Molecular logic operations based on surfactant nanoaggregates

ChemPhysChem

Volumn 9, Issue 13, 2008, Pages 1891-1898

  Qian, Junhong ^a   Xu, Yufang ^a   Qian, Xuhong ^a   Zhang, Shenyi ^a  

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

Author keywords

Fluorescence; Logic gates; Micelles; Molecular devices; Surfactants

Indexed keywords

CHARGE TRANSFER; FLUORESCENCE; LOGIC GATES; MICELLES; SODIUM DODECYL SULFATE; SODIUM SULFATE; SULFUR COMPOUNDS; SURFACE ACTIVE AGENTS;

EMISSION INTENSITY; FLUORESCENCE BEHAVIORS; INORGANIC SALTS; INTRA-MOLECULAR CHARGE TRANSFER; MOLECULAR DEVICE; MOLECULAR LOGIC GATES; OR LOGIC FUNCTION; SURFACTANT CONCENTRATIONS;

COMPUTER CIRCUITS;

EID: 53049105949     PISSN: 14394235     EISSN: 14397641     Source Type: Journal    
DOI: 10.1002/cphc.200800009     Document Type: Article

References (68)

1. A. P. de Silva, H. Q. N. Gunaratne, C. P. McCoy, Nature 1993, 364, 42-44.
2. a) A. P. de Silva, H. Q. N. Gunaratne, C. P. McCoy, J. Am. Chem. Soc. 1997, 119, 7891-7892;
3. b) H.-F. Ji, R. Dabestani, G. M. Brown, J. Am. Chem. Soc. 2000, 122, 9306-9307;
4. c) A. Credi, V. Balzani, S. J. Langford, J. F. Stoddart, J. Am. Chem. Soc. 1997, 119, 2679-2681;
5. d) D. C. Magri, G. D. Coen, R. L. Boyd, A. P. de Silva, Anal. Chim. Acta 2006, 568, 156-159;
6. e) J. Matsui, M. Mitsuishi, A. Aoki, T. Miyashita, Angew. Chem. 2003, 115, 2374-2377;
7. Angew. Chem. Int. Ed. 2003, 42, 2272-2275;
8. f) K. Szacilowski, W. Macyk, G. Stochel, J. Am. Chem. Soc. 2006, 128, 4550-4551;
9. g) A. Saghatelian, N. H. Völcker, K. M. Guckian, V. S.-Y. Lin, M. R. Ghadiri, J. Am. Chem. Soc. 2003, 125, 346-347;
10. h) B. M. Frezza, S. L. Cockroft, M. R. Ghadiri, J. Am. Chem. Soc. 2007, 129, 14 875-14 879;
11. i) H. T. Baytekin, E. U. Akkaya, Org. Lett. 2000, 2, 1725-1727.
12. a) S. J. Langford, T. Yann, J. Am. Chem. Soc. 2003, 125, 11 198-11 199;
13. b) R. Baron, O. Lioubashevski, E. Katz, T. Niazov, I. Willner, Angew. Chem. 2006, 118, 1602-1606;
14. Angew. Chem. Int. Ed. 2006, 45, 1572-1576;
15. c) A. Coskun, E. Deniz, E. U. Akkaya, Org. Lett. 2005, 7, 5187-5189;
16. d) M. N. Stojanovic, D. Stefanovic, J. Am. Chem. Soc. 2003, 125, 6673-6674;
17. e) D. Qu, Q. Wang, H. Tian, Angew. Chem. 2005, 117, 5430-5433;
18. Angew. Chem. Int. Ed. 2005, 44, 5296-5299;
19. f) X. Guo, D. Zhang, G. Zhang, D. Zhu, J. Phys. Chem. B 2004, 108, 11 942-11 945;
20. g) A. Okamoto, K. Tanaka, I. Saiti, J. Am. Chem. Soc. 2004, 126, 9458-9463;
21. h) D. Margulies, G. Melman, C. E. Felder, R. Arad-Yellin, A. Shanzer, J. Am. Chem. Soc. 2004, 126, 15 400-15 401;
22. i) D. Margulies, G. Melman, A. Shanzer, J. Am. Chem. Soc. 2006, 128, 4865-4871;
23. j) D. C. Magri, T. P. Vance, A. P. de Silva, Inorg. Chim. Acta 2007, 360, 751-764.
24. a) S. Uchiyama, G. D. McClean, K. Iwai, A. P. de Silva, J. Am. Chem. Soc. 2005, 127, 8920-8921;
25. b) H. Zhang, X. Lin, Y. Yan, L. Wu, Chem. Commun. 2006, 4575-4577;
26. c) A. Roque, F. Pina, S. Alves, R. Ballardini, M. Maestri, V. Balzani, J. Mater. Chem. 1999, 9, 2265-2269.
27. a) L. Brinchi, P. Di Profio, R. Germani, V. Giacomini, G. Savelli, C. A. Bunton, Langmuir 2000, 16, 222-226;
28. b) Y. S. Simanenko, E. A. Karpichev, T. M. Prokop'eva, B. V. Panchenko, C. A. Bunton, Langmuir 2001, 17, 581-582;
29. c) L. Brinchi, R. Germani, L. Goracci, G. Savelli, C. A. Bunton, Langmuir 2002, 18, 7821-7825;
30. d) K. Niikura, E. V. Anslyn, J. Org. Chem. 2003, 68, 10 156-10 157;
