<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-6HHMYFSJ</identifier><date>2026</date><creator>Edwards, Kathleen F.</creator><creator>Liebman, Joel F.</creator><creator>Ponikvar-Svet, Maja</creator><relation>documents/doc/6/URN_NBN_SI_doc-6HHMYFSJ_001.pdf</relation><relation>documents/doc/6/URN_NBN_SI_doc-6HHMYFSJ_001.txt</relation><format format_type="issue">1</format><format format_type="volume">73</format><format format_type="type">article</format><format format_type="extent">str. 31-38</format><identifier identifier_type="DOI">10.17344/acsi.2024.8870</identifier><identifier identifier_type="ISSN">1580-3155</identifier><identifier identifier_type="COBISSID_HOST">275841283</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-6HHMYFSJ</identifier><language>eng</language><publisher>Slovensko kemijsko društvo</publisher><source>Acta chimica slovenica</source><rights>BY</rights><subject language_type_id="slv">acetilaceton</subject><subject language_type_id="slv">Aceton</subject><subject language_type_id="eng">acetylacetone</subject><subject language_type_id="eng">keto-enol</subject><subject language_type_id="slv">Tavtomerija</subject><subject language_type_id="slv">Termokemija</subject><title>Acetylacetone</title><title>metal complexes and keto-enol tautomerism – which tautomer is more/less stable?</title></Record>