SciELO - Scientific Electronic Library Online

 
vol.65Synthesis of (S)-3-aminoethyl-1,2,3,4-tetrahydroisoquinoline (TIQ-diamine) via the Mitsunobu protocolThe determination of 11B/10B and 87Sr/86Sr isotope ratios by quadrupole-based ICP-MS for the fingerprinting of South African wine índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Artigo

Indicadores

Links relacionados

  • Em processo de indexaçãoCitado por Google
  • Em processo de indexaçãoSimilares em Google

Compartilhar


South African Journal of Chemistry

versão On-line ISSN 1996-840X
versão impressa ISSN 0379-4350

S.Afr.j.chem. (Online) vol.65  Durban  2012

 

RESEARCH ARTICLE

 

Preparation of Mg-doped Ce-Zr solid catalysts and their catalytic potency for the synthesis of 5-arylidene-2,4-thiazolidinediones via Knoevenagel condensation

 

 

Sandip RathodI; Madhukar NavgireII; Balasaheb ArbadII; Machhindra LandeII, *

IDepartment of Chemistry, Waghire Arts, Commerce & Science College, Saswad, Pune, (MS)-412301, India
IIDepartment of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, (MS)-431004, India

 

 


ABSTRACT

A series of Mg-doped Ce-Zr mixed oxides with different molar ratios were prepared by a simple co-precipitation method. The surface characterization of these materials were investigated by means of XRD, FT-IR, SEM-EDS, CO2-TPD and BET techniques. The catalytic activity of the prepared materials was tested by synthesizing of 5-arylidene-2,4-thiazolidinedione derivatives via a Knoevenagel condensation using aromatic aldehydes and 2,4-thiazolidinedione in ethanol:water medium. The best catalytic activity was obtained with Ce1Mg0.6Zr0.4O2. The particle size or crystallite size was estimated using the Debye-Scherrer equation. Addition of MgO to the Ce-Zr mixed metal oxides affected both particle size and catalytic activity.

Keywords: Mg-doped Ce-Zr oxide, surface characterization, co-precipitation, 5-arylidene-2,4-thiazolidinedione


 

 

Full text available only in PDF format.

Acknowledgements

The authors are grateful to the Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, for providing laboratory facilities. One of the authors (S.B. Rathod) would like to acknowledge the university authorities for awarding a Golden Jubilee research fellowship.

 

References

1 I.M. Labouta, H.M. Salama and N.H. Eshba, Eur. J. Med. Chem., 1987, 22, 485-489.         [ Links ]

2 A.J.S. Goes, M.C.A. DeLima and S.L. Galdino, Ann. Pharm. Franc., 1991, 49, 92-98.         [ Links ]

3 B.C.C. Cantello, M.A. Cawthorne, G.P. Cottam, P.T. Du, D. Haigh, R.M. Hindley, C.A. Lister and S.A. Smith, J. Med. Chem., 1994, 37, 3977-3985.         [ Links ]

4 A. Andreani, M. Rambaldi and A. Locatelli, Eur. J. Med. Chem., 1993, 28, 825-829.         [ Links ]

5 S.A.H. El-Feky, Pharmazie, 1993, 48, 894-896.         [ Links ]

6 J.D. Peuler, A.R. Lannussiand M.J. Hoderek, Am. J. Hypertens., 1996, 9, 188-192.         [ Links ]

7 G. Bruno, L. Costantino, C. Curinga, R. Maccari, F. Monforte, F. Nicolo and M.G. Ottana, Bioorg. J. Med. Chem., 2002, 10, 1077-1084.         [ Links ]

8 R.B. Lesyk and B.S. Zimenkovsky, Curr. Org. Chem., 2004, 8, 1547-1577.         [ Links ]

9 N. Sachan, S.S. Kadam and VM. Kulkarni, Ind. J. Hetro. Chem., 2007, 17, 57-62.         [ Links ]

10 O. Yoshitata, M. Teruo, N. Mishiko, J. Motoyuki and K. Norio, Chem. Phar. Bull., 1992, 40, 899-906.         [ Links ]

11 W. Hanefeld and M. Schlietzer, J. Hetero. Chem., 1995, 32, 1019-1025.         [ Links ]

12 T. Tashima, H. Kagechika, M. Tsuji, H. Fukasawa, K. Kawachi and Y. Hashimoto, Chem. Phar. Bull., 1997, 45, 1805-1813.         [ Links ]

13 K. Popov-Pergal, Z. Chekovich and M. Pergal, Zhur. Obschch. Khim. 1994, 61, 2112-2117.         [ Links ]

14 R.S. Mahalle, P.D. Netankar, S.P. Bondge and R.A. Mane, Green. Chem. Lett. Rev., 2008, 1, 103-106.         [ Links ]

15 F. Figueras, Top. Catal., 2004, 29, 189-196.         [ Links ]

16 H.H. Kung, Transition Metal Oxides: Surface Chemistry and Catalysis, Elsevier Science, Amsterdam, Netherlands, 1989.         [ Links ]

