Journal2016

Synthesis of spiropyran derivatives over 1-(carboxymethyl) pyridinium iodide as nanostructured pyridinium salt under aqueous media

Ahmad Reza Moosavi‐Zare, Mohammad Ali Zolfigol, Rasoul Salehi-Moratab, Ehsan Noroozizadeh

Canadian Journal of Chemistry Vol. 95, No. 2, 194–198

چکیده

In this work, acetic acid functionalized pyridinium salt, namely 1-(carboxymethyl)pyridinium iodide {[cmpy]I}, has been applied as reusable nanostructured catalyst for green, simple and efficient preparation of spiropyrans by the one-pot domino Knoevenagel–Michael–cyclization reaction of isatin derivatives or acenaphthenquinone, with malononitrile, and 1,3-dicarbonyl compounds under aqueous media. Moreover, 1H and 13C NMR, mass, CHN analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), thermal gravimetric analysis (TGA), differential thermal gravimetric (DTG), X-ray diffraction analysis (XRD), and calculation of crystallite size and interplaner distance of the catalyst have been studied.

موضوعات و کلیدواژه‌ها

Photochromic and Fluorescence ChemistryMulticomponent Synthesis of HeterocyclesBioactive Compounds and Antitumor AgentsChemistryPyridiniumMalononitrileThermogravimetric analysisKnoevenagel condensationFourier transform infrared spectroscopyAqueous solutionIodideCatalysisNuclear chemistryPolymer chemistryInorganic chemistryOrganic chemistryChemical engineering

ارجاع علمی

Ahmad Reza Moosavi‐Zare, Mohammad Ali Zolfigol, Rasoul Salehi-Moratab, Ehsan Noroozizadeh. “Synthesis of spiropyran derivatives over 1-(carboxymethyl) pyridinium iodide as nanostructured pyridinium salt under aqueous media.” Canadian Journal of Chemistry, 2016. https://doi.org/10.1139/cjc-2016-0374