Nanohybrid conjugated polyelectrolytes: highly photostable and ultrabright nanoparticles
Source abstract
Abstract
We present a general and straightforward one-step approach to enhance the photophysical properties of conjugated polyelectrolytes. Upon complexation with an amphiphilic polymer (polyvinylpyrrolidone), an anionic conjugated polyelectrolyte (poly[5-methoxy-2-(3-sulfopropoxy)-1,4-phenylenevinylene]) was prepared into small nanoparticles with exceptional photostability and brightness. The polymer fluorescence intensity was enhanced by 23 -fold and could be easily tuned by changing the order of addition. Single molecule experiments revealed a complete suppression of blinking. In addition, after only losing 18% of the original intensity, a remarkable amount of photons were emitted per particle (∼10(9), on average). This number is many folds greater than popular organic fluorescent dyes. We believe that an intimate contact between the two polymers is shielding the conjugated polyelectrolyte from the destructive photooxidation. The prepared nanohybrid particles will prove instrumental in single particle based fluorescent assays and can serve as a probe for the current state-of-the-art bioimaging fluorescence techniques.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Perovskite Materials and Applications · Polydiacetylene-based materials and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry
American University of Beirut
Beirut, Lebanon
Funding
Academy of Sciences for the Developing World
References (53)
Show source-provided references
1. Ngo · Pure Appl. Chem. · 2010 · 83 · 4310.1351/PAC-CON-10-11-02 ↗
2. Jiang · Angew. Chem., Int. Ed. · 2009 · 48 · 430010.1002/anie.200805456 ↗
3. Seo · J. Am. Chem. Soc. · 2011 · 133 · 841610.1021/ja2037673 ↗
4. He · Nat. Photonics · 2012 · 6 · 59110.1038/nphoton.2012.190 ↗
5. He · Adv. Mater. · 2011 · 23 · 463610.1002/adma.201103006 ↗
6. Lu · Langmuir · 2005 · 21 · 1015410.1021/la046987q ↗
7. Karam · Langmuir · 2014 · 30 · 1070410.1021/la502572u ↗
8. Ogawa · Langmuir · 2007 · 23 · 454110.1021/la0630108 ↗
9. Chemburu · J. Phys. Chem. B · 2008 · 112 · 1449210.1021/jp803358j ↗
10. Achyuthan · J. Mater. Chem. · 2005 · 15 · 264810.1039/b501314c ↗
11. Wang · Proc. Natl. Acad. Sci. U. S. A. · 2002 · 99 · 4910.1073/pnas.012581399 ↗
12. Liang · J. Mater. Chem. · 2013 · 4 · 1377
13. Pinto · Proc. Natl. Acad. Sci. U. S. A. · 2004 · 101 · 750510.1073/pnas.0402280101 ↗
14. Tan · Chem. Commun. · 2002 · 44610.1039/b109630c ↗
15. Thomas · Chem. Rev. · 2007 · 107 · 133910.1021/cr0501339 ↗
16. Zhou · J. Am. Chem. Soc. · 1995 · 117 · 701710.1021/ja00131a031 ↗
17. Gaylord · Proc. Natl. Acad. Sci. U. S. A. · 2002 · 99 · 1095410.1073/pnas.162375999 ↗
18. Gaylord · J. Am. Chem. Soc. · 2003 · 125 · 89610.1021/ja027152+ ↗
19. Liu · Chem. Mater. · 2004 · 16 · 446710.1021/cm049587x ↗
20. Zhao · Chem. Commun. · 2007 · 291410.1039/b706629e ↗
21. Chen · Proc. Natl. Acad. Sci. U. S. A. · 1999 · 96 · 1228710.1073/pnas.96.22.12287 ↗
22. Duarte · J. Am. Chem. Soc. · 2010 · 132 · 1256210.1021/ja105747b ↗
23. Dalgarno · J. Am. Chem. Soc. · 2013 · 135 · 718710.1021/ja311874f ↗
24. Pu · Adv. Funct. Mater. · 2011 · 21 · 340810.1002/adfm.201101153 ↗
25. Huser · Proc. Natl. Acad. Sci. U. S. A. · 2000 · 97 · 1118710.1073/pnas.97.21.11187 ↗
26. Karam · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · 1748010.1073/pnas.1008068107 ↗
27. Yan · Phys. Rev. Lett. · 1994 · 73 · 74410.1103/PhysRevLett.73.744 ↗
28. Barbara · Acc. Chem. Res. · 2005 · 38 · 60210.1021/ar040141w ↗
29. Montano · Chem. Commun. · 2004 · 2490–249110.1039/b401682c ↗
30. Ngo · Langmuir · 2009 · 26 · 674610.1021/la904100q ↗
31. Ngo · J. Am. Chem. Soc. · 2008 · 130 · 45710.1021/ja076217b ↗
32. Liu · Anal. Chem. · 2007 · 80 · 15010.1021/ac701672g ↗
33. Viger · J. Phys. Chem. C · 2011 · 115 · 297410.1021/jp109993a ↗
34. Lee · Macromolecules · 2011 · 44 · 474210.1021/ma200574d ↗
35. Jiang · J. Am. Chem. Soc. · 2004 · 126 · 1208410.1021/ja048912e ↗
36. Koenen · ACS Macro Lett. · 2014 · 3 · 40510.1021/mz500067k ↗
37. Scurlock · J. Am. Chem. Soc. · 1995 · 117 · 1019410.1021/ja00146a004 ↗
38. Dou · J. Phys. Chem. B · 2008 · 112 · 1268110.1021/jp805345d ↗
39. Liu · J. Am. Chem. Soc. · 2011 · 134 · 164810.1021/ja208437e ↗
40. Torchilin · Biomaterials · 2001 · 22 · 303510.1016/S0142-9612(01)00050-3 ↗
41. Huang · ACS Nano · 2010 · 4 · 715110.1021/nn101643u ↗
42. Lee · Macromol. Res. · 2007 · 15 · 54710.1007/BF03218829 ↗
43. Kamada · Cancer Res. · 2000 · 60 · 6416
44. Resch-Genger · Nat. Methods · 2008 · 5 · 76310.1038/nmeth.1248 ↗
45. Tretiak · Phys. Rev. Lett. · 2002 · 89 · 09740210.1103/PhysRevLett.89.097402 ↗
46. Godin · J. Phys. Chem. C · 2015 · 119 · 1287510.1021/acs.jpcc.5b03491 ↗
47. Wu · ACS Nano · 2008 · 2 · 241510.1021/nn800590n ↗
48. Schönle · Opt. Lett. · 1998 · 23 · 32510.1364/OL.23.000325 ↗
49. Schmidt · Single Molecules · 2002 · 3 · 32710.1002/1438-5171(200211)3:5/6<327::AID-SIMO327>3.0.CO;2-8 ↗
50. Wu · J. Am. Chem. Soc. · 2007 · 129 · 1290410.1021/ja074590d ↗
51. Wichterlová · Polymer · 2005 · 46 · 997410.1016/j.polymer.2005.06.125 ↗
52. Hadassah · Clin. Exp. Optom. · 2006 · 89 · 37410.1111/j.1444-0938.2006.00080.x ↗
53. Tian · NPG Asia Mater · 2014 · 6 · e13410.1038/am.2014.91 ↗