Structure and kinetics of novel cyclophane inclusion compounds

Author(s):  
Sylke Apel ◽  
Mátyás Czugler ◽  
Vivienne J. Griffith ◽  
Luigi R. Nassimbeni ◽  
Edwin Weber
1999 ◽  
Vol 10 (4) ◽  
pp. 235-241 ◽  
Author(s):  
M. R. Caira ◽  
A. Coetzee ◽  
L. R. Nassimbeni ◽  
E. Weber ◽  
A. Wierig

ChemInform ◽  
2010 ◽  
Vol 33 (6) ◽  
pp. no-no
Author(s):  
Elise de Vries ◽  
Luigi R. Nassimbeni ◽  
Hong Su

1999 ◽  
Vol 23 (7) ◽  
pp. 436-437
Author(s):  
Anita Coetzee ◽  
Luigi R. Nassimbeni ◽  
Hong Su

The kinetics of desolvation of the inclusion compounds formed between the diol host and 2-, 3- and 4-methylcyclohexanones show a compensation effect in their Arrhenius parameters.


2001 ◽  
Vol 57 (3) ◽  
pp. 394-398 ◽  
Author(s):  
Luigi R. Nassimbeni ◽  
Hong Su

The crystal structures of the inclusion compounds formed between the host 2,2′-dihydroxy-1,1′-binaphthyl and the three picoline isomers have been elucidated and their lattice energies calculated. The selectivities of enclathration by the host have been measured by competition experiments. The thermal stabilities and activation energies of desolvation of the compounds have been determined. The kinetics of desolvation are correlated to the structures.


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