English

• 
  
• 1. [1]

     Nayanathara, U.; Kottegoda, N.; Perera, I. C.; Mudiyanselage, T. K. Synthesis, photodegradable and antibacterial properties of polystyrene-cinnamaldehyde copolymer film. Polym. Degrad. Stab. 2018, 155, 195-207. doi: 10.1016/j.polymdegradstab.2018.07.021

  2. [2]

     Pan, G. Y.; Jia, H. R.; Zhu, Y. X.; Wu, F. G. Turning double hydrophilic into amphiphilic: IR825-conjugated polymeric nanomicelles for near-infrared fluorescence imaging-guided photothermal cancer therapy. Nanoscale 2018, 10, 2115-2127. doi: 10.1039/C7NR07495F

  3. [3]

     Fairbanks, B. D.; Singh, S. P.; Bowman, C. N.; Anseth, K. S. Photodegradable, photoadaptable hydrogels via radical-mediated disulfide fragmentation reaction. Macromolecules 2011, 44, 2444-2450. doi: 10.1021/ma200202w

  4. [4]

     Cao, Z.; Li, Q.; Wang, G. , Photodegradable polymer nanocapsules fabricated from dimethyldiethoxysilane emulsion templates for controlled release. Polym. Chem. 2017, 8, 6817-6823. doi: 10.1039/C7PY01153A

  5. [5]

     Käpyla, E.; Delgado, S. M.; Kasko, A. M. Shape-changing photodegradable hydrogels for dynamic 3D cell culture. ACS Appl. Mater. Interfaces 2016, 8, 17885-17893. doi: 10.1021/acsami.6b05527

  6. [6]

     McKinnon, D. D.; Brown, T. E.; Kyburz, K. A.; Kiyotake, E.; Anseth, K. S. Design and characterization of a synthetically accessible, photodegradable hydrogel for user-directed formation of neural networks. Biomacromolecules 2014, 15, 2808-2816. doi: 10.1021/bm500731b

  7. [7]

     Manouras, T.; Vamvakaki, M. Field responsive materials: photo-, electro-, magnetic- and ultrasound- sensitive polymers. Polym. Chem. 2017, 8, 74-96. doi: 10.1039/C6PY01455K

  8. [8]

     Yang, F. C.; Wang, J.; Chen, L.; Wang, X.; Chen, X. Y.; Zhang, X. Soluble and degradable polyimides with phenyl-2-pyridyl ether structure: synthesis and characterization. Chinese J. Polym. Sci. 2015, 33, 481-489. doi: 10.1007/s10118-015-1602-6

  9. [9]

     Liu, Y.; Yuan, J.; Zou, Y.; Li, Y. Research progress of the furan-containing fused ring conjugated organic molecules and polymers. Acta Chim. Sin. 2017, 75, 257-270. doi: 10.6023/A16090495

  10. [10]

      Hu, Y.; Han, T.; Yan, N.; Liu, J.; Liu, X.; Wang, W. X.; Lam, J. W. Y.; Tang B. Z. Visualization of biogenic amines and in vivo ratiometric mapping of intestinal pH by AIE-active polyheterocycles synthesized by metal-free multicomponent polymerizations. Adv. Funct. Mater. 2019, 1902240. doi: 10.1002/adfm.201902240

  11. [11]

      Wang, F.; Gu, H.; Swager, T. M. Carbon nanotube/polythiophene chemiresistive sensors for chemical warfare agents. J. Am. Chem. Soc. 2008, 130, 5392-5393. doi: 10.1021/ja710795k

  12. [12]

      Afzal, A.; Abuilaiwi, F. A.; Habib, A.; Awais, M.; Waje, S. B.; Atieh, M. A. Polypyrrole/carbon nanotube supercapacitors: Technological advances and challenges. J. Power Sources 2017, 352, 174-186. doi: 10.1016/j.jpowsour.2017.03.128

  13. [13]

      Tibaoui, T.; Zaidi, B.; Bouachrine, M.; Paris, M.; Alimi, K. A study of polymers obtained by oxidative coupling of furan monomers. Synth. Met. 2011, 161, 2220-2225. doi: 10.1016/j.synthmet.2011.07.007

  14. [14]

      Yeh, I. C.; Rinderspacher, B. C.; Andzelm, J. W.; Cureton, L. T.; La Scala, J. Computational study of thermal and mechanical properties of nylons and bio-based furan polyamides. Polymer 2014, 55, 166-174. doi: 10.1016/j.polymer.2013.11.009

  15. [15]

