Electronic Transmutation Concept: Is the Inverse Process Possible? An Evaluation of Main Group Compounds

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dc.contributor.affiliationUniversidad Andres Bello
dc.contributor.affiliationUniversidad de Las Americas - Chile
dc.contributor.affiliationUniversidad Arturo Prat
dc.contributor.authorBáez-Grez, Rodrigo
dc.contributor.authorYáñez, Osvaldo
dc.contributor.authorPino-Rios, Ricardo
dc.date.accessioned2024-09-03T19:21:23Z
dc.date.available2024-09-03T19:21:23Z
dc.date.issued2023-01-09
dc.description.abstractThe electronic transmutation (ET) concept states that when an element with atomic number Z gains an electron, it transmutes into a Z + 1 element, leading to species that possess similar chemical bonding patterns and geometric structures regarding the original (Z + 1) element. In this work, the opposite concept, that is, the inverse ET, is assessed. For this purpose, several main group compounds have been analyzed in terms of the adaptive natural density partitioning. The obtained results suggest that when an atom Z loses an electron, it transmutes into a Z - 1 atom, acquiring its geometrical structure and bonding pattern.
dc.description.sponsorshipFONDECYT Postdoctorado [3210037]; supercomputing infrastructure of the NLHPC of the Universidad de Chile [ECM-02]; R.B.-G. is grateful for financial support from FONDECYT Postdoctorado 3210037. Powered@NLHPC: this research was partially supported by the supercomputing infrastructure of the NLHPC (ECM-02) of the Universidad de Chile.
dc.format.mimetypeapplication/pdf
dc.identifier.citationACS Omega, 8(3), 2880-2886. https://doi.org/10.1021/acsomega.2c03865
dc.identifier.doihttps://doi.org/10.1021/acsomega.2c03865
dc.identifier.folio3210037
dc.identifier.issn2470-1343
dc.identifier.orcidhttps://orcid.org/0000-0001-9303-1559
dc.identifier.orcidhttps://orcid.org/0000-0001-8993-9353
dc.identifier.orcidhttps://orcid.org/0000-0003-4756-1115
dc.identifier.pmid36713707
dc.identifier.researcheridAAM-4876-2021
dc.identifier.rorhttps://ror.org/01qq57711
dc.identifier.rorhttps://ror.org/0166e9x11
dc.identifier.rorhttps://ror.org/01hrxxx24
dc.identifier.scopusauthorid57201096006
dc.identifier.scopusauthorid55794064800
dc.identifier.scopusauthorid56951201800
dc.identifier.urihttps://repositorio.udla.cl/handle/udla/1631
dc.language.isoeng
dc.publisherAmerican Chemical Society (ACS)
dc.relation.fundingFondo Nacional de Desarrollo Científico y Tecnológico, FONDECYT
dc.relation.fundingUniversidad de Chile, Uchile
dc.relation.fundingFONDECYT Postdoctorado [3210037]
dc.relation.fundingsupercomputing infrastructure of the NLHPC of the Universidad de Chile [ECM-02]
dc.relation.isindexedbyWeb of Science
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceACS OMEGA
dc.source.urihttps://pubs.acs.org/doi/10.1021/acsomega.2c03865
dc.subjectBOND
dc.subjectREACTIVITY
dc.subjectBENZENE
dc.subjectVALENCE
dc.subjectANALOGS
dc.subject.oecd21.4 Ciencias Químicas
dc.titleElectronic Transmutation Concept: Is the Inverse Process Possible? An Evaluation of Main Group Compounds
dc.title.alternativeElectronic Transmutation Concept: Is the Inverse Process Possible? An Evaluation of Main Group Compounds.
dc.typejournal article
dc.type.coarhttp://purl.org/coar/resource_type/c_6501
dc.type.driverinfo:eu-repo/semantics/article
dc.udla.catalogadorCBM
oaire.citation.endPage2886
oaire.citation.issue3
oaire.citation.startPage2880
oaire.citation.titleACS OMEGA
oaire.citation.volume8
oaire.fundingReference.awardNumber3210037
oaire.fundingReference.funderNameAgencia Nacional de Investigación y Desarrollo (ANID)
udla.curacion.controljmvg
udla.oecd.area2 Ingeniería y Tecnología
udla.oecd.subarea1.4 Ciencias Químicas

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