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Poly[4-pyridinyl-4´-(2-methacryloyloxyethoxy)styryl ketone-co-2- hydroxypropyl methacrylate]: Synthesis, Characterization, Thermal and Electrical properties, and Photocrosslinking behavior

Year 2018, Volume: 5 Issue: 1, 24 - 34, 31.01.2018
https://doi.org/10.31202/ecjse.339908

Abstract

Synthesis of a chalcone bearing pyridine ring, 4-pyridinyl-4´-(2-hydroxyethoxy)styryl ketone, was carried out from the reaction of 4-acetyl pyridine and 4-(2-hydroxyetoxy)benzaldehyde in an aqueous solution of NaOH. 4-Pyridinyl-4´-(2-methacryloyloxyethoxy)styryl ketone which is the methacrylate monomer bearing chalcone structure in side chain, was obtained from acylation of 4-pyridinyl-4´-(2-hydroxyethoxy)styryl ketone with methacryloyl chloride in the cold. The copolymer of 4-pyridinyl-4´-(2-methacryloyloxyethoxy)styryl ketone and 2-hydroxypropyl methacrylate was prepared by free radical polymerization in presence of AIBN at 70 oC. FTIR, 1H-NMR and 13C-APT spectroscopic techniques were used for structural characterization of the Chalcone, the monomer and the copolymer. Thermal characterization of the copolymer was carried out using DSC and TGA techniques. DSC curve shows that this copolymer has a glass transition temperature of 78 oC. The TGA curve shows that decomposition given volatile product started at 230 °C and a residue of 21% left at 500 °C. Dielectric constant (ε´) of the copolymer decreased rapidly from 8.8 to 4.2 with increasing frequency in the range of 100-1000 Hz, and after this frequency ε´ quantity remained constant at a value such as 4.2. ε´ Value of the copolymer increased only from 4.2 to 4.9 with increasing from 290 K to 385 K. The AC conductivity of the copolymer increases from 5.01x10-10 S/cm to 126.0x10-10 S/cm as the frequency increase from 100 Hz to 5000 Hz. The AC conductivity increases slightly with increasing temperature, 2.52x10-9 S/cm at 300 K, and 2.89x10-9 S/cm at 385 K. After a solution of the copolymer was irradiated using UV light at 365 nm at room temperature, the absorption band at 356 nm disappeared and a new band was seen at 284 nm.

