-
1
-
-
85042671105
-
-
a) E.E. Jelley, Nature 1936, 138, 1009-1010;
-
(1936)
Nature
, vol.138
, pp. 1009-1010
-
-
Jelley, E.E.1
-
2
-
-
42149112490
-
-
b) E. E. Jelley, Nature 1937, 139, 631-632;
-
(1937)
Nature
, vol.139
, pp. 631-632
-
-
Jelley, E.E.1
-
5
-
-
0016081438
-
-
e) E. Daltrozzo, G. Scheibe, K. Geschwind, F. Haimerl, Photogr. Sci. Eng. 1974, 18, 441-450;
-
(1974)
Photogr. Sci. Eng
, vol.18
, pp. 441-450
-
-
Daltrozzo, E.1
Scheibe, G.2
Geschwind, K.3
Haimerl, F.4
-
6
-
-
0343789627
-
-
f) H. von Berlepsch, C. Böttcher, L. Dahne, J. Phys. Chem. B 2000, 104, 8792-8799.
-
(2000)
J. Phys. Chem. B
, vol.104
, pp. 8792-8799
-
-
von Berlepsch, H.1
Böttcher, C.2
Dahne, L.3
-
7
-
-
0017556290
-
-
A. H. Herz, Adv. Colloid Interface Sci. 1977, 8, 237-298;
-
a) A. H. Herz, Adv. Colloid Interface Sci. 1977, 8, 237-298;
-
-
-
-
8
-
-
0029305073
-
-
b) D. Mobius, Adv. Mater. 1995, 7, 437-444;
-
(1995)
Adv. Mater
, vol.7
, pp. 437-444
-
-
Mobius, D.1
-
9
-
-
0003127039
-
-
Ed, T. Kobayashi, World Scientific, Singapore
-
c) H. Kuhn, C Kuhn in J-Aggregates (Ed.: T. Kobayashi), World Scientific, Singapore, 1996, pp. 1-40;
-
(1996)
J-Aggregates
, pp. 1-40
-
-
Kuhn, H.1
Kuhn in, C.2
-
10
-
-
0031187064
-
-
d) A. Pawlik, S. Kirstein, U. De Rossi, S. Dähne, J. Phys. Chem. B 1997, 101, 5646-5651;
-
(1997)
J. Phys. Chem. B
, vol.101
, pp. 5646-5651
-
-
Pawlik, A.1
Kirstein, S.2
De Rossi, U.3
Dähne, S.4
-
12
-
-
30444434841
-
-
a) A. Ajayaghosh, S. J. George, A. P. H. J. Schenning, Top. Curr. Chem. 2005, 258, 83-118;
-
(2005)
Top. Curr. Chem
, vol.258
, pp. 83-118
-
-
Ajayaghosh, A.1
George, S.J.2
Schenning, A.P.H.J.3
-
13
-
-
18044384227
-
-
b) F. J. M. Hoeben, P. Jonkheijm, E. W. Meijer, A. P. H. Schenning, Chem. Rev. 2005, 105, 1491-1546;
-
(2005)
Chem. Rev
, vol.105
, pp. 1491-1546
-
-
Hoeben, F.J.M.1
Jonkheijm, P.2
Meijer, E.W.3
Schenning, A.P.H.4
-
14
-
-
0033876519
-
-
for a review on phosphorescent assemblies, see: c
-
for a review on phosphorescent assemblies, see: c) L. Bruzzone, R. Badia, M. E. Diaz Garcia, Crit. Rev. Anal. Chem. 2000, 30, 163-178.
-
(2000)
Crit. Rev. Anal. Chem
, vol.30
, pp. 163-178
-
-
Bruzzone, L.1
Badia, R.2
Diaz Garcia, M.E.3
-
16
-
-
1542286016
-
-
Some fluorescent aggregates of perylene bisimides have been reported, but they do not display J-type characteristics, such as small Stokes shifts and narrow emission bands: a D. Liu, S. De Feyter, M. Cotlet, U.-M. Wiesler, T. Weil, A. Herrmann, K. Müllen, F. C. De Schryver, Macromolecules 2003, 36, 8489-8498;
-
Some fluorescent aggregates of perylene bisimides have been reported, but they do not display J-type characteristics, such as small Stokes shifts and narrow emission bands: a) D. Liu, S. De Feyter, M. Cotlet, U.-M. Wiesler, T. Weil, A. Herrmann, K. Müllen, F. C. De Schryver, Macromolecules 2003, 36, 8489-8498;
-
-
-
-
17
-
-
13244286584
-
-
b) P. Yan, A. Chowdhury, M. W. Holman, D. M. Adams, J. Phys. Chem. B 2005, 109, 724-730;
-
(2005)
J. Phys. Chem. B
, vol.109
, pp. 724-730
-
-
Yan, P.1
Chowdhury, A.2
Holman, M.W.3
Adams, D.M.4
-
18
-
-
33846238608
-
-
c) Z. Chen, V. Stepanenko, V. Dehm, P. Prins, L. D. A. Siebbeles, J. Seibt, P. Marquetand, V. Engel, F. Würthner, Chem. Eur. J. 2007, 13, 436-449.
