journal article·2017

Coordination coupling enhanced two-photon absorption of a ZnS-based microhybrid for two-photon microscopy imaging in HepG2

Lin Kong, Xiao-he Tian, Hui Wang, Yuan-hao Gao, Qiong Zhang, Jia-xiang Yang, Hong-ping Zhou, Sheng-yi Zhang, Yu-peng Tian

Nanoscale· Volume 9· Issue 23
Publisher page

Abstract

Coordination coupling induced self-assembly of ZnS microparticles was performed with the help of a π-conjugated sulphur-terminal Zn(II) complex ZnS2L (L = N-hexyl-3-{2-[4-2,2′:6′,2′′-terpyridin-4′-yl-phenyl]ethenyl}-carbazole). The interactions between ZnS and ZnS2L components at the interface, which were analyzed by far-IR and XPS, resulted in a tunable single-photon excited fluorescence and an enhanced nonlinear optical response, including a two-photon absorption cross section and a two-photon excited fluorescence. Such an enhancement in nonlinear optical properties was triggered by the coordination coupling effect between terminal S atoms of ZnS2L and naked Zn2+ ions at the surface of ZnS particles. Thus, the novel hybrid system displayed a unique two-photon excited fluorescence to facilitate promising two-photon microscopy imaging of HepG2 cells upon NIR light illumination at 840 nm. The hybrid shows a stronger ability to enter the cells than free ZnS2L.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nonlinear Optical Materials Studies · Luminescence and Fluorescent Materials · Quantum Dots Synthesis And Properties

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

References (52)

Show source-provided references
1. Cahalan · Nat. Rev. Immunol. · 2002 · 2 · 87210.1038/nri935 ↗
2. Impellizzeri · Chem. – Eur. J. · 2016 · 22 · 728110.1002/chem.201600218 ↗
3. Lavagnino · Sci. Rep. · 2016 · 6 · 2392310.1038/srep23923 ↗
4. Chen · Chem. Soc. Rev. · 2015 · 44 · 451710.1039/C5CS00005J ↗
5. Wu · Nat. Commun. · 2014 · 5 · 526210.1038/ncomms6262 ↗
6. Yuan · Nanoscale · 2015 · 7 · 306710.1039/C4NR06420H ↗
7. Li · Chem. – Asian J. · 2009 · 4 · 66810.1002/asia.200800402 ↗
8. Park II · Chem. Soc. Rev. · 2015 · 44 · 130210.1039/C4CS00173G ↗
9. Stellacci · J. Am. Chem. Soc. · 2003 · 125 · 32810.1021/ja0281277 ↗
10. Gao · Adv. Funct. Mater. · 2015 · 25 · 285710.1002/adfm.201500010 ↗
11. Albota · Science · 1998 · 281 · 165310.1126/science.281.5383.1653 ↗
12. Wu · Enzyme Microb. Technol. · 2012 · 51 · 4710.1016/j.enzmictec.2012.03.012 ↗
13. Hernández-Gordillo · Catal. Commun. · 2012 · 19 · 5110.1016/j.catcom.2011.12.026 ↗
14. Deng · Chem. Mater. · 2012 · 24 · 302910.1021/cm3015594 ↗
15. Wu · Chem. Soc. Rev. · 2016 · 45 · 378110.1039/C5CS00472A ↗
16. Zhang · Anal. Chem. · 2013 · 85 · 22810.1021/ac3025653 ↗
17. Zhang · ACS Nano · 2012 · 6 · 977710.1021/nn304154s ↗
18. Smith · ACS Nano · 2012 · 6 · 947510.1021/nn302288r ↗
19. Casciato · Ind. Eng. Chem. Res. · 2012 · 51 · 1171010.1021/ie301553g ↗
20. Gaury · J. Appl. Phys. · 2016 · 119 · 12510510.1063/1.4944597 ↗
21. Reiss · Chem. Rev. · 2016 · 116 · 1073110.1021/acs.chemrev.6b00116 ↗
22. Querner · J. Am. Chem. Soc. · 2004 · 126 · 1157410.1021/ja047882c ↗
23. Kern · ACS Nano · 2012 · 6 · 982810.1021/nn3033612 ↗
24. Owen · Science · 2015 · 347 · 61510.1126/science.1259924 ↗
25. Constable · Chem. Soc. Rev. · 2007 · 36 · 24610.1039/B601166G ↗
26. Gao · J. Am. Chem. Soc. · 2009 · 131 · 520810.1021/ja808606d ↗
27. Engel · Chem. Mater. · 2013 · 25 · 14910.1021/cm303049k ↗
28. Y. H. Sehlleier , A.Abdali, T.Hülser, H.Wiggers and C.Schulz, NanoFormulation, RSC Publishing, 2012
29. Zhang · J. Am. Chem. Soc. · 2007 · 129 · 352710.1021/ja0642109 ↗
30. He · Adv. Mater. · 2012 · 24 · 217110.1002/adma.201200525 ↗
31. Yang · Chem. Phys. · 2009 · 358 · 3910.1016/j.chemphys.2008.12.017 ↗
32. Xu · J. Opt. Soc. Am. B · 1996 · 13 · 48110.1364/JOSAB.13.000481 ↗
33. Ajami · J. Opt. Soc. Am. B · 2010 · 27 · 229010.1364/JOSAB.27.002290 ↗
34. Laajalehto · Appl. Surf. Sci. · 1994 · 81 · 1110.1016/0169-4332(94)90080-9 ↗
35. Pettenkofer · Phys. Chem. · 1991 · 95 · 560
36. Szargan · Poverkhnost · 1997 · 90
37. Golzhauser · Surf. Sci. · 1995 · 334 · 23510.1016/0039-6028(95)00251-0 ↗
38. Querner · J. Am. Chem. Soc. · 2004 · 126 · 1157410.1021/ja047882c ↗
39. Kern · ACS Nano · 2012 · 6 · 982810.1021/nn3033612 ↗
40. Gill · J. Phys. Chem. C · 2012 · 116 · 1668710.1021/jp305720q ↗
41. Vivas · J. Phys. Chem. C · 2013 · 117 · 853010.1021/jp400956k ↗
42. Retsch · Nano Lett. · 2011 · 11 · 138910.1021/nl2002445 ↗
43. Lykhach · Nat. Mater. · 2016 · 15 · 28410.1038/nmat4500 ↗
44. He · J. Am. Chem. Soc. · 2011 · 133 · 667510.1021/ja1113112 ↗
45. Husinsky · Opt. Commun. · 2012 · 285 · 272910.1016/j.optcom.2012.01.044 ↗
46. Oh · Part. Part. Syst. Charact. · 2013 · 30 · 45310.1002/ppsc.201200140 ↗
47. Zhao · Nanoscale · 2012 · 4 · 771210.1039/c2nr32196c ↗
48. Jeong · Adv. Funct. Mater. · 2004 · 14 · 6410.1002/adfm.200304478 ↗
49. Zhou · Anal. Chem. · 2015 · 87 · 562610.1021/acs.analchem.5b00691 ↗
50. Lim · Chem. – Asian J. · 2015 · 10 · 224010.1002/asia.201500314 ↗
51. Chen · Anal. Chem. · 2012 · 84 · 309910.1021/ac202810b ↗
52. Gao · Chem. Commun. · 2014 · 50 · 831210.1039/c4cc00452c ↗