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17
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85163238504
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note
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3CN.
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-
-
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18
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85163236327
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note
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[11] This is in accordance with the lower donor ability of MeCN compared to EtCN.
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19
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85163237106
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note
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2, which was too soluble to be crystallized out of an acetonitrile solution.
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20
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85163238666
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note
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Under millimolar conditions, the half-life time was ca. 5 minutes. Kinetic and mechanistic studies on the exchange process are under investigation.
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-
-
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21
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85163239895
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note
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2 an unusual up-field shift for the OMe resonance is observed. A Dreiding model in fact showed that these methoxy groups are situated in the anisotropic cone of the aromatic benzimidazole moieties.
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-
-
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22
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85163240035
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note
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3CN, with a broad resonance at δ = -0.7. This confirmed the presence of a coordinating acetonitrile molecule inside the aromatic cavity in solution; see ref. [11].
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-
-
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24
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0034680518
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Y. Rondelez, O. Sénèque, M.-N. Rager, A. Duprat, O. Reinaud, Chem. Eur. J. 2000, 6, 4218-4226.
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Rondelez, Y.1
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Duprat, A.4
Reinaud, O.5
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25
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-
85163241053
-
-
note
-
+) of pyrazole, pyridine, imidazole, and aliphatic amines are 2.5, 5.3, 7.0, and 9-11, respectively.
-
-
-
-
26
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0000862586
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S. Julia, C. Martinez-Martorell, J. Elguero, Heterocycles 1986, 24, 2233-2237.
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Julia, S.1
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27
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85153010997
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H. Skolink, J. G. Miller, A. R. Day, J. Am. Chem. Soc. 1943, 65, 1865-1856.
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Skolink, H.1
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Day, A.R.3
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28
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85163237480
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-
note
-
3). Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: (internat.) + 44-1223/336-033; E-mail: deposit@ccdc. ac. uk).
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