Skip to main content
Log in

Polymer supported nickel complex: Synthesis, structure and catalytic application

  • Published:
Journal of Chemical Sciences Aims and scope Submit manuscript

Abstract

In the present investigation, a new synthetic route for a novel recyclable free [3-MOBdMBn-Ni] and polystyrene-anchored [P-3-MOBdMBn-Ni] nickel complexes is presented. The free and polymer-anchored metal complexes were synthesized by the reaction of nickel (II) with one molar equivalent of unsupported N N-bis (2-Hydroxy-3-methoxybenzaldehyde) 4-Methylbenzene-1,2-diamine (3-MOBdMBn) or polymer-supported (P-3-MOBdMBn) Schiff-base ligand in methanol under nitrogen atmosphere. The advantages of these polymer-supported catalysts are the low cost of catalyst and recyclability up to six times, due to easy availability of materials and simple synthetic route. The higher efficiency of complexation of nickel on the polymer-anchored 3-MOBdMBn Schiff base than the unsupported analogue is another advantage of this catalyst system. The structural study reveals that nickel(II) complex of 3-MOBdMBn is square planar in geometry. The catalytic activity of nickel complex towards the oxidation of phenol was investigated in the presence of hydrogen peroxide. Experimental results indicate that the reactivity of P-3-MOBdMBn-Ni was dramatically affected by the polymer support compared to free 3-MOBdMBn-Ni. The rates of oxidation (Rp) for unsupported and supported catalysts are 1.37 × 10−6 mole dm−3 s−1 and 2.33 × 10−6 mole dm−3 s−1 respectively.

The catalytic activity of free [3-MOBdMBn-Ni] and polystyrene-anchored [P-3-MOBdMBn-Ni] nickel complexes were tested towards oxidation of phenol and the effect of the H2O2 concentration/phenol concentration/catalyst concentration is presented.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1
Scheme 1
Scheme 2
Scheme 3
Scheme 4
Scheme 5
Figure 2
Scheme 6
Scheme 7
Figure 3
Figure 4
Scheme 8

Similar content being viewed by others

References

  1. Gupta K C and Sutar A K 2008 Coord. Chem. Rev. 252 1420

  2. Chang Y, Zha F, Su B and Wang Y 2006 J. Macromol. Sci. Pure Appl. Chem. 43 923

  3. Ding K, Wang Z, Wang X, Liang Y and Wang X 2006 Chem. Eur. J. 12 5188

  4. Thomas S R and Janda K D 2000 J. Am. Chem. Soc. 122 6929

  5. Sutar A K, Maharana T, Dutta S, Chen C-T and Lin C-C 2010 Chem. Soc. Rev. 39 1724

  6. Vatankhah-Varnoosfaderani M, Pourmahdian S and Afshar-Taromi F 2011 Iran. Poly. J. 20(11) 897

  7. Grivani G and Akherati A 2013 Inorg. Chem. Comm. 28 90

  8. Gupta K C, Sutar A K and Lin C C 2009 Coord. Chem. Rev. 253 1926

  9. Yoo D W, Han J H, Nam S H, Kim H J, Kim C and Lee J K 2006 Inorg. Chem. Commun. 9 654

  10. Yue C, Fei Z, Bitao S and Yupu W 2006 J. Macromol. Sci. Part A Pure Appl. Chem. 43 (6) 923

  11. Kumar A and Srinivas D 2013 J Mol Catal A: Chem. 368 112

  12. Keav S, de los Monteros A E, Barbier Jr. J and Duprez D 2014 Appl. Catal. B: Environ. 150 402

  13. Bellardita M, Augugliaro V, Loddo V, Megna B, Palmisano G, Palmisano L and Puma M A 2012 Appl. Catal. A: Gen. 441 79

  14. Hernmert C, Renz M and Meunier B 1999 J. Mol. Catal. A. Chem. 137 205

  15. Walling C 1975 Acc. Chem. Res. 8 125

  16. Gupta K C and Sutar A K 2008 J. Mol. Catal. A Chem. 280 173

  17. Owsik I, Kolarz B N and Jezierska J 2006 J. Catal. Lett. 107 197

  18. Gupta K C and Sutar A K 2007 J. Mol. Catal. A Chem. 272 64

  19. Gupta K C and Sutar A K 2007 J. Macromol. Sci. Part A: Pure Appl. Chem. 44 1171

  20. Vogel A I 1978 In Textbook of practical organic chemistry (London: ELBS and Longman)

  21. Fraile J M, Mayoral J A, Royo A J, Salvador R V, Altava B, Luis S V, Burguete M I 1996 Tetrahedron 52(29) 9853

  22. Kowalak S, Weiss R C, Balkus K J 1991 J. Chem. Soc. Chem. Commun. 57 57

  23. Buijsman R C, van Vuuren E and Sterrenburg J G 2001 Org. Lett. 3(23) 3785

Download references

Acknowledgements

The authors are thankful to Department of Science and Technology (DST), Council of Scientific and Industrial Research (CSIR) and University Grants Commission (UGC), New Delhi, India for funding. The authors are also grateful to Ravenshaw University, KIIT University and National Institute of Technology, Raipur for providing research facilities.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to ALEKHA KUMAR SUTAR.

Additional information

Supporting Information

FTIR spectrum of unsupported 3-MOBdDMBn Schiff base and polymer-supported 3-MOBdDBn Schiff base,1H-NMR spectrum of 3-MOBdMBn Schiff base, time variation data for conversion of phenol by unsupported and polymer-supported nickel complex (Ni-3-MOBdMBn) are provided in supporting information (SI) available at www.ias.ac.in/chemsci.

Electronic supplementary material

Below is the link to the electronic supplementary material.

(DOC 1.25 MB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

SUTAR, A.K., MAHARANA, T., DAS, Y. et al. Polymer supported nickel complex: Synthesis, structure and catalytic application. J Chem Sci 126, 1695–1705 (2014). https://doi.org/10.1007/s12039-014-0728-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12039-014-0728-3

Keywords

Navigation