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NMR studies of inclusion complexes: naphthalene and natural cyclodextrins

Autor
Nowakowski, Michał
Ejchart, Andrzej
Wójcik, Jacek
Jopa, Sylwia
Data publikacji
2022
Abstrakt (EN)

Inclusion complexes of naphthalene (NP) with cyclodextrins (CD) have been investigated so far using non-NMR techniques resulting in inconsistent data. Here, the first application of high-field NMR spectroscopy in combination with a precise analysis of the results has allowed us to determine accurately the stoichiometry of complexes and their association constants. Titration measurements have been performed by H-1 NMR spectroscopy in D2O at a magnetic field B-0 of 18.8 T. NP and alpha CD form a 1 : 2 complex in which a single NP molecule is closed in a capsule made up of two alpha CD macrocycles. NP and beta CD build coexisting 2 : 1 and 2 : 2 complexes with large binding constants. Larger gamma CD host molecules form essentially similar complexes with NP as the beta CD but corresponding binding constants are smaller.

Słowa kluczowe EN
POLYCYCLIC AROMATIC-HYDROCARBONS
ASSOCIATION CONSTANTS
BETA-CYCLODEXTRIN
CHIRAL RECOGNITION
CHEMICAL-SHIFTS
Dyscyplina PBN
nauki chemiczne
Czasopismo
Physical Chemistry Chemical Physics
Tom
24
Zeszyt
22
Strony od-do
13690-13697
ISSN
1463-9076
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