<?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>2026-10-29T21:47:08Z</responseDate><request verb="GetRecord" identifier="oai:munzur-rdlopen.rawdatalibrary.net:munzur/4419" metadataPrefix="oai_dc">https://munzur-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:munzur-rdlopen.rawdatalibrary.net:munzur/4419</identifier><datestamp>2026-10-28T15:47:44Z</datestamp><setSpec>openaire</setSpec><setSpec>com_munzur_1</setSpec><setSpec>col_munzur_2</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>Cyano-complexes and salts with tetracyanonickellateII and N,N-bis(2-hydroxyethyl)-ethylenediamine: synthesis, IR spectra, magnetic properties, thermal analyses, and crystal structures</dc:title><dc:creator>Karadag, A.</dc:creator><dc:creator>Korkmaz, S. Aslan</dc:creator><dc:creator>Andaç, O.</dc:creator><dc:creator>Yerli, Y.</dc:creator><dc:creator>Topcu, Y.</dc:creator><dc:subject>Tetracyanonickellate(II)</dc:subject><dc:subject>Bimetallic complexes</dc:subject><dc:subject>N,N-Bis(2-hydroxyethyl)-ethylenediamine</dc:subject><dc:subject>Eight-coordination</dc:subject><dc:subject>Thermal analysis</dc:subject><dc:subject>Magnetic properties</dc:subject><dc:description>Four cyano complexes, [Ni(N-bishydeten)Ni(CN)(4)](n) (c1), [Cu(N-bishydeten)(2)][Ni(CN)(4)] (c2), [Zn-2(N-bishydeten)(2)Ni(CN)(4)](n) (c3), and [Cd(N-bishydeten)(2)][Ni(CN)(4)] (c4), have been synthesized and characterized by FT-IR, elemental, and thermal analyses. The structures of c2 and c4 were determined by single-crystal X-ray diffraction studies; both structures contain isolated cations and anions. The c2 consists of [Cu(N-bishydeten)(2)](2+) with octahedrally coordinated Cu-II and diamagnetic [Ni(CN)(4)](2-), but c4 consists of [Cd(N-bishydeten)(2)](2+), in which Cd-II is eight coordinate with two tetradentate N-bishydeten and diamagnetic [Ni(CN)(4)](2-). The value of the shape measure S (degrees) indicates that the coordination geometry around Cd-II lies along D-2d [dodecahedron; (dd)], C-2v [bicapped trigonal prism; (btp)], and D-4d [square antiprism; (sap)] but close to D-2d and D-4d. Variable temperature magnetic susceptibility measurements of c1 and c2 show the presence of little antiferromagnetic interaction below 20 K. Thermal analyses reveal that first neutral N-bishydeten and then cyano ligands were liberated from the complexes.</dc:description><dc:publisher>TAYLOR &amp; FRANCIS LTD</dc:publisher><dc:date>2012</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/munzur/4419</dc:identifier><dc:identifier>https://doi.org/10.1080/00958972.2012.678337</dc:identifier><dc:identifier>0095-8972</dc:identifier><dc:language>en</dc:language><dc:relation>JOURNAL OF COORDINATION CHEMISTRY</dc:relation><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://munzur-rdlopen.rawdatalibrary.net/tr/items/munzur/4419</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>