References

  • Yerragunta, V.; Kumaraswamy, T.; Suman, D.; Anusha, V.; Patil, P.; Samhitha, T., A review on Chalcones and its importance, Pharma.Tutor. 2013, 1(2): p. 54-59.
  • Chavan, B. B.; Gadekar, A. S.; Mehta, P. P.; Vawhal, P. K.; Kolsure, A. K.; Chabukswar, A. R., Synthesis and Medicinal Significance of Chalcones- A Review, Asian J. Biomed. Pharma. Sci., 2016, 6(56): p. 01-07.
  • Rusu, E.; Oncius, M., Polycondensates of 2´-(Chalcone-4-Oxy)-Ethyl-3,5-Diaminobenzoate with Some Aromatic Dicarboxylic Acids, J.M.S. Part A: Pure and Appl. Chem., 2005, 42: p.1025–1036.
  • Kaniappan, K.; Murugavel, S.C., Synthesis and Characterization of Photosensitive Phosphorus Based Polymers Containing ,β-Unsaturated Ketones in the Main Chain, J.M.S. Part A: Pure and Appl. Chem., 2005, 42: p.1589–1602.
  • Selvam, P.; Babu, K.C.; Penlidis, A.; Nanjundan, Dr. S., Copolymers of 4‐(3′,4′‐Dimethoxycinnamoyl)phenyl Acrylate and MMA: Synthesis, Characterization, Photocrosslinking Properties, and Monomer Reactivity Ratios, J.M.S. Part A: Pure and Appl. Chem., 2004, A41(7): p.791–809.
  • Faghihi, K.; Hajibeygi, M.; Shabanian, M., Photosensitive and Optically Active Poly(amide-imide)s Based on N,N- (pyromellitoyl)-bis-L-amino acid and Dibenzalacetone Moiety in the Main Chain: Synthesis and Characterization, J.M.S. Part A: Pure and Appl. Chem., 2010, 47: p.144-153.
  • Ahmed Rehab, Studies of Photoreactive Poly(Norbornene Derivatives) Bearing Chalcone Units, J.M.S. Part A: Pure and Appl. Chem., 2003, A40(7): p.689-703.
  • Perundevi, T.S.; Jonathan, D.R.; Kothai,S., Synthesis And Characterization of Certain Photocrosslinkable Random Copolyesters With Bischalcone Moiety, Int. J. Adv. Research, 2015, 3(3): p. 1147-1154.
  • Nanjundan, S.; Selvamalar, C.S.J., Synthesis, Characterization and Photocrosslinking Properties of Poly(1-(4-Methacrylamidophenyl)-1-(4-nitrophenyl)prop-1-en-3-one), J.M.S. Part A: Pure and Appl. Chem., 2006, 43: p.1189-1203.
  • Balaji, R.; Nanjundan,S., Studies on Photosensitive Homopolymer and Copolymers Having a Pendant Photocrosslinkable Functional Group, J. Appl. Polym. Sci., 2002, 86: p. 1023–1037.
  • Tamilvanan, M.; Pandurangan, A.; Subramanian, K.; Reddy, B.S.R., Synthesis and characterization of mono- and di-methoxy substituted acrylate polymers containing photocrosslinkable pendant chalcone moiety, Polym. Adv. Technol. 2008, 19: p.1218–1225.
  • Mahy, R.; Bouammali, B.; Oulmidi, A.; Challioui, A.; Derouet, D.; Brosse, J.C., Photosensitive polymers with cinnamate units in the side position of chains: Synthesis, monomer reactivity ratios and photoreactivity, Eur. Polym. J., 2006,42: p. 2389–2397.
  • Balajia, R.; Grande, D.; Nanjundan, S., Photoresponsive polymers having pendant chlorocinnamoyl moieties: synthesis, reactivity ratios and photochemical properties, Polymer, 2004, 45: p.1089–1099.
  • Rehab, A.; Salahuddin, N., (1999): Photocrosslinked polymers based on pendant extended chalcone as photoreactive moieties, Polymer, 1999, 40(9): p. 2197-2207.
  • Kawatsuki, N.; Yamamoto, T.; Ono, H., Photoinduced alignment control of photoreactive side-chain polymer liquid crystal by linearly polarized UV light, Appl. Phys. Lett., 1999, 74: p.935-937.
  • Book review, Reiser A., Photoreactive polymers. The science and technology of resists. by Arnost Reiser, John Wiley and Sons, New York, 1989, 409 pp.
  • Nagamatsu, G.; Inui, H., Photosensitive polymers. Tokyo: Kodansha, 1977.
