Microwave assisted sol-gel synthesis of MgO nanoparticles and their catalytic activity in the synthesis of Hantzsch 1,4-dihydropyridines

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 33, Issue 9, 2012, Pages 1502-1507

  Mirzaei, Hakimeh ^a   Davoodnia, Abolghasem ^a  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

Hantzsch 1,4 dihydropyridine; Magnesium oxide; Microwave assisted sol gel method; Nanoparticle

Indexed keywords

1 ,4-DIHYDROPYRIDINE; 1 ,4-DIHYDROPYRIDINES; ADSORPTION DESORPTION; AMMONIUM ACETATE; AROMATIC ALDEHYDE; CATALYTIC BEHAVIOR; ETHYLACETOACETATE; HIGH SPECIFIC SURFACE AREA; HIGH YIELD; MGO; MICROWAVE ASSISTED; MICROWAVE-ASSISTED SOL-GEL METHOD; NANO-SIZED; ONE-POT SYNTHESIS; PARTICLES SIZES; SOL-GEL SYNTHESIS; STRUCTURE AND MORPHOLOGY; WATER AS SOLVENT; XRD;

ALDEHYDES; AMMONIUM COMPOUNDS; CALCINATION; CATALYST ACTIVITY; DEIONIZED WATER; DYES; MAGNESIA; MAGNESIUM; NANOPARTICLES; SCANNING ELECTRON MICROSCOPY; SOL-GEL PROCESS; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION;

SYNTHESIS (CHEMICAL);

EID: 84867525578     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (48)

