메뉴 건너뛰기




Volumn 101, Issue 38, 1997, Pages 7494-7504

Two-dimensional emission quenching and charge separation using a Ru(II)-photosensitizer assembled with membrane-bound acceptors

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; DIFFUSION IN LIQUIDS; ELECTRON EMISSION; ELECTROSTATICS; MOLECULAR STRUCTURE; OXIDATION; PHOTOSENSITIVITY; SYNTHESIS (CHEMICAL);

EID: 0031235288     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp9710805     Document Type: Article
Times cited : (46)

References (74)
  • 1
    • 0029124427 scopus 로고
    • See e.g. (and references therein): (a) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849. (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C.; Balzani, V.; Barigelletti, F.; De Cola, L.; Flamigni, L. Chem. Rev. (Washington, DC) 1994, 94, 993. (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res 1993, 26, 198. (d) Wasielewski, M. R. Chem. Rev. (Washington, DC) 1992, 92, 435. (e) Balzani, V.; Scandola, F. Supramolecular Photochemistry; Ellis Horwood: UK, Chichester, 1991.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 849
    • Kurreck, H.1    Huber, M.2
  • 3
    • 11744372773 scopus 로고
    • See e.g. (and references therein): (a) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849. (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C.; Balzani, V.; Barigelletti, F.; De Cola, L.; Flamigni, L. Chem. Rev. (Washington, DC) 1994, 94, 993. (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res 1993, 26, 198. (d) Wasielewski, M. R. Chem. Rev. (Washington, DC) 1992, 92, 435. (e) Balzani, V.; Scandola, F. Supramolecular Photochemistry; Ellis Horwood: UK, Chichester, 1991.
    • (1993) Acc. Chem. Res , vol.26 , pp. 198
    • Gust, D.1    Moore, T.A.2    Moore, A.L.3
  • 4
    • 0040891425 scopus 로고
    • See e.g. (and references therein): (a) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849. (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C.; Balzani, V.; Barigelletti, F.; De Cola, L.; Flamigni, L. Chem. Rev. (Washington, DC) 1994, 94, 993. (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res 1993, 26, 198. (d) Wasielewski, M. R. Chem. Rev. (Washington, DC) 1992, 92, 435. (e) Balzani, V.; Scandola, F. Supramolecular Photochemistry; Ellis Horwood: UK, Chichester, 1991.
    • (1992) Chem. Rev. (Washington, DC) , vol.92 , pp. 435
    • Wasielewski, M.R.1
  • 5
    • 0004103426 scopus 로고
    • Ellis Horwood: UK, Chichester
    • See e.g. (and references therein): (a) Kurreck, H.; Huber, M. Angew. Chem., Int. Ed. Engl. 1995, 34, 849. (b) Sauvage, J.-P.; Collin, J.-P.; Chambron, J.-C.; Guillerez, S.; Coudret, C.; Balzani, V.; Barigelletti, F.; De Cola, L.; Flamigni, L. Chem. Rev. (Washington, DC) 1994, 94, 993. (c) Gust, D.; Moore, T. A.; Moore, A. L. Acc. Chem. Res 1993, 26, 198. (d) Wasielewski, M. R. Chem. Rev. (Washington, DC) 1992, 92, 435. (e) Balzani, V.; Scandola, F. Supramolecular Photochemistry; Ellis Horwood: UK, Chichester, 1991.
    • (1991) Supramolecular Photochemistry
    • Balzani, V.1    Scandola, F.2
  • 6
    • 0000757541 scopus 로고
    • For recent examples of noncovalent, pairwise assembly of donors and acceptors, see refs 2a-d and references therein. (a) Hayashi, T.; Takimura, T.; Ogoshi, H. J. Am. Chem. Soc. 1995, 117, 7, 11606. (b) Král, V.; Springs, S. L.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 7, 8881. (c) Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 8252. (d) Roberts, J. A.; Kirby, J. P.; Nocera, D. G. J. Am. Chem. Soc. 1995, 117, 8051. (e) Benniston, A. C.; Harriman, A. J. Am. Chem. Soc. 1994, 116, 11531.
    • (1995) J. Am. Chem. Soc. , vol.117 , Issue.7 , pp. 11606
    • Hayashi, T.1    Takimura, T.2    Ogoshi, H.3
  • 7
    • 0039762993 scopus 로고
    • For recent examples of noncovalent, pairwise assembly of donors and acceptors, see refs 2a-d and references therein. (a) Hayashi, T.; Takimura, T.; Ogoshi, H. J. Am. Chem. Soc. 1995, 117, 7, 11606. (b) Král, V.; Springs, S. L.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 7, 8881. (c) Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 8252. (d) Roberts, J. A.; Kirby, J. P.; Nocera, D. G. J. Am. Chem. Soc. 1995, 117, 8051. (e) Benniston, A. C.; Harriman, A. J. Am. Chem. Soc. 1994, 116, 11531.
    • (1995) J. Am. Chem. Soc. , vol.117 , Issue.7 , pp. 8881
    • Král, V.1    Springs, S.L.2    Sessler, J.L.3