-
(2007)
Chem. Eur. J
, vol.13
, pp. 436-449
-
-
Chen, Z.1
Stepanenko, V.2
Dehm, V.3
Prins, P.4
Siebbeles, L.D.A.5
Seibt, J.6
Marquetand, P.7
Engel, V.8
Würthner, F.9
-
20
-
-
0029637583
-
-
b) G. McDermott, S. M. Prince, A. A. Freer, A.M. Hawthornthwaite-Lawless, M. Z. Papiz, R. J. Cogdell, N. W. Isaacs, Nature 1995, 374, 517-521;
-
(1995)
Nature
, vol.374
, pp. 517-521
-
-
McDermott, G.1
Prince, S.M.2
Freer, A.A.3
Hawthornthwaite-Lawless, A.M.4
Papiz, M.Z.5
Cogdell, R.J.6
Isaacs, N.W.7
-
22
-
-
33646727998
-
-
d) T. S. Balaban, H. Tamiaki, A. R. Holzwarth, Top. Curr. Chem. 2005, 258, 1-38.
-
(2005)
Top. Curr. Chem
, vol.258
, pp. 1-38
-
-
Balaban, T.S.1
Tamiaki, H.2
Holzwarth, A.R.3
-
23
-
-
0033804502
-
-
V. I. Prokhorenko, D. B. Steensgard, A. R. Holzwarth, Biophys. J. 2000, 79, 2105-2120.
-
(2000)
Biophys. J
, vol.79
, pp. 2105-2120
-
-
Prokhorenko, V.I.1
Steensgard, D.B.2
Holzwarth, A.R.3
-
25
-
-
14744297685
-
-
b) T. Yamaguchi, T. Kimura, H. Matsuda, T. Aida, Angew. Chem. 2004, 116, 6510-6515;
-
(2004)
Angew. Chem
, vol.116
, pp. 6510-6515
-
-
Yamaguchi, T.1
Kimura, T.2
Matsuda, H.3
Aida, T.4
-
26
-
-
11144297945
-
-
Angew. Chem. Int. Ed. 2004, 43, 6350-6355;
-
(2004)
Chem. Int. Ed
, vol.43
, pp. 6350-6355
-
-
Angew1
-
27
-
-
33744492652
-
-
c) J. A. A. W. Elemans, R. van Hameren, R. J. M. Nolte, A. E. Rowan, Adv. Mater. 2006, 18, 1251-1266.
-
(2006)
Adv. Mater
, vol.18
, pp. 1251-1266
-
-
Elemans, J.A.A.W.1
van Hameren, R.2
Nolte, R.J.M.3
Rowan, A.E.4
-
29
-
-
4644284199
-
-
V. Percec, M. Glodde, T. K. Bera, Y. Miura, I. Shiyanovskaya, K. D. Singer, V. S. K. Balagurusamy, P. A. Heiney, I. Schnell, A. Rapp, H.-W. Spiess, S. D. Hudson, H. Duan, Nature 2002, 417, 384-387.
-
(2002)
Nature
, vol.417
, pp. 384-387
-
-
Percec, V.1
Glodde, M.2
Bera, T.K.3
Miura, Y.4
Shiyanovskaya, I.5
Singer, K.D.6
Balagurusamy, V.S.K.7
Heiney, P.A.8
Schnell, I.9
Rapp, A.10
Spiess, H.-W.11
Hudson, S.D.12
Duan, H.13
-
31
-
-
34547423308
-
-
The perylene bisimide 1 was characterized by NMR spectroscopy, mass spectrometry, and elemental analysis: m.p. 246-247°C; 1H NMR (CDCl3, 400.13 MHz, 300 K, TMS, δ, 8.31 (s, 2H, NH, 8.17 (s, 4H, Hpery, 7.33 (s, 8H, Haryl, 7.15-7.10 (m, 8H, Haryl, 6.97-6.92 (m, 8H, Haryl, 4.02-3.93 (m, 24H, OCH2, 1.85-1.62 (m, 24H, CH2, 1.55-1.35 (m, 24H, CH 2, 1.35-1.10 (m, 192 H, CH2, 0.84-0.78 ppm (m, 36 H, CH3, MS (MALDI-TOF, positive mode, DCTB, m/z calcd for C220H332N2O28: 3450.46 [M+2H, found: 3450.40; UV/Vis (CH2Cl2, λmax (ε, 570 (41 600, 533 (26 800, 444 nm (19000 M-1 cm-1, fluorescence CH2Cl2, λex, 535 nm, λmax, 602 nm, Φfl= 0.93 ±
-
2O (3466.46): C 76.17, H 9.65, N 0.81; found: C 76.04, H 9.55, N 0.89.
-
-
-
-
32
-
-
0000409284
-
-
Transition dipole moments were calculated according to a reported method: W. Liptay, R. Wortmann, H. Schaffrin, O. Burkhard, W. Reitinger, N. Detzer, Chem. Phys. 1988, 120, 429-438. The molar extinction coefficient and the transition dipole moment for the aggregate are given as the values per aggregatebound monomelic unit.
