Paal–Knorr reaction catalyzed by metal–organic framework IRMOF-3 as an efficient and reusable heterogeneous catalyst

[Display omitted] ► IRMOF-3 was synthesized and characterized. ► IRMOF-3 was used as catalyst for the Paal–Knorr reaction. ► High conversions were achieved using catalytic amounts of the IRMOF-3. ► The catalyst could be reused. A highly porous metal–organic framework (IRMOF-3) was synthesized from t...

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Published inJournal of molecular catalysis. A, Chemical Vol. 363-364; pp. 178 - 185
Main Authors Phan, Nam T.S., Nguyen, Tung T., Luu, Quang H., Nguyen, Lien T.L.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.11.2012
Elsevier
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ISSN1381-1169
1873-314X
DOI10.1016/j.molcata.2012.06.007

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Summary:[Display omitted] ► IRMOF-3 was synthesized and characterized. ► IRMOF-3 was used as catalyst for the Paal–Knorr reaction. ► High conversions were achieved using catalytic amounts of the IRMOF-3. ► The catalyst could be reused. A highly porous metal–organic framework (IRMOF-3) was synthesized from the reaction of zinc nitrate hexahydrate and 2-amino-1,4-benzenedicarboxylic acid by solvothermal method. Physical characterizations of the material were achieved by using a variety of different techniques, including X-ray powder diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR), atomic absorption spectrophotometry (AAS), and nitrogen physisorption measurements. The IRMOF-3 was used as an efficient heterogeneous catalyst for the Paal–Knorr reaction of benzyl amine with 2,5-hexanedione. Excellent conversions were obtained under mild conditions in the presence of 3mol% catalyst. The IRMOF-3 catalyst could be reused several times without a significant degradation in catalytic activity.
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ISSN:1381-1169
1873-314X
DOI:10.1016/j.molcata.2012.06.007