  • 8
    • 0001167158 scopus 로고
    • For recent examples of noncovalent, pairwise assembly of donors and acceptors, see refs 2a-d and references therein. (a) Hayashi, T.; Takimura, T.; Ogoshi, H. J. Am. Chem. Soc. 1995, 117, 7, 11606. (b) Král, V.; Springs, S. L.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 7, 8881. (c) Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 8252. (d) Roberts, J. A.; Kirby, J. P.; Nocera, D. G. J. Am. Chem. Soc. 1995, 117, 8051. (e) Benniston, A. C.; Harriman, A. J. Am. Chem. Soc. 1994, 116, 11531.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8252
    • Berman, A.1    Izraeli, E.S.2    Levanon, H.3    Wang, B.4    Sessler, J.L.5
  • 9
    • 0007083260 scopus 로고
    • For recent examples of noncovalent, pairwise assembly of donors and acceptors, see refs 2a-d and references therein. (a) Hayashi, T.; Takimura, T.; Ogoshi, H. J. Am. Chem. Soc. 1995, 117, 7, 11606. (b) Král, V.; Springs, S. L.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 7, 8881. (c) Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 8252. (d) Roberts, J. A.; Kirby, J. P.; Nocera, D. G. J. Am. Chem. Soc. 1995, 117, 8051. (e) Benniston, A. C.; Harriman, A. J. Am. Chem. Soc. 1994, 116, 11531.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8051
    • Roberts, J.A.1    Kirby, J.P.2    Nocera, D.G.3
  • 10
    • 0001105962 scopus 로고
    • For recent examples of noncovalent, pairwise assembly of donors and acceptors, see refs 2a-d and references therein. (a) Hayashi, T.; Takimura, T.; Ogoshi, H. J. Am. Chem. Soc. 1995, 117, 7, 11606. (b) Král, V.; Springs, S. L.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 7, 8881. (c) Berman, A.; Izraeli, E. S.; Levanon, H.; Wang, B.; Sessler, J. L. J. Am. Chem. Soc. 1995, 117, 8252. (d) Roberts, J. A.; Kirby, J. P.; Nocera, D. G. J. Am. Chem. Soc. 1995, 117, 8051. (e) Benniston, A. C.; Harriman, A. J. Am. Chem. Soc. 1994, 116, 11531.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 11531
    • Benniston, A.C.1    Harriman, A.2
  • 12
    • 0002294319 scopus 로고
    • Springer-Verlag: Berlin
    • Several examples exist where electrostatic forces have been used to assemble sensitizers and acceptors at surfactant aggregates. For reviews, see e.g.: (a) Fox, M. A. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 68. (b) Willner, I,; Willner, B. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 153. (c) Rabani, J. In Photoinduced Electron Transfer, Part B; Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam, 1988; p 642. (d) Grätzel, M. Heterogeneous Photochemical Electron Transfer; CRC Press: Boca Raton, FL, 1989. (e) Matsuo, T. J. Photochem. 1985, 29, 41.
    • (1991) Photoinduced Electron-Transfer III; Top. Curr. Chem. , vol.159 , pp. 68
    • Fox, M.A.1
  • 13
    • 0002708701 scopus 로고
    • Springer-Verlag: Berlin
    • Several examples exist where electrostatic forces have been used to assemble sensitizers and acceptors at surfactant aggregates. For reviews, see e.g.: (a) Fox, M. A. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 68. (b) Willner, I,; Willner, B. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 153. (c) Rabani, J. In Photoinduced Electron Transfer, Part B; Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam, 1988; p 642. (d) Grätzel, M. Heterogeneous Photochemical Electron Transfer; CRC Press: Boca Raton, FL, 1989. (e) Matsuo, T. J. Photochem. 1985, 29, 41.
    • (1991) Photoinduced Electron-Transfer III; Top. Curr. Chem. , vol.159 , pp. 153
    • Willner, I.1    Willner, B.2
  • 14
    • 0011161030 scopus 로고
    • Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam
    • Several examples exist where electrostatic forces have been used to assemble sensitizers and acceptors at surfactant aggregates. For reviews, see e.g.: (a) Fox, M. A. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 68. (b) Willner, I,; Willner, B. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 153. (c) Rabani, J. In Photoinduced Electron Transfer, Part B; Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam, 1988; p 642. (d) Grätzel, M. Heterogeneous Photochemical Electron Transfer; CRC Press: Boca Raton, FL, 1989. (e) Matsuo, T. J. Photochem. 1985, 29, 41.
    • (1988) Photoinduced Electron Transfer, Part B , pp. 642
    • Rabani, J.1
  • 15
    • 0004214038 scopus 로고
