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developed stationary phase would be able to separate the biologically important chiral amino acids. CDs are extensively used in chiral separations due to their unique property to form inclusion compounds with other smaller hydrophobic molecules [ 18 ]. To

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306 : 147 – 155 10.1016/S0008-6215(97)10046-5 . 23. Andini , S , Castronuovo , G , Elia , V , Gallotta , E 1991 Inclusion compounds in water. Calorimetric and spectroscopic studies

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analysis of inclusion compounds of calixarenes, providing a comprehensive method to analyze trends of molecular forces involved in the complexation, quantitatively. The azocalix[ n ]arene molecular complexes form small molecules with variable

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temperature increasing to 380 °C. However, as mentioned above, partial structure of the catalyst was collapsed, converting to ZnO phase when the reduction temperature was at 380 °C. Thus, the best catalytic activity was achieved when the inclusion compound Ni

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