Synthesis of new poly(1,2,3-triazolyl-benzenesulfonamide)s via step-growth polymerization and characterization of their structures
dc.contributor.author | Ay E. | |
dc.date.accessioned | 2024-07-22T08:02:20Z | |
dc.date.available | 2024-07-22T08:02:20Z | |
dc.date.issued | 2023 | |
dc.description.abstract | In this article, three new poly(1,2,3-triazolyl-benzenesulfonamide)s (4-6) were synthesized from the new molecule 4-azido-N-(prop-2ʹ-yn-1ʹ-yl)benzenesulfonamide (3). The synthesis and step-growth click polyaddition reaction of a new AB-type monomer containing terminal alkyne and azide groups were described. Copper (I)-catalyzed azide-alkyne cycloaddition (CuAAC) and Huisgen click polymerization were performed to prepare sulfonamide, a derivative of poly(1,2,3-triazole)s. The CuAAC polymerization regioselectively led to 1,4-disubstituted triazole ring and hence to a stereoregular polymer. In contrast, the thermal polymerization also produced 1,5-disubstituted triazole units. The structure of the new poly(1,2,3-triazolyl-benzenesulfonamide)s (4-6) obtained from (4-azido-N-(prop-2ʹ-yn-1ʹ-yl)benzenesulfonamide) were characterized by FTIR, 1H-, and 13C- NMR spectroscopy. The resulting polymers had weight-average molecular weights in the 7,700-58,650 range and were determined by Gel Permeation Chromatography (GPC). The resulting polymers 4, 5 and 6, lossing about 50% of their weights, showed a decomposition temperature of 406, 474, and 451 °C in a nitrogen atmosphere, respectively. The glass transition temperature of all polymers were at 128 °C. In addition, the surface morphology was studied via Scanning Electron Microscopy with Energy Dispersive Spectroscopy (SEM/EDS). This paper is dedicated to the 100th Annivesary of Repuclic of Türkiye. © 2023, The Polymer Society, Taipei. | |
dc.identifier.DOI-ID | 10.1007/s10965-023-03734-2 | |
dc.identifier.issn | 10229760 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/11807 | |
dc.language.iso | English | |
dc.publisher | Springer Science and Business Media B.V. | |
dc.subject | Copper compounds | |
dc.subject | Energy dispersive spectroscopy | |
dc.subject | Fourier transform infrared spectroscopy | |
dc.subject | Gel permeation chromatography | |
dc.subject | Glass transition | |
dc.subject | Hydrocarbons | |
dc.subject | Morphology | |
dc.subject | Nuclear magnetic resonance spectroscopy | |
dc.subject | Scanning electron microscopy | |
dc.subject | Sulfur compounds | |
dc.subject | Surface morphology | |
dc.subject | Synthesis (chemical) | |
dc.subject | Benzenesulfonamide | |
dc.subject | Click reaction | |
dc.subject | CuAAC | |
dc.subject | Huisgen reaction | |
dc.subject | Poly(1,2,3-triazole) | |
dc.subject | Polyaddition reactions | |
dc.subject | Step-growth polymerizations | |
dc.subject | Sulphonamides | |
dc.subject | Synthesised | |
dc.subject | Terminal alkyne | |
dc.subject | Polymerization | |
dc.title | Synthesis of new poly(1,2,3-triazolyl-benzenesulfonamide)s via step-growth polymerization and characterization of their structures | |
dc.type | Article |