-
1
-
-
15844424533
-
-
T. Brixner, J. Stenger, H. M. Vaswani, M. Cho, R. E. Blankenship, G. R. Fleming, Nature 2005, 434, 625-628
-
(2005)
Nature
, vol.434
, pp. 625-628
-
-
Brixner, T.1
Stenger, J.2
Vaswani, H.M.3
Cho, M.4
Blankenship, R.E.5
Fleming, G.R.6
-
2
-
-
0036335537
-
-
L. M. Yoder, A. G. Cole, R. J. Sension, Photosynth. Res. 2002, 72, 147-158
-
(2002)
Photosynth. Res.
, vol.72
, pp. 147-158
-
-
Yoder, L.M.1
Cole, A.G.2
Sension, R.J.3
-
7
-
-
33947395582
-
-
For light harvesting energy-transfer system based on synthetic protein assemblies, see R. A. Miller, A. D. Presley, M. B. Francis, J. Am. Chem. Soc. 2007, 129, 3104-3109
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 3104-3109
-
-
Miller, R.A.1
Presley, A.D.2
Francis, M.B.3
-
8
-
-
35748956777
-
-
M. Endo, M. Fujitsuka, T. Majima, Chem. Eur. J. 2007, 13, 8660-8666
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 8660-8666
-
-
Endo, M.1
Fujitsuka, M.2
Majima, T.3
-
9
-
-
0033963393
-
-
Y. Z. Hu, S. Tsukiji, S. Shinkai, S. Oishi, I. Hamachi, J. Am. Chem. Soc. 2000, 122, 241-253.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 241-253
-
-
Hu, Y.Z.1
Tsukiji, S.2
Shinkai, S.3
Oishi, S.4
Hamachi, I.5
-
10
-
-
67650566587
-
-
E. R. Young, J. Rosenthal, J. M. Hodgkiss, D. G. Nocera, J. Am. Chem. Soc. 2009, 131, 7678-7684
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 7678-7684
-
-
Young, E.R.1
Rosenthal, J.2
Hodgkiss, J.M.3
Nocera, D.G.4
-
11
-
-
46049098107
-
-
G. Fernández, E. M. Pérez, L. Sánchez, N. Martín, Angew. Chem. 2008, 120, 1110-1113
-
(2008)
Angew. Chem.
, vol.120
, pp. 1110-1113
-
-
Fernández, G.1
Pérez, E.M.2
Sánchez, L.3
Martín, N.4
-
12
-
-
38849152258
-
-
Angew. Chem. Int. Ed. 2008, 47, 1094-1097
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 1094-1097
-
-
-
13
-
-
34249035443
-
-
P. G. A. Janssen, J. Vandenbergh, J. L. J. VanDongen, E. W. Meijer, A. P. H. J. Schenning, J. Am. Chem. Soc. 2007, 129, 6078-6079
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 6078-6079
-
-
Janssen, P.G.A.1
Vandenbergh, J.2
Vandongen, J.L.J.3
Meijer, E.W.4
Schenning, A.P.H.J.5
-
14
-
-
29844456001
-
-
A. DelGuerzo, A. G. L. Olive, J. Reichwagen, H. Hopf, J. P. Desvergne, J. Am. Chem. Soc. 2005, 127, 17984-17985.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17984-17985
-
-
Delguerzo, A.1
Olive, A.G.L.2
Reichwagen, J.3
Hopf, H.4
Desvergne, J.P.5
-
15
-
-
77951613692
-
-
R. J. Brea, C. Reiriz, J. R. Granja, Chem. Soc. Rev. 2010, 39, 1448-1456
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1448-1456
-
-
Brea, R.J.1
Reiriz, C.2
Granja, J.R.3
-
16
-
-
77956766226
-
-
(Eds: J.A. Schwarz, C.I. Contescu, K. Putyera), Marcel Dekker Inc, New York
-
R. J. Brea, J. R. Granja, in Dekker Encyclopedia of Nanoscience and Nanotechnology (Eds:, J.A. Schwarz, C.I. Contescu, K. Putyera,), Marcel Dekker Inc, New York, 2004, pp. 3439-3457
-
(2004)
Dekker Encyclopedia of Nanoscience and Nanotechnology
, pp. 3439-3457
-
-
Brea, R.J.1
Granja, J.R.2
-
17
-
-
0011477170
-
-
G. R. Patzke, F. Krumeich, R. Nesper, Angew. Chem. 2002, 114, 2554-2571
-
(2002)
Angew. Chem.
