Skip to main content
SpringerLink
Log in

Fluorescent naphthalene-based benzene tripod for selective recognition of fluoride in physiological condition

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

Abstract

Aluminium complex of a naphthalene-based benzene tripod ligand system has been reported for the selective recognition of fluoride in aqueous medium in physiological condition. The ligand can selectively recognize Al3+ through enhancement in the fluorescence intensity and this in situ formed aluminium complex recognizes fluoride through quenching of fluorescence. The receptor system detects fluoride in nanomolar range. The sensing property was extended for practical utility to sense fluoride in tap water, pond water and river water.

A highly fluorescent tripodal aluminum complex was used for the sensing of fluoride in physiological condition and in waste water.

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

Access this article

Log in via an institution

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

Instant access to the full article PDF.

Institutional subscriptions

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

Similar content being viewed by others

References

  1. (a) Lee C H, Miyaji H, Yoon D W and Sessler J L 2008 Chem. Commun. 24; (b) Yoon J, Kim S K, Singh N J and Kim K S 2006 Chem. Soc. Rev. 35 355; (c) Gunnlaugsson T, Glynn M, Tocci G. M, Kruger P E and Pfeffer F M 2006 Coord. Chem. Rev. 250, 3094; (d) Gale P A 2006 Acc. Chem. Res. 39 465; (e) Beer P D and Gale P A 2001 Angew. Chem., Int. Ed. 40 486; (f) Martínez-Máñez R and Sancenón F 2003 Chem. Rev. 103 4419; (g) Kim S K, Lee D H, Hong J I and Yoon J 2009 Acc. Chem. Res. 42 23; (h) Lee H N, Xu Z, Kim S K, Swamy K M K, Kim Y, Kim S J and Yoon J 2007 J. Am. Chem. Soc. 129 3828

  2. (a) Ripa L W 1993 J. Publ. Health Dent. 53 17; (b) McDonagh M S, Whiting P F, Wilson P M, Sutton A J, Chestnutt I, Cooper J, Misso K, Bradley M, Treasure E and Kleijnen J 2000 Br. Med. J. 321 855

  3. (a) Jagtap S, Yenkie M K, Labhsetwar N and Rayalu S 2012 Chem. Rev. 112 2454; (b) Wu R, Qian S S, Hao F, Cheng H, Zhu D and Zhang J 2011 Environ. Sci. Technol. 45 6041

  4. (a) Gazzano E, Bergandi L, Riganti C, Aldieri E, Doublier S, Costamagna C, Bosia A and Ghigo D 2010 Curr. Med. Chem. 17 2431; (b) Spittle B 2011 Fluoride 44 117; (c) Grandjean P and Landrigan P J 2006 Lancet 368 2167; (d) Olivier B L Arreola M and Luz M D R 2010 Chem.–Biol. Interact. 188 319

  5. (a) Zhang M, Wang A G, Xia T and He P 2008 Toxicol. Lett. 179 1; (b) Wurtz T, Houari S, N Mauro, MacDougall M, Peters H and Berdal A 2008 Toxicology 249 26

  6. Baker J L, Sudarsan N, Weinberg Z, Roth A, Stockbridge R B and Breaker R R 2012 Science 335 233

  7. Clark J H 1980 Chem. Rev. 80 429

  8. (a) Reddy M A and Fichtner M 2011 J. Mater. Chem. 21 17059; (b) Subbaiyan N K, Hill J P, Ariga K, Fukuzumi S and D’Souza F 2011 Chem. Commun. 47 6003; (c) Cook G J R, Parker C, Chua S, Johnson B, Aksnes A K and Lewington V J 2011 EJNMMI Res. 1 4; (d) Li Y, Schiepers C, Lake R, Dadparvar S and Berenji G R 2012 Bone 50 128; (e) Grochala W 2009 J. Mater. Chem. 19 6949; (f) Trewin A, Darling G R and Cooper A I 2008 New J. Chem. 32 17

