synthesis of phthalocyanine derivatives by synergistic effect of catalysts over nanodimensional zeolites under solvent-free conditions
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abstract
copper (ii) phthalocyanine and 2,9,16,23 tetrakis nitro copper (ii) phthalocyaninehas been synthesized respectively from phthalonitrile and 4-nitro phthalonitrile under solvent-free condition using two different catalystsovernanodimensionalzeolites. 4-nitro phthalonitrile synthesized from phthalimide in three steps. the newly prepared compounds have been characterized by ir, uv-vis, 1hnmr and ms spectra.
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Synthesis of Phthalocyanine derivatives by synergistic effect of catalysts over nanodimensional zeolites under solvent-free conditions
Copper (II) phthalocyanine and 2,9,16,23 tetrakis nitro copper (II) phthalocyaninehas been synthesized respectively from phthalonitrile and 4-nitro phthalonitrile under solvent-free condition using two different catalystsovernanodimensionalzeolites. 4-Nitro phthalonitrile synthesized from phthalimide in three steps. The newly prepared compounds have been characterized by IR, UV-Vis, 1</sup...
full textSynthesis of phthalocyanine derivatives by synergistic effect of catalysts over nanodimensional zeolites under solvent-free conditions
Copper (II) phthalocyanine and 2, 9, 16, 23 tetrakis nitro copper (II) phthalocyanine has been synthesized respectively from phthalonitrile and 4-nitro phthalonitrile under solvent-free condition using two different catalysts over nanodimensional zeolites. 4-Nitro phthalonitrile synthesized from phthaimide in three steps. The newly prepared compounds have been characterized by IR, UV-Vis,1H N...
full textSynthesis of Phthalocyanine derivatives by synergistic effect of catalysts over nanodimensional zeolites under solvent-free conditions
Copper (II) phthalocyanine and 2,9,16,23 tetrakis nitro copper (II) phthalocyaninehas been synthesized respectively from phthalonitrile and 4-nitro phthalonitrile under solvent-free condition using two different catalystsovernanodimensionalzeolites. 4-Nitro phthalonitrile synthesized from phthalimide in three steps. The newly prepared compounds have been characterized by IR, UV-Vis, 1</sup...
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Protonation of the highly reactive 1:1 intermediates, produced in the reaction between triphenylphosphine and acetylenic esters, by NH-acids such as azathioprine, imidazole or theophylline leads to the formation of vinyltriphenylphosphonium salts, which undergo a Michael addition reaction with a conjugate base to produce phosphorus ylides. Silica nanoparticles (silica NPs were prepared by therm...
full textSynthesis of electron-poor N-Vinylimidazole derivatives catalyzed by Silica nanoparticles under solvent-free conditions
Protonation of the highly reactive 1:1 intermediates, produced in the reaction between triphenylphosphine and acetylenic esters, by NH-acids such as azathioprine, imidazole or theophylline leads to the formation of vinyltriphenylphosphonium salts, which undergo a Michael addition reaction with a conjugate base to produce phosphorus ylides. Silica nanoparticles (silica NPs were prepared by therm...
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Journal title:
international journal of nano dimensionجلد ۵، شماره ۱، صفحات ۳۵-۳۹
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