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Volumn 16, Issue 4, 2000, Pages 1924-1930

Introduction of [2]catenanes into Langmuir films and Langmuir-Blodgett multilayers. A possible strategy for molecular information storage materials

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; HYDROPHOBICITY; ISOTHERMS; MOLECULAR DYNAMICS; MOLECULAR STRUCTURE; MOLECULES; MULTILAYERS; PHOSPHORUS COMPOUNDS; POSITIVE IONS; ULTRAVIOLET SPECTROSCOPY; X RAY SCATTERING;

EID: 0033893479     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la990791m     Document Type: Article
Times cited : (72)

References (84)
  • 6
    • 0001384399 scopus 로고
    • Nobel Lecture
    • (a) Cram, D. J. (Nobel Lecture) Angew. Chem. 1988, 100, 1041-1052; Angew. Chem., Int. Ed. Engl. 1988, 27, 1009-1020.
    • (1988) Angew. Chem. , vol.100 , pp. 1041-1052
    • Cram, D.J.1
  • 7
    • 84990085627 scopus 로고
    • (a) Cram, D. J. (Nobel Lecture) Angew. Chem. 1988, 100, 1041- 1052; Angew. Chem., Int. Ed. Engl. 1988, 27, 1009-1020.
    • (1988) Angew. Chem., Int. Ed. Engl. , vol.27 , pp. 1009-1020
  • 8
    • 0001295376 scopus 로고
    • Nobel Lecture
    • (b) Pedersen, C. J. (Nobel Lecture) Angew. Chem. 1988, 100, 1053-1059; Angew. Chem., Int. Ed. Engl. 1988, 27, 1021-1027.
    • (1988) Angew. Chem. , vol.100 , pp. 1053-1059
    • Pedersen, C.J.1
  • 9
    • 84990101529 scopus 로고
    • (b) Pedersen, C. J. (Nobel Lecture) Angew. Chem. 1988, 100, 1053-1059; Angew. Chem., Int. Ed. Engl. 1988, 27, 1021-1027.
    • (1988) Angew. Chem., Int. Ed. Engl. , vol.27 , pp. 1021-1027
  • 32
    • 0025668818 scopus 로고
    • (a) Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1990, 29, 1304- 1319; Angew. Chem. 1990, 102, 1347-1363.
    • (1990) Angew. Chem. , vol.102 , pp. 1347-1363
  • 36
    • 0025047522 scopus 로고
    • (b) Langer, R. Science 1990, 249, 1527-1533.
    • (1990) Science , vol.249 , pp. 1527-1533
    • Langer, R.1
  • 45
    • 0033583549 scopus 로고    scopus 로고
    • Fitzmaurice, D.; Nagaraja Rao, S.; Preece, J. A.; Stoddart, J. F.; Wenger, S.; Zaccheroni, N. Angew. Chem. 1999, 111, 1220-1224; Angew. Chem., Int. Ed. 1999, 38, 1147-1150.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 1147-1150
  • 49
    • 0030822095 scopus 로고    scopus 로고
    • (a) Diederich, F.; Gomez-Lopez, M.; Nierengarten, J.-F.; Preece, J. A.; Raymo, F. M.; Stoddart, J. F. Angew. Chem. 1997, 109, 1611- 1614; Angew. Chem., Int. Ed. Engl. 1997, 36, 1448-1451.
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 1448-1451
  • 56
    • 33748229714 scopus 로고
    • (a) Ballardini, R.; Balzani, V.; Gandolfi, M. T.; Prodi, L.; Venturi, M.; Philp, D.; Ricketts, H. G.; Stoddart, J. F. Angew. Chem. 1993, 105, 1362-1364; Angew. Chem., Int. Ed. Engl. 1993, 32, 1301-1303.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1301-1303
  • 65
    • 0001457235 scopus 로고
    • 6 which has been self-assembled in high yield (70%) by appealing to the template direction resulting from the molecular recognition between the π-electron-accepting bipyridinium units in the cyclophane component and the π-electron-donating hydroquinone rings in the crown ether component. See: (b) Ashton, P. R.; Goodnow, T. T.; Kaifer, A. E.; Reddington, M. V.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Vicent, C.; Williams, D. J. Angew. Chem. 1989, 101, 1404-1408; Angew. Chem., Int. Ed. Engl. 1989, 28, 1396-1399.
