Prediction of the most preferable rotamer of meta-aminophenol in β-cyclodextrin cavity in aqueous medium by using spectroscopic and DFT computational studies-Reference-Cited by-同舟云学术

Prediction of the most preferable rotamer of meta-aminophenol in β-cyclodextrin cavity in aqueous medium by using spectroscopic and DFT computational studies

Published:2020-02-12 Issue:1-2 Volume:97 Page:77-86
ISSN:1388-3127
Container-title:Journal of Inclusion Phenomena and Macrocyclic Chemistry
language:en
Short-container-title:J Incl Phenom Macrocycl Chem

Author:

Majhi Koushik,Bandyopadhyay Prasanta,Khatun Rijia,Sinha Subrata^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Condensed Matter Physics,General Chemistry,Food Science,Condensed Matter Physics,General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s10847-020-00985-0.pdf

Reference40 articles.

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3. Prashanthi, S., Kumar, P.H., Siva, D., Bangal, P.R.: Investigation of supramolecular stoichiometry and dynamic for inclusion complex of water soluble porphyrin with cucurbit [7] uril by fluorescence correlation spectroscopy. J. Photochem. Photobiol. A 284, 27–35 (2014)

4. Reis, S., Liberto, N.A., Fernandes, S.A., de Fátima, A., Almeida, W.B.D., Guimarães, L., Nascimento Jr., C.S.: Theoretical investigation on the molecular inclusion process of urease inhibitors into p-sulfonic acid calix[4,6]arenes. Chem. Phys. Lett. 692, 117–123 (2018)

5. Crini, G.: Review: a history of cyclodextrins. Chem. Rev. 114, 10940–10975 (2014)

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