, vol.114
, pp. 2554-2571
-
-
Patzke, G.R.1
Krumeich, F.2
Nesper, R.3
-
18
-
-
0037099441
-
-
Angew. Chem. Int. Ed. 2002, 41, 2446-2461
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2446-2461
-
-
-
19
-
-
0001482044
-
-
D. T. Bong, T. D. Clark, J. R. Granja, M. R. Ghadiri, Angew. Chem. 2001, 113, 1016-1041
-
(2001)
Angew. Chem.
, vol.113
, pp. 1016-1041
-
-
Bong, D.T.1
Clark, T.D.2
Granja, J.R.3
Ghadiri, M.R.4
-
20
-
-
0035857549
-
-
Angew. Chem. Int. Ed. 2001, 40, 988-1011.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 988-1011
-
-
-
22
-
-
34548378697
-
-
E. S. Barrett, T. J. Dale, J. Rebek, Jr., J. Am. Chem. Soc. 2007, 129, 8818-8824
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 8818-8824
-
-
Barrett, E.S.1
Dale, T.J.2
Rebek Jr., J.3
-
24
-
-
11144293462
-
-
M. V. Ovchinnikov, A. M. Brown, X. Liu, C. A. Mirkin, L. N. Zakharov, A. L. Rheingold, Inorg. Chem. 2004, 43, 8233-8235.
-
(2004)
Inorg. Chem.
, vol.43
, pp. 8233-8235
-
-
Ovchinnikov, M.V.1
Brown, A.M.2
Liu, X.3
Mirkin, C.A.4
Zakharov, L.N.5
Rheingold, A.L.6
-
25
-
-
11144319853
-
-
P. M. Bowers, S. J. Cokus, D. Eisenberg, T. O. Yeates, Science 2004, 306, 2246-2249
-
(2004)
Science
, vol.306
, pp. 2246-2249
-
-
Bowers, P.M.1
Cokus, S.J.2
Eisenberg, D.3
Yeates, T.O.4
-
29
-
-
0037251326
-
-
M. R. Young, H.-S. Yang, N. H. Colburn, Trends Mol. Med. 2003, 9, 36-41
-
(2003)
Trends Mol. Med.
, vol.9
, pp. 36-41
-
-
Young, M.R.1
Yang, H.-S.2
Colburn, N.H.3
-
30
-
-
0037462454
-
-
R. Eferl, R. Ricci, L. Kenner, R. Zenz, J.-P. David, M. Rath, E. F. Wagner, Cell 2003, 112, 181-192.
-
(2003)
Cell
, vol.112
, pp. 181-192
-
-
Eferl, R.1
Ricci, R.2
Kenner, L.3
Zenz, R.4
David, J.-P.5
Rath, M.6
Wagner, E.F.7
-
31
-
-
70350097624
-
-
C. Reiriz, M. Amorín, R. García-Fandiño, L. Castedo, J. R. Granja, Org. Biomol. Chem. 2009, 7, 4358-4361
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 4358-4361
-
-
Reiriz, C.1
Amorín, M.2
García-Fandiño, R.3
Castedo, L.4
Granja, J.R.5
-
33
-
-
27744590590
-
-
M. Amorín, L. Castedo, J. R. Granja, Chem. Eur. J. 2005, 11, 6543-6551
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 6543-6551
-
-
Amorín, M.1
Castedo, L.2
Granja, J.R.3
-
34
-
-
27144476831
-
-
M. Amorín, R. J. Brea, L. Castedo, J. R. Granja, Org. Lett. 2005, 7, 4681-4684
-
(2005)
Org. Lett.
