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dc.contributor.authorFathalla, Eman M.
dc.contributor.authorAbu-Youssef, Morsy A. M.
dc.contributor.authorSharaf, Mona M.
dc.contributor.authorEl-Faham, Ayman
dc.contributor.authorBarakat, Assem
dc.contributor.authorHaukka, Matti
dc.contributor.authorSoliman, Saied M.
dc.date.accessioned2023-05-30T06:04:38Z
dc.date.available2023-05-30T06:04:38Z
dc.date.issued2023
dc.identifier.citationFathalla, E. M., Abu-Youssef, M. A. M., Sharaf, M. M., El-Faham, A., Barakat, A., Haukka, M., & Soliman, S. M. (2023). Synthesis, X-ray Structure of Two Hexa-Coordinated Ni(II) Complexes with s-Triazine Hydrazine Schiff Base Ligand. <i>Inorganics</i>, <i>11</i>(5), Article 222. <a href="https://doi.org/10.3390/inorganics11050222" target="_blank">https://doi.org/10.3390/inorganics11050222</a>
dc.identifier.otherCONVID_183332459
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/87285
dc.description.abstractThe hydrazine s-triazine ligand (E)-4,4’-(6-(2-(1-(pyridin-2-yl)ethylidene)hydrazinyl)-1,3,5-triazine-2,4-diyl)dimorpholine (DMPT) was used to synthesize two new Ni(II) complexes via a self-assembly technique. The two complexes were synthesized by a one-pot synthesis strategy and characterized by elemental analysis, FTIR and single-crystal X-ray diffraction analysis to be [Ni(DMPT)(H2O)3](NO3)2.3H2O (1) and [Ni(DMPT)(H2O)3](NO3)2.H2O (2). The structures of both complexes were very similar regarding the coordination sphere and counter anions, but differ only in the number of the crystal water molecules. In the case of complex 1, there are three water molecules instead of one H2O molecule as in complex 2. In the two complexes, the DMPT ligand acts as a neutral tridentate NNN-chelate via three Ni–N coordination interactions. The coordination sphere of the Ni(II) ion is completed by three water molecules. As a result, the two complexes exhibit distorted octahedral geometry. The Hirshfeld surfaces around each entity in both complexes have been computed. Subsequently, their corresponding intermolecular interactions were quantified separately. Because the number of crystal water molecules is different in both complexes, their monomeric units are connected differently in their crystal structures where the crystal water molecules act as both hydrogen bond donor and acceptor. The polar O…H interactions are the most dominant in all entities of both complexes. As a result, strong O…H interactions are the driving force in the crystal packing of both complexes, and this is attributed to the presence of the nitrate anions and water molecules. The antimicrobial activity of the free ligand and complex 1 were determined against two selected fungal species, Gram-negative and Gram-positive bacterial strains. The free ligand was found to be inactive against all microbial species. On the other hand, the Ni(II) complex 1 was found active against the Gram-positive bacterial species Bacillus subtilis and also the Gram-negative bacterial species Escherichia coli. The respective inhibition zone diameter of the Ni(II) complex was 12 and 11 mm, respectively.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherMDPI AG
dc.relation.ispartofseriesInorganics
dc.rightsCC BY 4.0
dc.subject.others-triazine hydrazone
dc.subject.othermolecular packing
dc.subject.otherX-ray
dc.subject.otherNi(II) complexes
dc.subject.otherHirshfeld surface
dc.subject.otherantimicrobial
dc.titleSynthesis, X-ray Structure of Two Hexa-Coordinated Ni(II) Complexes with s-Triazine Hydrazine Schiff Base Ligand
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202305303342
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineEpäorgaaninen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.contributor.oppiaineInorganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2304-6740
dc.relation.numberinseries5
dc.relation.volume11
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 by the authors. Licensee MDPI, Basel, Switzerland
dc.rights.accesslevelopenAccessfi
dc.subject.ysoantimikrobiset yhdisteet
dc.subject.ysokompleksiyhdisteet
dc.subject.ysonikkeli
dc.subject.ysoröntgenkristallografia
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p21949
jyx.subject.urihttp://www.yso.fi/onto/yso/p30190
jyx.subject.urihttp://www.yso.fi/onto/yso/p19926
jyx.subject.urihttp://www.yso.fi/onto/yso/p29058
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3390/inorganics11050222
jyx.fundinginformationThe authors would like to extend their sincere appreciation to the Researchers Supporting Project (RSP2023R64), King Saud University, Riyadh, Saudi Arabia.
dc.type.okmA1


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