Copper(II)-directed static excimer formation of an anthracene-based highly selective fluorescent receptor

Tetrahedron Letters

Volumn 56, Issue 1, 2015, Pages 162-167

  Malkondu, Sait ^a   Turhan, Dilek ^a   Kocak, Ahmet ^a  

^a SELCUK UNIVERSITY   (Turkey)

Author keywords

Anthracene; Copper; Disassociation; Excimer; PET

Indexed keywords

ANTHRACENE; CUPRIC ION; FLUORESCENT RECEPTOR; METHYL 3 [(ANTHRACEN 9 YLMETHYLENE)AMINO]BENZOATE; MONOMER; RECEPTOR; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; CONCENTRATION (PARAMETERS); ELECTRON TRANSPORT; FLUORESCENCE SPECTROSCOPY; ISOMERIZATION; TEMPERATURE;

EID: 84918551139     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.11.055     Document Type: Article

References (52)

1. H.J. Kim, Y.S. Park, S. Yoon, and J.S. Kim Tetrahedron 64 2008 1294 1300
2. Y. Zheng, K.M. Gatta's-Asfura, V. Konka, and R.M. Leblance Chem. Commun. 2002 2350 2351
3. Z. Xu, Y. Xiao, X. Qian, J. Cui, and D. Cui Org. Lett. 7 2005 889 892
4. S. Malkondu, and S. Erdemir Tetrahedron 70 2014 5494 5498
5. R. Krämer Angew. Chem., Int. Ed. 37 1998 772 773
6. B.E. Kim, T. Nevitt, and D.J. Thiele Nat. Chem. Biol. 4 2008 176 185
7. R.A. Lovstad Biometals 17 2004 111 113
8. P.L. Malvankar, and V.M. Shinde Analyst 116 1991 1081 1084
9. C. Vulpe, B. Levinson, S. Whiteny, S. Packman, and J. Gitschier Nat. Genet. 3 1993 7 13
10. P.C. Bull, G.R. Thomas, J.M. Rommens, J.R. Forbes, and D.W. Cox Nat. Genet. 5 1993 327 337
11. Y. Liu, P. Liang, and L. Guo Talanta 68 2005 25 30
12. J.S. Becker, A. Matusch, C. Depboylu, J. Dobrowolska, and M.V. Zoriy Anal. Chem. 79 2007 6074 6080
13. A.P.S. Gonzales, M.A. Firmino, C.S. Nomura, F.R.P. Rocha, P.V. Oliveira, and I. Gaubeur Anal. Chim. Acta 636 2009 198 204
14. Y. Oztekin, Z. Yazicigil, A. Ramanaviciene, and A. Ramanavicius Talanta 85 2011 1020 1027
15. E.L. Que, D.W. Domaille, and C.J. Chang Chem. Rev. 108 2008 1517 1549
16. J. Du, M. Hu, J. Fan, and X. Peng Chem. Soc. Rev. 41 2012 4511 4535
17. C.Y. Tsai, and Y.W. Lin Analyst 138 2013 1232 1238
18. A.W. Varnes, R.B. Dodson, and E.L. Wehry J. Am. Chem. Soc. 94 1972 946 950
19. M. Turel, A. Duerkop, A. Yegorova, Y. Scripinets, A. Lobnik, and N. Samec Anal. Chim. Acta 644 2009 53 60
20. S. Khatua, S.H. Choi, J. Lee, J.O. Huh, Y. Do, and D.G. Churchill Inorg. Chem. 48 2009 1799 1801
21. H.Q. Chen, A.N. Liang, L. Wang, Y. Liu, and B.B. Qian Microchim. Acta 164 2009 453 458
22. S. Erdemir, and S. Malkondu J. Lumin. 158 2015 86 90
23. C.W. Yu, J. Zhang, R. Wang, and L.X. Chen Org. Biomol. Chem. 8 2010 5277 5279
24. M.H. Lee, H.J. Kim, S. Yoon, N. Park, and J.S. Kim Org. Lett. 10 2008 213 216
25. Z.Q. Hu, X.M. Wang, Y.C. Feng, L. Ding, and H.Y. Lu Dyes Pigments 88 2011 257 261
26. 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 1566
27. B. Valeur, and I. Leray Coord. Chem. Rev. 205 2000 3 40
28. L. Prodi, F. Bolletta, M. Montalti, and N. Zaccheroni Coord. Chem. Rev. 205 2000 59 83
29. Z. Xu, J. Yoon, and D.R. Spring Chem. Commun. 2010 2563 2565
30. K. Baek, M.S. Eom, S. Kim, and M.S. Han Tetrahedron Lett. 54 2013 1654 1657
31. S.A. Ingale, and F. Seela J. Org. Chem. 77 2012 9352 9356
32. G. Nishimura, H. Maehara, Y. Shiraishi, and T. Hirai Chem. Eur. J. 14 2008 259 271
33. X.H. Huang, Y.B. He, C.G. Hu, and Z.H. Chen Eur. J. Org. Chem. 2009 1549 1553
34. X.H. Huang, Y. Lu, Y.B. He, and Z.H. Chen Eur. J. Org. Chem. 2010 1921 1927
35. S. Sarkar, S. Roy, A. Sikdar, R.N. Saha, and S.S. Panja Analyst 138 2013 7119 7126
36. W. Lin, L. Yuan, and J. Feng Eur. J. Org. Chem. 22 2008 3821 3825
37. H.S. Jung, M. Park, D.Y. Han, E. Kim, C. Lee, S. Ham, and J.S. Kim Org. Lett. 11 2009 3378 3381
38. H.J. Kim, J. Hong, A. Hong, S. Ham, J.H. Lee, and J.S. Kim Org. Lett. 10 2008 1963 1966
39. L. Praveen, J. Babu, M.L.P. Reddy, and R.L. Varma Tetrahedron Lett. 53 2012 3951 3954
40. Z. Xu, S. Kim, K.-H. Lee, and J. Yoon Tetrahedron Lett. 48 2007 3797 3800
41. L.D. Shirtcliff, H. Xu, and F. Diederich Eur. J. Org. Chem. 2010 846 855
42. M. Shellaiah, Y.H. Wu, A. Singh, M.V. Ramakrishnam Raju, and H.C. Lin J. Mater. Chem. A 1 2013 1310 1318
43. F. Huang, and G. Feng RSC Adv. 4 2014 474 484
44. D. Parker, and J.A.G. Williams J. Chem. Soc., Perkin Trans. 2 1995 1305 1314
45. A. Beeby, D. Parker, and J.A.G. Williams J. Chem. Soc., Perkin Trans. 2 1996 1565 1579
46. S. Yoon, A.E. Albert, A.P. Wong, and C.J. Chang J. Am. Chem. Soc. 127 2005 16030 16031
47. M. Licchelli, A.O. Biroli, A. Poggi, D. Sacchi, C. Sangermania, and M. Zema Dalton Trans. 2003 4537 4545
48. J.K. Choi, S.H. Kim, J. Yoon, K.H. Lee, R.A. Bartsch, and J.S. Kim J. Org. Chem. 71 2006 8011 8015
49. J.S. Yang, C.S. Linand, and C.Y. Hwang Org. Lett. 3 2001 889 892
50. S. Erdemir, and S. Malkondu Sens. Actuators, B-Chem. 188 2013 1225 1229
51. H.A. Benesi, and J.H. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707
52. B. Valeur Molecular Fluorescence: Principles and Applications 2001 VCH Weinheim, Germany 200 224