Complexation with diol host compounds. Part 24. Kinetics of desolvation of inclusion compounds of 2,7-substituted 2,2′-bis(9-hydroxy-9-fluorenyl)biphenyl hosts with acetone

1997 ◽  
pp. 237-242 ◽  
Author(s):  
Mino R. Caira ◽  
Anita Coetzee ◽  
Luigi R. Nassimbeni ◽  
Edwin Weber ◽  
Andreas Wierig
Keyword(s):  
Inclusion Compounds ◽  
Kinetics Of

Kinetics of Desolvation of Related Organic Inclusion Compounds

1999 ◽  
Vol 10 (4) ◽  
pp. 235-241 ◽  
Author(s):  
M. R. Caira ◽  
A. Coetzee ◽  
L. R. Nassimbeni ◽  
E. Weber ◽  
A. Wierig
Keyword(s):  
Inclusion Compounds ◽  
Organic Inclusion ◽  
Kinetics Of

ChemInform Abstract: Inclusion Compounds of Binaphthol with Lutidines - Structures, Selectivity and Kinetics of Desolvation.

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

Structure and kinetics of novel cyclophane inclusion compounds

1997 ◽  
pp. 1949-1953 ◽  
Author(s):  
Sylke Apel ◽  
Mátyás Czugler ◽  
Vivienne J. Griffith ◽  
Luigi R. Nassimbeni ◽  
Edwin Weber
Keyword(s):  
Inclusion Compounds ◽  
Kinetics Of

scholarly journals Thermal Stabilities and Kinetics of Desolvation of Related Inclusion Compounds of trans-9,10-Dihydroxy-9,10-diphenyl-9,10-dihydroanthracene

1999 ◽  
Vol 23 (7) ◽  
pp. 436-437
Author(s):  
Anita Coetzee ◽  
Luigi R. Nassimbeni ◽  
Hong Su
Keyword(s):  
Inclusion Compounds ◽  
Compensation Effect ◽  
Thermal Stabilities ◽  
Arrhenius Parameters ◽  
Kinetics Of

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.

Inclusion compounds of binaphthol with picolines: structures, selectivity and kinetics of desolvation

2001 ◽  
Vol 57 (3) ◽  
pp. 394-398 ◽  
Author(s):  
Luigi R. Nassimbeni ◽  
Hong Su
Keyword(s):  
Crystal Structures ◽  
Inclusion Compounds ◽  
Activation Energies ◽  
Thermal Stabilities ◽  
Lattice Energies ◽  
Kinetics Of

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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