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Utilizing the Azaazulene Scaffolds in the Design of New Organic Superbases

Barić, Danijel (2019) Utilizing the Azaazulene Scaffolds in the Design of New Organic Superbases. ACS Omega, 4 (12). pp. 15197-15207. ISSN 2470-1343

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Abstract

New neutral organic superbases with 1- azaazulene(s) as a molecular backbone are computationally designed, employing two basic substituents: dimethylaminocyclopropenimines (CPI) and dimethylaminocyclopropeniminophosphazenes (CPI- P). Their proton affinities, gas basicities, and pKa values in acetonitrile are obtained using density functional theory. Azaazulenes substituted with CPI have a computed PA in the gas phase ranging between 272.9 and 306.8 kcal mol–1, with pKa values in acetonitrile between 28.8 and 36 units. The substitution with the CPI-P group resulted in even stronger superbases, with a PA from 296.5 to 335.2 kcal mol–1 and corresponding pKa values from 33.9 to 50 units. This exceptionally strong thermodynamic basicity is accompanied by very high kinetic basicity as well ; contrary to typical proton sponges, the release of a proton from the conjugate superbase does not demand high activation energy. Because synthetic routes for both substituents and azaazulenes are already known, newly designed superbases represent suitable targets for synthesis and application.

Item Type: Article
Uncontrolled Keywords: 1-azaazulene ; density functional theory ; dimethylaminocyclopropenimines, dimethylaminocyclopropeniminophosphazenes ; superbasicity
Subjects: NATURAL SCIENCES > Chemistry
Divisions: Division of Physical Chemistry
Depositing User: Sofija Konjević
Date Deposited: 03 Oct 2019 13:48
Last Modified: 03 Oct 2019 13:48
URI: http://fulir.irb.hr/id/eprint/5023
DOI: 10.1021/acsomega.9b02087

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