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dc.contributor.authorHannachi, Anissa
dc.contributor.authorGarcía, Carlos J Gómez
dc.contributor.authorValkonen, Arto
dc.contributor.authorSmirani, Wajda
dc.date.accessioned2024-02-15T08:59:08Z
dc.date.available2024-02-15T08:59:08Z
dc.date.issued2022
dc.identifier.citationHannachi, A., García, C. J. G., Valkonen, A., & Smirani, W. (2022). Synthesis and characterization of a novel coordination compound based on 2, 6-dimethylpiperazine. <i>Journal of Molecular Structure</i>, <i>1267</i>, Article 133569. <a href="https://doi.org/10.1016/j.molstruc.2022.133569" target="_blank">https://doi.org/10.1016/j.molstruc.2022.133569</a>
dc.identifier.otherCONVID_148841362
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/93410
dc.description.abstractHere we show the synthesis and complete characterization, including single crystal X-ray structure determination, of the first compound containing the monoprotonated 2,6-dimethylpiperazinium cation: (C6H15N2)+. Compound [Co(NCS)4(C6H15N2)2] (1) crystallizes in the monoclinic P21/n space group and contains an octahedral Co(II) ion surrounded by four -NCS and two protonated 2,6-dimethylpiperazine ligands (C6H15N2)+. There are some N-H•••S intermolecular hydrogen bonds that generate a three-dimensional H-bonded network. Compound 1 has been characterized by single-crystal and powder X-Ray diffraction, infrared, UV-Vis and RMN spectroscopies, thermogravimetric analysis (TGA) and differential thermal analysis (DTA). The magnetic properties in the temperature range indicate the presence of isolated high spin Co(II) ions with the expected spin-orbit coupling. The antibacterial activity of compound 1 shows a higher antibacterial activity than other related complexes due to the presence of the piperazine-derivative ligands.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesJournal of Molecular Structure
dc.rightsCC BY-NC-ND 4.0
dc.subject.otherisothiocyanate
dc.subject.other2,6-dimethylpiperazine
dc.subject.othercoordination
dc.subject.otherbiological activity
dc.titleSynthesis and characterization of a novel coordination compound based on 2, 6-dimethylpiperazine
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202402151888
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0022-2860
dc.relation.volume1267
dc.type.versionacceptedVersion
dc.rights.copyright© 2022 Elsevier
dc.rights.accesslevelopenAccessfi
dc.subject.ysobiologinen aktiivisuus
dc.subject.ysokoboltti
dc.subject.ysospektroskopia
dc.subject.ysovetysidokset
dc.subject.ysokemialliset sidokset
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p24582
jyx.subject.urihttp://www.yso.fi/onto/yso/p15221
jyx.subject.urihttp://www.yso.fi/onto/yso/p10176
jyx.subject.urihttp://www.yso.fi/onto/yso/p38131
jyx.subject.urihttp://www.yso.fi/onto/yso/p10130
dc.rights.urlhttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.relation.doi10.1016/j.molstruc.2022.133569
jyx.fundinginformationThe authors gratefully acknowledge the support of the Tunisian Ministry of Higher Education and Scientific Research. We also thank the Generalidad Valenciana (Prometeo/2019/076) and the grant CTQ2017-87201-P funded by MCIN/AEI/10.13039/ 501100011033 and by “ERDF A way of making Europe” for financial support.
dc.type.okmA1


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