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15N NMR study of protonation position determination in 2-(6-methoxynaphthalen-2-yl)vinyl diazine chromophores

dc.contributor.authorLyčka, Antonín
dc.contributor.authorNoirbent, Guillaume
dc.contributor.authorAchelle, Sylvain
dc.date.accessioned2026-08-17T09:19:56Z
dc.date.issued2026
dc.description.abstractThe 1H-15N HMBC spectra were successfully used for protonation position determination in 4-[(E)-2-(6-methoxynaphthalen-2-yl)vinyl]pyrimidine (1), 2-[(E)-2-(6-methoxynaphthalen-2-yl)-vinyl]quinoxaline (2), 2-[(E)-2-(6-methoxynaphthalen-2-yl)vinyl]pyrazine (3), and 3-[(E)-2-(6-methoxynaphthalen-2-yl)vinyl]pyridazine (4). Mono protonation was proved. In three cases (compounds 1, 2 and 4) only one nitrogen was protonated while in pyrazine compound 3 the equilibrium between regioisomers was observed.eng
dc.formatp. "Article Number: 143980"
dc.identifier.doi10.1016/j.molstruc.2025.143980
dc.identifier.issn0022-2860
dc.identifier.obd43882360
dc.identifier.scopus2-s2.0-105015768182
dc.identifier.urihttps://hdl.handle.net/20.500.12603/2912
dc.identifier.wos001586744900004
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherElsevier
dc.relation.ispartofJournal of molecular structure, volume 1350, issue: 1eng
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0022286025026262?via%3Dihub
dc.rights.accessOpen Access
dc.rights.licenseCC BY 4.0
dc.source.urlhttps://www.sciencedirect.com/science/article/pii/S0022286025026262?via%3Dihub
dc.subjectDiazineseng
dc.subject15N NMReng
dc.subjectProtonationeng
dc.subjectIntramolecular charge transfereng
dc.title15N NMR study of protonation position determination in 2-(6-methoxynaphthalen-2-yl)vinyl diazine chromophoreseng
dc.typearticle

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