-
1
-
-
39749137246
-
-
Eds, M. Crego-Calama, D.N. Reinhoudt, Springer, New York
-
a) Supramolecular Chirality. Topics in Current Chemistry, Vol. 265 (Eds.: M. Crego-Calama, D.N. Reinhoudt), Springer, New York, 2006;
-
(2006)
Supramolecular Chirality. Topics in Current Chemistry
, vol.265
-
-
-
2
-
-
4444384013
-
-
b) M. A. Mateos-Timoneda, M. Crego-Calama, D. N. Reinhoudt, Chem. Soc. Rev. 2004, 33, 363 - 372.
-
(2004)
Chem. Soc. Rev
, vol.33
, pp. 363-372
-
-
Mateos-Timoneda, M.A.1
Crego-Calama, M.2
Reinhoudt, D.N.3
-
3
-
-
22844441238
-
-
and references therein
-
J. Zhang, M. T. Albelda, Y. Liu, J.W. Canary, Chirality 2005, 17, 404-420, and references therein.
-
(2005)
Chirality
, vol.17
, pp. 404-420
-
-
Zhang, J.1
Albelda, M.T.2
Liu, Y.3
Canary, J.W.4
-
4
-
-
1842844521
-
-
R. Paolesse, D. Monti, L. La Monica, M. Venanzi, A. Froiio, S. Nardis, C. Di Natale, E. Martinelli, A. D'Amico, Chem. Eur. J. 2002, 8, 2476 -2483.
-
(2002)
Chem. Eur. J
, vol.8
, pp. 2476-2483
-
-
Paolesse, R.1
Monti, D.2
La Monica, L.3
Venanzi, M.4
Froiio, A.5
Nardis, S.6
Di Natale, C.7
Martinelli, E.8
D'Amico, A.9
-
5
-
-
0031780556
-
-
a) R. F. Pasternack, E. J. Gibbs, P. J. Collings, J. C. dePaula, L. C. Turzo, A. Terracina, J. Am. Chem. Soc. 1998, 120, 5873-5878;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 5873-5878
-
-
Pasternack, R.F.1
Gibbs, E.J.2
Collings, P.J.3
dePaula, J.C.4
Turzo, L.C.5
Terracina, A.6
-
6
-
-
75249094572
-
-
b) R. F. Pasternack, E. J. Gibbs, D. Bruzewicz, D. Stewart, K. S. Eng- strom, J. Am. Chem. Soc. 2001, 123, 3533-3539;
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 3533-3539
-
-
Pasternack, R.F.1
Gibbs, E.J.2
Bruzewicz, D.3
Stewart, D.4
Eng- strom, K.S.5
-
7
-
-
0032477280
-
-
c) E. Bellacchio, R. Lauceri, S. Guerrieri, L. Monsù Scolaro, A. Romeo, R. Purrello, J. Am. Chem. Soc. 1998, 120, 12353-12354;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 12353-12354
-
-
Bellacchio, E.1
Lauceri, R.2
Guerrieri, S.3
Monsù Scolaro, L.4
Romeo, A.5
Purrello, R.6
-
8
-
-
0034319624
-
-
d) R. Purrello, A Raudino, L. Monsu Scolaro, A. Loisi, E. Bellacchio, R. Lauceri, J. Phys. Chem. B 2000, 104, 10900-10908;
-
(2000)
J. Phys. Chem. B
, vol.104
, pp. 10900-10908
-
-
Purrello, R.1
Raudino, A.2
Monsu Scolaro, L.3
Loisi, A.4
Bellacchio, E.5
Lauceri, R.6
-
9
-
-
0037065677
-
-
e) R. Lauceri, A. Raudino, Monsu Scolaro, N. Micali, R. Purrello, J. Am. Chem. Soc. 2002, 124, 894-895;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 894-895
-
-
Lauceri, R.1
Raudino, A.2
Scolaro, M.3
Micali, N.4
Purrello, R.5
-
10
-
-
26944432898
-
-
f) M. Balaz, M. De Napoli, A. E. Holmes, A. Mammana, K. Nakanishi, N. Berova, R. Purrello, Angew. Chem. 2005, 117, 4074-4077;
-
(2005)
Angew. Chem
, vol.117
, pp. 4074-4077
-
-
Balaz, M.1
De Napoli, M.2
Holmes, A.E.3
Mammana, A.4
Nakanishi, K.5
Berova, N.6
Purrello, R.7
-
11
-
-
21244490493
-
-
Angew. Chem. Int. Ed. 2005, 44, 4006-4009;
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 4006-4009
-
-
-
12
-
-
34447129729
-
-
and references therein;
-
g) A. Mam- mana, A. D'Urso, R. Lauceri, R. Purrello, J. Am. Chem. Soc. 2007, 129, 8062- 8063, and references therein;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 8062-8063
-
-
Mam- mana, A.1
D'Urso, A.2
Lauceri, R.3
Purrello, R.4
-
13
-
-
58149198803
-
-
A chiral porphyrin array has also been obtained by incorporating a porphyrin-substituted nu- cleotide into DNA as scaffold: I. Bouamaied, T. N. Nguyen, T. Rühl, E. Stulz, Org. Biomol. Chem. 2008, 6, 3888-3891
-
h) A chiral porphyrin array has also been obtained by incorporating a porphyrin-substituted nu- cleotide into DNA as scaffold: I. Bouamaied, T. N. Nguyen, T. Rühl, E. Stulz, Org. Biomol. Chem. 2008, 6, 3888-3891.
