Fabrication of a Novel Cholic Acid Modified OPE-Based Fluorescent Film and Its Sensing Performances to Inorganic Acids in Acetone
Source abstract
Abstract
A self-assembled monolayer (SAM)-based fluorescent film was designed and prepared by chemical immobilization of a novel oligo(p-phenylene- ethynylene) (OPE) with cholic acid moieties at the ends of its side chains (Film 1). As a control, a similar film, Film 2, of which OPE brings no side chains, was also prepared. The structures of the films were characterized by contact angle, XPS, ATR-IR and fluorescence measurements. Fluorescence studies revealed that the emission of Film 1 is sensitive to the presence of trace amount of some inorganic acids in acetone, such as HCl, H(2)SO(4), HNO(3), and H(3)PO(4), etc., whereas the acids as studied showed little effect on the emission of Film 2. The difference in the sensing performances of the two films have been rationalized by considering presence or absence of a possible cavity, a substructure appearing above the OPE adlayer which is something like a dimer of cholic acid (CholA) formed at specific environment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Conducting polymers and applications · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Applied Surface and Colloid Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi’an 710062, P. R. China
References (37)
Show source-provided references
1. Zaks A. · Proc. Natl. Acad. Sci. U.S.A. · 1985 · 82 · 319210.1073/pnas.82.10.3192 ↗
2. Klibanov A. M. · Nature · 1995 · 374 · 59610.1038/374596a0 ↗
3. Staahl M. · J. Am. Chem. Soc. · 1991 · 113 · 936610.1021/ja00024a051 ↗
4. Lousa D. · Protein Sci. · 2011 · 20 · 37910.1002/pro.569 ↗
5. Klibanov A. M. · Nature · 2001 · 409 · 24110.1038/35051719 ↗
6. Carrea G. · Angew. Chem., Int. Ed. · 2000 · 39 · 222610.1002/1521-3773(20000703)39:13<2226::AID-ANIE2226>3.0.CO;2-L ↗
7. Hudson E. P. · Curr. Opin. Biotechnol. · 2005 · 16 · 63710.1016/j.copbio.2005.10.004 ↗
8. Lee M. Y. · Curr. Opin. Biotechnol. · 2002 · 13 · 37610.1016/S0958-1669(02)00337-3 ↗
9. Koryta J. · Anal. Chim. Acta · 1984 · 159 · 110.1016/S0003-2670(00)84279-8 ↗
10. Bates, R. G.InDetemination of pH, Theory and Practice;Wiley:New York, 1973; Vol.11, p372.
11. Javanbakht M. · Electroanal · 1999 · 11 · 8110.1002/(SICI)1521-4109(199902)11:2<81::AID-ELAN81>3.0.CO;2-Q ↗
12. Naddo T. · J. Am. Chem. Soc. · 2007 · 129 · 697810.1021/ja070747q ↗
13. de Silva A. P. · Chem. Rev. · 1997 · 97 · 151510.1021/cr960386p ↗
14. Basabe-Desmonts L. · Chem. Soc. Rev. · 2007 · 36 · 99310.1039/b609548h ↗
15. Zhang S. J. · Langmuir · 2007 · 23 · 158410.1021/la062773s ↗
16. Lü F. T. · Langmuir · 2006 · 22 · 84110.1021/la052866u ↗
17. Gao L. N. · Appl. Surf. Sci. · 2006 · 252 · 388410.1016/j.apsusc.2005.06.002 ↗
18. Albert K. J. · Chem. Rev. · 2000 · 100 · 259510.1021/cr980102w ↗
19. Wu X. · Macromolecules · 2010 · 43 · 891710.1021/ma1019413 ↗
20. Swager T. M. · Acc. Chem. Res. · 1998 · 31 · 20110.1021/ar9600502 ↗
21. McQuade D. T. · Chem. Rev. · 2000 · 100 · 253710.1021/cr9801014 ↗
22. Kim Y. · J. Am. Chem. Soc. · 2005 · 127 · 1212210.1021/ja052828x ↗
23. Yang Y. · Adv. Funct. Mater. · 2010 · 20 · 209310.1002/adfm.200901904 ↗
24. Yang J. S. · J. Am. Chem. Soc. · 1998 · 120 · 1186410.1021/ja982293q ↗
25. Thomas S. W. · Chem. Rev. · 2007 · 107 · 133910.1021/cr0501339 ↗
26. Lee W. E. · Angew. Chem., Int. Ed. · 2010 · 49 · 140610.1002/anie.200906621 ↗
27. Feng X. L. · Angew. Chem., Int. Ed. · 2009 · 48 · 531610.1002/anie.200901555 ↗
28. Lee K. · Angew. Chem., Int. Ed. · 2007 · 46 · 466710.1002/anie.200700419 ↗
29. Ding L. P. · Chem. Soc. Rev. · 2010 · 39 · 425810.1039/c003028g ↗
30. He G. · Chem. Mater. · 2009 · 21 · 149410.1021/cm900013f ↗
31. He G. · Macromolecules · 2011 · 44 · 70310.1021/ma102769b ↗
32. Wang H. Y. · J. Mater. Chem. · 2012 · 22 · 752910.1039/c2jm16637b ↗
33. Bandyopadhyay P. · J. Am. Chem. Soc. · 2001 · 123 · 769110.1021/ja010926m ↗
34. Mukhopadhyay S. a. M. · Curr. Sci. India · 2004 · 87 · 1666
35. Zhu X. X. · Acc. Chem. Res. · 2002 · 35 · 53910.1021/ar0101180 ↗
36. Flink S. · Adv. Mater. · 2000 · 12 · 131510.1002/1521-4095(200009)12:18<1315::AID-ADMA1315>3.0.CO;2-K ↗
37. Lakowicz, J. R.InPrinciples of Fluorescence Spectroscopy,3rd ed.Springer-Verlag:Berlin, 2006; Vol.8, p278.