Reaction of Amines with NO at room temperature and atmospheric pressure: is nitroxyl a reaction intermediate?

Author:

Hamer Mariana1ORCID,Suarez Sebastián A.23ORCID,Muñoz Martina23,Álvarez Lucía23ORCID,Marti Marcelo45ORCID,Doctorovich Fabio23ORCID

Affiliation:

1. CONICET-Instituto de Nanosistemas, Universidad de San Martin , San Martin , Buenos Aires CP1650, Argentina

2. Departamento de Química Inorgánica , Analítica y Química Física, Facultad de Ciencias Exactas y Naturales , Universidad de Buenos Aires , Buenos Aires , Argentina

3. and INQUIMAE-CONICET, Ciudad Universitaria , Buenos Aires , C1428EHA, Argentina

4. Departamento de Química Biológica , Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires , Buenos Aires , Argentina

5. IQUIBICEN-CONICET, Ciudad Universitaria , Buenos Aires , C1428EHA, Argentina

Abstract

Abstract The novelty of this work lies in the experimental confirmation that alkylamines react with Nitric oxide (NO) in aqueous solution at room temperature and atmospheric pressure conditions releasing HNO. We combined spectroscopic, electrochemical, and kinetic techniques to describe the reactions intermediates and characterized end products determined by UV–vis, NMR, and GC-MS. Nitrosamine and propene were detected for the reactions of diethylamine and isopropylamine, showing differential mechanisms between primary and secondary alkylamines. Finally, mechanistic analysis using ab-initio methods was performed and compared with the molecular mechanism proposed for the decomposition of NONOates. The results are discussed in the context of the growing interest in the NO/HNO interconversion reactions, required to understand their overlapping and different reactivity.

Funder

Universidad de Buenos Aires

Fondo para la Investigación Científica y Tecnológica

Agencia Nacional de Promoción Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Reference26 articles.

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2. M. Hamer, M. A. Morales Vásquez, F. Doctorovich. The Chemistry and Biology of Nitroxyl (HNO), pp. 1–9. Elsevier (2017).

3. M. D. Bartberger, W. Liu, E. Ford, K. M. Miranda, C. Switzer, J. M. Fukuto, P. J. Farmer, D. A. Wink, K. N. Houk. Proc. Natl. Acad. Sci.99, 10958–10963 (2002).

4. W. Flores-Santana, D. J. Salmon, S. Donzelli, C. H. Switzer, D. Basudhar, L. Ridnour, R. Cheng, S. A. Glynn, N. Paolocci, J. M. Fukuto, K. M. Miranda, D. A. Wink. Antioxid. Redox Signal.14, 1659–1674 (2011).

5. M. Hamer, S. A. Suarez, N. I. Neuman, L. Alvarez, M. Muñoz, M. A. Marti, F. Doctorovich. Inorg. Chem.54, 9342–9350 (2015).

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