Skip to main content
Log in

Synthesis, characterization and self-assembly of Co3+ complexes appended with phenol and catechol groups

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

Abstract

This work presents the syntheses, characterization and hydrogen bonding based self-assembly of Co3+ complexes of pyridine-amide based bidentate ligands containing appended phenol and catechol groups. Placement of multiple hydrogen bond donors (phenolic OH and amidic NH groups) and acceptors (Oamide groups) in these molecules results in interesting self-assembled architectures.

Cobalt complexes of pyridine-amide based bidentate ligands containing appended phenol and catechol groups are discussed. Placement of multiple hydrogen bond donors and acceptors in these coordination complexes results in interesting self-assembly.

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.

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

Similar content being viewed by others

References

  1. Kumar G and Gupta R 2013 Chem. Soc. Rev. 42 9403

  2. (a) Desiraju G R 1995 Angew. Chem. Int. Ed. 34 2311; (b) Desiraju G R 2001 Nature 412 397; (c) Desiraju G R 2007 Cryst. Eng. Comm. 9 91; (d) Prins L J, Reinhoudt D N and Timmerman P 2001 Angew. Chem. Int. Ed. 40 2382; (e) Steiner T 2002 Angew. Chem. Int. Ed. 41 48; (e) Wuest J D 2005 Chem. Commun. 5830; (f) Suslick K S, Bhyrappa P, Chou J S, Kosal M E, Nakagaki S, Smithenry D W and Wilson S R 2005 Acc. Chem. Res. 38 283; (f) Beatty A M 2003 Coord. Chem. Rev. 246 131

  3. Ali A, Hundal G and Gupta R 2012 Cryst. Growth Des. 12 1308

  4. Kumar G, Aggarwal H and Gupta R 2013 Cryst. Growth Des. 13 74

  5. (a) Sarma R J and Baruah J B 2007 Cryst. Growth Des. 7 989 and references cited therein; (b) Sarma R J and Baruah J B 2005 Cryst. Eng. Comm. 7 706; (c) Sarma R J and Baruah J B 2006 Chem. Eur. J. 12 4994

  6. (a) Aitipanula S, Thallapally P K, Thaimattam R, Jaskolsiki M and Desiraju G R 2002 Org. Lett. 4 921; (b) Thallapally P K, Katz A K, Carrell H L and Desiraju G R 2002 Chem. Commun. 344; (c) Aitipanula S, Desiraju G R, Jaskolsiki M, Nangia A and Thaimattam R 2003 Cryst. Eng. Comm. 5 447; (d) Vangala V R, Mondal R, Broder C K, Howard J A K and Desiraju G R 2005 Cryst. Growth Des. 5 99

  7. (a) Malek N, Maris T, Perron M E and Wuest J D 2005 Angew. Chem. Int. Ed. 44 4021; (b) Malek N, Maris T, Simard M and Wuest J D 2005 J. Am. Chem. Soc. 127 5910; (c) Saied O, Maris T, Wang X, Simard M and Wuest J D 2005 J. Am. Chem. Soc. 127 10008; (d) Fournier J H, Maris T, Simard M and Wuest J D 2003 Cryst. Growth Des. 3 535

  8. (a) Tanaka K, Okada T and Toda F 1993 Angew. Chem. Int. Ed. 32 1147; (b) Urbanczyk-Lipkowska Z, Yoshizawa K, Toyota S and Toda F 2003 Cryst. Eng. Comm. 5 114; (c) Yoshizawa K, Toyota S, Toda F, Kato M and Csöregh I 2007 Cryst. Eng. Comm. 9 786; (d) Goldberg I, Stein Z, Kai A and Toda F 1987 Chem. Lett. 1617; (e) Toda F, Tanaka K, Hyoda T and Mak T C W 1988 Chem. Lett. 107

  9. (a) Thakuria R, Sarma B and Nangia A 2010 New J. Chem. 34 623; (b) Aitipamula S and Nangia A 2005 Chem.–Eur. J. 11 6727; (c) Sarma B, Roy S and Nangia A 2006 Chem. Commun. 4918; (d) Aitipanula S and Nangia A 2005 Chem. Commun.3159;(e) Jagadeesh, N and Nangia A 2006 Cryst. Growth Des. 6 1995

