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For recent reviews of organic compounds with covalently bonded nitric oxide, see: (a) Wang, P. G.; Xian, M.; Tang, X.; Wu, X.; Wen, Z.; Cai, T.; Janczuk, A. J. Chem. Rev. 2002, 102, 1091. (b) Hrabie, J. A.; Keefer, L. K. Chem. Rev. 2002, 102, 1135.
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85087596377
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Cyclophane hosts: Binding of lipophilic and cationic guests
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Cyclophane related synthetic hosts for recognition discrimination of nonpolar structures in aqueous solutions and at membrane surfaces
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42
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85087598331
-
-
note
-
500) refer to the high (340) and low energy (500) bands, respectively, in all complexes (although the actual maxima of the corresponding bands varied somewhat).
-
-
-
-
43
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85087598648
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note
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15b
-
-
-
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44
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0034674284
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(b) Rathore, R.; Lindeman, S. V.; Rao, K. S.; Sun, D.-L.; Kochi, J. K. Angew. Chem. Int. Ed. 2000, 39, 2123.
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60
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0038136132
-
-
note
-
In complexes with bis-coordinated nitrosonium, there are also transitions from the noninteracting orbitals of the arene to the antibonding molecular orbital; but they are expected to be much less intense (similar to the low-energy bands VL in 1:1 complexes) and are overshadowed by the nonbonding-to-antibonding transition.
-
-
-
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65
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0042291889
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Astruc, D., Ed.; VCH-Wiley: New York
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66
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85087595545
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-
note
-
CT = -RT ln K) is considered instead of the equilibrium constant to allow direct comparison with different donor/acceptor stoichiometries.
-
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67
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4243281514
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70
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0038812863
-
-
note
-
The energy (enthalpy) gain of [1:1] and [2:1] complexes is mainly connected with the relocation of two electrons initially residing on the donor orbital to lower-lying molecular orbitals of the complex. The second electron pair in [2:1] complexes resides on the nonbonding orbital.
-
-
-
-
72
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-
0038812864
-
-
note
-
max at 380 and 780 nm).
-
-
-
-
73
-
-
85087596782
-
-
note
-
. in vacuo.
-
-
-
-
74
-
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85087594759
-
-
note
-
20 The problem is related to the apparent mismatch of the diarene cavity to the requirements of the guest.
-
-
-
-
75
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0038812866
-
-
note
-
(a) Particularly in nonaqueous solutions.
-
-
-
-
76
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0037798398
-
-
note
-
(b) Note that this procedure circumvents the kinetic lability of arene cation radicals.
-
-
-
-
77
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0038136129
-
-
note
-
(c) From the results in Table 1 (eq 2), we estimate the intrinsic NO sensitivity to be ∼1 μM on the basis of a spectrophotometric resolution of 0.01 in the optical density; but for a solid-state device, the practical sensitivity will depend on its design, particularly for application to an aqueous environment.
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79
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