, vol.7
, pp. 4681-4684
-
-
Amorín, M.1
Brea, R.J.2
Castedo, L.3
Granja, J.R.4
-
35
-
-
0037433498
-
-
M. Amorín, L. Castedo, J. R. Granja, J. Am. Chem. Soc. 2003, 125, 2844-2845.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2844-2845
-
-
Amorín, M.1
Castedo, L.2
Granja, J.R.3
-
36
-
-
53849146070
-
-
M. Amorín, L. Castedo, J. R. Granja, Chem. Eur. J. 2008, 14, 2100-2111.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 2100-2111
-
-
Amorín, M.1
Castedo, L.2
Granja, J.R.3
-
37
-
-
70350639426
-
-
For α,γ-peptide nanotube formation, see R. García-Fandiño, J. R. Granja, D. A. Marco, M. Orozco, J. Am. Chem. Soc. 2009, 131, 15678-15686
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 15678-15686
-
-
García-Fandiño, R.1
Granja, J.R.2
Marco, D.A.3
Orozco, M.4
-
38
-
-
68849122340
-
-
C. Reiriz, R. J. Brea, R. Arranz, J. L. Carrascosa, A. Garibotti, B. Manning, J. M. Valpuesta, R. Eritja, L. Castedo, J. R. Granja, J. Am. Chem. Soc. 2009, 131, 11335-11337.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11335-11337
-
-
Reiriz, C.1
Brea, R.J.2
Arranz, R.3
Carrascosa, J.L.4
Garibotti, A.5
Manning, B.6
Valpuesta, J.M.7
Eritja, R.8
Castedo, L.9
Granja, J.R.10
-
39
-
-
53849127445
-
-
R. J. Brea, M. Amorín, L. Castedo, J. R. Granja, Angew. Chem. 2005, 117, 5856-5859
-
(2005)
Angew. Chem.
, vol.117
, pp. 5856-5859
-
-
Brea, R.J.1
Amorín, M.2
Castedo, L.3
Granja, J.R.4
-
40
-
-
24944550968
-
-
Angew. Chem. Int. Ed. 2005, 44, 5710-5713.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 5710-5713
-
-
-
41
-
-
77951110595
-
-
For theoretical studies carried out with homo-and heterodimers, see:, R. García-Fandiño, L. Castedo, J. R. Granja, S. Vázquez, J. Phys. Chem. B 2010, 114, 4973-4983.
-
(2010)
J. Phys. Chem. B
, vol.114
, pp. 4973-4983
-
-
García-Fandiño, R.1
Castedo, L.2
Granja, J.R.3
Vázquez, S.4
-
42
-
-
1642280493
-
-
For heteromeric peptide nanotube formation driven mainly by side-chain/side-chain interactions, see K. Rosenthal-Aizman, G. Svensson, A. Undén, J. Am. Chem. Soc. 2004, 126, 3372-3373
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3372-3373
-
-
Rosenthal-Aizman, K.1
Svensson, G.2
Undén, A.3
-
43
-
-
0037189896
-
-
J. Sánchez-Quesada, M. P. Isler, M. R. Ghadiri, J. Am. Chem. Soc. 2002, 124, 10004-10005.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 10004-10005
-
-
Sánchez-Quesada, J.1
Isler, M.P.2
Ghadiri, M.R.3
-
44
-
-
34248360332
-
-
For donor-acceptor systems based on α,γ-CP heterodimer formation, see R. J. Brea, M. A. Herranz, L. Sánchez, L. Castedo, W. Seitz, D. M. Guldi, N. Martín, J. R. Granja, Proc. Natl. Acad. Sci. USA 2007, 104, 5291-5294
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 5291-5294
-
-
Brea, R.J.1
Herranz, M.A.2
Sánchez, L.3
Castedo, L.4
Seitz, W.5
Guldi, D.M.6
Martín, N.7
Granja, J.R.8
-
45
-
-
33846979505
-
-
R. J. Brea, M. E. Vázquez, M. Mosquera, L. Castedo, J. R. Granja, J. Am. Chem. Soc. 2007, 129, 1653-1657.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1653-1657
-
-
Brea, R.J.1
Vázquez, M.E.2
Mosquera, M.3
Castedo, L.4
Granja, J.R.5
-
48
-
-
0023008334
-
-
(Eds: C.B. Anfinsen, J.T. Edsall, F.M. Richards), Academic Press, Orlando
-
S. Krimm, J. Bandekar, in Advances in Protein Chemistry (Eds:, C.B. Anfinsen, J.T. Edsall, F.M. Richards,), Academic Press, Orlando, 1986, pp. 181-364.
-
(1986)
Advances in Protein Chemistry
, pp. 181-364
-
-
Krimm, S.1
Bandekar, J.2
-
49
-
-
13444287737
-
-
M. Amorin, V. Villaverde, L. Castedo, J. R. Granja, J. Drug Delivery Sci. Technol. 2005, 15, 87-92.
-
(2005)
J. Drug Delivery Sci. Technol.
, vol.15
, pp. 87-92
-
-
Amorin, M.1
Villaverde, V.2
Castedo, L.3
Granja, J.R.4
-
50
-
-
78650793777
-
-
DOI:10.1002/chem.201002271
-
For a recent studies of molecular tweezers based on α,γ-CP dimer/porphyrin hybrids, see: L.P. Hernández-Eguía, R.J. Brea, L. Castedo, P. Ballester, J.R. Granja Chem. Eur. J. 2010, DOI:10.1002/chem. 201002271.