-
-
-
-
14
-
-
75249104487
-
-
Z. El-Hachemi, G. Mancini, J. M. Ribo, A. Sorrenti, J. Am. Chem. Soc. 2009, 131, 15176-15184.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 15176-15184
-
-
El-Hachemi, Z.1
Mancini, G.2
Ribo, J.M.3
Sorrenti, A.4
-
16
-
-
0037050539
-
-
a) V. Král, F. P. Schmidtchen, K. Lang, M. Berger, Org. Lett. 2002, 4, 51 -54;
-
(2002)
Org. Lett
, vol.4
, pp. 51-54
-
-
Král, V.1
Schmidtchen, F.P.2
Lang, K.3
Berger, M.4
-
18
-
-
3242725250
-
-
a) V. V. Borovkov, G. A. Hembury, Y. Inoue, Acc. Chem. Res. 2004, 37, 449-459;
-
(2004)
Acc. Chem. Res
, vol.37
, pp. 449-459
-
-
Borovkov, V.V.1
Hembury, G.A.2
Inoue, Y.3
-
19
-
-
0344871274
-
-
b) V. Borovkov, T. Harada, G. A. Hembury, Y. Inoue, R. Kuroda, Angew. Chem. 2003, 115, 1788-1791;
-
(2003)
Angew. Chem
, vol.115
, pp. 1788-1791
-
-
Borovkov, V.1
Harada, T.2
Hembury, G.A.3
Inoue, Y.4
Kuroda, R.5
-
20
-
-
0037879264
-
-
Angew. Chem. Int. Ed. 2003, 42, 1746-1749;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 1746-1749
-
-
-
21
-
-
8544284818
-
-
c) V. Borovkov, T. Harada, G. A. Hem- bury, Y. Inoue, Angew. Chem. 2003, 115, 5468-5472;
-
(2003)
Angew. Chem
, vol.115
, pp. 5468-5472
-
-
Borovkov, V.1
Harada, T.2
Hem- bury, G.A.3
Inoue, Y.4
-
22
-
-
0344875953
-
-
Angew. Chem. Int. Ed. 2003, 42, 5310-5314;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 5310-5314
-
-
-
23
-
-
75249087901
-
-
V. V. Borovkov, T. Harada, G. A. Hembury, Y. Inoue, R. Kuroda, Angew. Chem. 2003, 115, 17881791;
-
d) V. V. Borovkov, T. Harada, G. A. Hembury, Y. Inoue, R. Kuroda, Angew. Chem. 2003, 115, 17881791;
-
-
-
-
24
-
-
0037879264
-
-
Angew. Chem. Int. Ed. 2003, 42, 1746-1749;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 1746-1749
-
-
-
25
-
-
0344871274
-
-
e) V. V. Borov- kov, T. Harada, Y. Inoue, R. Kuroda, Angew. Chem. 2003, 115, 1788-1791;
-
(2003)
Angew. Chem
, vol.115
, pp. 1788-1791
-
-
Borov- kov, V.V.1
Harada, T.2
Inoue, Y.3
Kuroda, R.4
-
26
-
-
0037879264
-
-
Angew. Chem. Int. Ed. 2003, 42, 1746-1749;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 1746-1749
-
-
-
27
-
-
0037868251
-
-
f) G. Pesci- telli, S. Gabriel, Y. Wang, J. Fleischhauer, R. W. Woody, N. Berova, J. Am. Chem. Soc. 2003, 125, 7613-7626;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 7613-7626
-
-
Pesci- telli, G.1
Gabriel, S.2
Wang, Y.3
Fleischhauer, J.4
Woody, R.W.5
Berova, N.6
-
28
-
-
75249088900
