<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" href="https://www.eurjchem.com/lib/pkp/xml/oai2.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>2026-04-30T06:19:33Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/1774" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/1774</identifier>
				<datestamp>2018-12-31T07:23:25Z</datestamp>
				<setSpec>eurjchem:ART</setSpec>
				<setSpec>driver</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 xml:lang="en-US">Synthesis, characterization and crystal structure of platinum(II) complexes with thiourea derivative ligands</dc:title>
	<dc:creator>Keskin, Ebru</dc:creator>
	<dc:creator>Solmaz, Ummuhan</dc:creator>
	<dc:creator>Binzet, Gun</dc:creator>
	<dc:creator>Gumus, Ilkay</dc:creator>
	<dc:creator>Arslan, Hakan</dc:creator>
	<dc:subject xml:lang="en-US">Thiourea</dc:subject>
	<dc:subject xml:lang="en-US">Synthesis</dc:subject>
	<dc:subject xml:lang="en-US">Platinum complexes</dc:subject>
	<dc:subject xml:lang="en-US">Benzamide derivative</dc:subject>
	<dc:subject xml:lang="en-US">Supramolecular structure</dc:subject>
	<dc:subject xml:lang="en-US">Single crystal X‐ray diffraction</dc:subject>
	<dc:description xml:lang="en-US">Thiourea derivatives [N-(di-n-propylcarbamothioyl)-4-fluorobenzamide (HL1) and N-(di-n-propylcarbamothioyl)-4-bromobenzamide (HL2)] and their platinum complexes have been successfully synthesized and structurally characterized by spectroscopic 1H NMR, 13C NMR, COSY, HMQC, and FT-IR techniques. The structure of both complexes was also confirmed by single crystal X-ray diffraction studies. The study of X-ray single crystal diffraction shows that the supramolecular aggregation of the complexes is stabilized via weak interactions as well as stacking interactions such as C-H⋅⋅⋅π and π⋅⋅⋅π. The cis-[Pt(L1-S,O)2 showed C–H⋯π and π⋯π stacking interactions, whereas only C–H⋯π stacking interaction was observed in cis-[Pt(L2-S,O)2]. In addition, the strong classical and non-classical intermolecular hydrogen bonds are not found in the prepared complexes. Therefore, it can be said that the C–H⋯π and π⋯π stacking interactions play an important role in the formation of supramolecular structures of the complexes.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2018-12-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:format>text/plain</dc:format>
	<dc:format>text/plain</dc:format>
	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1774</dc:identifier>
	<dc:identifier>10.5155/eurjchem.9.4.360-368.1774</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 9 No. 4 (2018): December 2018; 360-368</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/1774/pdf_1774</dc:relation>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/1774/2622</dc:relation>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/1774/2623</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2018 Authors</dc:rights>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
