High Catalytic Ability of Fe3O4/EDTA Magnetic Nanocatalyst in Comparison with Various Deep Eutectic Solvents for One-Pot Synthesis of 4H-Pyrans
Author(s):
Article Type:
Research/Original Article (بدون رتبه معتبر)
Abstract:
In this work, various 3-cyano-4-aryl-4H-pyran derivatives were prepared efficiently through a one-pot,multicomponent synthesis between aromatic aldehyde, malononitrile and acetophenone derivativesor ethyl acetoacetate using Fe3O4/EDTA magnetic nanocatalyst and ethanol as solvent. The reactionswere completed at room temperature in 10 min using 5 mg of catalyst and 2 mL of solvent to prepare1 mmol of the product. The employed catalyst has consisted of magnetite nanoparticles core, whichcoated with EDTA to modify its surface and prevent the aggregation. In addition, the catalytic abilitiesof different deep eutectic solvents (DESs) such as choline chloride/tin (II) chloride, choline chloride/zinc chloride and choline chloride/urea were compared with the nanomagnetic catalyst via thissynthesis. The nanomagnetic catalyst showed higher ability in comparison with various DESs for thetitle reaction. The employed nanomagnetic catalyst has been recycled 4 times without important lossof its activity which shows its high efficiency and small leaching.
Keywords:
Language:
English
Published:
Journal of Nanoanalysis, Volume:5 Issue: 1, Mar 2018
Pages:
49 to 57
magiran.com/p2606385
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یکساله به مبلغ 1,390,000ريال میتوانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
- حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران میشود.
- پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانههای چاپی و دیجیتال را به کاربر نمیدهد.
In order to view content subscription is required
Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!