Strong fluorescence of poly ( N-vinylpyrrolidone) and its oxidized hydrolyzate

Macromolecular Rapid Communications

Volumn 36, Issue 3, 2015, Pages 278-285

  Song, Guoshan ^a   Lin, Yannan ^a   Zhu, Zhongcheng ^a   Zheng, Heying ^a   Qiao, Jinping ^a   He, Changcheng ^a   Wang, Huiliang ^a  

^a BEIJING NORMAL UNIVERSITY   (China)

Author keywords

Aggregation induced emission; Fl uorescence; Hydrolyzates; Poly( N vinylpyrrolidone); Secondary amine oxides

Indexed keywords

METAL IONS; POLYMERS;

AGGREGATION-INDUCED EMISSIONS; HYDROLYZATES; MOLECULAR COMPOUNDS; N VINYLPYRROLIDONE; N-METHYLPYRROLIDONE; N-VINYL-2-PYRROLIDONE; POLY-N-VINYLPYRROLIDONE; SECONDARY AMINES;

OXIDATION;

2 PYRROLIDONE DERIVATIVE; N-VINYL-2-PYRROLIDINONE; POLYMER;

CHEMISTRY; FLUORESCENCE;

CHEMISTRY; FLUORESCENCE; POLYMERS; PYRROLIDINONES;

EID: 84964303675     PISSN: 10221336     EISSN: 15213927     Source Type: Journal    
DOI: 10.1002/marc.201400516     Document Type: Article

References (46)