-
-
g) H. Ishii, Y. Chen, R. A. Miller, S. Karady, K. Nakanishi, N. Berova, Chirality 2005, 17, 305315;
-
(2005)
Chirality
, vol.17
, pp. 305315
-
-
Ishii, H.1
Chen, Y.2
Miller, R.A.3
Karady, S.4
Nakanishi, K.5
Berova, N.6
-
29
-
-
3142757190
-
-
h) Y. Kubo, Y. Ishii, T. Yoshizawa, S. Tokita, Chem. Commun. 2004, 1394-1395;
-
(2004)
Chem. Commun
, pp. 1394-1395
-
-
Kubo, Y.1
Ishii, Y.2
Yoshizawa, T.3
Tokita, S.4
-
30
-
-
0034927033
-
-
i) D. Monti, L. La Monica, A. Scipioni, G. Mancini, New J. Chem. 2001, 25, 780-781;
-
(2001)
New J. Chem
, vol.25
, pp. 780-781
-
-
Monti, D.1
La Monica, L.2
Scipioni, A.3
Mancini, G.4
-
31
-
-
3142757190
-
-
j) Y. Kubo, Y. Ishii, T. Yoshiza- wa, S. Tokita, Chem. Commun. 2004, 1394-1395;
-
(2004)
Chem. Commun
, pp. 1394-1395
-
-
Kubo, Y.1
Ishii, Y.2
Yoshiza- wa, T.3
Tokita, S.4
-
33
-
-
75249083781
-
-
a) R. Rubires, J.-A. Farrera, J. M. Ribó, Chem. Eur. J. 2001, 7, 436446;
-
(2001)
Chem. Eur. J
, vol.7
, pp. 436446
-
-
Rubires, R.1
Farrera, J.-A.2
Ribó, J.M.3
-
34
-
-
0035874999
-
-
b) J. M. Ribó, J. Crusats, F. Sagués, J. M. Claret, R. Rubires, Science 2001, 292, 2063 -2066;
-
(2001)
Science
, vol.292
, pp. 2063-2066
-
-
Ribó, J.M.1
Crusats, J.2
Sagués, F.3
Claret, J.M.4
Rubires, R.5
-
35
-
-
0037804258
-
-
c) J. Crusats, J. M. Claret, I. Díez-Pérez, Z. El-Hachemi, García-Ortega, R. Rubires, F. Sagués, J. M. Ribó, Chem. Commun. 2003, 1588-1589;
-
(2003)
Chem. Commun
, pp. 1588-1589
-
-
Crusats, J.1
Claret, J.M.2
Díez-Pérez, I.3
El-Hachemi, Z.4
García-Ortega, R.5
Rubires, F.6
Sagués, J.7
Ribó, M.8
-
36
-
-
36049032533
-
-
d) C. Escudero, J. Crusatz, I. Díez-Pérez, Z. El-Hachemi, J. M. Ribó, Angew. Chem. 2006, 118, 8200-8203;
-
(2006)
Angew. Chem
, vol.118
, pp. 8200-8203
-
-
Escudero, C.1
Crusatz, J.2
Díez-Pérez, I.3
El-Hachemi, Z.4
Ribó, J.M.5
-
37
-
-
33845480078
-
-
Angew. Chem. Int. Ed. 2006, 45, 8032-8035.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 8032-8035
-
-
-
38
-
-
50649109314
-
-
a) Y. Zhang, P. Chen, M. Liu, Chem. Eur. J. 2008, 14, 1793-1803;
-
(2008)
Chem. Eur. J
, vol.14
, pp. 1793-1803
-
-
Zhang, Y.1
Chen, P.2
Liu, M.3
-
39
-
-
33751252838
-
-
P. Chen, X. Ma, P. Duan, M. Liu, ChemPhysChem 2006, 7, 24192423;
-
b) P. Chen, X. Ma, P. Duan, M. Liu, ChemPhysChem 2006, 7, 24192423;
-
-
-
-
40
-
-
22044437434
-
-
c) Z. Guo, J. Yuan, Y. Cui, F. Chang, W. Sun, M. Liu, Chem. Eur. J. 2005, 11, 4155-4162.