  • Ferreira, P.; Coelho,J.F.J.; J. F. Almeida, J.F.; Gil, M.H., Photocrosslinkable Polymers for Biomedical Applications, Biomedical Engineering - Frontiers and Challenges Edited by Prof. Reza Fazel, 2011, ISBN: 978-953-307-309-5.
  • Mene, B.; Kerman, K.; Ozkan, D.; Kara, P.; Erdem, A.; Kucukoglu, O.; Ereiyas, E.; Ozsoz, M., Electrochemical Biosensor for the interaction of DNA with the alkylating agent, 4,4'-dihydroxy chalcone based on guanine and adenine signals, J. Pharm. Biomed. Anal., 2002, 30: p.1339-1346.
  • Doroshenko, A.O.; Grigorovich, A.V.; Posokhov, E.A.; Pivovarenko, V.G.; Demchenko, A.P., Bis-Azacrown Derivative of Di-Benzilidene-Cyclopentanone as Alkali Earth Ion Chelating Probe: Spectroscopic Properties, Proton Accepting Ability and Complex Formation with Mg2+ and Ba2+ Ions, Mol. Eng., 1999, 8(3): p.199-205.
  • Marcotte, N.; Fery-Forgues, S.; Lavabre, D.; Marguet, S.; Pivovarenko, V.G., Spectroscopic study of a symmetrical bis-crown fluoroionophore of the diphenylpertadienone series, J. Phys. Chem., A , 1999, 103: p.3163-3170.
  • Ayaz, N.; Bezgin, F.; Demırellı, K., Polymers Based on Methacrylate Bearing Coumarin Side Group: Synthesis via Free Radical Polymerization,Monomer Reactivity Ratios, Dielectric Behavior, and Thermal Stabilities, ISRN Polym. Sci., 2012, Article ID 352759, doi:10.5402/2012/352759.
  • Pandey, A.S.; Dhar, R.; Achalkumar, A.S.; Yelamaggad, C.V., Thermodynamic, optical and dielectric properties of the twisted grain boundary phases of the homologous series of 4-n-alkyloxy-4′-(cholesteryloxycarbonyl-1-butyloxy) chalcone, Liquid Crystals, 2011, 38(6): p.775–784.
  • Coşkun, M.; Seven, P., Synthesis, characterization and investigation of dielectric properties of two-armed graft copolymers prepared with methyl methacrylate and styrene onto PVC using atom transfer radical polymerization, React. Funct. Polym.,2011, 71: p.395-401.
  • Tamilvanan, M.; Pandurangan, A.; Reddy, B.S.R.; Subramanian, K., Synthesis, characterization and properties of photoresponsive polymers comprising photocrosslinkable pendant chalcone moieties, Polym. Int.,2007, 56: p.104–111.
  • CROW logo Polymer Properties Database, Copyright © 2015 polymerdatabase.com.
  • http://www.polysciences.com/skin/frontend/default/polysciences/images/logo.png, CAS#: 25703-79-1.
  • Yilmaz, S.; Coşkun, M., Synthesis of an ABC Type Triblock Copolymer on MWCNT Surface: Structural, Thermal, Electrical and SEM Characterization, El-Cezerî J. Sci. Eng., 2017, 4(2): p.177-189.
  • So, H. H.; Cho, J. W.; Sahoo, N. G., Effect of carbon nanotubes on mechanical and electrical properties of polyimide/carbon nanotubes nanocomposites, Eur. Polym. J., 2007, 43: 3750–3756.
  • Yılmaz, S.; Coşkun, M., Thermal and electrical behaviors of acid functionalized MWCNT/ABC-type triblock copolymer grafted-MWCNT nanocomposites, J.M.S. Part A: Pure Appl. Chem., 2017, https://doi.org/10.1080/10601325.2017.1336723.
  • Balaji, R.; Nanjundan, S., Synthesis and characterization of photocrosslinkable functional polymer having pendant chalcone moiety, React. Funct. Polym. 2001, 49: p. 77– 86.
  • Subramanian, K.; Nanjundan, S.; Reddy, A.V.R., Synthesis and characterization of copolymers with a photosensitive group, Eur. Polym. J., 2001, 37: p.691-698.
  • Santhi, R.; Babu, K.V.; Penlidis, A.; Nanjundan, S., Studies on copolymers of 3-methacryloyloxystyryl-4´-methylphenyl ketone and methyl methacrylate, React. Funct. Polym. 2006, 66: p. 1215-1226.
  • Selvam, P.; Nanjundan, S., Synthesis and characterization of new photoresponsive acrylamide polymers having pendant chalcone moieties, React. Funct. Polym. 2005, 62: p. 179– 193.

