IR–Raman, NMR and density functional methods in the examination of tautomerism and features of N-methyl substituted 9-acridinamine derivatives
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference62 articles.
1. Theoretical studies on the prototropic tautomerism, structure, and features of acridine and 9-acridinamine free bases and their protonated forms
2. Experimental and INDO CI calculations of the electronic absorption spectra of acridine and 9-acridinamine free bases and their protonated forms with regard to tautomeric phenomena
3. Theoretical Studies on the Effect of the Medium on Tautomeric Phenomena in Neutral and Protonated Acridin-9-amine. Mechanism of Tautomerization in Neutral Entities
4. Hartree−Fock and Density Functional Methods and IR and NMR Spectroscopies in the Examination of Tautomerism and Features of Neutral 9-Acridinamine in Gaseous and Condensed Media
5. Stationary and time-resolved fluorescence investigations combined with studies of tautomeric phenomena in neutral and protonated 9-acridinamine
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1. Tautomerism of N-substituted acridin-9-amines in the context of dynamic NMR and matrix isolation-FT-IR spectroscopy supported by DFT calculations and structural analysis;Journal of Molecular Structure;2020-10
2. A review on acridinylthioureas and its derivatives: biological and cytotoxic activity;Journal of Applied Toxicology;2017-03-31
3. Synthesis and Radioiodination of Some 9-Aminoacridine Derivatives;European Journal of Organic Chemistry;2004-09
4. Interaction of Antimalarial Drug Quinacrine with Nucleic Acids of Variable Sequence Studied by Spectroscopic Methods;Journal of Biomolecular Structure and Dynamics;2000-12
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