betadex and alpha-aminopyridine

betadex has been researched along with alpha-aminopyridine* in 2 studies

Other Studies

2 other study(ies) available for betadex and alpha-aminopyridine

ArticleYear
Selective Removal of the Genotoxic Compound 2-Aminopyridine in Water using Molecularly Imprinted Polymers Based on Magnetic Chitosan and β-Cyclodextrin.
    International journal of environmental research and public health, 2017, 08-31, Volume: 14, Issue:9

    To develop efficient materials with enhanced adsorption and selectivity for genotoxic 2-aminopyridine in water, based on magnetic chitosan (CTs) and β-cyclodextrin (β-CD), the magnetic molecularly imprinted polymers (MMIPs) of Fe₃O₄-CTs@MIP and Fe₃O₄-MAH-β-CD@MIP were synthesized by a molecular imprinting technique using 2-aminopyridine as a template. The selective adsorption experiments for 2-aminopyridine were performed by four analogues including pyridine, aniline, 2-amino-5-chloropyridine and phenylenediamine. Results showed the target 2-aminopyridine could be selectively adsorbed and quickly separated by the synthesized MMIPs in the presence of the above structural analogues. The coexisting ions including Na⁺, K⁺, Mg

    Topics: Adsorption; Aminopyridines; beta-Cyclodextrins; Chitosan; Molecular Imprinting; Polymers; Waste Disposal, Fluid; Water Pollutants, Chemical

2017
Intramolecular proton transfer effects on 2,6-diaminopyridine.
    Journal of fluorescence, 2010, Volume: 20, Issue:1

    The photophysical behaviour of 2,6-diaminopyridine (DAP) has been studied in solvents of different polarity, pH, beta-cyclodextrin (beta-CD) and compared with 2-amino pyridine (2AP). The inclusion complex of both molecules with beta-CD are analysed by UV-visible, fluorimetry, FT-IR, (1)H NMR, SEM and AM1 methods. The solvent studies shows i) DAP gives more red shifted absorption and emission maxima than 2AP molecule and ii) addition of amino group in 2AP effectively increase the resonance interaction in the pyridine ring. A regular red shift observed in acidic pH solutions suggests intramolecular proton transfer (IPT) present in both molecules. beta-CD studies indicates i) in pH approximately 7, a regular red shifted absorption and emission maxima observed in AP molecules suggests pyridine ring encapsulated in to the beta-CD cavity (1:1 inclusion complex formed) and ii) in pH approximately 1, a blue shifted absorption maxima noticed in 2AP, is due to protonated amino group deeply encapsulated in to the hydrophobic part of the beta-CD cavity.

    Topics: Aminopyridines; beta-Cyclodextrins; Hydrogen-Ion Concentration; Magnetic Resonance Spectroscopy; Microscopy, Electron, Scanning; Models, Molecular; Molecular Conformation; Protons; Pyridines; Solvents; Spectrometry, Fluorescence

2010