    • (1993) Langmuir , vol.9 , pp. 1534-1544
    • Ahuja, R.C.1    Caruso, P.-L.2    Möbius, D.3    Wildberg, G.4    Ringsdorf, H.5    Philp, D.6    Preece, J.A.7    Stoddart, J.F.8
  • 66
    • 0000433056 scopus 로고
    • 6 which has been self-assembled in high yield (70%) by appealing to the template direction resulting from the molecular recognition between the π-electron-accepting bipyridinium units in the cyclophane component and the π-electron- donating hydroquinone rings in the crown ether component. See: (b) Ashton, P. R.; Goodnow, T. T.; Kaifer, A. E.; Reddington, M. V.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Vicent, C.; Williams, D. J. Angew. Chem. 1989, 101, 1404-1408; Angew. Chem., Int. Ed. Engl. 1989, 28, 1396-1399.
    • (1989) Angew. Chem. , vol.101 , pp. 1404-1408
    • Ashton, P.R.1    Goodnow, T.T.2    Kaifer, A.E.3    Reddington, M.V.4    Slawin, A.M.Z.5    Spencer, N.6    Stoddart, J.F.7    Vicent, C.8    Williams, D.J.9
  • 67
    • 84990151906 scopus 로고
    • 6 which has been self-assembled in high yield (70%) by appealing to the template direction resulting from the molecular recognition between the π-electron-accepting bipyridinium units in the cyclophane component and the π-electron- donating hydroquinone rings in the crown ether component. See: (b) Ashton, P. R.; Goodnow, T. T.; Kaifer, A. E.; Reddington, M. V.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Vicent, C.; Williams, D. J. Angew. Chem. 1989, 101, 1404-1408; Angew. Chem., Int. Ed. Engl. 1989, 28, 1396-1399.
    • (1989) Angew. Chem., Int. Ed. Engl. , vol.28 , pp. 1396-1399
  • 73
    • 0025498632 scopus 로고
    • 17 It may still be possible to exploit this methodology for incorporating switchable (supra)molecular structures into thin films and acheive the switching action. (For a demonstration of the use of azobenzene as a data-storage material, see: (a) Liu, Z. F.; Hashimoto, K.; Fujishima, A. Nature 1990, 347, 658-660 .) However, the solution to this is not simple, and the challenge still remains! It should be noted that there are several examples in which azobenzenze units have been photoisomerized in Langmuir-Blodgett films. For selected examples see: (b) Goldenberg, L. M.; Bryce, M. R.; Wegener, S.; Petty, M. C.; Cresswell, J. P.; Lednev, I. K.; Hester, R. E.; Moore, J. N. J. Mater. Chem. 1997, 7, 2033-2037. (c) Maack, J.; Ahuja, R. C.; Möbius, D.; Tachibana, H.; Matsumoto, H. Thin Solid Films 1994, 242, 122-126. (d) Nishiyama, K.; Fujihara, M. Chem. Lett. 1988, 1257-1260.
