Issue 14, 2017, Issue in Progress

Lewis acid stabilization and activation of primary N-nitrosamides

Abstract

The primary nitrosamides, here exemplified by the N-nitrosoalkylcarbamates, ROC(O)NHNO [R = CH3 (1), R = C2H5 (2)], show a markedly Lewis acid dependent chemistry. Although their alkali metal salts M[ROC(O)NNO] [M = K, R = CH3 (3), M = Na, R = CH3 (3-Na), M = K, R = C2H5 (4), M = Na, R = C2H5 (4-Na)] are stable isolable yellow solids, in solution they undergo pH dependent decomposition to give nitrogen and nitrous oxide as the primary nitrogen containing gaseous products. However chelation to a transition metal, [Re(L)(CO)2(PPh3)2], L = ROC(O)NNO gives rise to isomeric kinetic and thermodynamic products. Both are thermally stable and together illustrate the stability provided by a chelating low valent transition metal. The preparation, IR, NMR, and X-ray crystallographic characterization of these derivatives are reported. Taken together, these results demonstrate that the Lewis acid identity is an important factor in primary nitrosamide chemistry.

Graphical abstract: Lewis acid stabilization and activation of primary N-nitrosamides

Supplementary files

Article information

Article type
Paper
Submitted
30 Sep 2016
Accepted
09 Jan 2017
First published
10 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 8205-8219

Lewis acid stabilization and activation of primary N-nitrosamides

D. S. Bohle, Z. Chua, I. Perepichka and K. Rosadiuk, RSC Adv., 2017, 7, 8205 DOI: 10.1039/C6RA24421A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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