Poli[4-piridinil-4´-(2-metakriloiloksietoksi)stiril keton-ko-2-hidroksipropil metakrilat]: Sentezi, Karakterizasyonu, Termal ve Elektriksel Özellikleri ve Fotoçaprazbağlanma Davranışı

Year 2018, Volume: 5 Issue: 1, 24 - 34, 31.01.2018
https://doi.org/10.31202/ecjse.339908

Abstract



Piridin halkası taşıyan kalkonun sentezi, 4-piridinil-4´-(2-hidroksietoksi)stiril keton, 4-asetil piridin ve 4-(2-hidroksietoksi)benzaldehitin NaOH in sulu çözeltisinde reaksiyonundan gerçekleştirildi. Yan zincirinde kalkon yapısı taşıyan bir metakrilat monomeri olan 4-piridinil-4´-(2-metakriloiloksietoksi)stiril keton, 4-piridinil-4´-(2-hidroksietoksi)stiril ketonun metakriloil klorürle soğukta açillenmesinden elde edildi. 4-piridinil-4´-(2-metakriloiloksietoksi)stiril keton ve 2-hidroksipropil metakrilatın kopolimeri, AİBN yanında 70 oC de serbest radikal polimerizasyonuyla elde edildi. Kalkon, monomer ve kopolimerin yapısal karakterizasyonunda FTIR, 1H-NMR ve 13C-APT spektroskopik teknikleri kullanıldı. Kopolimerin termal karakterizasyonu DSC ve TGA teknikleriyle gerçekleştirildi. DSC eğrisi kopolimerin camsı geçiş sıcaklığının 78 oC olduğunu gösterdi. TGA eğrisi uçucu madde veren temel parçalanmanın 230 oC de başladığını ve 500 oC de %21 artık bıraktığını gösterdi. Kopolimerin dielektrik sabiti (ε´) 100-1000 Hz aralığında artan frekansla 8.8 den 4.2 ye hızla düştü ve bu frekanstan sonra ε´ niceliği 4.2 gibi bir değerdeDielectric constant (ε´) of the copolymer decreased rapidly from 8.8 to 4.2 with increasing frequency in the range of 100-1000 Hz, and after this frequency ε´ quantity remained constant at a value such as 4.2. ε´ Value of the copolymer increased only from 4.2 to 4.9 with increasing from 290 K to 385 K. The AC conductivity of the copolymer increases from 5.01x10-10 S/cm to 126.0x10-10 S/cm as the frequency increase from 100 Hz to 5000 Hz. The AC conductivity increases slightly with increasing temperature, 2.52x10-9 S/cm at 300 K, and 2.89x10-9 S/cm at 385 K. After a solution of the copolymer was irradiated using UV light at 365 nm at room temperature, the absorption band at 356 nm disappeared and a new band was seen at 284 nm. sabit kaldı. Kopolimerin ε´ değeri, sıcaklık 290 K den 385 K e artarken sadece 4.2 den 4.9´a yükseldi. Kopolimerin AC iletkenliği, frekansın 100 Hz´den 5000 Hz´e çıkmasıyla 5.01x10-10 S/cm´den 126.0x10-10 S/cm´ye arttı. AC iletkenliği artan sıcaklıkla çok az yükseldi, 300 K´de 2.52x10-9 S/cm ve 385 K´de 2.89x10-9 S/cm. Kopolimerin bir çözeltisi 365 nm dalga boylu UV ışığa maruz bırakıldığında 356 nm´deki band kayboldu ve 284 nm´de yeni bir band oluştu.



