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Detalle de: Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as "Octet" 1,3-Dipoles

Title Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as "Octet" 1,3-Dipoles
Abstract

Theoretical calculations at the G4MP2 level of theory demonstrate that it is possible to activate dinitrogen to make it react in dipolar cycloadditions using neutral beryllium derivatives and other neutral metallic compounds. For the particular case of beryllium, the barrier decreases more than 40 kJ·mol –1 with respect to the non-catalysed reaction. The activation achieved is lower than using diazonium salts (models of protonated N 2 ), but still in a range that can be experimentally attainable.

Apa Reference Montero-Campillo, M. M., Alkorta, I., & Elguero, J. (2017). Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as “Octet” 1,3-Dipoles. Scientific Reports, 7(1). 10.1038/s41598-017-05708-z
Doi 10.1038/s41598-017-05708-z
Publication Date 21 Jul 2017
Publication Type Article
Researcher María de la Merced Montero-Campillo
Ontology
Research Groups
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