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0343901508
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note
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Although Umezawa reported the synthesis of thiourea 2 and its excellent binding ability toward phosphate anion, its self-aggregation behavior was not referred to (ref. 2).
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17
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0342595787
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note
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3, respectively.
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18
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0343901507
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note
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-3. Such non-linear concentration dependence precluded the calculation of the association constant on the assumption that monomer-dimer equilibrium is dominant in this concentration range.
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20
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0343029922
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note
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-3. The data collection was done at 293 K using graphite monochromated Mo-Ka radiation (λ= 0.71069 Å). The structure was solved by direct methods (SHELXS86) and refined by full-matrix least-squares techniques (SHELXL93) to R = 0.070 (Rw = 0.206) for 1730 independent reflections having I > 2σ(I). Due to the disorder of the tert-butyl group and the large thermal parameters of the side-chain terminals, the structure data are not good enough to discuss the bond lengths and angles in detail. However, the crystallographic analysis certainly confirms the novel hydrogen-bonded dimer structure. Full crystallographic details are deposited in the Cambridge Crystallographic Data Centre.
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22
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33749118948
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b) Ottens-Hildebrandt, S.; Meier, S.; Schmidt, W.; Vögtle, F. Angew. Chem., Int. Ed. Engl. 1994, 33, 1767-1770.
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23
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c) Johnston, A. G.; Leigh, D. A.; Pritchard, R. J.; Deegan, M. D. ibid. 1995, 34, 1209-1212.
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24
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33749120997
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d) Johnston, A. G.; Leigh, D. A.; Nezhat, L.; Smart, J. P.; Deegan, M. D. ibid. 1995, 34, 1212-1216. For a review see, Vögtle, F.; Dünnwald, T.; Schmidt, T. Acc. Chem. Res. 1996, 29, 451-460.
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Johnston, A.G.1
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Deegan, M.D.5
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25
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d) Johnston, A. G.; Leigh, D. A.; Nezhat, L.; Smart, J. P.; Deegan, M. D. ibid. 1995, 34, 1212-1216. For a review see, Vögtle, F.; Dünnwald, T.; Schmidt, T. Acc. Chem. Res. 1996, 29, 451-460.
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Vögtle, F.1
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