-
(2005)
Chem. Eur. J
, vol.11
, pp. 4155-4162
-
-
Guo, Z.1
Yuan, J.2
Cui, Y.3
Chang, F.4
Sun, W.5
Liu, M.6
-
41
-
-
34249781693
-
-
a) D. Monti, M. Venanzi, M. Stefanelli, A. Sorrenti, G. Mancini, C. Di Natale, R. Paolesse, J. Am. Chem. Soc. 2007, 129, 6688-6689;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 6688-6689
-
-
Monti, D.1
Venanzi, M.2
Stefanelli, M.3
Sorrenti, A.4
Mancini, G.5
Di Natale, C.6
Paolesse, R.7
-
42
-
-
20044386130
-
-
b) D. Monti, M. Venanzi, M. Mancini, C. Di Natale, R. Paolesse, Chem. Commun. 2005, 2471-2473;
-
(2005)
Chem. Commun
, pp. 2471-2473
-
-
Monti, D.1
Venanzi, M.2
Mancini, M.3
Di Natale, C.4
Paolesse, R.5
-
43
-
-
2442549431
-
-
c) D. Monti, V. Cantonetti, M. Venanzi, C. Bombelli, F. Ceccacci, G. Mancini, Chem. Commun. 2004, 972-973;
-
(2004)
Chem. Commun
, pp. 972-973
-
-
Monti, D.1
Cantonetti, V.2
Venanzi, M.3
Bombelli, C.4
Ceccacci, F.5
Mancini, G.6
-
44
-
-
33847693635
-
-
d) P. Štěpánek, M. Dukh, D. Šaman, J. Moravcová, L. Kniežo, D. Monti, M. Venanzi, G. Mancini, P. Drasar, Org. Biomol. Chem. 2007, 5, 960-970;
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 960-970
-
-
Štěpánek, P.1
Dukh, M.2
Šaman, D.3
Moravcová, J.4
Kniežo, L.5
Monti, D.6
Venanzi, M.7
Mancini, G.8
Drasar, P.9
-
45
-
-
57049095166
-
-
e) D. Monti, M. Venanzi, E. Gatto, G. Mancini, A. Sorrenti, P. Štěpánek, P. Drašar, New J. Chem. 2008, 32, 2127 -2133;
-
(2008)
New J. Chem
, vol.32
, pp. 2127-2133
-
-
Monti, D.1
Venanzi, M.2
Gatto, E.3
Mancini, G.4
Sorrenti, A.5
Štěpánek, P.6
Drašar, P.7
-
46
-
-
0037050539
-
-
f)V. Král, F. P. Schmidtchen, K. Lang M. Berger, Org. Lett. 2002, 4, 51-54.
-
(2002)
Org. Lett
, vol.4
, pp. 51-54
-
-
Král, V.1
Schmidtchen, F.P.2
Lang, K.3
Berger, M.4
-
47
-
-
59549096698
-
-
For other related structural examples, but in which studies on chiral supramolecular assembly have not been undertaken, see: g
-
For other related structural examples, but in which studies on chiral supramolecular assembly have not been undertaken, see: g) P. lavicoli, M. Simon-Sorbed, D. B. Amabilino, New J. Chem. 2009, 33, 358-365;
-
(2009)
New J. Chem
, vol.33
, pp. 358-365
-
-
lavicoli, P.1
Simon-Sorbed, M.2
Amabilino, D.B.3
-
48
-
-
26944483098
-
-
For examples chiral self-assembled porphyrin structures in organic solvents see
-
h) E. Biron, N. Voyer, Chem. Commun. 2005, 4652 -4654. For examples chiral self-assembled porphyrin structures in organic solvents see:
-
(2005)
Chem. Commun
, pp. 4652-4654
-
-
Biron, E.1
Voyer, N.2
-
49
-
-
34547788913
-
-
i) F. J. M. Hoeben, M. Wolffs, J. Zhang, S. De Feyter, F. Lacière, A. P. H. J. Schenning, E. W. Meijer, J. Am. Chem. Soc. 2007, 129, 9819-9828;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 9819-9828
-
-
Hoeben, F.J.M.1
Wolffs, M.2
Zhang, J.3
De Feyter, S.4
Lacière, F.5
Schenning, A.P.H.J.6
Meijer, E.W.7
-
50
-
-
0345302444
-
-
j) T. S. Bala- ban, A. D. Bhise, M. Fischer, M. Linke-Schaetzel, C. Roussel, N. Vanthuyne, Angew. Chem. 2003, 115, 2190-2194;
-
(2003)
Angew. Chem
, vol.115
, pp. 2190-2194
-
-
Bala- ban, T.S.1
Bhise, A.D.2
Fischer, M.3
Linke-Schaetzel, M.4
Roussel, C.5
Vanthuyne, N.6
-
51
-
-
0038245254
-
-
Angew. Chem. Int. Ed. 2003, 42, 2140-2144.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 2140-2144
-
-
-
52
-
-
67649349565
-
-
S. Borocci, F. Ceccacci, O. Cruciani, G. Mancini, A. Sorrenti, Synlett 2009, 7, 1023-1033.
-
(2009)
Synlett
, vol.7
, pp. 1023-1033
-
-
Borocci, S.1
Ceccacci, F.2
Cruciani, O.3
Mancini, G.4
Sorrenti, A.5
-
53
-
-
33845184268
-
-
a) M. M. Green, M. P. Rediy, R. J. Johnson, G. Darling, D. J. O'Leary, G. J. Williamson, J. Am. Chem. Soc. 1989, 111, 6452 -6454;
-
(1989)
J. Am. Chem. Soc
, vol.111
, pp. 6452-6454
-
-
Green, M.M.1
Rediy, M.P.2
Johnson, R.J.3
Darling, G.4
O'Leary, D.J.5
Williamson, G.J.6
-
54
-
-
26444617549
-
-
and references therein;
-
b) J. J. D. de Jong, T. D. Tiemersma-Wegman, J. H. van Esch, B. L. Feringa, J. Am. Chem. Soc. 2005, 127, 13804-13805, and references therein;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 13804-13805
-
-
de Jong, J.J.D.1
Tiemersma-Wegman, T.D.2
van Esch, J.H.3
Feringa, B.L.4
-
55
-
-
0035944450
-
-
c) L. J. Prins, P. Timmerman, D. N. Reinhoudt, . Am. Chem. Soc. 2001, 123, 10153-10163.
