Journals / Celal Bayar Üniversitesi Fen Bilimleri Dergisi / 2019 / Cilt: 15 - Sayı: 4

Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties

Pages
329–336
Publication Date
2019-12-30
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The carbonized materials were further characterized by XRD and SEM/EDX.

📌 3 Key Takeaways

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Objective & Hypothesis:Azobenzene polymers have great potential and impact on fundamental and applied research.
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Key Findings & Data:Herein, nine conjugated main chain azobenzene polymers were synthesized using the nitroamine derivatives of some diphenylene compounds such as 4-amino-4′-nitrobiphenyl 1, 4-amino-4′-nitrobiphenyl ether 2 and 4-amino-4′-nitrobiphenyl sulfide 3, and comonomers triphenylamine A, N-methyldiphenyl amine B and triphenylphosphine C via diazo coupling reaction.
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Conclusion & Impact:The carbonized materials were further characterized by XRD and SEM/EDX.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Main chain azobenzene polymers · intumescent flame retardant additive · thermal stability

Abstract

Azobenzene polymers have great potential and impact on fundamental and applied research. However little is known about their thermal stability and degradation behaviours. Herein, nine conjugated main chain azobenzene polymers were synthesized using the nitroamine derivatives of some diphenylene compounds such as 4-amino-4′-nitrobiphenyl 1, 4-amino-4′-nitrobiphenyl ether 2 and 4-amino-4′-nitrobiphenyl sulfide 3, and comonomers triphenylamine A, N-methyldiphenyl amine B and triphenylphosphine C via diazo coupling reaction. These heteroatom containing polymers were characterized by 1H- and 31P-NMR, FTIR, UV–Vis and Raman spectroscopy. The thermal stability and degradation behaviour of these polymers were studied by means of TGA technique. Electronic spectra of the polymers recorded in DMF showed two strong maxima at ca. 280 and 380 nm. They were resistant to heat up to 270 °C and, produced 41-61% char under a nitrogen atmosphere at 800 °C. UL 94 burning tests performed for TPU Ravathane® (TPE-U) with added azobenzene polymer revealed that these polymers could be used as an intumescent reactive flame retardant additive, particularly for polyurethanes and elastomers, due to their high char yield at relatively high temperatures (e.g 800 °C). The carbonized materials were further characterized by XRD and SEM/EDX.

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Cite This Article

BAYAZİT, M. K., BİLEN, Z., BUDAK, E., OZARSLAN, O. (2019). Synthesis of Aromatic Conjugated Main Chain Azobenzene Polymers and Their Properties. Celal Bayar Üniversitesi Fen Bilimleri Dergisi, Cilt: 15 - Sayı: 4, 329–336. https://ajindex.com/articles/35004

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References (15)

  1. Izumi A, Nomura R, Masuda T. Design and synthesis of stimuli-responsive conjugated polymers having azobenzene units in the main chain. Macromolecules 2001;34:4342-7
  2. Yager KG, Barrett CJ. Azobenzene Polymers for Photonic Applications. Smart Light-Responsive Materials: John Wiley & Sons, Inc.; 2008. p. 1-46
  3. Yager KG, Barrett CJ. Amorphous Azobenzene Polymers for Light-Induced Surface Patterning. Smart Light-Responsive Materials: John Wiley & Sons, Inc.; 2008. p. 145-75
  4. Zollinger H. Front Matter. Diazo Chemistry I: Wiley-VCH Verlag GmbH & Co. KGaA; 2004. p. i-xiii
  5. Nuyken O, Scherer C, Baindl A, Brenner AR, Dahn U, Gartner R, et al. Azo-group-containing polymers for use in communications technologies. Progress in Polymer Science 1997;22:93-183
  6. Xie S, Natansohn A, Rochon P. Recent Developments in Aromatic Azo Polymers Research. Chemistry of Materials 1993;5:403-11
  7. Viswanathan NK, Kim DY, Bian SP, Williams J, Liu W, Li L, et al. Surface relief structures on azo polymer films. Journal of Materials Chemistry 1999;9:1941-55
  8. Cojocariu C, Rochon P. Light-induced motions in azobenzene-containing polymers. Pure and Applied Chemistry 2004;76:1479-97
  9. Jiang XY, Chen XB, Yue XG, Zhang JJ, Guan SW, Zhang HB, et al. Synthesis and characterization of photoactive poly(arylene ether sulfone)s containing azobenzene moieties in their main chains. Reactive & Functional Polymers 2010;70:616-21
  10. Jung WH, Ha EJ, Chung ID, Lee JO. Synthesis of aniline-based azopolymers for surface relief grating. Macromolecular Research 2008;16:532-8
  11. Apaydin DH, Akpinar H, Sendur M, Toppare L. Electrochromism in multichromic conjugated polymers: Thiophene and azobenzene derivatives on the main chain. Journal of Electroanalytical Chemistry 2012;665:52-7
  12. Acierno D, Amendola E, Bugatti V, Concilio S, Giorgini L, Iannelli P, et al. Synthesis and characterization of segmented liquid crystalline polymers with the azo group in the main chain. Macromolecules 2004;37:6418-23
  13. Faghihi K, Hagibeygi M. New aromatic polyamide with Azo and phosphine oxide groups in the main chain. Turkish Journal of Chemistry 2007;31:65-73
  14. Balasubramanian S, Kim J, Kim DY, Kumar J, Tripathy SK. Water soluble, conjugated main chain azo polymer: Synthesis and characterization. Macromolecular Rapid Communications 1996;17:853-7
  15. Wu YL, Natansohn A, Rochon P. Photoinduced birefringence and surface relief gratings in novel polyurethanes with azobenzene groups in