Please use this identifier to cite or link to this item:
http://hdl.handle.net/11452/23745
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Büyükgüngör, Orhan | - |
dc.date.accessioned | 2021-12-30T06:08:00Z | - |
dc.date.available | 2021-12-30T06:08:00Z | - |
dc.date.issued | 2010-03-30 | - |
dc.identifier.citation | Güney, E. vd. (2010). "Dimeric and polymeric silver(I) saccharinato complexes of two bis(pyridine) ligands: Synthesis, structural, spectroscopic, fluorescent and thermal properties". Polyhedron, 29(5), 1437-1442. | en_US |
dc.identifier.issn | 0277-5387 | - |
dc.identifier.uri | https://doi.org/10.1016/j.poly.2010.01.019 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0277538710000410 | - |
dc.identifier.uri | http://hdl.handle.net/11452/23745 | - |
dc.description.abstract | The reaction of silver(I) with 1,2-bis[1-(pyridin-2-yl)ethylidene]hydrazine (bpeh) and N,N-bis(pyridin-2-ylmethyl)amine (bpma) in the presence of Na(sac) (sac = saccharinate) yielded [Ag-2(sac)(2)(bpeh)] (1) and [Ag(sac)(bpma)](n) (2) with conformational chirality. Both complexes have been characterized by elemental analysis, IR, thermal analysis and X-ray single crystal diffraction. Complex 1 displays a binuclear composition, in which each silver(I) ion is bound to one monodentate sac ligand and one of the bidentate pyridylimino groups of the bpeh ligand in a distorted trigonal coordination geometry. Complex 2 is a one-dimensional helical polymer, in which silver(I) centers are bridged by tridentate bpma ligands, and each silver(I) ion is coordinated in a distorted tetrahedral geometry by one monodentate sac ligand, a bidentate pyridylamine group of one bpma ligand, and a pyridylimino group of another bpma ligand. Weak intermolecular C-H center dot center dot center dot O hydrogen bonds and C-H center dot center dot center dot pi interactions lead to assembly of 1 and 2 into threedimensional supramolecular frameworks. Spectral and thermal analysis data for 1 and 2 are in agreement with the crystal structures. In addition, both complexes in the solid state display intraligand pi-pi* fluorescence. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Pergamon-Elsevier Science | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Saccharinate | en_US |
dc.subject | 1,2-Bis[1-(pyridin-2yl)ethylidenelhydrazine | en_US |
dc.subject | N,N-bis(pyridin-2-ylmethyl)amine | en_US |
dc.subject | Chirality | en_US |
dc.subject | Coordination polymer | en_US |
dc.subject | Silver(I) | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Crystallography | en_US |
dc.title | Dimeric and polymeric silver(I) saccharinato complexes of two bis(pyridine) ligands: Synthesis, structural, spectroscopic, fluorescent and thermal properties | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000276720400010 | tr_TR |
dc.identifier.scopus | 2-s2.0-77649269879 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü. | tr_TR |
dc.contributor.orcid | 0000-0002-2849-3332 | tr_TR |
dc.identifier.startpage | 1437 | tr_TR |
dc.identifier.endpage | 1442 | tr_TR |
dc.identifier.volume | 29 | tr_TR |
dc.identifier.issue | 5 | tr_TR |
dc.relation.journal | Polyhedron | en_US |
dc.contributor.buuauthor | Güney, Emel | - |
dc.contributor.buuauthor | Yılmaz, Veysel Turan | - |
dc.contributor.researcherid | L-7238-2018 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.subject.wos | Chemistry, inorganic & nuclear | en_US |
dc.subject.wos | Crystallography | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 25027291500 | tr_TR |
dc.contributor.scopusid | 7006269202 | tr_TR |
dc.subject.scopus | Benzisothiazole; Palladium; 2-Phenylpyridine | en_US |
Appears in Collections: | Scopus Web of Science |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.