Towards a molecular understanding of cation‐anion interactions and self‐aggregation of adeninate salts in DMSO by NMR and UV spectroscopy and crystallography

dc.contributor.authorBuyens, Dominique M. S.
dc.contributor.authorPilcher, Lynne A.
dc.contributor.authorRoduner, Emil
dc.date.accessioned2024-08-20T13:42:14Z
dc.date.available2024-08-20T13:42:14Z
dc.date.issued2021de
dc.date.updated2023-11-14T02:57:29Z
dc.description.abstractRare anionic forms of nucleic acids play a significant biological role and lead to spontaneous mutations and replication and translational errors. There is a lack of information surrounding the stability and reactivity of these forms. Ion pairs of mono‐sodium and ‐potassium salts of adenine exist in DMSO solution with possible cation coordination sites at the N1, N7 and N9 atoms of the purine ring. At increasing concentrations π‐π stacked dimers are the predominant species of aggregates followed by higher order aggregation governed by coordination to metal cations in which the type of counter ion present has a central role in the aggregate formation.en
dc.description.sponsorshipNational Research Foundationde
dc.identifier.issn1439-7641
dc.identifier.issn1439-4235
dc.identifier.other1899365109
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-148639de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/14863
dc.identifier.urihttp://dx.doi.org/10.18419/opus-14844
dc.language.isoende
dc.relation.uridoi:10.1002/cphc.202100098de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subject.ddc540de
dc.titleTowards a molecular understanding of cation‐anion interactions and self‐aggregation of adeninate salts in DMSO by NMR and UV spectroscopy and crystallographyen
dc.typearticlede
ubs.fakultaetChemiede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutInstitut für Physikalische Chemiede
ubs.institutFakultätsübergreifend / Sonstige Einrichtungde
ubs.publikation.seiten2025-2033de
ubs.publikation.sourceChemPhysChem 22 (2021), S. 2025-2033de
ubs.publikation.typZeitschriftenartikelde

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