31. e) A. Mallick, M. C. Mandal, B. Haldar, A. Chakrabarty, P. Das, N. Chattopadhyay, J. Am. Chem. Soc. 2006, 128, 3126-3127;
32. f) Y. Zhao, Z. Zhong, Org. Lett. 2006, 8, 4715-4717.
33. a) K. S. Birdi, S. Backlund, K. Sørensen, T. Krag, S. Dalsager, J. Colloid Interface Sci. 1978, 66, 118-123;
34. b) B. T. Imae, C. Mori, S. Ikeda, J. Chem. Soc. Faraday Trans. 1, 1982, 78, 1359-1367;
35. c) Z. Zhou, B. Chu, V. M. Nace, Langmuir 1996, 12, 5016-5021;
36. d) D. P. Bossev, M. Matsumoto, M. Nakahara, J. Phys. Chem. B 1999, 103, 8251-8258;
37. e) T. Shimizu, J. Phys. Chem. B 2003, 107, 8228-8231;
38. f) M. Khamis, B. Bulos, F. Jumean, A. Manassra, M. Dakiky, Dyes Pigm. 2005, 66, 179-183.
39. a) S. S. Atik, L. A. Singer, J. Am. Chem. Soc. 1979, 101, 6759-6761;
40. b) M. G. Neumann, M. H. Gehlen, J. Colloid Interface Sci. 1990, 135, 209-217;
41. c) M. E. C. D. Real Oliveira, J. A. Ferreira, S. M. Nascimento, J. Chem. Soc. Faraday Trans. 1995, 3913-3917;
42. d) K. Toerne, R. Rogers, R. von Wandruszka, Langmuir 2001, 17, 6119-6121;
43. e) S. K. Ghosh, A. Pal, S. Kundu, M. Mandal, S. Nath, T. Pal, Langmuir 2004, 20, 5209-5213;
44. f) T. Sakai, Y. Kaneko, K. Taujii, Langmuir 2006, 22, 2039-2044.
45. a) S. G. Bertolotti, O. E. Zimmerman, J. J. Cosa, C. M. Previtali, J. Lumin. 1993, 55, 105-113;
46. b) N. Jiang, P. Li, Y. Wang, J. Wang, H. Yan, R. K. Thomas, J. Colloid Interface Sci. 2005, 286, 755-760;
47. c) M. M. Knock, C. D. Bain, Langmuir 2000, 16, 2857-2865.
48. a) R. A. Bissell, A. P. de Silva, H. Q. N. Gunaratne, P. L. M. Lynch, G. E. M. Maguire, K. R. A. S. Sandanayake, Chem. Soc. Rev. 1992, 21, 187-195;
49. b) S. Uchiyama, Y. Matsumura, A. P. de Silva, K. Iwai, Anal. Chem. 2004, 76, 1793-1798;
50. c) M. Licchelli, A. O. Biroli, A. Poggi, Org. Lett. 2006, 8, 915-918;
51. d) N. A. O'Connor, S. T. Sakata, H. Zhu, K. J. Shea, Org. Lett. 2006, 8, 1581-1584;
52. e) O. van den Berg, W. F. Jager, S. J. Picken, J. Org. Chem. 2006, 71, 2666-2676.
53. a) T. A. Fayed, J. Photochem. Photobiol. A 1999, 121, 17-25;
54. b) A. P. de Silva, N. D. McClenaghan, J. Am. Chem. Soc. 2000, 122, 3965-3966;
55. c) T. Yoshihara, S. I. Druzhinin, K. A. Zachariasse, J. Am. Chem. Soc. 2004, 126, 8535-8539;
56. d) J. Seo, S. Kim, S. Y. Park, J. Am. Chem. Soc. 2004, 126, 11 154-11 155;
57. e) Z. Xu, X. Qian, J. Cui, Org. Lett. 2005, 7, 3029-3032;
58. f) J. Wang, X. Qian, J. Cui, J. Org. Chem. 2006, 71, 4308-4311.
59. a) J. F. Callan, A. P. de Silva, J. Ferguson, A. J. M. Huxley, A. M. O'Brien, Tetrahedron 2004, 60, 11 125-11 131;
60. b) V. Thiagarajan, P. Ramamurthy, D. Thirumalai, V. T. Ramakrishnan, Org. Lett. 2005, 7, 657-660.
61. S)], where subscripts S and R represent the sample and reference, respectively; φ, F, and A are the fluorescence quantum yield, the integral of the emission band, and the absorbance at excited wavelength, respectively.
62. The cmc of SDS at 25°C in the literature is in the range of 7.2-8.1 mM; a) A. Yamagishi, J. Colloid Interface Sci. 1981, 81, 511-518;
63. b) Ref. [7e].
64. -6 M.
65. a) P. Bilski, R. N. Holt, C. F. Chignell, J. Photochem. Photobiol. A, 1997, 110, 67-74;
66. b) T. A. Fayed, S. E.-D. H. Etaiw, N. Z. Saleh, J. Lumin. 2006, 121, 431-440;
67. c) R. V. Pereira, M. H. Gehlen, Spectrochim. Acta Part A 2005, 61, 2926-2932.
68. Recently, we studied the molecular logic functions operated in surfactant systems. J. Qain, X. Qian, Y. Xu, S. Zhang, Chem. Commun. 2008, DOI: 10.1039/〈B805876H〉.