Abstract
IR Fourier spectra of pharmacologically active sterically hindered phenols in CCl4 solutions are studied. A relationship between the absorption intensity in the spectral range of the free vibrations of OH-groups and the antimicrobial activity of the phenols is discovered. If the hydroxyl groups are in an ortho-position within a molecule, then intramolecular hydrogen bonds are formed. The hindered phenols with nonassociated hydroxyl groups are the most pharmacologically active.
Sign-in/Register to access full text options 
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.