17 V.E. Henrich and P.A. Cox, The Surface Science of Metal Oxides, Cambridge University Press, Cambridge, UK, 1994.         [ Links ]

18 C. Noguera, Physics and Chemistry at Oxide Surfaces, Cambridge University Press Cambridge, UK, 1996.         [ Links ]

19 B.M. Reddy, Redox properties of metal oxides, in Metal Oxides: Chemistry and Application (J.L.G.Fierro, ed.), CRC Press, Boca Raton, FL, U.S.A., 1994.         [ Links ]

20 I. Spasova, G. Ivanov, V Georgescu and D.J.J. Mehandjiev, Univ. Chem Techno Metall , 2006, 41, 225-228.         [ Links ]

21 W. Feng, X. Jie, X. Li and Z. Lipeng, Adv. Synth. Catal., 2005, 347, 1987-1992.         [ Links ]

22 R. Lagnathan and B. Viswanathan, Bull. Catal. Soc. India, 2008, 7, 50-55.         [ Links ]

23 M.B. Gawande and R.V. Jayaram, Catal. Commun., 2006, 7, 931-935.         [ Links ]

24 T.F. Susana and D.A. Gloriya, React. Kinet. Catal. Lett., 2007, 92, 361-368.         [ Links ]

25 Z. Fakhroueian and M.J. Ghandi, J. Sci. Islamic Republic ofIran, 2007, 18, 303-309.         [ Links ]

26 J. Jose,J. Ameta and P.B. Punjabi, Bull. Catal. Soc. India, 2007, 6, 110-118.         [ Links ]

27 A.B. Gambhire, M.K. Lande and B.R. Arbad, Bull. Catal. Soc. India, 2008, 7, 28-40.         [ Links ]

28 H. Hattori, Chem. Rev., 1995, 95, 537-558.         [ Links ]

29 A. Cormaand R.M. Martin-Aranda, Appl. Catal. A., 1993, 105, 271-279.         [ Links ]

30 A. Corma, S.V. Forne, R.M. Martin-Aranda and F. Rey, J. Catal., 1992, 134, 58-65.         [ Links ]

31 A. Guida, M.H. Lhouty, F. Figueras and P. Geneste, Appl. Catal. A., 1997, 164 251-264.         [ Links ]

32 A. Corma, S. Iborra, S. Miquel and J. Primo, J. Catal., 1998, 173, 315-321.         [ Links ]

33 Y. Abrouki, M. Zahouily, A. Rayadh and S. Sebti, Tetrahedron Lett., 2002, 43, 8951-8953.         [ Links ]

34 X. Chunli, J.K. Bartley, D.W. Knight and G.J. Hutchings, Synthesis, 2005, 1 3468-3476.         [ Links ]

35 D. Zhang, Korean J. Chem. Eng., 2008, 25, 1205-1207.         [ Links ]

36 (a) S.B. Rathod, A.B. Gambhire, B.R. Arbad and M.K. Lande, Bull. Korean Chem. Soc., 2010, 31, 339-343.         [ Links ] (b) S.B. Rathod, B.R. Arbad and M.K. Lande, Chinese J. Catal., 2010, 31, 631-636.         [ Links ]; (c) S.S. Katkar, M.K. Lande, B.R. Arbad and S.B. Rathod, Bull. Korean Chem. Soc., 2010, 31, 1301-1304.         [ Links ]

37 H. Hattori, Chem. Rev., 1995, 95, 537-558.         [ Links ]

38 H. Hattori, Appl. Catal. A. Gen., 2001, 222, 247-259.         [ Links ]

39 H. Tsuji and H. Hattori, Catal. Today, 2006, 116, 239-243.         [ Links ]

40 M. Alifanti, B. Baps and N. Blangenois, J. Chem. Mater., 2003, 15, 395-403.         [ Links ]

41 H.W. Kim and M.H. Kong, Acta Phys. Pol. A., 2008, 29, 113-117.         [ Links ]

42 B.G. Mishra and G.R. Rao, Bull. Mater. Sci., 2002, 25, 155-162.         [ Links ]

43 O. Bozdag, G. Ayhan-Kilcigil and M. Tuncbilek, Turk. J. Chem., 1999, 23, 163-170.         [ Links ]

 

 

Received 3 May 2012
Revised 12 June 2012
Accepted 25 June 2012

 

 

* To whom correspondence should be addressed. E-mail: mkl_chem@yahoo.com

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons