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aminalsamine imines
amine imides
Compounds formally derived from the attachment of an amine R3N to a nitrene RN:. The structure R3N+–N−R expresses the 1,2-dipolar character of amine imides. They may be named systematically as substituted diazan-2-ium-1-ides, e.g. Me3N+–N−Me, 1,2,2,2-tetramethyldiazan-2-ium-1-ide or trimethylamine N-methylimide.
See also: ylides
Source:
PAC, 1995, 67, 1307 (Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995)) on page 1316
See also:
PAC, 1993, 65, 1357 (Revised nomenclature for radicals, ions, radical ions and related species (IUPAC Recommendations 1993)) on page 1357
InChI=1/C4H12N2/c1-5-6(2,3)4/h1-4H3
NTEPJNPCOMATCY-UHFFFAOYAS
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Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A.Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2008-09-12; version: 2.0.1.
DOI of this term: doi:10.1351/goldbook.A00271.
Original PDF version (may be out of date): http://www.iupac.org/goldbook/A00271.pdf.
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