      Streifel, B. C.; Martínez Hardigree, J. F.; Katz, H. E.; Tovar, J. D. Heteroaromatic variation in amorphous 1, 6-methano[10]annulene-based charge-transporting organic semiconductors. J. Mater. Chem. C 2014, 2, 7851-7858. doi: 10.1039/C4TC01326C

  16. [16]

      Sousa, A. F.; Vilela, C.; Fonseca, A. C.; Matos, M.; Freire, C. S. R.; Gruter, G. -J. M.; Coelho, J. F. J.; Silvestre, A. J. D. Biobased polyesters and other polymers from 2, 5-furandicarboxylic acid: a tribute to furan excellency. Polym. Chem. 2015, 6, 5961-5983. doi: 10.1039/C5PY00686D

  17. [17]

      Kaur, S.; Findlay, N. J.; Coomer, F. C.; Berridge, R.; Skabara, P. J. Poly([1, 4]dithiino[2, 3-c]Furan): The synthesis, electrochemistry, and optoelectronic properties of a furan-containing polymer. Macromol. Rapid Commun. 2013, 34, 1330-1334. doi: 10.1002/marc.v34.16

  18. [18]

      Song, B.; Hu, K.; Qin, A.; Tang, B. Z. Oxygen as a crucial comonomer in alkyne-based polymerization toward functional poly(tetrasubstituted furan)s. Macromolecules 2018, 51, 7013-7018. doi: 10.1021/acs.macromol.8b01293

  19. [19]

      Deng, H.; Hu, R. Zhao, E.; Chan, C. Y. K.; Lam, J. W. Y.; Tang, B. Z. One-pot three-component tandem polymerization toward functional poly(arylene thiophenylene) with aggregation-enhanced emission characteristics. Macromolecules 2014, 47, 4920-4929. doi: 10.1021/ma501190g

  20. [20]

      Huang, Y.; Chen, P.; Wei, B.; Hu, R.; Tang, B. Z. Aggregation-induced emission-active hyperbranched poly(tetrahydropyrimidine)s synthesized from multicomponent tandem polymerization. Chinese J. Polym. Sci. 2019, 37, 428-436. doi: 10.1007/s10118-019-2230-3

  21. [21]

      Hu, R.; Li, W.; Tang, B, Z. Recent advances in alkyne-based multicomponent polymerizations. Macromol. Chem. Phys. 2016, 217, 213-224. doi: 10.1002/macp.201500291

  22. [22]

      Kayser, L, V.; Vollmer, M.; Welnhofer, M.; Krikcziokat, H.; Meerholz, K.; Arndtsen, B, A. Metal-free, multicomponent synthesis of pyrrole-based π-conjugated polymers from imines, acid chlorides, and alkynes. J. Am. Chem. Soc. 2016, 138, 10516–10521. doi: 10.1021/jacs.6b05035

  23. [23]

      Fu, W.; Dong, L.; Shi, J.; Tong, B.; Cai, Z.; Zhi J.; Dong, Y. Synthesis of polyquinolines via one-pot polymerization of alkyne, aldehyde, and aniline under metal-free catalysis and their properties. Macromolecules 2018, 51, 3254-3263. doi: 10.1021/acs.macromol.7b02494

  24. [24]

      Liu, Y.; Qin, A.; Tang, B. Z. Polymerizations based on triple-bond building blocks. Prog. Polym. Sci. 2018, 78, 92-138. doi: 10.1016/j.progpolymsci.2017.09.004

  25. [25]

      Fu, W.; Dong, L.; Shi, J.; Tong, B.; Cai, Z.; Zhi J.; Dong, Y. Multicomponent spiropolymerization of diisocyanides, alkynes and carbon dioxide for constructing 1, 6-dioxospiro[4, 4]nonane-3, 8-diene as structural units under one-pot catalyst-free conditions. Polym. Chem. 2018, 9, 5543-5550. doi: 10.1039/C8PY01336E

  26. [26]

      Deng, X. X.; Li, L.; Li, Z. L.; Lv, A.; Du, F. S.; Li, Z. C. Sequence regulated poly(ester-amide)s based on passerini reaction. ACS Macro Lett. 2012, 1, 1300−1303. doi: 10.1021/mz300456p

  27. [27]

      Fu, W.; Kong, L.; Shi, J.; Tong, B.; Cai, Z.; Zhi J.; Dong, Y. Synthesis of poly(amine-furan-arylene)s through a one-pot catalyst-free in situ cyclopolymerization of diisocyanide, dialkylacetylene dicarboxylates and dialdehyde. Macromolecules 2019, 52, 729-737. doi: 10.1021/acs.macromol.8b02251

  28. [28]

      Mao, L.; Sakurai, H.; Hirao, T. Facile Synthesis of 2, 3-Disubstituted Quinoxalines by Suzuki-Miyaura Coupling. Synthesis 2004, 15, 2535-2539.

