<?xml version="1.0" encoding="UTF-8"?><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>2026-10-18T23:14:55Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12759" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/12759</identifier><datestamp>2026-10-18T20:43:10Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Synthesis, electrochemical and spectroscopic properties of ferrocene-based compounds</dc:title><dc:creator>Taşkor Önel, Gülce</dc:creator><dc:creator>Özgül Karaaslan, Emine</dc:creator><dc:creator>Ösken, İpek</dc:creator><dc:creator>Saygılı, Nezire</dc:creator><dc:subject>Cross-coupling</dc:subject><dc:subject>Cyclic voltammetry</dc:subject><dc:subject>Ferrocene derivatives</dc:subject><dc:subject>Palladium catalyst</dc:subject><dc:subject>UV–vis spectroscopy</dc:subject><dc:description>Ferrocene derivatives have been synthesized by the Suzuki cross-coupling reaction of ferroceneboronic acid with various aryl/heteroaryl halides. The reactions yield ferrocenyl derivatives with overall yields varying between 35 and 98%. The derivatives have been characterized by 1H NMR, 13C NMR, IR, HRMS and elemental analysis. The structure–property relationship has been investigated based on UV/Vis spectroscopy and cyclic voltammetry. Cyclic voltammetry studies revealed when the side group of ferrocenes were an electron-donating, lower oxidation was displayed. On the other hand, the strong electron-withdrawing group had a higher oxidation potential. Graphical abstract: [Figure not available: see fulltext.] © 2021, Institute of Chemistry, Slovak Academy of Sciences.</dc:description><dc:publisher>Springer Science and Business Media Deutschland GmbH</dc:publisher><dc:date>2022</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/12759</dc:identifier><dc:identifier>https://doi.org/10.1007/s11696-021-02034-7</dc:identifier><dc:identifier>0366-6352</dc:identifier><dc:language>en</dc:language><dc:relation>Chemical Papers</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/12759</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>