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51949116417
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-
Two out of nine amide NH protons could not be observed because of the overlapping with aromatic resonances see Supporting Information
-
Two out of nine amide NH protons could not be observed because of the overlapping with aromatic resonances (see Supporting Information).
-
-
-
-
38
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51949110193
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-
6,7
-
6,7
-
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39
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0000033171
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-
For example
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For example: Polese, A.; Formaggio, F.; Crisma, M.; Valle, G.; Toniolo, C.; Bonora, G. M.; Broxterman, Q. B.; Kamphuis, J. Chem. - Eur. J. 1996, 2, 1104-1111.
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Polese, A.1
Formaggio, F.2
Crisma, M.3
Valle, G.4
Toniolo, C.5
Bonora, G.M.6
Broxterman, Q.B.7
Kamphuis, J.8
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40
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0842341771
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Dewar, M. J. S.; Zoebisch, E. G.; Healy, E. F.; Stewart, J. J. P. J. Am. Chem. Soc. 1985, 107, 3902-3909.
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Stewart, J.J.P.4
-
41
-
-
51949094550
-
-
The molecular graphics were drawn with: Thompson, M. A. ArgusLab 4.0.1; Planaria Software LLC: Seattle, WA, 2004 (http://www.arguslab.com).
-
The molecular graphics were drawn with: Thompson, M. A. ArgusLab 4.0.1; Planaria Software LLC: Seattle, WA, 2004 (http://www.arguslab.com).
-
-
-
-
42
-
-
51949112280
-
-
The solution stood for over 30 min at room temperature before CD measurement to establish an equilibrium state.
-
The solution stood for over 30 min at room temperature before CD measurement to establish an equilibrium state.
-
-
-
-
43
-
-
51949119616
-
-
6a) (Figure S5).
-
6a) (Figure S5).
-
-
-
-
44
-
-
51949097888
-
-
Induced CD intensity of 1 with equimolar mixture of L-2 and 3 was about one-half the value as compared with that of 1 with L-2 (Figure S6).
-
Induced CD intensity of 1 with equimolar mixture of L-2 and 3 was about one-half the value as compared with that of 1 with L-2 (Figure S6).
-
-
-
-
45
-
-
84985628243
-
-
Hummel, R.-P.; Toniolo, C.; Jung, G. Angew. Chem., Int. Ed. Engl. 1987, 26, 1150-1152.
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(1987)
Angew. Chem., Int. Ed. Engl
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, pp. 1150-1152
-
-
Hummel, R.-P.1
Toniolo, C.2
Jung, G.3
-
46
-
-
51949118864
-
-
In methanol/chloroform (77/3; v/v) mixed solution which prevents interaction between 1 and L-2, kinetic and thermodynamic parameters of 1 were also obtained; Ea, 93.4 kJ mol-1, ΔG420, 85.1 kJ mol -1, ΔH‡, 91.1 kJ mol-1, and ΔS‡, 20.5 J mol-1 K-1 Figures S8-S9 and Table S1, These values are comparable to those of the complex 1·3. Thus, there is little effect of guest binding on the rate of helix inversion of 1
-
-1 (Figures S8-S9 and Table S1). These values are comparable to those of the complex 1·3. Thus, there is little effect of guest binding on the rate of helix inversion of 1.
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-
-
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