journal article·2009

Synthesis of highly luminescent cobalt(ii)-bis(8-hydroxyquinoline) nanosheets as isomeric aromatic amine probes

Haibing Li, Yuling Li

Nanoscale· Volume 1· Issue 1
Publisher page

Abstract

Highly luminescent and water-soluble cobalt(ii)-bis(8-hydroxyquinoline) (CoQ(2)) nanosheets have been successfully synthesized via a simple, rapid sonochemical method. The water-soluble CoQ(2) nanosheets were characterized by luminescence spectroscopy, UV-vis spectroscopy, FT-IR spectroscopy and transmission electron microscopy (TEM). The CoQ(2) nanosheets allow highly sensitive and selective determination of p-nitroaniline via fluorescence quenching. Under optimal conditions, the relative fluorescence intensities of nanosheets decreased linearly with increasing p-nitroaniline. However, the sensitivity of CoQ(2) nanosheets toward other aromatic amines including o-diaminobenzene, m-diaminobenzene, p-diaminobenzene, p-toluidine, o-nitroaniline, m-nitroaniline, p-chloroaniline and aniline is negligible. It is found that p-nitroaniline can quench the luminescence of CoQ(2) nanosheets in a concentration-dependent manner that is best described by a Stern-Volmer-type equation. The possible underlying mechanism is discussed.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Luminescence and Fluorescent Materials · Lanthanide and Transition Metal Complexes

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

References (28)

Show source-provided references
1. Zimmermann · Anal. Chem. · 2004 · 76 · 102810.1021/ac035098p ↗
2. Weiss · J. Chromatogr., B: Anal. Technol. Biomed. Life Sci. · 2002 · 778 · 17910.1016/S0378-4347(01)00542-4 ↗
3. Singh · J. Chromatogr., A · 2003 · 1010 · 24310.1016/S0021-9673(03)01123-3 ↗
4. Marengo · J. Chromatogr., A · 1999 · 863 · 110.1016/S0021-9673(99)00914-0 ↗
5. Caudron · J. Chromatogr., A · 2005 · 1072 · 14910.1016/j.chroma.2005.02.028 ↗
6. Clark · Anal. Chem. · 1999 · 71 · 483110.1021/ac990629o ↗
7. Park · Anal. Chem. · 2003 · 75 · 378410.1021/ac0342323 ↗
8. Bakalova · J. Am. Chem. Soc. · 2005 · 127 · 1132810.1021/ja051089h ↗
9. Zhang · J. Am. Chem. Soc. · 2006 · 128 · 532410.1021/ja060537y ↗
10. Chen · Chem. Commun. · 2006 · 26310.1039/B512677K ↗
11. Kaewsuya · Anal. Chim. Acta · 2008 · 626 · 11110.1016/j.aca.2008.08.002 ↗
12. Li · J. Mater. Chem. · 2007 · 17 · 353610.1039/b705743a ↗
13. Li · Chem. Mater. · 2007 · 19 · 414810.1021/cm0700089 ↗
14. Fu · Angew. Chem., Int. Ed. · 2003 · 42 · 288310.1002/anie.200350961 ↗
15. Chiu · Adv. Mater. · 2003 · 15 · 136110.1002/adma.200304918 ↗
16. Sapochak · J. Am. Chem. Soc. · 2002 · 124 · 611910.1021/ja0201909 ↗
17. Zhao · Adv. Funct. Mater. · 2006 · 16 · 198510.1002/adfm.200600070 ↗
18. Hu · Chem. Commun. · 2007 · 308310.1039/b704106c ↗
19. Farruggia · J. Am. Chem. Soc. · 2006 · 128 · 34410.1021/ja056523u ↗
20. Pan · J. Phys. Chem. B · 2007 · 111 · 576710.1021/jp0703049 ↗
21. Hossain · Electrochim. Acta · 1997 · 42 · 257710.1016/S0013-4686(96)00453-7 ↗
22. Nayak · J. Anal. Appl. Pyrolysis · 2003 · 70 · 69910.1016/S0165-2370(03)00041-X ↗
23. Phillips · Anal. Chim. Acta · 1957 · 17 · 23110.1016/S0003-2670(00)87019-1 ↗
24. Tackett · Inorg. Chem. · 1964 · 3 · 69210.1021/ic50015a021 ↗
25. Li · Inorg. Chem. Commun. · 2008 · 11 · 137510.1016/j.inoche.2008.09.010 ↗
26. Wang · Dyes Pigm. · 2007 · 72 · 35710.1016/j.dyepig.2005.09.017 ↗
27. Zahn · Angew. Chem., Int. Ed. · 2002 · 41 · 422510.1002/1521-3773(20021115)41:22<4225::AID-ANIE4225>3.0.CO;2-3 ↗
28. Yamaguchi · J. Am. Chem. Soc. · 2001 · 123 · 1208710.1021/ja016692o ↗