<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-05T19:34:32Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/47830" metadataPrefix="qdc">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/47830</identifier><datestamp>2022-01-06T22:16:12Z</datestamp><setSpec>com_10324_28542</setSpec><setSpec>com_10324_952</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_28543</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
<dc:title>Molecular rotation spectrum of tetracyclic quinolizidines: Observation of trans-Matrine and the elusive cis-Matrine</dc:title>
<dc:creator>Juanes San José, Marcos</dc:creator>
<dc:creator>Saragi, Rizalina Tama</dc:creator>
<dc:creator>Enríquez Giraudo, María Lourdes</dc:creator>
<dc:creator>Jaraíz Maldonado, Martín</dc:creator>
<dc:creator>Lesarri Gómez, Alberto Eugenio</dc:creator>
<dcterms:abstract>We characterized the bis-quinolizidine tetracyclic alkaloid (5S, 6S, 7R, 11R)-matrine in a supersonic jet expansion, using chirped-pulsed broadband microwave spectroscopy. Previous crystal diffraction analyses suggested 16 diastereoisomers associated with matrine’s four carbon stereocenters but were inconclusive whether the lactamic nitrogen atom would additionally produce separated trans-/cis- diastereoisomers or if both species may interconvert through low potential barriers. Our experiment simultaneously detected trans- and cis-matrine through their rotational spectrum, confirming the possibility of conformational rearrangement in matrine alkaloids. The two matrine conformers mainly differ in the envelope or half-chair lactamic ring, as evidenced by the experimental rotational and nuclear quadrupole coupling parameters. Molecular orbital calculations with ab initio (MP2) and density functional methods (B3LYP-D3(BJ) and MN15) were tested against the experiment, additionally offering an estimation of the cis-/trans- barrier of 24.9–26.9 kJ mol–1. The experiment illustrates the structural potential of chirped-pulsed broadband microwave spectroscopy for high-resolution rotational studies of biomolecules in the range of 20–40 atoms.</dcterms:abstract>
<dcterms:dateAccepted>2021-07-30T08:21:58Z</dcterms:dateAccepted>
<dcterms:available>2021-07-30T08:21:58Z</dcterms:available>
<dcterms:created>2021-07-30T08:21:58Z</dcterms:created>
<dcterms:issued>2021</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>The Journal of Organic Chemistry, 2021, vol. 86, n. 2. p. 1861–1867</dc:identifier>
<dc:identifier>1520-6904</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/47830</dc:identifier>
<dc:identifier>10.1021/acs.joc.0c02689</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://pubs.acs.org/doi/10.1021/acs.joc.0c02689</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© 2021 ACS Publications</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>ACS Publications</dc:publisher>
</qdc:qualifieddc></metadata></record></GetRecord></OAI-PMH>