-
(2010)
Chem. Eur. J.
-
-
Hernández-Eguía, L.P.1
-
51
-
-
33745464977
-
-
V. A. Azov, A. Schlegel, F. Diederich, Angew. Chem. 2005, 117, 4711-4715
-
(2005)
Angew. Chem.
, vol.117
, pp. 4711-4715
-
-
Azov, V.A.1
Schlegel, A.2
Diederich, F.3
-
52
-
-
22844446166
-
-
Angew. Chem. Int. Ed. 2005, 44, 4635-4638
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 4635-4638
-
-
-
54
-
-
0141678910
-
-
R. B. Martin, K. Fu, H. Li, D. Cole, Y.-P. Sun, Chem. Commun. 2003, 2368-2369.
-
(2003)
Chem. Commun.
, pp. 2368-2369
-
-
Martin, R.B.1
Fu, K.2
Li, H.3
Cole, D.4
Sun, Y.-P.5
-
55
-
-
32044443628
-
-
N. Ashkenasy, W. S. Horne, M. R. Ghadiri, Small 2006, 2, 99-102
-
(2006)
Small
, vol.2
, pp. 99-102
-
-
Ashkenasy, N.1
Horne, W.S.2
Ghadiri, M.R.3
-
56
-
-
14544281493
-
-
W. S. Horne, N. Ashkenasy, M. R. Ghadiri, Chem. Eur. J. 2005, 11, 1137-1144.
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 1137-1144
-
-
Horne, W.S.1
Ashkenasy, N.2
Ghadiri, M.R.3
-
57
-
-
38049047105
-
-
For pyrene/perylene FRET pair, see D. Lindegaard, A. S. Madsen, I. V. Astakhova, A. D. Malakhov, B. R. Babu, V. A. Korshunb, J. Wengel, Bioorg. Med. Chem. 2008, 16, 94-99
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 94-99
-
-
Lindegaard, D.1
Madsen, A.S.2
Astakhova, I.V.3
Malakhov, A.D.4
Babu, B.R.5
Korshunb, V.A.6
Wengel, J.7
-
58
-
-
0034654675
-
-
M. Masuko, S. Ohuchi, K. Sode, H. Ohtani, A. Shimadzu, Nucleic Acids Res. 2000, 28, 34e
-
(2000)
Nucleic Acids Res.
, vol.28
-
-
Masuko, M.1
Ohuchi, S.2
Sode, K.3
Ohtani, H.4
Shimadzu, A.5
-
59
-
-
33947277312
-
-
J. N. Wilson, J. Gao, E. T. Kool., Tetrahedron 2007, 63, 3427-3433
-
(2007)
Tetrahedron
, vol.63
, pp. 3427-3433
-
-
Wilson, J.N.1
Gao, J.2
Kool, E.T.3
-
60
-
-
67849104948
-
-
Y. N. Teo, J. N. Wilson, E. T. Kool, J. Am. Chem. Soc. 2009, 131, 3923-3933
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3923-3933
-
-
Teo, Y.N.1
Wilson, J.N.2
Kool, E.T.3
-
61
-
-
77049104967
-
-
H. Kashida, T. Takatsu, K. Sekiguchi, H. Asanuma, Chem. Eur. J. 2010, 16, 2479-2486.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 2479-2486
-
-
Kashida, H.1
Takatsu, T.2
Sekiguchi, K.3
Asanuma, H.4
-
62
-
-
29744457739
-
-
For the preparation of perylen-3-ylmethanol (14), see:, M. V. Skorobogatyi, A. A. Pchelintseva, A. L. Petrunina, I. A. Stepanova, V. L. Andronova, G. A. Galegov, A. D. Malakhov, V. A. Korshun, Tetrahedron 2006, 62, 1279-1287.
