A simple 1,10-phenanthroline-based fluorescent receptor in solution and 1,10-phenanthroline in solid state for urea recognition

Journal of Luminescence

Volumn 130, Issue 8, 2010, Pages 1475-1480

  Mahapatra, Ajit Kumar ^a   Sahoo, Prithidipa ^a   Hazra, Giridhari ^a   Goswami, Shyamaprosad ^a   Fun, Hoong Kun ^b  

^a INDIAN INSTITUTE OF ENGINEERING SCIENCE AND TECHNOLOGY   (India)

^b SCHOOL OF PHYSICS   (Malaysia)

Author keywords

1,10 Phenanthroline; Fluorescent receptor; Supramolecular assemblies; Urea binding

Indexed keywords

CHEMOSENSOR; FLUORESCENT RECEPTOR; HYDROGEN-BONDED COMPLEXES; PHENANTHROLINES; SINGLE CRYSTAL X-RAY DIFFRACTION ANALYSIS; SPECTROSCOPIC METHOD; SUPRAMOLECULAR ASSEMBLIES; UV-VISIBLE;

FLUORESCENCE; SINGLE CRYSTALS; SPECTROSCOPIC ANALYSIS; SUPRAMOLECULAR CHEMISTRY; UREA; X RAY DIFFRACTION; X RAY DIFFRACTION ANALYSIS;

METABOLISM;

EID: 77955231920     PISSN: 00222313     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jlumin.2010.03.015     Document Type: Article

References (28)

1. M.-E. Lee, van der Vegt, F.A.N. 2006, 128, 4948-4949.
2. I.J. Cooke Nature 194 1962 1262
3. J.B. Coombe, and D.E. Tribe Nature 182 1958 116
4. J.G. Morris, and E.J. Payne Agri. Sci. 74 1970 259
5. A.P. De Silva, H.Q.N. Gunaratne, T. Gunnlaugsson, A.J.M. Huxley, C.P. McCoy, J.T. Rademacher, and T.E. Rice Chem. Rev. 97 1997 1515
6. L. Fabbrizzi Acc. Chem. Res. 32 1999 846
7. R.W. Cattarall Chemical Sensors 1997 Oxford University Press New York p 2350
8. H.-C. Chou, C.-H. Hsu, Y.-M. Cheng, C.-C. Cheng, H.-W. Liu, S.-C. Pu, and P.-T. Chou J. Am. Chem. Soc. 126 2004 1650
9. K. Ghosh, S. Adhikari, and R. Frohlich Tetrahedron Lett. 49 2008 5063
10. K. Ghosh, and T. Sen Tetrahedron Lett. 50 2009 4096
11. R.M. Claramunt, F. Herranz, M.D. Santa Maria, E. Pinilla, M.R. Torres, and J. Elguero Tetrahedron 61 2005 5089
12. F. Herranz, M.D. Santa Maria, and R.M. Claramunt J. Org. Chem. 71 2006 2944
13. S. Goswami, and S. Dey J. Org. Chem. 71 2006 7280
14. C.J. Pedersen J. Org. Chem. 36 1971 1690
15. C.J. van Staveren, V.M.L.J. Aarts, P.D.J. Grootenhuis, W.J.H. Droppers, J. van Eerden, S. Harkema, and D.N. Reinhoudt J. Am. Chem. Soc. 110 1988 8134
16. C.J. van Staveren, J. van Eerden, F.C. Veggel, J.M. Herkema, and D.N. Reinhoudt J. Am. Chem. Soc. 110 1988 4994
17. T.W. Bell, and J.J. Liu J. Am. Chem. Soc. 110 1988 3673
18. M.G. Fisher, P.A. Gale, and M.E. Light N. J. Chem. 31 2007 1583
19. B. Chetia, and P.K. Iyer Tetrahedron Lett. 47 2006 8115
20. S. Goswami, R. Mukherjee, and J. Ray Org. Lett. 7 2005 1283
21. S. Goswami, and R. Mukherjee Tetrahedron Lett. 38 1997 1619
22. W.R. Cannon, J.D. Madura, R.P. Thummel, and J.A. McCammon J. Am. Chem. Soc. 115 1993 879
23. V. Hegde, C.Y. Hung, P. Madhukar, R. Cunningham, T. Hopfner, and R.P. Thummel J. Am. Chem. Soc. 115 1993 872
24. V. Hegde, P. Madhukar, J.D. Madura, and R.P. Thummel J. Am. Chem. Soc. 112 1990 4549
25. Semi-empirical AM1 (MOPAC) calculations were performed using CS Chem 3D (version 7.0).
26. -3.
27. F. Pina, M.A. Bernardo, and E. Garća-España Eur. J. Inorg. Chem. 2000 2143
28. P.T. Chou, G.R. Wu, C.Y. Wei, C.C. Cheng, C.P. Chang, and F.T. Hung J. Phys. Chem. B 104 2000 7818