References

  • Yerragunta, V.; Kumaraswamy, T.; Suman, D.; Anusha, V.; Patil, P.; Samhitha, T., A review on Chalcones and its importance, Pharma.Tutor. 2013, 1(2): p. 54-59.
  • Chavan, B. B.; Gadekar, A. S.; Mehta, P. P.; Vawhal, P. K.; Kolsure, A. K.; Chabukswar, A. R., Synthesis and Medicinal Significance of Chalcones- A Review, Asian J. Biomed. Pharma. Sci., 2016, 6(56): p. 01-07.
  • Rusu, E.; Oncius, M., Polycondensates of 2´-(Chalcone-4-Oxy)-Ethyl-3,5-Diaminobenzoate with Some Aromatic Dicarboxylic Acids, J.M.S. Part A: Pure and Appl. Chem., 2005, 42: p.1025–1036.
  • Kaniappan, K.; Murugavel, S.C., Synthesis and Characterization of Photosensitive Phosphorus Based Polymers Containing ,β-Unsaturated Ketones in the Main Chain, J.M.S. Part A: Pure and Appl. Chem., 2005, 42: p.1589–1602.
  • Selvam, P.; Babu, K.C.; Penlidis, A.; Nanjundan, Dr. S., Copolymers of 4‐(3′,4′‐Dimethoxycinnamoyl)phenyl Acrylate and MMA: Synthesis, Characterization, Photocrosslinking Properties, and Monomer Reactivity Ratios, J.M.S. Part A: Pure and Appl. Chem., 2004, A41(7): p.791–809.
  • Faghihi, K.; Hajibeygi, M.; Shabanian, M., Photosensitive and Optically Active Poly(amide-imide)s Based on N,N- (pyromellitoyl)-bis-L-amino acid and Dibenzalacetone Moiety in the Main Chain: Synthesis and Characterization, J.M.S. Part A: Pure and Appl. Chem., 2010, 47: p.144-153.
  • Ahmed Rehab, Studies of Photoreactive Poly(Norbornene Derivatives) Bearing Chalcone Units, J.M.S. Part A: Pure and Appl. Chem., 2003, A40(7): p.689-703.
  • Perundevi, T.S.; Jonathan, D.R.; Kothai,S., Synthesis And Characterization of Certain Photocrosslinkable Random Copolyesters With Bischalcone Moiety, Int. J. Adv. Research, 2015, 3(3): p. 1147-1154.
  • Nanjundan, S.; Selvamalar, C.S.J., Synthesis, Characterization and Photocrosslinking Properties of Poly(1-(4-Methacrylamidophenyl)-1-(4-nitrophenyl)prop-1-en-3-one), J.M.S. Part A: Pure and Appl. Chem., 2006, 43: p.1189-1203.
  • Balaji, R.; Nanjundan,S., Studies on Photosensitive Homopolymer and Copolymers Having a Pendant Photocrosslinkable Functional Group, J. Appl. Polym. Sci., 2002, 86: p. 1023–1037.
  • Tamilvanan, M.; Pandurangan, A.; Subramanian, K.; Reddy, B.S.R., Synthesis and characterization of mono- and di-methoxy substituted acrylate polymers containing photocrosslinkable pendant chalcone moiety, Polym. Adv. Technol. 2008, 19: p.1218–1225.
  • Mahy, R.; Bouammali, B.; Oulmidi, A.; Challioui, A.; Derouet, D.; Brosse, J.C., Photosensitive polymers with cinnamate units in the side position of chains: Synthesis, monomer reactivity ratios and photoreactivity, Eur. Polym. J., 2006,42: p. 2389–2397.
  • Balajia, R.; Grande, D.; Nanjundan, S., Photoresponsive polymers having pendant chlorocinnamoyl moieties: synthesis, reactivity ratios and photochemical properties, Polymer, 2004, 45: p.1089–1099.
  • Rehab, A.; Salahuddin, N., (1999): Photocrosslinked polymers based on pendant extended chalcone as photoreactive moieties, Polymer, 1999, 40(9): p. 2197-2207.
  • Kawatsuki, N.; Yamamoto, T.; Ono, H., Photoinduced alignment control of photoreactive side-chain polymer liquid crystal by linearly polarized UV light, Appl. Phys. Lett., 1999, 74: p.935-937.
  • Book review, Reiser A., Photoreactive polymers. The science and technology of resists. by Arnost Reiser, John Wiley and Sons, New York, 1989, 409 pp.
  • Nagamatsu, G.; Inui, H., Photosensitive polymers. Tokyo: Kodansha, 1977.
  • Ferreira, P.; Coelho,J.F.J.; J. F. Almeida, J.F.; Gil, M.H., Photocrosslinkable Polymers for Biomedical Applications, Biomedical Engineering - Frontiers and Challenges Edited by Prof. Reza Fazel, 2011, ISBN: 978-953-307-309-5.
  • Mene, B.; Kerman, K.; Ozkan, D.; Kara, P.; Erdem, A.; Kucukoglu, O.; Ereiyas, E.; Ozsoz, M., Electrochemical Biosensor for the interaction of DNA with the alkylating agent, 4,4'-dihydroxy chalcone based on guanine and adenine signals, J. Pharm. Biomed. Anal., 2002, 30: p.1339-1346.