-
(2001)
Am. Chem. Soc
, vol.123
, pp. 10153-10163
-
-
Prins, L.J.1
Timmerman, P.2
Reinhoudt, D.N.3
-
56
-
-
75249090189
-
-
M. Takeuchi, S. Tanaka, S. Shinkai, Chem. Commun. 2005, 55395541;
-
a) M. Takeuchi, S. Tanaka, S. Shinkai, Chem. Commun. 2005, 55395541;
-
-
-
-
57
-
-
0031210116
-
-
b) K. Kano, H. Minamizono, T. Kitae, S. Negi, J. Phys. Chem. A 1997, 101, 6118-6124.
-
(1997)
J. Phys. Chem. A
, vol.101
, pp. 6118-6124
-
-
Kano, K.1
Minamizono, H.2
Kitae, T.3
Negi, S.4
-
58
-
-
34447629078
-
-
L-Proline was recently employed in the construction of homochiral metal-organic frameworks based on hydrogen bonds: M. Ingleson, J. Becsa, M. J. Rosseinsky, Chem. Commun. 2007, 3036-3038
-
L-Proline was recently employed in the construction of homochiral metal-organic frameworks based on hydrogen bonds: M. Ingleson, J. Becsa, M. J. Rosseinsky, Chem. Commun. 2007, 3036-3038.
-
-
-
-
60
-
-
75249096849
-
-
for a recent overview of binding mechanisms in supramolecular chemistry, see: H.-J. Schneider, Angew. Chem. 2009, 121, 39824036;
-
b) for a recent overview of binding mechanisms in supramolecular chemistry, see: H.-J. Schneider, Angew. Chem. 2009, 121, 39824036;
-
-
-
-
61
-
-
70349782154
-
-
Angew. Chem. Int. Ed. 2009, 48, 3924-3977.
-
(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 3924-3977
-
-
-
62
-
-
75249100102
-
-
Copper porphyrin derivatives form pentacoordinate complexes only in the presence of high concentrations of strong nitrogen ligands, such as pyridines and the like
-
Copper porphyrin derivatives form pentacoordinate complexes only in the presence of high concentrations of strong nitrogen ligands, such as pyridines and the like.
-
-
-
-
63
-
-
75249094571
-
-
Synthesis and Properties of Metalloporphyrins: J.W. Buchler in The Porphyrins, 1 (Ed.: D. Dolphin), Academic Press, New York, 1978, Chapter 10, pp. 389483;
-
a) "Synthesis and Properties of Metalloporphyrins": J.W. Buchler in The Porphyrins, Vol.1 (Ed.: D. Dolphin), Academic Press, New York, 1978, Chapter 10, pp. 389483;
-
-
-
-
64
-
-
75249101890
-
-
J. K. M. Sanders, N. Bampos, Z. Clyde-Watson, S. L. Darling, J. C. Hawley, H.-J. Kim, C. C. Mak, S. J. Webb, Axial Coordination Chemistry of Metalloporphyrins, in The Porphyrin Handbook, 3 (Eds. : K. K. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, 2000, Chapter 15, pp. 1-48.
-
b) J. K. M. Sanders, N. Bampos, Z. Clyde-Watson, S. L. Darling, J. C. Hawley, H.-J. Kim, C. C. Mak, S. J. Webb, Axial Coordination Chemistry of Metalloporphyrins, in The Porphyrin Handbook, Vol. 3 (Eds. : K. K. Kadish, K. M. Smith, R. Guilard), Academic Press, San Diego, 2000, Chapter 15, pp. 1-48.
-
-
-
-
65
-
-
0036433643
-
-
a) M. A. Castriciano, A. Romeo, L. Monsù Scolaro, J. Porphyrins Phthalocyanines 2002, 6, 431-438.
-
(2002)
J. Porphyrins Phthalocyanines
, vol.6
, pp. 431-438
-
-
Castriciano, M.A.1
Romeo, A.2
Monsù Scolaro, L.3
-
66
-
-
0035887268
-
-
The term extinction is more correct than the term absorbance, owing to the contribution of an RLS component to the UV/Vis and CD spectral bands. For a discussion on this topic, see : N. Micali, F. Mallamace, M. Castriciano, A. Romeo, L. Monsú Scolaro, Anal. Chem. 2001, 73, 4958-4963.
