-
1
-
-
0000674963
-
-
M. N. Berberan-Santos, J. Canceill, J. C. Brochon, L. Jullien, J. M. Lehn, J. Pouget, P. Tauc, B. Valeur, J. Am. Chem. Soc. 1992, 114, 6427-6436.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 6427-6436
-
-
Berberan-Santos, M.N.1
Canceill, J.2
Brochon, J.C.3
Jullien, L.4
Lehn, J.M.5
Pouget, J.6
Tauc, P.7
Valeur, B.8
-
2
-
-
0000890509
-
-
M. N. Berberan-Santos, J. Pouget, B. Valeur, J. Canceill, L. Jullien, J.-M. Lehn, J. Phys. Chem. 1993, 97, 11376-11379.
-
(1993)
J. Phys. Chem.
, vol.97
, pp. 11376-11379
-
-
Berberan-Santos, M.N.1
Pouget, J.2
Valeur, B.3
Canceill, J.4
Jullien, L.5
Lehn, J.-M.6
-
4
-
-
0007440826
-
-
L. Jullien, J. Canceill, B. Valeur, E. Bardez, J.-M. Lehn, Angew. Chem. 1994, 106, 2582-2584; Angew. Chem. Int. Ed. Engl. 1994, 33, 2438-2439.
-
(1994)
Angew. Chem.
, vol.106
, pp. 2582-2584
-
-
Jullien, L.1
Canceill, J.2
Valeur, B.3
Bardez, E.4
Lehn, J.-M.5
-
5
-
-
0000369981
-
-
L. Jullien, J. Canceill, B. Valeur, E. Bardez, J.-M. Lehn, Angew. Chem. 1994, 106, 2582-2584; Angew. Chem. Int. Ed. Engl. 1994, 33, 2438-2439.
-
(1994)
Angew. Chem. Int. Ed. Engl.
, vol.33
, pp. 2438-2439
-
-
-
6
-
-
0003019274
-
-
M. N. Berberan-Santos, J. Canceill, G. Gratton, L Jullien, J.-M. Lehn, P. Peter So, J. Sutin, B. Valeur, J. Phys. Chem. 1996, 100, 15-20.
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 15-20
-
-
Berberan-Santos, M.N.1
Canceill, J.2
Gratton, G.3
Jullien, L.4
Lehn, J.-M.5
Peter So, P.6
Sutin, J.7
Valeur, B.8
-
7
-
-
0029953291
-
-
L. Jullien, J. Canceill, B. Valeur, E. Bardez, J.-P. Lefèvre, J.-M. Lehn, V. Marchi-Artzner, R. Pansu, J. Am. Chem. Soc. 1996, 118, 5432-5442.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 5432-5442
-
-
Jullien, L.1
Canceill, J.2
Valeur, B.3
Bardez, E.4
Lefèvre, J.-P.5
Lehn, J.-M.6
Marchi-Artzner, V.7
Pansu, R.8
-
8
-
-
0000635180
-
-
P. Wang, L. Jullien, B. Valeur, J.-S. Filhol, J. Canceill, J.-M. Lehn, New J. Chem. 1996, 20, 895-907.
-
(1996)
New J. Chem.
, vol.20
, pp. 895-907
-
-
Wang, P.1
Jullien, L.2
Valeur, B.3
Filhol, J.-S.4
Canceill, J.5
Lehn, J.-M.6
-
9
-
-
0031007383
-
-
M. Nowakowska, N. Loukine, D. M. Gravett, N. A. D. Burke, J. E. Guillet, J. Am. Chem. Soc. 1997, 119, 4364-4368.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 4364-4368
-
-
Nowakowska, M.1
Loukine, N.2
Gravett, D.M.3
Burke, N.A.D.4
Guillet, J.E.5
-
11
-
-
0033599566
-
-
M. N. Berberan-Santos, P. Choppinet, A. Fedorov, L. Jullien, B. Valeur, J. Am. Chem. Soc. 1999, 121, 2526-2533.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 2526-2533
-
-
Berberan-Santos, M.N.1
Choppinet, P.2
Fedorov, A.3
Jullien, L.4
Valeur, B.5
-
12
-
-
0029637583
-
-
a) G. Mc Dermott, 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
-
-
Dermott, G.M.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
-
14
-
-
0002516698
-
-
c) R. Van Grondelle, R. Monshouwer, L. Valkunas, Ber. Bunsenges. Phys. Chem. 1996, 100, 1950-1957;
-
(1996)
Ber. Bunsenges. Phys. Chem.
, vol.100
, pp. 1950-1957
-
-
Van Grondelle, R.1
Monshouwer, R.2
Valkunas, L.3
-
16
-
-
0027111711
-
-
a) H. H. Baer, Y. Shen, F. S. Gonzalez, A. V. Berenguel, J. I. Garcia, Carbohydr. Res. 1992, 235, 129-139;
-
(1992)
Carbohydr. Res.