  • Doroshenko, A.O.; Grigorovich, A.V.; Posokhov, E.A.; Pivovarenko, V.G.; Demchenko, A.P., Bis-Azacrown Derivative of Di-Benzilidene-Cyclopentanone as Alkali Earth Ion Chelating Probe: Spectroscopic Properties, Proton Accepting Ability and Complex Formation with Mg2+ and Ba2+ Ions, Mol. Eng., 1999, 8(3): p.199-205.
  • Marcotte, N.; Fery-Forgues, S.; Lavabre, D.; Marguet, S.; Pivovarenko, V.G., Spectroscopic study of a symmetrical bis-crown fluoroionophore of the diphenylpertadienone series, J. Phys. Chem., A , 1999, 103: p.3163-3170.
  • Ayaz, N.; Bezgin, F.; Demırellı, K., Polymers Based on Methacrylate Bearing Coumarin Side Group: Synthesis via Free Radical Polymerization,Monomer Reactivity Ratios, Dielectric Behavior, and Thermal Stabilities, ISRN Polym. Sci., 2012, Article ID 352759, doi:10.5402/2012/352759.
  • Pandey, A.S.; Dhar, R.; Achalkumar, A.S.; Yelamaggad, C.V., Thermodynamic, optical and dielectric properties of the twisted grain boundary phases of the homologous series of 4-n-alkyloxy-4′-(cholesteryloxycarbonyl-1-butyloxy) chalcone, Liquid Crystals, 2011, 38(6): p.775–784.
  • Coşkun, M.; Seven, P., Synthesis, characterization and investigation of dielectric properties of two-armed graft copolymers prepared with methyl methacrylate and styrene onto PVC using atom transfer radical polymerization, React. Funct. Polym.,2011, 71: p.395-401.
  • Tamilvanan, M.; Pandurangan, A.; Reddy, B.S.R.; Subramanian, K., Synthesis, characterization and properties of photoresponsive polymers comprising photocrosslinkable pendant chalcone moieties, Polym. Int.,2007, 56: p.104–111.
  • CROW logo Polymer Properties Database, Copyright © 2015 polymerdatabase.com.
  • http://www.polysciences.com/skin/frontend/default/polysciences/images/logo.png, CAS#: 25703-79-1.
  • Yilmaz, S.; Coşkun, M., Synthesis of an ABC Type Triblock Copolymer on MWCNT Surface: Structural, Thermal, Electrical and SEM Characterization, El-Cezerî J. Sci. Eng., 2017, 4(2): p.177-189.
  • So, H. H.; Cho, J. W.; Sahoo, N. G., Effect of carbon nanotubes on mechanical and electrical properties of polyimide/carbon nanotubes nanocomposites, Eur. Polym. J., 2007, 43: 3750–3756.
  • Yılmaz, S.; Coşkun, M., Thermal and electrical behaviors of acid functionalized MWCNT/ABC-type triblock copolymer grafted-MWCNT nanocomposites, J.M.S. Part A: Pure Appl. Chem., 2017, https://doi.org/10.1080/10601325.2017.1336723.
  • Balaji, R.; Nanjundan, S., Synthesis and characterization of photocrosslinkable functional polymer having pendant chalcone moiety, React. Funct. Polym. 2001, 49: p. 77– 86.
  • Subramanian, K.; Nanjundan, S.; Reddy, A.V.R., Synthesis and characterization of copolymers with a photosensitive group, Eur. Polym. J., 2001, 37: p.691-698.
  • Santhi, R.; Babu, K.V.; Penlidis, A.; Nanjundan, S., Studies on copolymers of 3-methacryloyloxystyryl-4´-methylphenyl ketone and methyl methacrylate, React. Funct. Polym. 2006, 66: p. 1215-1226.
  • Selvam, P.; Nanjundan, S., Synthesis and characterization of new photoresponsive acrylamide polymers having pendant chalcone moieties, React. Funct. Polym. 2005, 62: p. 179– 193.
There are 34 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Makaleler
Authors

Ela Nur Aygün This is me

Mehmet Coşkun

Publication Date January 31, 2018
Submission Date September 25, 2017
Acceptance Date October 20, 2017
Published in Issue Year 2018 Volume: 5 Issue: 1

Cite

IEEE E. N. Aygün and M. Coşkun, “Poly[4-pyridinyl-4´-(2-methacryloyloxyethoxy)styryl ketone-co-2- hydroxypropyl methacrylate]: Synthesis, Characterization, Thermal and Electrical properties, and Photocrosslinking behavior”, El-Cezeri Journal of Science and Engineering, vol. 5, no. 1, pp. 24–34, 2018, doi: 10.31202/ecjse.339908.
Creative Commons License El-Cezeri is licensed to the public under a Creative Commons Attribution 4.0 license.
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