-
b) The term extinction is more correct than the term absorbance, owing to the contribution of an RLS component to the UV/Vis and CD spectral bands. For a discussion on this topic, see : N. Micali, F. Mallamace, M. Castriciano, A. Romeo, L. Monsú Scolaro, Anal. Chem. 2001, 73, 4958-4963.
-
-
-
-
67
-
-
0033936839
-
-
R. F. Pasternack, C. Fleming, S. Herring, P. J. Collings, J. dePaula, G. DeCastro, E. J. Gibbs, Biophys. J. 2000, 79, 550-560.
-
(2000)
Biophys. J
, vol.79
, pp. 550-560
-
-
Pasternack, R.F.1
Fleming, C.2
Herring, S.3
Collings, P.J.4
dePaula, J.5
DeCastro, G.6
Gibbs, E.J.7
-
68
-
-
0033716607
-
-
a) N. Micali, F. Mallamace, A. Romeo, R. Purrello, L. Monsu Scolaro, J. Phys. Chem. B 2000, 104, 5897-5904;
-
(2000)
J. Phys. Chem. B
, vol.104
, pp. 5897-5904
-
-
Micali, N.1
Mallamace, F.2
Romeo, A.3
Purrello, R.4
Monsu Scolaro, L.5
-
69
-
-
0036467727
-
-
b) L. Monsù Scolaro, M. Castriciano, A. Romeo, A. Mazzaglia, F. Mallamace, N. Micali, Physica 2002, 304, 158-169;
-
(2002)
Physica
, vol.304
, pp. 158-169
-
-
Monsù Scolaro, L.1
Castriciano, M.2
Romeo, A.3
Mazzaglia, A.4
Mallamace, F.5
Micali, N.6
-
70
-
-
18344364686
-
-
c)F. Mallamace, L. Monsu Scolaro, A. Romeo, N. Micali, Phys. Rev. Lett. 1999, 82, 3480-3483.
-
(1999)
Phys. Rev. Lett
, vol.82
, pp. 3480-3483
-
-
Mallamace, F.1
Monsu Scolaro, L.2
Romeo, A.3
Micali, N.4
-
71
-
-
12044257185
-
-
a) R. F. Pasternack, C. Bustamante, P. J. Collings, A. Giannetto, E. J. Gibbs, J. Am. Chem. Soc. 1993, 115, 5393-5399;
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 5393-5399
-
-
Pasternack, R.F.1
Bustamante, C.2
Collings, P.J.3
Giannetto, A.4
Gibbs, E.J.5
-
72
-
-
0028821365
-
-
b) J. C. dePaula, J. H. Robblee, R. F. Pasternack, Biophys. J. 1995, 68, 335-341.
-
(1995)
Biophys. J
, vol.68
, pp. 335-341
-
-
dePaula, J.C.1
Robblee, J.H.2
Pasternack, R.F.3
-
73
-
-
8344263764
-
-
Salt-promoted aggregation at 25% of water is too fast to be followed by the usual spectroscopic means. We surmised that such moderate variation of the solvent composition should only influence the rate of the reaction, and not dramatically affect the intimate nature of the self-assembly process. Note, however, that the overall rate is lower than those observed in the absence of added salt, undoubtedly a consequence of the chosen ethanol-richer composition of the medium, in which detailed kinetic studies can be conveniently carried out. For other examples, see: F. I. Simplicio, R. Ribeiro da Silva Soares, F. Maionchi, O. S. Filho, N. Hioka, J. Phys. Chem. A 2004, 108, 9384-9389.
-
Salt-promoted aggregation at 25% of water is too fast to be followed by the usual spectroscopic means. We surmised that such moderate variation of the solvent composition should only influence the rate of the reaction, and not dramatically affect the intimate nature of the self-assembly process. Note, however, that the overall rate is lower than those observed in the absence of added salt, undoubtedly a consequence of the chosen ethanol-richer composition of the medium, in which detailed kinetic studies can be conveniently carried out. For other examples, see: F. I. Simplicio, R. Ribeiro da Silva Soares, F. Maionchi, O. S. Filho, N. Hioka, J. Phys. Chem. A 2004, 108, 9384-9389.
