journal article·2013-06-25

A “Plug-and-Play” Method to Prepare Water-Soluble Photoresponsive Encapsulated Upconverting Nanoparticles Containing Hydrophobic Molecular Switches

Tuoqi Wu, John-Christopher Boyer, Madeleine Barker, Danielle Wilson, Neil R. Branda

Chemistry of Materials· Volume 25· Issue 12
Publisher page

Abstract

A convenient and versatile protocol to encapsulate lanthanide doped upconverting nanoparticles by an amphiphilic polymer shell containing photoresponsive diarylethene chromophores was developed. The assemblies are all water-soluble and fluoresce in the visible region of the spectrum when excited with 980 nm near-infrared light. The fluorescent emission can be selectively and reversibly modulated by alternatively irradiating the photoresponsive nanoparticles with UV light and visible light, which triggers ring-closing and ring-opening reactions of the chromophores, respectively. Fluorescence lifetime experiments suggest that the quenching mechanism is a combination of energy transfer and emission-reabsorption processes. These photoresponsive upconverting nanoparticles have the potential to advance bioimaging and other applications in nanophotonics.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Porphyrin and Phthalocyanine Chemistry · Quantum Dots Synthesis And Properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

4D LABS, Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, BC, Canada V5A 1S6

References (53)

Show source-provided references
1. Lakowicz J. R. · 200610.1007/978-0-387-46312-4 ↗
2. Murphy D. B. · 2001
3. Chandler D. · 2009
4. Yuste R. · Nat. Methods · 2005 · 2 · 90210.1038/nmeth1205-902 ↗
5. Lichtman J. · Nat. Methods. · 2005 · 2 · 91010.1038/nmeth817 ↗
6. Huang B. · Annu. Rev. Biochem. · 2009 · 78 · 99310.1146/annurev.biochem.77.061906.092014 ↗
7. Fölling J. · Angew. Chem., Int. Ed. · 2007 · 46 · 626610.1002/anie.200702167 ↗
8. Fölling J. · Chem. Phys. Chem. · 2008 · 9 · 32110.1002/cphc.200700655 ↗
9. Bossi M. · Nano Lett. · 2008 · 8 · 246310.1021/nl801471d ↗
10. Berns M. W. · J. Photochem. Photobiol., B: Biol. · 2004 · 75 · 5110.1016/j.jphotobiol.2004.05.002 ↗
11. Zou Y. · J. Am. Chem. Soc. · 2008 · 130 · 1575010.1021/ja8043163 ↗
12. Yildiz I. · Chem. Soc. Rev. · 2009 · 38 · 185910.1039/b804151m ↗
13. Cusido J. · Eur. J. Org. Chem. · 2009 · 203110.1002/ejoc.200801244 ↗
14. Klajn R. · Chem. Soc. Rev. · 2010 · 39 · 220310.1039/b920377j ↗
15. Medintz I. · J. Am. Chem. Soc. · 2004 · 126 · 3010.1021/ja037970h ↗
16. Medintz I. · Proc. SPIE-Int. Soc. Opt. Eng. · 2004 · 5593 · 300
17. Zhu L. · J. Am. Chem. Soc. · 2005 · 127 · 896810.1021/ja0423421 ↗
18. Jares-Erijman E. A. · Mol. Cryst. Liq. Cryst. · 2005 · 430 · 25710.1080/15421400590946479 ↗
19. Tomasulo M. · Aust. J. Chem. · 2006 · 59 · 17510.1071/CH05332 ↗
20. Binder W. · J. Mater. Chem. · 2007 · 17 · 212510.1039/B618510J ↗
21. 10.1021/ar300058510.1021/ar3000585 ↗
22. Chan W. C. W. · Science · 1998 · 281 · 201610.1126/science.281.5385.2016 ↗
23. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
24. Boyer J.-C. · J. Am. Chem. Soc. · 2010 · 132 · 1576610.1021/ja107184z ↗
25. Carling C.-J. · Org. Biomol. Chem. · 2012 · 10 · 615910.1039/c2ob25368b ↗
26. Boyer J. C. · Chem.—Eur. J. · 2012 · 18 · 312210.1002/chem.201103767 ↗
27. Zhou Z. · Chem. Commun. · 2008 · 478610.1039/b809021a ↗
28. Zhang C. · Adv. Mater. · 2010 · 22 · 63310.1002/adma.200901722 ↗
29. Nyk M. · Nano Lett. · 2008 · 8 · 383410.1021/nl802223f ↗
30. Haase M. · Angew. Chem., Int. Ed. · 2011 · 50 · 580810.1002/anie.201005159 ↗
31. Feringa B. L. · 2010
32. Tian H. · Chem. Soc. Rev. · 2004 · 33 · 8510.1039/b302356g ↗
33. Ubaghs L. · 2009 · 2
34. Carling C.-J. · J. Am. Chem. Soc. · 2009 · 131 · 1083810.1021/ja904746s ↗
35. Jiang W. · Chem. Mater. · 2006 · 18 · 87210.1021/cm051393+ ↗
36. Mattoussi H. · J. Am. Chem. Soc. · 2000 · 122 · 1214210.1021/ja002535y ↗
37. Goldman E. R. · J. Am. Chem. Soc. · 2002 · 124 · 637810.1021/ja0125570 ↗
38. Uyeda H. T. · J. Am. Chem. Soc. · 2005 · 127 · 387010.1021/ja044031w ↗
39. Susumu K. · J. Am. Chem. Soc. · 2007 · 129 · 1398710.1021/ja0749744 ↗
40. Liu W. · J. Am. Chem. Soc. · 2008 · 130 · 127410.1021/ja076069p ↗
41. Pellegrino T. · Nano Lett. · 2004 · 4 · 70310.1021/nl035172j ↗
42. Gao X. H. · Nat. Biotechnol. · 2004 · 22 · 96910.1038/nbt994 ↗
43. Yu W. W. · J. Am. Chem. Soc. · 2007 · 129 · 287110.1021/ja067184n ↗
44. Lin C. J. · Small · 2008 · 4 · 33410.1002/smll.200700654 ↗
45. Díaz S. A. · J. Am. Chem. Soc. · 2013 · 135 · 320810.1021/ja3117813 ↗
46. Yildiz I. · J. Am. Chem. Soc. · 2011 · 133 · 87110.1021/ja107341f ↗
47. Díaz S. A. · ACS Nano · 2011 · 5 · 279510.1021/nn103243c ↗
48. Genovese D. · Chem. Commun. · 2011 · 47 · 1097510.1039/c1cc14800a ↗
49. Cusido J. · Chem.—Eur. J. · 2012 · 18 · 1039910.1002/chem.201201184 ↗
50. Edelsztein V. C. · J. Mater. Chem. · 2012 · 22 · 2185710.1039/c2jm34891h ↗
51. Pu S. · Dyes Pigm. · 2010 · 84 · 2510.1016/j.dyepig.2009.06.018 ↗
52. Peters A. · J. Am. Chem. Soc. · 2003 · 125 · 340410.1021/ja028764x ↗
53. Das G. K. · J. Phys. Chem. Lett. · 2012 · 3 · 52410.1021/jz201664h ↗