - 0022-4936

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