Volume 57, Issue 8 pp. o786-o787

An isoindoline EPR label: 5-acet­amido-1,1,3,3-tetra­methyl­isoindolin-2-yl­oxyl

Graham Smith

Graham Smith

Centre for Instrumental and Developmental Chemistry, Queensland University of Technology, GPO Box 2434, Brisbane 4001, Australia

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Steven E. Bottle

Steven E. Bottle

Centre for Instrumental and Developmental Chemistry, Queensland University of Technology, GPO Box 2434, Brisbane 4001, Australia

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Damien A. Reid

Damien A. Reid

Centre for Instrumental and Developmental Chemistry, Queensland University of Technology, GPO Box 2434, Brisbane 4001, Australia

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Raymond C. Bott

Raymond C. Bott

Centre for Instrumental and Developmental Chemistry, Queensland University of Technology, GPO Box 2434, Brisbane 4001, Australia

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First published: 03 August 2004
Graham Smith, e-mail: [email protected]

Abstract

The crystal structure of the isoindoline nitro­xide amide 5-acet­amido-1,1,3,3-tetra­methyl­isoindolin-2-yl­oxyl, C14H19N2O2, which has utility as an EPR label, shows a characteristically stable tetra­methyl-substituted nitro­xide ring system which is essentially coplanar with the amide side-chain substituent. A single intermolecular hydrogen bond between the amide H atom and the nitro­xide O atom links the mol­ecules head-to-tail into an infinite polymeric chain.

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