Synthesis, characterization, optical, and electrochemical properties of thermal stable novel poly(azomethine-ether)s
dc.authorid | AVCI, Ali/0000-0003-3097-8782 | |
dc.authorid | Kaya, Ismet/0000-0002-9813-2962 | |
dc.contributor.author | Kaya, İsmet | |
dc.contributor.author | Avci, Ali | |
dc.contributor.author | Kolcu, Feyza | |
dc.contributor.author | Culhaoglu, Suleyman | |
dc.date.accessioned | 2025-01-27T20:43:36Z | |
dc.date.available | 2025-01-27T20:43:36Z | |
dc.date.issued | 2014 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | In this study, the novel Schiff base monomers were synthesized by condensation reactions. Then, these monomers were converted to poly(azomethine-ether)s by oxidative polycondensation (OP) reactions in an aqueous alkaline medium. The structural characterizations of compounds were carried out by FT-IR, NMR, and size exclusion chromatography (SEC). According to the SEC analysis, the calculated number-average molecular weight (M-n), weight average molecular weight (M-w), and polydispersity index values of P-2 and P-4 were found to be 17,500gmol(-1), 24,400gmol(-1), and 1.39; and 18,700gmol(-1), 25,600gmol(-1), and 1.36, respectively. The HOMO-LUMO energy levels, electrochemical (E-g'), and optical (E-g) band gaps of polymers were calculated from cyclic voltammetry (CV) and UV-vis measurements, respectively. CV was used to determine the electrochemical oxidation-reduction characteristics of polymers. Thermal characterizations of compounds were made by using TG-DTA and DSC techniques. According to TG analysis, polymers with higher initial degradation temperatures (T-on) than those of their monomers indicate that the synthesized polyphenols have higher thermal stabilities than their monomer species. | |
dc.description.sponsorship | Canakkale Onsekiz Mart University scientific research project commission [FBA-2013-111] | |
dc.description.sponsorship | The authors thank Canakkale Onsekiz Mart University scientific research project commission for support with the project number (Project No. FBA-2013-111). | |
dc.identifier.doi | 10.1080/15685551.2013.867581 | |
dc.identifier.endpage | 490 | |
dc.identifier.issn | 1385-772X | |
dc.identifier.issn | 1568-5551 | |
dc.identifier.issue | 5 | |
dc.identifier.scopus | 2-s2.0-84892439565 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 481 | |
dc.identifier.uri | https://doi.org/10.1080/15685551.2013.867581 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/24289 | |
dc.identifier.volume | 17 | |
dc.identifier.wos | WOS:000329546400002 | |
dc.identifier.wosquality | Q1 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Ltd | |
dc.relation.ispartof | Designed Monomers and Polymers | |
dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.snmz | KA_WoS_20250125 | |
dc.subject | poly(azomethine-ether)s | |
dc.subject | thermal analysis | |
dc.subject | thermally stable polymers | |
dc.subject | cyclic voltammetry | |
dc.subject | band gap | |
dc.title | Synthesis, characterization, optical, and electrochemical properties of thermal stable novel poly(azomethine-ether)s | |
dc.type | Article |