, vol.235
, pp. 129-139
-
-
Baer, H.H.1
Shen, Y.2
Gonzalez, F.S.3
Berenguel, A.V.4
Garcia, J.I.5
-
17
-
-
58149325748
-
-
b) F. Guillo, B. Hamelin, L. Jullien, J. Canceill, J.-M. Lehn, L. De Robertis, H. Driguez, Bull. Soc. Chim. Fr. 1995, 132, 857-866.
-
(1995)
Bull. Soc. Chim. Fr.
, vol.132
, pp. 857-866
-
-
Guillo, F.1
Hamelin, B.2
Jullien, L.3
Canceill, J.4
Lehn, J.-M.5
De Robertis, L.6
Driguez, H.7
-
20
-
-
0002413436
-
-
(Ed. O. Sinanoglu), Academic Press, New York
-
T. Förster, in Modern Quantum Chemistry, Part III (Ed. O. Sinanoglu), p. 93-137, Academic Press, New York, 1965.
-
(1965)
Modern Quantum Chemistry
, Issue.PART III
, pp. 93-137
-
-
Förster, T.1
-
22
-
-
0003407246
-
-
Plenum, 6th ed., New York
-
b) J. O'M. Bockris, A. K. N. Reddy, in Modern Electrochemistry, Plenum, 6th ed., New York, 1977.
-
(1977)
Modern Electrochemistry
-
-
Bockris, J.O'M.1
Reddy, A.K.N.2
-
23
-
-
85088810231
-
-
note
-
a between the two carboxylic groups of MOD-St essentially originates from the repulsive electrostatic interaction between both ionized carboxylate in the doubly charged form. See note [18].
-
-
-
-
24
-
-
0348212897
-
-
note
-
a are about between 4 and 10. At pH 6 the total charge is then about 4.5 whereas it is about 13.5 at pH 10.
-
-
-
-
27
-
-
0001291104
-
-
b) D. T. McQuade, D. G. Barrett, J. M. Desper, R. K. Hayashi, S. H. Gellman, J. Am. Chem. Soc. 1995, 117, 4862-4869;
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 4862-4869
-
-
McQuade, D.T.1
Barrett, D.G.2
Desper, J.M.3
Hayashi, R.K.4
Gellman, S.H.5
-
28
-
-
0001025460
-
-
c) Y. Cheng, D. M. Ho, C. R. Gottlieb, D. Kahne, M. A. Bruck, J. Am. Chem. Soc. 1992, 114, 7319-7320;
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 7319-7320
-
-
Cheng, Y.1
Ho, D.M.2
Gottlieb, C.R.3
Kahne, D.4
Bruck, M.A.5
-
29
-
-
0000676012
-
-
d) P. Venkatesan, Y. Cheng, D. Kahne, J. Am. Chem. Soc. 1994, 116, 6955-6956;
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 6955-6956
-
-
Venkatesan, P.1
Cheng, Y.2
Kahne, D.3
-
31
-
-
0029892370
-
-
f) V. Janout, M. Lanier, S. L. Regen, J. Am. Chem. Soc. 1996, 118, 1573-1574;
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 1573-1574
-
-
Janout, V.1
Lanier, M.2
Regen, S.L.3
-
32
-
-
0033046267
-
-
g) B. Hamelin, L. Jullien, A. Laschewsky, C Hervé du Penhoat, Chem. Eur. J. 1999, 5, 546-556.
-
(1999)
Chem. Eur. J.
, vol.5
, pp. 546-556
-
-
Hamelin, B.1
Jullien, L.2
Laschewsky, A.3
Hervé Du Penhoat, C.4
-
33
-
-
0025158146
-
-
Ox725 has been already used as a guest for complexation by the native β-cyclodextrin, see: W. G. Herkstroeter, P. A. Martic, S. Farid, J. Am. Chem. Soc. 1990, 112, 3583-3589.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 3583-3589
-
-
Herkstroeter, W.G.1
Martic, P.A.2
Farid, S.3
-
34
-
-
0347583239
-
-
note
-
At larger concentrations, the inner-filter effects appear.
-
-
-
-
35
-
-
0000453184
-
-
G. S. Levinson, W. T. Simpson, W. Curtis, J. Am. Chem. Soc. 1957, 79, 4314-4320.
-
(1957)
J. Am. Chem. Soc.
, vol.79
, pp. 4314-4320
-
-
Levinson, G.S.1
Simpson, W.T.2
Curtis, W.3
-
36
-
-
85088810089
-
-
note
-
tot. These expressions are then introduced in Eq. (2a) to yield Eq. (2b).
-
-
-
-
37
-
-
0348212890
-
-
note
-
The method for correcting the contribution of direct excitation has been reported in a previous paper, see ref. [6].