  10. (a) Kobayashi K, Shirasaka T, Horn E and Furukawa N 2000 Tetrahedron Lett. 41 89; (b) Kobayashi K, Shirasaka T, Sato A, Horn E and Furukawa N 1999 Angew. Chem. Int. Ed. 38 3483; (c) Sawaki T, Endo K, Kobayashi K, Hayashida O and Aoyama Y 1997 Bull. Chem. Soc. Jpn. 70 3075; (d) Kobayashi K, Kobayashi N, Ikuta M, Therrien B, Sakamoto S and Yamaguchi K 2005 J. Org. Chem. 70 749; (e) Tanaka T, Tasaki T and Aoyama Y 2002 J. Am. Chem. Soc. 124 12453; (f) Kobayashi K, Endo K, Aoyama Y and Masuda H 1993 Tetrahedron Lett. 34 7929

  11. (a) Tominaga M, Katagiri K, and Azumaya I 2009 Cryst. Growth Des. 9 3692; (b) Tominaga M, Katagiri K and Azumaya I 2010 Cryst. Eng. Comm. 12 1164; (c) Tominaga M, Masu H and Azumaya I 2011 Cryst. Growth Des. 11 542; (d) Tominaga M, Masu H and Azumaya I 2011 Cryst. Eng. Comm. 13 5299

  12. (a) Aitipamula S, Nangia A, Thaimattam R and Jaskolski M 2003 Acta Crystallogr. 39 481; (b) Venkataramanan B, Guan James W L, Vittal J J and Suresh V 2004 Cryst. Growth Des. 4 553; (c) Pigge F C, Dighe M K and Rath N P 2006 Cryst. Growth Des. 6 2732

  13. Perrin D D, Armarego W L F and Perrin D R 1980 In Purification of Laboratory Chemicals (Oxford: Pergamon Press)

  14. Ali A, Bansal D, Kaushik N K, Kaushik N, Choi E H and Gupta R 2014 J. Chem. Sci. 126 1091

  15. SMART: Bruker Molecular Analysis Research Tool, version 5.618, Bruker Analytical X-ray System: Madison, WI, 2000

  16. SAINT-NT, Version 6.04, Bruker Analytical X-ray System: Madison, WI, 2001

  17. SHELXTL-NT, Version 6.10, Bruker Analytical X-ray System: Madison, WI, 2000

  18. Altomare A, Cascarano G, Giacovazzo C and Guagliardi A 1993 J. Appl. Crystallogr. 26 343

  19. Sheldrick G M 2008 Acta Crystallogr. Sec. A 64 112

  20. Farrugia, L J WinGX version 1.64, An Integrated System of Windows Programs for the Solution, Refinement and Analysis of Single-Crystal X-ray Diffraction Data; Department of Chemistry, University of Glasgow, 2003

  21. Spek A L, PLATON, A Multipurpose Crystallographic Tool, Utrecht University, The Netherlands, 2002

  22. Geary W J 1971 Coord. Chem. Rev. 7 81

  23. Mishra A, Kaushik N K, Verma A K and Gupta R 2008 Eur. J. Med. Chem. 43 2189

  24. Mishra A, Ali A, Upreti S and Gupta R 2008 Inorg. Chem. 47 154

  25. (a) Das A, Peng S –M, Lee G –H and Bhattacharya S 2004 New. J. Chem. 28 712; (b) Bag N, Lahiri G K, Bhattacharya S, Falvello LR and Chakravorty A 1988 Inorg. Chem. 27 4396; (c) Ellis R M, Quilligan J D, William N H and Yandell J K 1989 Aust. J. Chem. 42 1; (d) Barral M C, Aparicio R J, Royer E C, Saucedo M J, Urbanos F A, Puebla E G and Valero C R 1991 J. Chem. Soc., Dalton Trans. 1609

Download references

Acknowledgements

Authors thank Science and Engineering Research Board (SERB), Govt. of India for the generous financial support and CIF-USIC of this university for the instrumental facilities. AA and DB thank University Grant Commission (UGC) for their fellowships.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to RAJEEV GUPTA.

Additional information

Supplementary Information

Figures for absorption spectra, NMR spectra and thermal analysis; and tables for NMR spectra data. The electronic supplementary information can be seen at www.ias.ac.in/chemsci. CCDC 994231-994234 contain the crystallographic data for this paper. These data can be obtained free of charges from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.

Electronic supplementary material

Below is the link to the electronic supplementary material.

(DOC 1.42 MB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

ALI, A., BANSAL, D. & GUPTA, R. Synthesis, characterization and self-assembly of Co3+ complexes appended with phenol and catechol groups. J Chem Sci 126, 1535–1546 (2014). https://doi.org/10.1007/s12039-014-0703-z

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12039-014-0703-z

Keywords

Navigation