Abstract
β-Cyclodextrin 6-O-monobenzoate has been synthesized and its complex stability constants (Ks) for acyclic and cyclic hydrocarbons of different size, shape and rigidity evaluated in 1 : 1 methanol–water and/or water by means of differential circular dichroism spectrometry. In the absence of the dipole–dipole and hydrogen-bonding interactions which usually play significant roles in the inclusion complexation of cyclodextrins, the Ks values obtained for the modified cyclodextrin may be more explicitly understood in terms of the size, conformation and rigidity of the guest molecules.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