-
(2006)
Tetrahedron
, vol.62
, pp. 1279-1287
-
-
Skorobogatyi, M.V.1
Pchelintseva, A.A.2
Petrunina, A.L.3
Stepanova, I.A.4
Andronova, V.L.5
Galegov, G.A.6
Malakhov, A.D.7
Korshun, V.A.8
-
65
-
-
0008499166
-
-
A. Ueno, I. Suzuki, T. Osa, J. Am. Chem. Soc. 1989, 111, 6391-6397.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 6391-6397
-
-
Ueno, A.1
Suzuki, I.2
Osa, T.3
-
66
-
-
78650792520
-
-
A was determined, taking in consideration ratios between alternated and eclipse forms calculated by NMR experiments, by least-squares analysis fitting to appropriate equations using Kaleidagraph 3.5 (Synergy Software, Reading, PA). For model and equation used, see
-
A was determined, taking in consideration ratios between alternated and eclipse forms calculated by NMR experiments, by least-squares analysis fitting to appropriate equations using Kaleidagraph 3.5 (Synergy Software, Reading, PA). For model and equation used, see
-
-
-
-
67
-
-
0042338504
-
-
J. W. Park, H. E. Song, S. Y. Lee, J. Org. Chem. 2003, 68, 7071-7076
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7071-7076
-
-
Park, J.W.1
Song, H.E.2
Lee, S.Y.3
-
69
-
-
0003109459
-
-
M. R. Ghadiri, K. Kobayashi, J. R. Granja, R. K. Chadha, D. E. McRee, Angew. Chem. 1995, 107, 76-78
-
(1995)
Angew. Chem.
, vol.107
, pp. 76-78
-
-
Ghadiri, M.R.1
Kobayashi, K.2
Granja, J.R.3
Chadha, R.K.4
McRee, D.E.5
-
71
-
-
0032500342
-
-
T. D. Clark, J. M. Buriak, K. Kobayashi, M. P. Isler, D. E. McRee, M. R. Ghadiri, J. Am. Chem. Soc. 1998, 120, 8949-8962.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 8949-8962
-
-
Clark, T.D.1
Buriak, J.M.2
Kobayashi, K.3
Isler, M.P.4
McRee, D.E.5
Ghadiri, M.R.6
-
72
-
-
78650790725
-
-
-1
-
-1.
-
-
-
-
73
-
-
78650799885
-
-
Fluorescence studies of 12c carried out in milliQ water did not show the appearance of the pyrene excimer-emission band, which suggests that the formation of the corresponding dimer is not possible in water or that the solubility of the peptide is much lower
-
Fluorescence studies of 12c carried out in milliQ water did not show the appearance of the pyrene excimer-emission band, which suggests that the formation of the corresponding dimer is not possible in water or that the solubility of the peptide is much lower.
-
-
-
-
74
-
-
78650793776
-
-
-1
-
-1.
-
-
-
-
75
-
-
78650783031
-
-
Perylene-based CP 12f present only one band with the typical vibronic structure, so it could not be used for association constant determination through excimer formation, because its characteristic lower energy peak than the monomer emission could not be detected even at high concentration. This was attributed to the short lifetime and low quantum yields of the perylene moiety, which precludes the excimer formation and detection if it is not previously preformed
-
Perylene-based CP 12f present only one band with the typical vibronic structure, so it could not be used for association constant determination through excimer formation, because its characteristic lower energy peak than the monomer emission could not be detected even at high concentration. This was attributed to the short lifetime and low quantum yields of the perylene moiety, which precludes the excimer formation and detection if it is not previously preformed.
-
-
-
-
76
-
-
78650800742
-
-
11c-12c. Furthermore, addition of 1-pyreneacetic acid to 12f did not induce any change in its emission intensity, a finding consistent with the absence of the heterodimeric species
-
11c-12c. Furthermore, addition of 1-pyreneacetic acid to 12f did not induce any change in its emission intensity, a finding consistent with the absence of the heterodimeric species.
-
-
-
-
77
-
-
78650775069
-
-
Perylene life times could not be precisely measured in heterodimeric species, owing to the perturbation caused by the presence of other supramolecular entities with similar lifetimes
-
Perylene life times could not be precisely measured in heterodimeric species, owing to the perturbation caused by the presence of other supramolecular entities with similar lifetimes.
-
-
-
-
79
-
-
21544450820
-
-
A. Rieche, H. Gross, E. Höft, Chem. Ber. 1960, 93, 88-94.
-
(1960)
Chem. Ber.
, vol.93
, pp. 88-94
-
-
Rieche, A.1
Gross, H.2
Höft, E.3
|