-
-
-
-
74
-
-
49449085692
-
-
R. Lauceri, G. F. Fasciglione, A. D'Urso, S. Marini, R. Purrello, M. Coletta, J. Am. Chem. Soc. 2008, 130, 10476-10477.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 10476-10477
-
-
Lauceri, R.1
Fasciglione, G.F.2
D'Urso, A.3
Marini, S.4
Purrello, R.5
Coletta, M.6
-
75
-
-
75249088899
-
-
This is also in striking contrast to that observed in the case of the aggregation of 3H2 in the presence of added salts, in which annihilation of the CD features is observed.[11b]This indicates that the stereochemical induction is strictly controlled by a large variety of interactions, for example, hydrogen bonding, π interactions and electrostatic and dispersion forces. For a discussion of the effect of the solvent on chiral induction of porphyrin derivatives, see: reference [8a] and [8c
-
[11b]This indicates that the stereochemical induction is strictly controlled by a large variety of interactions, for example, hydrogen bonding, π interactions and electrostatic and dispersion forces. For a discussion of the effect of the solvent on chiral induction of porphyrin derivatives, see: reference [8a] and [8c].
-
-
-
-
76
-
-
0033936839
-
-
R. F. Pasternack, C. Fleming, S. Herring, P. J. Collings, J. dePaula, G. DeCastro, E. J. Gibbs, Biophys. J. 2000, 79, 550-560.
-
(2000)
Biophys. J
, vol.79
, pp. 550-560
-
-
Pasternack, R.F.1
Fleming, C.2
Herring, S.3
Collings, P.J.4
dePaula, J.5
DeCastro, G.6
Gibbs, E.J.7
-
77
-
-
0037057106
-
-
and references therein
-
E. Malinowska, L. Gorski, M. E. Meyerhoff, Anal. Chim. Acta 2002, 468, 133 -141, and references therein.
-
(2002)
Anal. Chim. Acta
, vol.468
, pp. 133-141
-
-
Malinowska, E.1
Gorski, L.2
Meyerhoff, M.E.3
-
78
-
-
36849080923
-
-
For a recent discussion of this topic see, for example
-
For a recent discussion of this topic see, for example : A. F. Thomas, A. H. Elcock, J. Am. Chem. Soc. 2007, 129, 14887-14898;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 14887-14898
-
-
Thomas, A.F.1
Elcock, A.H.2
-
79
-
-
33846387917
-
-
b) X. Tadeo, M. Pons, O. Millet, Biochemistry 2007, 46, 917-923.
-
(2007)
Biochemistry
, vol.46
, pp. 917-923
-
-
Tadeo, X.1
Pons, M.2
Millet, O.3
-
80
-
-
0242333944
-
-
The independence of the structure of deposited aggregates on substrates of different nature has been also reported by others: A. D. Schwab, D. E. Smith, C. S. Rich, E. R. Young, W. F. Smith, J. C. de Paula, J. Phys. Chem. B 2003, 107, 11339-11345. In different cases of direct absorption of porphyrin derivatives, we found that the nature of the surface could have a strong influence on the structure of the porphyrin adlayers. See, for example
-
a) The independence of the structure of deposited aggregates on substrates of different nature has been also reported by others: A. D. Schwab, D. E. Smith, C. S. Rich, E. R. Young, W. F. Smith, J. C. de Paula, J. Phys. Chem. B 2003, 107, 11339-11345. In different cases of direct absorption of porphyrin derivatives, we found that the nature of the surface could have a strong influence on the structure of the porphyrin adlayers. See, for example:
-
-
-
-
81
-
-
36248946171
-
-
M. Scarselli, P. Castrucci, D. Monti, M. De Crescenzi, Surf. Sci. 2007, 601, 55265532, and references therein.
-
b) M. Scarselli, P. Castrucci, D. Monti, M. De Crescenzi, Surf. Sci. 2007, 601, 55265532, and references therein.
-
-
-
-
82
-
-
75249089795
-
-
a) F. Dini, E. Martinelli, G. Pomarico, R. Paolesse, D. Monti, D. Fili- ppini, A. D'Amico, C. Di Natale, I. Lundstrom, Nanotechnology 2009, 20;
-
(2009)
Nanotechnology
, vol.20
-
-
Dini, F.1
Martinelli, E.2
Pomarico, G.3
Paolesse, R.4
Monti, D.5
Fili- ppini, D.6
D'Amico, A.7
Di Natale, C.8
Lundstrom, I.9
-
83
-
-
53849129995
-
-
b) D. Filippini, A. Alimelli, C. Di Natale, R. Paolesse, A. D'Amico, I. Lundstrom, Angew. Chem. 2006, 118, 3884 - 3887;
-
(2006)
Angew. Chem
, vol.118
, pp. 3884-3887
-
-
Filippini, D.1
Alimelli, A.2
Di Natale, C.3
Paolesse, R.4
D'Amico, A.5
Lundstrom, I.6
-
84
-
-
33746265849
-
-
Angew. Chem. Int. Ed. 2006, 45, 3800-3803;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 3800-3803
-
-
-
85
-
-
33748135573
-
-
c) L. S. Dolci, E. Marzocchi, M. Montalti, L. Prodi, D. Monti, C. Di Natale, A. D'Amico, R. Paolesse, Biosens. Bioelectron. 2006, 22, 399-404;
-
(2006)
Biosens. Bioelectron
, vol.22
, pp. 399-404
-
-
Dolci, L.S.1
Marzocchi, E.2
Montalti, M.3
Prodi, L.4
Monti, D.5
Di Natale, C.6
D'Amico, A.7
Paolesse, R.8
-
86
-
-
47849099773
-
-
d) A. G. Mignani, D. Monti, M. Mastroianni, R. Paolesse, IEEE Sens. J. 2008, 8, 1342-1354;
-
(2008)
IEEE Sens. J
, vol.8
, pp. 1342-1354
-
-
Mignani, A.G.1
Monti, D.2
Mastroianni, M.3
Paolesse, R.4
-
87
-
-
6344294752
-
-
e) D. Monti, M. Venanzi, M. Russo, G. L. Bussetti, C. Goletti, M. Montalti, N. Zaccheroni, L. Prodi, R. Rella, M. G. Manera, G. Mancini, C. Di Natale, R. Paolesse, New J. Chem. 2004, 28, 1123-1128.