  29. [29]

      Sandmann, B.; Happ, B.; Vitz, J.; Paulus, R. M.; Hager, M. D.; Burtscher, P.; Moszner, N.; Schubert, U. S. Metal-Free cycloaddition of internal alkynes and multifunctional azides under solvent-free conditions. Macromol. Chem. Phys. 2014, 215, 1603-1608. doi: 10.1002/macp.v215.17

  30. [30]

      Song, B.; He, B.; Qin, A.; Tang, B. Z. Direct polymerization of carbon dioxide, diynes, and alkyl dihalides under mild reaction conditions. Macromolecules 2017, 51, 42-48. doi: 10.1021/acs.macromol.7b02109

  31. [31]

      We, B.; Li, W.; Zhao, Z.; Qin, A.; Hu, R.; Tang, B, Z. Metal-free multicomponent tandem polymerizations of alkynes, amines, and formaldehyde toward structure- and sequence- controlled luminescent polyheterocycles. J. Am. Chem. Soc. 2017, 139, 5075-5084. doi: 10.1021/jacs.6b12767

  32. [32]

      Alizadeh, A.; Rostamnia, S.; Zhu, L. G. Competition of the R3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: a novel binucleophilic system for three-component synthesis of 2-aminofurans. Synthesis 2008, 2008 (11), 1788-1792. doi: 10.1055/s-2008-1067028

  33. [33]

      Urdl, K.; Weiss, S.; Karpa, A.; Perić, M.; Zikulnig-Rusch, E.; Brecht, M.; Kandelbauer, A.; Müller, U.; Kern, W. Furan-functionalised melamine-formaldehyde particles performing Diels-Alder reactions. Eur. Polym. J. 2018, 108, 225-234. doi: 10.1016/j.eurpolymj.2018.08.023

  34. [34]

      Suzuki, Y.; Higashihara, T.; Ando, S.; Ueda, M. Synthesis and characterization of high refractive index and high abbe’s number poly(thioether sulfone)s based on tricyclo[5. 2. 1. 02, 6]decane moiety. Macromolecules 2012, 45, 3402-3408. doi: 10.1021/ma300379w

  35. [35]

      Cai, Z.; Zhang, Y.; Song, Y.; Cheng, Q.; Zheng, Y.; Cui, Z.; Shi, Z.; Chen, C.; Zhang, D. Optically transparent fluorine-containing polycarbonates with high refractive indices for thermo-optic switches. Mater. Chem. Front. 2017, 1, 2031-2038. doi: 10.1039/C7QM00209B

  36. [36]

      Faurie, A.; Mallet, C.; Allain, M.; Skene, W. G.; Frère, P. Topological and packing mode modification for solid-state emission enhancement of bis(perfluorostyryl)furan derivatives. New J. Chem. 2016, 40, 6728-6734. doi: 10.1039/C5NJ03561A

  37. [37]

      Qiu, Z.; Liu, X.; Lam, J. W. Y.; Tang, B. Z. The marriage of aggregation-induced emission with polymer science. Macromol. Rapid Commun. 2019, 40, 1800568. doi: 10.1002/marc.201800568

  38. [38]

      Hu, R.; Xin, D. H.; Qin, A. J.; Tang, B. Z. Polymers with aggregation-induced emission characteristics. Acta Polymerica Sinica (in Chinese) 2018, 18, 132-144.

  39. [39]

      Dong, H.; Zhu, H.; Meng, Q.; Gong, X.; Hu, W. Organic photoresponse materials and devices. Chem. Soc. Rev. 2012, 41, 1754-1808. doi: 10.1039/C1CS15205J

  40. [40]

      Yildirim, Y. Influence of g-ray irradiation on the thermal stability and conductivity of polyfuran. Asian J. Chem. 2013, 25, 7582-7586. doi: 10.14233/ajchem

  41. [41]

      Christensen, E.; Fioroni, G. M.; Kim, S.; Fouts, L.; Gjersing, E.; Paton, R. S.; McCormick, R. L. Experimental and theoretical study of oxidative stability of alkylated furans used as gasoline blend components. Fuel 2018, 212, 576-585. doi: 10.1016/j.fuel.2017.10.066

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