1. a) Z. Song, Y. Hong, R. T. K. Kwok, J. W. Y. Lam, B. Liu, B. Z. Tang, J. Mater. Chem. B 2014, 2, 1717
2. (b) W. Zhang, L. Xu, J. Qin, C. Yang, Macromol. Rapid Commun. 2013, 34, 442.
3. a) L. Bai, W. Li, J. Chen, F. Bo, B. Gao, H. Liu, J. Li, Y. Wu, X. Ba, Macromol. Rapid Commun. 2013, 34, 539
4. (b) Y.-X. Wu, J.-B. Li, L.-H. Liang, D.-Q. Lu, J. Zhang, G.-J. Mao, L.-Y. Zhou, X.-B. Zhang, W. Tan, G.-L. Shen, R.-Q. Yu, Chem. Commun. 2014, 50, 2040
5. (c) H. Shi, H. Sun, H. Yang, S. Liu, G. Jenkins, W. Feng, F. Li, Q. Zhao, B. Liu, W. Huang, Adv. Funct. Mater. 2013, 23, 3268
6. (d) M. Chen, M. Yin, Prog. Polym. Sci. 2014, 39, 365.
7. a) F. Qiu, D. Wang, Q. Zhu, L. Zhu, G. Tong, Y. Lu, D. Yan, X. Zhu, Biomacromolecules 2014, 15, 1355
8. (b) B. Kang, M. M. Afifi, L. A. Austin, M. A. El-Sayed, ACS Nano 2013, 7, 7420.
9. J. N. Brantley, C. B. Bailey, J. R. Cannon, K. A. Clark, D. A. Vanden Bout, J. S. Brodbelt, A. T. Keatinge-Clay, C. W. Bielawski, Angew. Chem. Int. Ed. 2014, 53, 5088.
10. a) A. P. Alivisatos, Science 1996, 271, 933
11. (b) Y. Song, S. Zhu, B. Yang, RSC Adv. 2014, 4, 27184
12. (c) A. Lourenco, T. Casimiro, V. D. B. Bonifacio, Talanta 2014, 125, 319.
13. a) M. Li, L.-H. Feng, H.-Y. Lu, S. Wang, C.-F. Chen, Adv. Funct. Mater. 2014, 24, 4405
14. (b) A. Braganca, M. Araujo, V. D. B. Bonifacio, Part. Part. Syst. Charact. 2014, DOI: 10.1002/ppsc.201400120.
15. a) C. Munkholm, D. R. Parkinson, D. R. Walt, J. Am. Chem. Soc. 1990, 112, 2608
16. (b) B.-P. Jiang, D.-S. Guo, Y.-C. Liu, K.-P. Wang, Y. Liu, ACS Nano 2014, 8, 1609.
17. a) J. Luo, Z. Xie, J. W. Y. Lam, L. Cheng, H. Chen, C. Qiu, H. S. Kwok, X. Zhan, Y. Liu, D. Zhu, B. Z. Tang, Chem. Commun. 2001, 1740
18. (b) Y. Hong, J. W. Y. Lam, B. Z. Tang, Chem. Soc. Rev. 2011, 40, 5361
19. (c) A. Qin, J. W. Y. Lam, B. Z. Tang, Prog. Polym. Sci. 2012, 37, 182.
20. T. Huang, Z. Wang, A. Qin, J. Z. Sun, B. Z. Tang, Acta Chim. Sinica 2013, 71, 979.
21. a) G. A. Crosby, J. N. Demas, J. Phys. Chem. 1971, 75, 991
22. (b) W. I. Lee, Y. Bae, A. J. Bard, J. Am. Chem. Soc. 2004, 126, 8358
23. (c) L. Cao, W. Yang, C. Wang, S. Fu, J. Macromol. Sci., Part A 2007, 44, 417
24. (d) W. Yang, C.-Y. Pan, Macromol. Rapid Commun. 2009, 30, 2096
25. (e) Y.-Z. You, Z.-Q. Yu, M.-M. Cui, C.-Y. Hong, Angew. Chem. Int. Ed. 2010, 49, 1099
26. (f) D. Wang, Z.-Q. Yu, C.-Y. Hong, Y.-Z. You, Eur. Polym. J. 2013, 49, 4189.
27. a) D. C. Wu, Y. Liu, C. B. He, S. H. Goh, Macromolecules 2005, 38, 9906
28. (b) M. Sun, C.-Y. Hong, C.-Y. Pan, J. Am. Chem. Soc. 2012, 134, 20581.
29. Y. Lin, J.-W. Gao, H.-W. Liu, Y.-S. Li, Macromolecules 2009, 42, 3237.
30. R. B. Restani, P. I. Morgado, M. P. Ribeiro, I. J. Correia, A. Aguiar-Ricardo, V. D. B. Bonifácio, Angew. Chem. Int. Ed. 2012, 51, 5162.
31. C. M. Xing, J. W. Y. Lam, A. J. Qin, Y. Q. Dong, M. Haussler, W. T. Yang, B. Z. Tang, Polym. Mater. Sci. Eng. 2007, 96, 418.
32. A. Pucci, R. Rausa, F. Ciardelli, Macromol. Chem. Phys. 2008, 209, 900.
33. J.-J. Yan, Z.-K. Wang, X.-S. Lin, C.-Y. Hong, H.-J. Liang, C.-Y. Pan, Y.-Z. You, Adv. Mater. 2012, 24, 5617.
34. T. Trellenkamp, H. Ritter, Macromolecules 2010, 43, 5538.
35. D. Darwis, N. Hilmy, L. Hardiningsih, T. Erlinda, Radiat. Phys. Chem. 1993, 42, 907.
36. a) T. M. Zima, I. A. Vorsina, N. Z. Lyakhov, Inorg. Mater. 2009, 45, 524
37. (b) M. Yin, Y. Ye, M. Sun, N. Kang, W. Yang, Macromol. Rapid Commun. 2013, 34, 616.
38. a) T.-H. Wu, C.-P. Liu, C.-T. Chien, S.-Y. Lin, Chem. Eur. J. 2013, 19, 11672
39. (b) M. Thiverny, E. Demory, B. Baptiste, C. Philouze, P. Y. Chavant, V. Blandin, Tetrahedron: Asymmetry 2011, 22, 1266
40. (c) S.-I. Murahashi, T. Shiota, Tetrahedron Lett. 1987, 28, 2383.
41. E. Pretsch, P. Bühlmann, C. Affolter, Structure Determination of Organic Compounds: Tables of Spectral Data, Springer, Berlin 2000, p. 295.
42. C. G. Freeman, M. J. McEwan, R. F. C. Claridge, L. F. Phillips, Chem. Phys. Lett. 1971, 8, 77.
43. N. Tokman, S. Akman, C. Ozeroglu, Talanta 2004, 63, 699.
44. T. Çaykara, R. Inam, Z. Öztürk, O. Güven, Colloid. Polym. Sci. 2004, 282, 1282.
45. D. Wang, T. Imae, J. Am. Chem. Soc. 2004, 126, 13204.
46. S.-F. Shiau, T.-Y. Juang, H.-W. Chou, M. Liang, Polymer 2013, 54, 623 .