Molecular Engineering of Hybrid Dye–Silica Fluorescent Nanoparticles: Influence of the Dye Structure on the Distribution of Fluorophores and Consequent Photoemission Brightness
Source abstract
Abstract
This work was addressed to the elucidation of molecular parameters that rule the distribution of organic fluorophores throughout the nascent inorganic network during the synthesis of hybrid dye–silica nanoparticles by the reverse microemulsion method, which involves the partition of reactants among bulk oil phase, surfactant palisade, and inner water core. The evolution of the photophysical properties (absorption and steady-state and time-resolved photoluminescence) of three cyanine dyes, differing for the number of sulfonic substituents, from the starting microemulsion to the final nanoparticles provided evidence of the key role of the hydrophilicity of the fluorophores in ruling the dispersion within the SiO 2 matrix.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Porphyrin and Phthalocyanine Chemistry · Photochemistry and Electron Transfer Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Torino, via P. Giuria 7, 10125 Torino, Italy
NIS (Nanostructured Interfaces and Surfaces) Interdepartmental Centre of Excellence, at the Centre for Innovation, via G. Quarello 11/a, 10135, Torino, Italy
References (46)
Show source-provided references
1. Paquet C. · Mater. Today · 2008 · 11 · 4810.1016/S1369-7021(08)70056-7 ↗
2. Fang X. S. · Crit. Rev. Solid State Mater. Sci. · 2009 · 34 · 19010.1080/10408430903245393 ↗
3. Kalinowski J. · Coord. Chem. Rev. · 2011 · 255 · 240110.1016/j.ccr.2011.01.049 ↗
4. Uthirakumar P. · J. Lumin. · 2008 · 128 · 28710.1016/j.jlumin.2007.07.021 ↗
5. Sailor M. J. · Adv. Funct. Mater. · 2009 · 19 · 319510.1002/adfm.200900535 ↗
6. Somers R. C. · Chem. Soc. Rev · 2007 · 36 · 57910.1039/b517613c ↗
7. Coto-Garcia A. M. · Anal. Bioanal. Chem. · 2011 · 399 · 2910.1007/s00216-010-4330-3 ↗
8. Boisselier E. · Chem. Soc. Rev. · 2009 · 38 · 175910.1039/b806051g ↗
9. Liu L. · Forensic Sci. Int. · 2008 · 176 · 16310.1016/j.forsciint.2007.08.006 ↗
10. Theaker B. J. · Forensic Sci. Int. · 2008 · 174 · 2610.1016/j.forsciint.2007.02.030 ↗
11. Resch-Genger U. · Nat. Methods · 2008 · 5 · 76310.1038/nmeth.1248 ↗
12. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
13. Fercher A. · ACS Nano · 2011 · 5 · 549910.1021/nn200807g ↗
14. Tong R. · Microsc. Res. Tech. · 2010 · 73 · 90110.1002/jemt.20824 ↗
15. Zhao X. · Adv. Mater. · 2004 · 16 · 17310.1002/adma.200305622 ↗
16. Lian W. · Anal. Biochem. · 2004 · 334 · 13510.1016/j.ab.2004.08.005 ↗
17. Gianotti E. · Appl. Mater. Interfaces · 2009 · 1 · 67810.1021/am800196r ↗
18. Abarkan I. · Polyhedron · 2006 · 25 · 176310.1016/j.poly.2005.11.031 ↗
19. Arriagada F. J. · J. Colloid Interface Sci. · 1995 · 170 · 810.1006/jcis.1995.1064 ↗
20. Huang S. · J. Fluoresc. · 2009 · 19 · 109510.1007/s10895-009-0509-4 ↗
21. Bharali D. J. · Proc. Natl. Acad. Sci. U.S.A. · 2005 · 102 · 1153910.1073/pnas.0504926102 ↗
22. Rosi N. L. · Chem. Rev. · 2005 · 105 · 154710.1021/cr030067f ↗
23. Santra S. · Anal. Chem. · 2001 · 73 · 498810.1021/ac010406+ ↗
24. Van Blaaderen A. · Langmuir · 1992 · 8 · 292110.1021/la00048a013 ↗
25. Van Blaaderen A. · J. Colloid Interface Sci. · 1993 · 156 · 110.1006/jcis.1993.1073 ↗
26. Stöber W. · J. Colloid Interface Sci. · 1968 · 26 · 6210.1016/0021-9797(68)90272-5 ↗
27. Rampazzo E. · J. Am. Chem. Soc. · 2007 · 129 · 1425110.1021/ja073150j ↗
28. Larson D. R. · Chem. Mater. · 2008 · 20 · 267710.1021/cm7026866 ↗
29. Osseo-Asare K. · J. Colloid Interface Sci. · 1999 · 218 · 6810.1006/jcis.1999.6232 ↗
30. Osseo-Asare K. · Colloids Surf. · 1990 · 50 · 32110.1016/0166-6622(90)80273-7 ↗
31. Bagwe R. P. · Langmuir · 2004 · 20 · 833610.1021/la049137j ↗
32. Mishra A. · Chem. Rev. · 2000 · 100 · 197310.1021/cr990402t ↗
33. Alberto A. · J. Phys. Chem. C · 2009 · 113 · 2104810.1021/jp907415q ↗
34. Bonacchi S. · Angew. Chem. Int. Ed. · 2011 · 50 · 405610.1002/anie.201004996 ↗
35. Santra S. · J. Biomed. Opt. · 2001 · 6 · 16010.1117/1.1353590 ↗
36. Waggoner A. S. · Bioconjugate Chem. · 1993 · 4 · 10510.1021/bc00020a001 ↗
37. Bertolino C. A. · Chem. Phys. · 2006 · 330 · 5210.1016/j.chemphys.2006.07.045 ↗
38. Lackowicz J. R. · 200610.1007/978-0-387-46312-4 ↗
39. achapter 19, p629;
40. bchapter 1, pp7–8.
41. Kachkovski A. D. · Dyes Pigm. · 1994 · 24 · 17110.1016/0143-7208(94)80008-1 ↗
42. Baraldi I. · Chem. Phys. · 2002 · 275 · 14910.1016/S0301-0104(01)00530-4 ↗
43. Mustroph H. · Angew. Chem., Int. Ed. · 2006 · 45 · 201610.1002/anie.200502820 ↗
44. Miletto I. · Dyes Pigm. · 2010 · 84 · 12110.1016/j.dyepig.2009.07.004 ↗
45. Kortüm G. · 196910.1007/978-3-642-88071-1 ↗
46. Arriagada F. J. · Colloids Surf. A · 1999 · 154 · 31110.1016/S0927-7757(98)00870-X ↗