    • CRC Press: Boca Raton, FL
    • Several examples exist where electrostatic forces have been used to assemble sensitizers and acceptors at surfactant aggregates. For reviews, see e.g.: (a) Fox, M. A. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 68. (b) Willner, I,; Willner, B. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 153. (c) Rabani, J. In Photoinduced Electron Transfer, Part B; Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam, 1988; p 642. (d) Grätzel, M. Heterogeneous Photochemical Electron Transfer; CRC Press: Boca Raton, FL, 1989. (e) Matsuo, T. J. Photochem. 1985, 29, 41.
    • (1989) Heterogeneous Photochemical Electron Transfer
    • Grätzel, M.1
  • 16
    • 0001863118 scopus 로고
    • Several examples exist where electrostatic forces have been used to assemble sensitizers and acceptors at surfactant aggregates. For reviews, see e.g.: (a) Fox, M. A. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 68. (b) Willner, I,; Willner, B. Photoinduced Electron-Transfer III; Top. Curr. Chem.; Springer-Verlag: Berlin, 1991; Vol. 159, p 153. (c) Rabani, J. In Photoinduced Electron Transfer, Part B; Fox, M. A., Chanon, M., Eds.; Elsevier: Amsterdam, 1988; p 642. (d) Grätzel, M. Heterogeneous Photochemical Electron Transfer; CRC Press: Boca Raton, FL, 1989. (e) Matsuo, T. J. Photochem. 1985, 29, 41.
    • (1985) J. Photochem. , vol.29 , pp. 41
    • Matsuo, T.1
  • 19
  • 22
    • 0003074065 scopus 로고
    • Cevc, G., Ed.; Marcel Dekker: New York
    • (b) Blume, A. In Phospholipids Handbook; Cevc, G., Ed.; Marcel Dekker: New York, 1993; p 455.
    • (1993) Phospholipids Handbook , pp. 455
    • Blume, A.1
  • 23
    • 4043133637 scopus 로고    scopus 로고
    • For monolayer values, see refs 7d and 27 and references therein
    • (c) For monolayer values, see refs 7d and 27 and references therein.
  • 36
    • 4043150566 scopus 로고
    • Bartok, W.; Rosenfeld, D. D.; A. Schriesheim, A. J. Org. Chem. 1963, 28, 410-412. This type of oxidation is also described, without experimental details, in: Potts, K. T. Bull. Soc. Chim. Belg. 1990, 99, 741-768.
    • (1963) J. Org. Chem. , vol.28 , pp. 410-412
    • Bartok, W.1    Rosenfeld, D.D.2    A. Schriesheim, A.3
  • 37
    • 84988110401 scopus 로고
    • Bartok, W.; Rosenfeld, D. D.; A. Schriesheim, A. J. Org. Chem. 1963, 28, 410-412. This type of oxidation is also described, without experimental details, in: Potts, K. T. Bull. Soc. Chim. Belg. 1990, 99, 741-768.
    • (1990) Bull. Soc. Chim. Belg. , vol.99 , pp. 741-768
    • Potts, K.T.1
  • 46
    • 4043130783 scopus 로고    scopus 로고
    • note
    • A biexponential decay was reported in ref 20, with the shorter lifetime between 1 and 20 ns at pH = 0-7. This was attributed to a protonation/deprotonation equilibration in the excited state. However, the intermediate, uncharged form was a poorer emitter than both the fully protonated and the fully dissociated forms. Therefore, such an equilibration would have produced both decreasing and increasing components in the pH interval examined by the authors. Also, the reported lifetime of 20 ns is to short to be explained by a protonation at pH = 7, and the fraction of even singly protonated excited species is expected to be ≪ 1% at pH = 7 and therefore not be detectable in the emission experiments. Thus, it is likely that the fast component of the biexponential decay reported in ref 20 may rather be explained by an impurity or an experimental artifact.
  • 56
    • 85087582134 scopus 로고    scopus 로고
    • note
    • - was assumed to contribute by roughly 0.1 nm. Due to the membrane, the nonspherical viologen headgroups were probably not randomly oriented in the encounter complexes, which makes the value r = 1.1 nm somewhat uncertain. However, for the purpose of the present investigation this was not critical.
  • 66
    • 85087580289 scopus 로고    scopus 로고
    • note
    • 5 contributes to another 0.1 V difference.
  • 68
    • 0039886146 scopus 로고
    • Cevc, G., Ed.; Marcel Dekker: New York
    • (a) Cevc, G. In Phospholipids Handbook; Cevc, G., Ed.; Marcel Dekker: New York, 1993; p 639.
    • (1993) Phospholipids Handbook , pp. 639
    • Cevc, G.1
  • 72
    • 4043048585 scopus 로고    scopus 로고
    • note
    • An X-ray investigation is being pursued presently.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.