1. Wagner G W, Bartram P W, Koper O, Klabunde K J. J Phys Chem B, 1999, 103: 3225
2. Davini P, Tartarelli R. Fuel, 1985, 64: 380
3. Duyar O, Durusoy H Z. Turk J Phys, 2004, 28: 139
4. Phillips J M. Appl Phys, 1996, 79: 1829
5. Hamet J F, Mercey B, Hervieu M, Raveau B. Physica C, 1992, 193: 465
6. Liu S W, Weaver J, Yuan Z, Donner W, Chen C L, Jiang J C, Meletis E I, Chang W, Kirchoefer S W, Horwitz J, Bhalla A. Appl Phys Lett, 2005, 87: 142905/1
7. Hattori H. Chem Rev, 1995, 95: 537
8. Mishakov I V, Bedilo A F, Richards R M, Chesnokov V V, Volodin A M, Zaikovskii V I, Buyanov R A, Klabunde K J. J Catal, 2002, 206: 40
9. Chesnokov V V, Bedilo A F, Heroux D S, Mishakov I V, Klabunde K J. J Catal, 2003, 218: 438
10. Kumar D, Reddy V B, Mishra B G, Rana R K, Nadagoudac M N, Varmac R S. Tetrahedron, 2007, 63: 3093
11. Climent M J, Corma A, Iborra S, Mifsud M. J Catal, 2007, 247: 223
12. Zelmanov G, Semiat R. Water Res, 2008, 42: 492
13. Pucher P, Benmami M, Azouani R, Krammer G, Chhor K, Bocquet J F, Kanaev A V. Appl Catal A, 2007, 332: 297
14. Mirjafary Z, Saeidian H, Sadeghi A, Matloubi Moghaddam F. Catal Commun, 2008, 9: 299
15. Xue C H, Palaniappan K, Arumugam G, Hackney S A, Liu J, Liua H Y. Catal Lett, 2007, 116: 94
16. Jiu J T, Kurumada K I, Tanigaki M, Adachi M, Yoshikawa S. Mater Lett, 2004, 58: 44
17. Chadwick A V, Poplett I J F, Maitland D T S, Smith M E. Chem Mater, 1998, 10: 864
18. Bokhimi X, Morales A, Portilla M, Garcia-Ruiz A. Nanostruct Mater, 1999, 12: 589
19. Subramania A, Kumar G V, Priya A R S, Vasudevan T. Nanotechnology, 2007, 18: 225601/1
20. Lopez T, Gomez R, Navarrete J, Lopez-Salinas E. J Sol-Gel Sci Technol, 1998, 13: 1043
21. Utamapanya S, Klabunde K J, Schlup J R. Chem Mater, 1991, 3: 175
22. Liang S H, Gay I D. Langmuir, 1985, 1: 593
23. Klabunde K J, Stark J, Koper O, Mohs C, Park D G, Decker S, Jiang Y, Lagadic I, Zhang D J. J Phys Chem, 1996, 100: 12142
24. Bokhimi X, Morales A, Lopez T, Gomez R. J Solid State Chem, 1995, 115: 411
25. Xu B Q, Wei J M, Wang H Y, Sun K Q, Zhu Q M. Catal Today, 2001, 68: 217
26. Matthews J S, Just O, Obi-Johnson B, Rees W S. Chem Vapor Depos, 2000, 6: 129
27. El-Shall M S, Slack W, Vann W, Kane D, Hanley D. J Phys Chem, 1994, 98: 3067
28. Ding Y, Zhang G T, Wu H, Hai B, Wang L B, Qian Y T. Chem Mater, 2001, 13: 435
29. Helble J J. J Aerosol Sci, 1998, 29: 721
30. Krishnakumar T, Jayaprakash R, Parthibavarman M, Phani A R, Singh V N, Mehta B R. Mater Lett, 2009, 63: 896
31. Davoodnia A, Rahimizadeh M, Atapour-Mashhad H, Tavakoli-Hoseini N. Heteroat Chem, 2009, 20: 346
32. Parida K M, Parija S. Sol Energy, 2006, 80: 1048
33. Moghaddam F M, Saeisian H. Mater Sci Engin B, 2007, 139: 265
34. Davoodnia A, Heravi M M, Rezaei-Daghigh L, Tavakoli-Hoseini N. Chin J Chem, 2010, 28: 429
35. Davoodnia A, Khojastehnezhad A, Tavakoli-Hoseini N. Bull Korean Chem Soc, 2011, 32: 2243
36. Zeinali-Dastmalbaf M, Davoodnia A, Heravi M M, Tavakoli-Hoseini N, Khojastehnezhad A, Zamani H A. Bull Korean Chem Soc, 2011, 32: 656
37. Khojastehnezhad A, Davoodnia A, Bakavoli M, Tavakoli-Hoseini N, Zeinali-Dastmalbaf M. Chin J Chem, 2011, 29: 297
38. Davoodnia A, Tavakoli-Nishaburi A, Tavakoli-Hoseini N. Bull Korean Chem Soc, 2011, 32: 635
39. Jenkins R, Snyder R L. Chemical Analysis: Introduction to X-Ray Powder Diffractometry. New York: Wiley, 1996. 90
40. Klug H P, Alexander L E. X-Ray Diffraction Procedures. 2nd Ed. New York: Wiley, 1974. 656
41. Antonyraj C A, Kannan S. Appl Catal A, 2008, 338: 121
42. Debache A, Ghalem W, Boulcina R, Belfaitah A, Rhouati S, Carboni B. Tetrahedron Lett, 2009, 50: 5248
43. Heydari A, Khaksar S, Tajbakhsh M, Bijanzadeh H R. J Fluorine Chem, 2009, 130: 609
44. Murthy Y L N, Rajack A, Taraka Ramji M, Jeson Babu J, Praveen Ch, Aruna Lakshmi K. Bioorg Med Chem Lett, 2012, in press
45. Adharvana Chari M, Syamasundar K. Catal Commun, 2005, 6: 624
46. Sridhar R, Perumal P T. Tetrahedron, 2005, 61: 2465
47. Bamoharram F F. Synth React Inorg Met-Org Nano-Met Chem, 2011, 41: 571
48. Diez V K, Apesteguia C R, Di Cosimo J I. Catal Today, 2000, 63: 53