-
-
-
-
40
-
-
0000223084
-
-
and references therein
-
Y. Inoue, T. Hakushi, Y. Liu, L. H. Tong, B. J. Shen, D. S. Jin, J. Am. Chem. Soc. 1993, 115, 475-481, and references therein.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 475-481
-
-
Inoue, Y.1
Hakushi, T.2
Liu, Y.3
Tong, L.H.4
Shen, B.J.5
Jin, D.S.6
-
41
-
-
0348212889
-
-
Freeman, New York
-
C. R. Cantor, P. R. Schimmel, Biophysical Chemistry, Part II, Freeman, New York, 1980.
-
(1980)
Biophysical Chemistry
, Issue.PART II
-
-
Cantor, C.R.1
Schimmel, P.R.2
-
42
-
-
0348212887
-
-
note
-
The DCMOH orientation within the CD-NA cavity was analyzed by circular dichroism by using established correlations between the guest orientation and the shape of the CD signal, see ref. 6. In view of the intrinsic chirality of the steroid walls, it was impossible to use the same methodology in the CD-St case.
-
-
-
-
43
-
-
84984085914
-
-
T. Tao, Biopolymers 1972, 8, 609-632.
-
(1972)
Biopolymers
, vol.8
, pp. 609-632
-
-
Tao, T.1
-
46
-
-
0032569193
-
-
B. Hamelin, L. Jullien, C. Derouet, C. Hervé du Penhoat, P. Berthault, J. Am. Chem. Soc. 1998, 120, 8438-8447.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 8438-8447
-
-
Hamelin, B.1
Jullien, L.2
Derouet, C.3
Hervé Du Penhoat, C.4
Berthault, P.5
-
48
-
-
0348212881
-
-
note
-
77 = 0.70 at 0.005M ionic strength).
-
-
-
-
49
-
-
0007425498
-
-
I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4292-4304; I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4305-4313; U. Mohanty, B. W. Ninham, I. Oppenheim, Proc. Natl. Acad. Sci. USA 1996, 93, 4342-4344.
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 4292-4304
-
-
Rouzina, I.1
Bloomfield, V.A.2
-
50
-
-
0012848624
-
-
I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4292-4304; I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4305-4313; U. Mohanty, B. W. Ninham, I. Oppenheim, Proc. Natl. Acad. Sci. USA 1996, 93, 4342-4344.
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 4305-4313
-
-
Rouzina, I.1
Bloomfield, V.A.2
-
51
-
-
0029958889
-
-
I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4292-4304; I. Rouzina, V. A. Bloomfield, J. Phys. Chem. 1996, 100, 4305-4313; U. Mohanty, B. W. Ninham, I. Oppenheim, Proc. Natl. Acad. Sci. USA 1996, 93, 4342-4344.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 4342-4344
-
-
Mohanty, U.1
Ninham, B.W.2
Oppenheim, I.3
-
52
-
-
0000285072
-
-
crit = 1. If one assimilates both CD-NA and CD-St cyclodextrins as rings (radius ≃ 1 nm) of regularly spaced elementary charges (7 for CD-NA and 14 for CD-St at pH 10; vide supra), one finds ξ = 0.8 for CD-NA whereas ξ = 1.6 for CD-St.
-
(1995)
J. Phys. Chem.
, vol.99
, pp. 17877-17885
-
-
Hamelin, B.1
Jullien, L.2
Guillo, F.3
Lehn, J.-M.4
Jardy, A.5
De Robertis, L.6
Driguez, H.7
-
53
-
-
0017895903
-
-
crit = 1. If one assimilates both CD-NA and CD-St cyclodextrins as rings (radius ≃ 1 nm) of regularly spaced elementary charges (7 for CD-NA and 14 for CD-St at pH 10; vide supra), one finds ξ = 0.8 for CD-NA whereas ξ = 1.6 for CD-St.
-
(1978)
Q. Rev. Biophys.
, vol.11
, pp. 179-246
-
-
Manning, G.S.1
-
55
-
-
0346952180
-
-
3OH. The compound melting at 245-250°C was identified as the bisdehydromarrianolic acid from its melting point already reported in the literature (J. Heer, J. R. Billeter, K. Miescher, Helv. Chim. Acta 1945, 28, 991-1003). It can be converted into the compound melting at 226°C by dissolution in 1M NaOH.
-
(1945)
Helv. Chim. Acta
, vol.28
, pp. 991-1003
-
-
Heer, J.1
Billeter, J.R.2
Miescher, K.3
-
60
-
-
0024751658
-
-
J. Pouget, J. Mugnier, B. Valeur, J. Phys. E Sci. Instr. 1989, 22, 855-862.
-
(1989)
J. Phys. E Sci. Instr.
, vol.22
, pp. 855-862
-
-
Pouget, J.1
Mugnier, J.2
Valeur, B.3
|