    • (1990) Nature , vol.347 , pp. 658-660
    • Liu, Z.F.1    Hashimoto, K.2    Fujishima, A.3
  • 74
    • 0001760780 scopus 로고    scopus 로고
    • 17 It may still be possible to exploit this methodology for incorporating switchable (supra)molecular structures into thin films and acheive the switching action. (For a demonstration of the use of azobenzene as a data-storage material, see: (a) Liu, Z. F.; Hashimoto, K.; Fujishima, A. Nature 1990, 347, 658-660 .) However, the solution to this is not simple, and the challenge still remains! It should be noted that there are several examples in which azobenzenze units have been photoisomerized in Langmuir-Blodgett films. For selected examples see: (b) Goldenberg, L. M.; Bryce, M. R.; Wegener, S.; Petty, M. C.; Cresswell, J. P.; Lednev, I. K.; Hester, R. E.; Moore, J. N. J. Mater. Chem. 1997, 7, 2033-2037. (c) Maack, J.; Ahuja, R. C.; Möbius, D.; Tachibana, H.; Matsumoto, H. Thin Solid Films 1994, 242, 122-126. (d) Nishiyama, K.; Fujihara, M. Chem. Lett. 1988, 1257-1260.
    • (1997) J. Mater. Chem. , vol.7 , pp. 2033-2037
    • Goldenberg, L.M.1    Bryce, M.R.2    Wegener, S.3    Petty, M.C.4    Cresswell, J.P.5    Lednev, I.K.6    Hester, R.E.7    Moore, J.N.8
  • 75
    • 0028405286 scopus 로고
    • 17 It may still be possible to exploit this methodology for incorporating switchable (supra)molecular structures into thin films and acheive the switching action. (For a demonstration of the use of azobenzene as a data-storage material, see: (a) Liu, Z. F.; Hashimoto, K.; Fujishima, A. Nature 1990, 347, 658-660 .) However, the solution to this is not simple, and the challenge still remains! It should be noted that there are several examples in which azobenzenze units have been photoisomerized in Langmuir-Blodgett films. For selected examples see: (b) Goldenberg, L. M.; Bryce, M. R.; Wegener, S.; Petty, M. C.; Cresswell, J. P.; Lednev, I. K.; Hester, R. E.; Moore, J. N. J. Mater. Chem. 1997, 7, 2033-2037. (c) Maack, J.; Ahuja, R. C.; Möbius, D.; Tachibana, H.; Matsumoto, H. Thin Solid Films 1994, 242, 122-126. (d) Nishiyama, K.; Fujihara, M. Chem. Lett. 1988, 1257-1260.
    • (1994) Thin Solid Films , vol.242 , pp. 122-126
    • Maack, J.1    Ahuja, R.C.2    Möbius, D.3    Tachibana, H.4    Matsumoto, H.5
  • 76
    • 0001760780 scopus 로고    scopus 로고
    • 17 It may still be possible to exploit this methodology for incorporating switchable (supra)molecular structures into thin films and acheive the switching action. (For a demonstration of the use of azobenzene as a data-storage material, see: (a) Liu, Z. F.; Hashimoto, K.; Fujishima, A. Nature 1990, 347, 658-660 .) However, the solution to this is not simple, and the challenge still remains! It should be noted that there are several examples in which azobenzenze units have been photoisomerized in Langmuir-Blodgett films. For selected examples see: (b) Goldenberg, L. M.; Bryce, M. R.; Wegener, S.; Petty, M. C.; Cresswell, J. P.; Lednev, I. K.; Hester, R. E.; Moore, J. N. J. Mater. Chem. 1997, 7, 2033-2037. (c) Maack, J.; Ahuja, R. C.; Möbius, D.; Tachibana, H.; Matsumoto, H. Thin Solid Films 1994, 242, 122-126. (d) Nishiyama, K.; Fujihara, M. Chem. Lett. 1988, 1257-1260.