-
(2004)
New J. Chem
, vol.28
, pp. 1123-1128
-
-
Monti, D.1
Venanzi, M.2
Russo, M.3
Bussetti, G.L.4
Goletti, C.5
Montalti, M.6
Zaccheroni, N.7
Prodi, L.8
Rella, R.9
Manera, M.G.10
Mancini, G.11
Di Natale, C.12
Paolesse, R.13
-
88
-
-
0035542911
-
-
For overviews on the construction of chiral supramolecular architectures, see: a
-
For overviews on the construction of chiral supramolecular architectures, see: a) J. J. L. M. Cornelissen, A. E. Rowan, R. J. M. Nolte, N. A. J. M. Sommerdijk, Chem. Rev. 2001, 101, 4039-4070;
-
(2001)
Chem. Rev
, vol.101
, pp. 4039-4070
-
-
Cornelissen, J.J.L.M.1
Rowan, A.E.2
Nolte, R.J.M.3
Sommerdijk, N.A.J.M.4
-
89
-
-
20344394407
-
-
b) D. Bradshaw, J. B. Claridge, E. J. Cussen, T. J. Prior, M. J. Rosseinsky, Acc. Chem. Res. 2005, 38, 273 -282.
-
(2005)
Acc. Chem. Res
, vol.38
, pp. 273-282
-
-
Bradshaw, D.1
Claridge, J.B.2
Cussen, E.J.3
Prior, T.J.4
Rosseinsky, M.J.5
-
90
-
-
70349137169
-
-
and references therein. For a recent example of porphyrin-based hybrid functional materials, see
-
c) For a recent example of porphyrin-based hybrid functional materials, see : G. De Luca, A. Romeo, V. Villari, N. Micali, I. Foltran, E. Foresti, I. G. Lesci, N. Roveri, T. Zuccheri, L. Monsu Scolaro, J. Am. Chem. Soc. 2009, 131, 6920-6921, and references therein.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 6920-6921
-
-
De Luca, G.1
Romeo, A.2
Villari, V.3
Micali, N.4
Foltran, I.5
Foresti, E.6
Lesci, I.G.7
Roveri, N.8
Zuccheri, T.9
Monsu Scolaro, L.10
-
91
-
-
1542315467
-
-
a) R. Luguya, L. Jaquinod, F. R. Fronczek, M. G. H. Vicente, K. M. Smith, Tetrahedron 2004, 60, 2757-2763;
-
(2004)
Tetrahedron
, vol.60
, pp. 2757-2763
-
-
Luguya, R.1
Jaquinod, L.2
Fronczek, F.R.3
Vicente, M.G.H.4
Smith, K.M.5
-
92
-
-
58249106298
-
-
M. Stefanelli, D. Monti, V. Van Axel Castelli, G. Ercolani, M. Venanzi, G. Pomarico, R. Pao- lesse, J. Porphyrins Phthalocyanines 2008, 12, 1279-1288.
-
b) M. Stefanelli, D. Monti, V. Van Axel Castelli, G. Ercolani, M. Venanzi, G. Pomarico, R. Pao- lesse, J. Porphyrins Phthalocyanines 2008, 12, 1279-1288.
-
-
-
-
93
-
-
3142715245
-
-
V. Cantonetti, D. Monti, M. Venanzi, C. Bombelli, F. Ceccacci, G. Mancini, Tetrahedron: Asymmetry 2004, 15, 1969-1977.
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 1969-1977
-
-
Cantonetti, V.1
Monti, D.2
Venanzi, M.3
Bombelli, C.4
Ceccacci, F.5
Mancini, G.6
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