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- sensing with boronic acid derivatives: N. DiCesare and J. R. Lakowicz, Anal. Biochem., 2002, 301, 111 or utilizing the remarkable dual emission features of aminobenzonitriles: K. Kobiro and Y. Inoue, J. Am. Chem. Soc., 2003, 125, 421.
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Szumna, A.1
Jurczak, J.2
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5044221088
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note
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Concentration-dependent studies on 1 always yielded results similar to those in Table 1, ruling out excited-state chromophore interaction.
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25
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5044236310
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note
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For the impact of the differences in the molecular structure of the tilted arms of both solvates on the π-π interactions and packing in the crystals, see discussion in Section 2.3, ESI.
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26
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5044223840
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note
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The analysis of the non-bonding distances shows that a more planar conformation would have created unusually short distances between the guest and the aromatic ortho-hydrogens H13A and H13′A.
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27
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5044220580
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note
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- were more pronounced changes found, consistent with a deprotonation of 1 due to the high reactivity of this ion in such kind of solvent mixtures.
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28
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5044219943
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note
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