    • (1988) Chem. Lett. , pp. 1257-1260
    • Nishiyama, K.1    Fujihara, M.2
  • 79
    • 33749154871 scopus 로고
    • Ahuja, R. C.; Caruso, P.-L.; Möbius, D.; Paulus, W.; Ringsdorf, H.; Wildburg, G. Angew. Chem. 1993, 105, 1082-1091; Angew. Chem., Int. Ed. Engl. 1993, 32, 1033-1036.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1033-1036
  • 80
    • 0343150742 scopus 로고
    • For a collection of papers dealing with bottom-up and top-down approaches to (molecular) devices, see: Philos. Trans. R. Soc. London, Ser. A 1995, 353, 279-293. These papers are a collective theme on the "perspectives on the limits of fabrication and measurement" compiled and edited by M. E. Weiland and J. K. Gimzewski, and also see a special issue of the Jounal of Materials Chemistry (J. Mater. Chem. 1999, 9, 1853-2275) on Functional Organic Materials for Devices.
    • (1995) Philos. Trans. R. Soc. London, Ser. A , vol.353 , pp. 279-293
  • 81
    • 0342716228 scopus 로고    scopus 로고
    • For a collection of papers dealing with bottom-up and top-down approaches to (molecular) devices, see: Philos. Trans. R. Soc. London, Ser. A 1995, 353, 279-293. These papers are a collective theme on the "perspectives on the limits of fabrication and measurement" compiled and edited by M. E. Weiland and J. K. Gimzewski, and also see a special issue of the Jounal of Materials Chemistry (J. Mater. Chem. 1999, 9, 1853-2275) on Functional Organic Materials for Devices.
    • Jounal of Materials Chemistry
    • Weiland, M.E.1    Gimzewski, J.K.2
  • 82
    • 0032885210 scopus 로고    scopus 로고
    • For a collection of papers dealing with bottom-up and top-down approaches to (molecular) devices, see: Philos. Trans. R. Soc. London, Ser. A 1995, 353, 279-293. These papers are a collective theme on the "perspectives on the limits of fabrication and measurement" compiled and edited by M. E. Weiland and J. K. Gimzewski, and also see a special issue of the Jounal of Materials Chemistry (J. Mater. Chem. 1999, 9, 1853-2275) on Functional Organic Materials for Devices.
    • (1999) J. Mater. Chem. , vol.9 , pp. 1853-2275
  • 83
    • 0033575366 scopus 로고    scopus 로고
    • Recently, a combination of "top-down" and "bottom-up" approaches has provided, utilizing Langmuir-Blodgett films of the closely related rotaxane (see ref 11) molecular materials, electronically configurable molecular-based logic gates. See: Collier, C. P.; Wong, E. W.; Belohradsky, M.; Raymo, F. M.; Stoddart, J. F.; Kuekes, P. J.; Williams, R. S.; Heath, J. R. Science 1999, 285, 391-394. Additionally, the pseudorotaxane architecture has been introduced into LB films. See: Lynch, D. E.; Hamilton, D. G.; Calos, N. J.; Wood, B.; Sanders, J. K. M. Langmuir 1999, 15, 5600-5605.
    • (1999) Science , vol.285 , pp. 391-394
    • Collier, C.P.1    Wong, E.W.2    Belohradsky, M.3    Raymo, F.M.4    Stoddart, J.F.5    Kuekes, P.J.6    Williams, R.S.7    Heath, J.R.8
  • 84
    • 0032598451 scopus 로고    scopus 로고
    • Recently, a combination of "top-down" and "bottom-up" approaches has provided, utilizing Langmuir-Blodgett films of the closely related rotaxane (see ref 11) molecular materials, electronically configurable molecular-based logic gates. See: Collier, C. P.; Wong, E. W.; Belohradsky, M.; Raymo, F. M.; Stoddart, J. F.; Kuekes, P. J.; Williams, R. S.; Heath, J. R. Science 1999, 285, 391-394. Additionally, the pseudorotaxane architecture has been introduced into LB films. See: Lynch, D. E.; Hamilton, D. G.; Calos, N. J.; Wood, B.; Sanders, J. K. M. Langmuir 1999, 15, 5600-5605.
    • (1999) Langmuir , vol.15 , pp. 5600-5605
    • Lynch, D.E.1    Hamilton, D.G.2    Calos, N.J.3    Wood, B.4    Sanders, J.K.M.5


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