A novel ratiometric sensor for the fast detection of palladium species with large red-shift and high resolution both in aqueous solution and solid state

Analytica Chimica Acta

Volumn 786, Issue , 2013, Pages 139-145

  Cui, Lei ^a,b   Zhu, Weiping ^a   Xu, Yufang ^a   Qian, Xuhong ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b UNIVERSITY OF SHANGHAI FOR SCIENCE AND TECHNOLOGY   (China)

Author keywords

Excited state intramolecular proton transfer; Fluorescent probe; Palladium; Paper strip; Solid state fluorescence

Indexed keywords

EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER; FLUORESCENT PROBES; MAXIMUM EMISSIONS; PALLADIUM SPECIES; RATIOMETRIC SENSORS; SOLID-STATE FLUORESCENCE; SUZUKI-MIYAURA COUPLING REACTION; TSUJI-TROST REACTION;

CATALYSIS; EMISSION SPECTROSCOPY; FLUORESCENCE; FLUOROPHORES; PALLADIUM;

SOLUTIONS;

BENZAMIDE; FLUORESCENT DYE; N [3 (BENZO[D]THIAZOL 2 YL) 4 (HYDROXYPHENYL) BENZAMIDE]; PALLADIUM; UNCLASSIFIED DRUG;

ABSORPTION; AQUEOUS SOLUTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CONTROLLED STUDY; FLUORESCENCE SPECTROSCOPY; HYDROLYSIS; LIMIT OF DETECTION; PH; PRIORITY JOURNAL; RATIOMETRIC SENSOR; SENSOR; SOLID STATE; SUZUKI REACTION; SYNTHESIS;

BIOSENSING TECHNIQUES; FLUORESCENT DYES; PALLADIUM; SOLUTIONS; SPECTROMETRY, FLUORESCENCE; TIME FACTORS; WATER;

EID: 84879307227     PISSN: 00032670     EISSN: 18734324     Source Type: Journal    
DOI: 10.1016/j.aca.2013.05.011     Document Type: Article

References (27)

1. Lafrance M., Fagnou K. J. Am. Chem. Soc. 2006, 128:16496.
2. Hodge V.F., Stallard M.O. Environ. Sci. Technol. 1986, 20:1058.
3. Iwasawa T., Tokunaga M., Obora Y., Tsuji Y. J. Am. Chem. Soc. 2004, 126:6554.
4. International Programme on Chemical Safety Palladium; Environmental Health Criteria Series 226 2002, World Health Organization, Geneva.
5. Fu S.H., Liu Z.F., Liu S.P., Liu J.T., Yi A.E. Anal. Chim. Acta 2007, 599:271.
6. Locatelli C., Melucci D., Torsi G. Anal. Bioanal. Chem. 2005, 382:1567.
7. Dimitrova B., Benkhedda K., Ivanova E., Adams F. J. Anal. Atom. Spectrom. 2004, 19:1394.
8. Yang Y., Zhao Q., Feng W., Li F. Chem. Rev. 2013, 113:192.
9. Jun M.E., Roy B., Ahn K.H. Chem. Commun. 2011, 47:7583.
10. Jou M.J., Chen X., Swamy K.M., Kim H.N., Kim H.J., Lee S.G., Yoon J. Chem. Commun. 2009, 45:7218.
11. Liu B., Tian H. Chem. Commun. 2005, 41:3156.
12. Kumar M., Kumar N., Bhalla V. RSC Adv. 2013, 3:1097.
13. Garner A.L., Koide K. Chem. Commun. 2009, 44:83.
14. Garner A.L., Koide K. J. Am. Chem. Soc. 2008, 130:16472.
15. Song F., Garner A.L., Koide K. J. Am. Chem. Soc. 2007, 129:12354.
16. Li H., Fan J., Du J., Guo K., Sun S., Liu X., Peng X. Chem. Commun. 2010, 46:1079.
17. Zhang X., Xiao Y., Qian X. Angew. Chem. Int. Ed. 2008, 47:8025.
18. Henary M.M., Wu Y.G., Fahrni C.J. Chem.-Eur. J. 2004, 10:3015.
19. Scheiner S. J. Phys. Chem. A 2000, 104:5898.
20. Grando S.R., Pessoa C.M., Gallas M.R., Costa T.M.H., Rodembusch F.S., Benvenutti E.V. Langmuir 2009, 25:13219.
21. Hu R., Feng J.A., Hu D.H., Wang S.Q., Li S.Y., Li Y., Yang G.Q. Angew. Chem. Int. Ed. 2010, 49:4915.
22. Garner A.L., Song F.L., Koide K. J. Am. Chem. Soc. 2009, 131:5163.
23. Liu B., Wang H., Wang T., Bao Y., Du F., Tian J., Li Q., Bai R. Chem. Commun. 2012, 48:2867.
24. Chen W., Wright B.D., Pang Y. Chem. Commun. 2012, 48:3824.
25. Kürti L., Czakó B. Strategic Applications of Named Reactions in Organic Synthesis 2005, 458-459. Elsevier Academic Press, London.
26. Barni E., Savarino P., Marzona M., Piva M. J. Heterocycl. Chem. 1983, 20:1517.
27. Irving H.M.N.H., Freiser H., West T.S. IUPAC Compendium of Analytical Nomenclature, Definitive Rules 1981, Pergamon Press, Oxford.