-
Transition dipole moments were calculated according to a reported method: W. Liptay, R. Wortmann, H. Schaffrin, O. Burkhard, W. Reitinger, N. Detzer, Chem. Phys. 1988, 120, 429-438. The molar extinction coefficient and the transition dipole moment for the aggregate are given as the values per aggregatebound monomelic unit.
-
-
-
-
33
-
-
33846242192
-
-
Z. Chen, U. Baumeister, C. Tschierske, F. Würthner, Chem. Eur. J. 2007, 13, 450-465.
-
(2007)
Chem. Eur. J
, vol.13
, pp. 450-465
-
-
Chen, Z.1
Baumeister, U.2
Tschierske, C.3
Würthner, F.4
-
34
-
-
1842332153
-
-
R. P. Sijbesma, F. H. Beijer, L. Brunsveld, B.J. B. Folmer, J. H. K. K. Hirschberg, R. F. M. Lange, J. K. L. Lowe, E.W. Meijer, Science 1997, 278, 1601-1604.
-
(1997)
Science
, vol.278
, pp. 1601-1604
-
-
Sijbesma, R.P.1
Beijer, F.H.2
Brunsveld, L.3
Folmer, B.J.B.4
Hirschberg, J.H.K.K.5
Lange, R.F.M.6
Lowe, J.K.L.7
Meijer, E.W.8
-
35
-
-
84913521777
-
-
M. Kasha, H. R. Rawls, M. A. El-Bayoumi, Pure Appl. Chem. 1965, 11, 371-392.
-
(1965)
Pure Appl. Chem
, vol.11
, pp. 371-392
-
-
Kasha, M.1
Rawls, H.R.2
El-Bayoumi, M.A.3
-
36
-
-
34547477744
-
-
For a discussion, see the Supporting Information
-
For a discussion, see the Supporting Information.
-
-
-
-
37
-
-
34547416065
-
-
For further details, see the Supporting Information
-
For further details, see the Supporting Information.
-
-
-
-
38
-
-
0035910094
-
-
a) R. M. Jones, L. D. Lu, R. Helgeson, T. S. Bergstedt, D. W. McBranch, D. G. Whitten, Proc. Natl. Acad. Sci. USA 2001, 98, 14769-14772;
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 14769-14772
-
-
Jones, R.M.1
Lu, L.D.2
Helgeson, R.3
Bergstedt, T.S.4
McBranch, D.W.5
Whitten, D.G.6
-
39
-
-
17644363642
-
-
b) A. Rose, Z. G. Zhu, C. F. Madigan, T. M. Swager, V. Bulovic, Nature 2005, 434, 876-879.
-
(2005)
Nature
, vol.434
, pp. 876-879
-
-
Rose, A.1
Zhu, Z.G.2
Madigan, C.F.3
Swager, T.M.4
Bulovic, V.5
-
40
-
-
0003146848
-
-
Previously reported fluorescence quantum yields for cyaninedye J-aggregates are about 40% at room temperature and 70% at 77 K; see: a I. G. Scheblykin, O. P. Varnavsky, M. M. Bataiev, O. Sliusarenko, M. van der Auweraer, A. G. Vitukhnovsky, Chem. Phys. Lett. 1998, 298, 341-350;
-
Previously reported fluorescence quantum yields for cyaninedye J-aggregates are about 40% at room temperature and 70% at 77 K; see: a) I. G. Scheblykin, O. P. Varnavsky, M. M. Bataiev, O. Sliusarenko, M. van der Auweraer, A. G. Vitukhnovsky, Chem. Phys. Lett. 1998, 298, 341-350;
-
-
-
-
41
-
-
0001939480
-
-
b) I. G. Scheblykin, M. Bataiev, M. van der Auweraer, A. G. Vitukhnovsky, Chem. Phys. Lett. 2000, 316, 37-44.
-
(2000)
Chem. Phys. Lett
, vol.316
, pp. 37-44
-
-
Scheblykin, I.G.1
Bataiev, M.2
van der Auweraer, M.3
Vitukhnovsky, A.G.4
-
42
-
-
4043098304
-
-
fwhm,agg = √V (G. Busse, B. Frederichs, N. K. Petrov, S. Techert, Phys. Chem. Chem. Phys. 2004, 6, 3309-3314).
-
fwhm,agg = √V (G. Busse, B. Frederichs, N. K. Petrov, S. Techert, Phys. Chem. Chem. Phys. 2004, 6, 3309-3314).
-
-
-
-
43
-
-
0037188025
-
-
S. S. Lampoura, C. Spitz, S. Dähne, J. Knoester, K. Duppen, J. Phys. Chem. B 2002, 106, 3103-3111.
-
(2002)
J. Phys. Chem. B
, vol.106
, pp. 3103-3111
-
-
Lampoura, S.S.1
Spitz, C.2
Dähne, S.3
Knoester, J.4
Duppen, K.5
|