dc.creator | Báez-Grez, Rodrigo | |
dc.creator | Pino-Rios, Ricardo | |
dc.date.accessioned | 2023-10-23T02:50:49Z | |
dc.date.accessioned | 2024-05-02T14:58:17Z | |
dc.date.available | 2023-10-23T02:50:49Z | |
dc.date.available | 2024-05-02T14:58:17Z | |
dc.date.created | 2023-10-23T02:50:49Z | |
dc.date.issued | 2023-06 | |
dc.identifier | ACS Omega, Volume 8, Issue 25, Pages 23168 - 2317327, June 2023 | |
dc.identifier | 24701343 | |
dc.identifier | https://repositorio.unab.cl/xmlui/handle/ria/53536 | |
dc.identifier | 10.1021/acsomega.3c02663 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/9260884 | |
dc.description.abstract | In this article, we studied the capability of bulky groups to contribute to the stabilization of a given compound in addition to the well-known steric effect related to substituents due to their composition (alkyl chains and aromatic groups, among others). For this purpose, the recently synthesized 1-bora-3-boratabenzene anion which contains large substituents was analyzed by means of the independent gradient model (IGM), natural population analysis (NPA) at the TPSS/def2-TZVP level, force field-based energy decomposition analysis (EDA-FF) applying the universal force field (UFF), and molecular dynamics calculations under the GFN2-xTB approach. The results indicate that the bulky groups should not only be considered for their steric effects but also for their ability to stabilize a system that could be very reactive. © 2023 The Authors. Published by American Chemical Society. | |
dc.language | en | |
dc.publisher | American Chemical Society | |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.rights | CC BY-NC-ND 4.0 DEED
Attribution-NonCommercial-NoDerivs 4.0 International | |
dc.title | On the Importance of Noncovalent Interactions in the Stabilization of Nonconventional Compounds Using Bulky Groups | |
dc.type | Artículo | |