  9. (a) An B K, Wang X, Burn P L and Meredith P 2010 Chem. Phys. Chem. 11 3517; (b) Qu Y, Hua J and Tian H 2010 Org. Lett. 12 3320; (c) Bhosale S V, Bhosale S V, Kalyankar M B and Langford S J 2009 Org. Lett. 11 5418; (d) Jung H S, Kim H J, Vicens J and Kim J S 2009 Tetrahedron Lett. 50 983; (e) Hudnall T W and Gabbaï F P 2008 Chem. Commun. 4596; (f) Dorsey C L, Jewula P, Hudnall T W, Hoefelmeyer J D, Taylor T J, Honesty N R, Chiu C W, Schulte M and Gabbaï F P 2008 Dalton Trans. 4442; (g) Jiang X, Vieweger M C, Bollinger J C, Dragnea B and Lee D 2007 Org. Lett. 9 3579; (h) Tan W, Zhang D, Wang Z, Liu C and Zhu D 2007 J. Mater. Chem. 17 1964; (i) Parab K, Venkatasubbaiah K and Jäkle F 2006 J. Am. Chem. Soc. 128 12879; (j) Lin Z, Ou S, Duan C, Zhang B and Bai Z 2006 Chem. Commun. 624; (k) Vázquez M, Fabbrizzi L, Taglietti A, Pedrido R M, González-Noya A M and Bermejo M R 2004 Angew. Chem. Int. Ed. 43 1962; (l) Kim T H and Swager T M 2003 Angew. Chem., Int. Ed. 42 4803; (m) Cho E J, Moon J W, Ko S W, Lee J Y, Kim S K, Yoon J and Nam K C 2003 J. Am. Chem. Soc. 125 12376; (n) Yamagushi S, Akiyama S and Tamao K 2001 J. Am. Chem. Soc. 123 11372; (o) Black C B, Andrioletti B, Try A C, Ruiperez C and Sessler J L 1999 J. Am. Chem. Soc. 121 10438

  10. (a) Guha S and Saha S 2010 J. Am. Chem. Soc. 132 17674; (b) Wang F, Wu J, Zhuang X, Zhang W, Liu W, Wang P and Wu S 2010 Sens. Actuators B 146 260; (c) Yang X F, Qi H, Wang L, Su Z and Wang G 2009 Talanta 80 92; (d) Kim S Y and Hong J I 2007 Org. Lett. 9 3109; (e) Gao X, Zheng H, Shang G q and Xu J G 2007 Talanta 73 770; (f) Lee M H, Agou T, Kobayashi J, Kawashima T and Gabbaï F P 2007 Chem. Commun. 1133; (g) Zhu C Q, Chen J L, Zheng H, Wu Y Q and Xu J G 2005 Anal. Chim. Acta. 539 311; (h) Takahashi Y, Tanaka D A P, Matsunaga H and Suzuki T M 2002 J. Chem. Soc., Perkin Trans. 2 759; (i) Cooper C R, Spencer N and James T D 1998 Chem. Commun. 1365

  11. (a) Andolina C M and Morrow J R 2011 Eur. J. Inorg. Chem. 154; (b) Hu R, Feng J, Hu D, Wang S, Li S, Li Y and Yang G 2010 Angew. Chem., Int. Ed. 49 4915; (c) Kim Y and Gabbaï F P 2009 J. Am. Chem. Soc. 131 3363; (d) Kim S Y, Park J, Koh M, Park S B and Hong J I 2009 Chem. Commun. 4735; (e) Matsunaga H, Kanno C, Yamada H, Takahashi Y and Suzuki T M 2006 Talanta 68 1000; (f) Yamamoto H, Ori A, Ueda K, Dusemund C and Shinkai S 1996 Chem. Commun. 407

  12. Housecroft C E and Sharpe A G 2008 Inorganic chemistry, 3rd edn (Harlow: Pearson Education Ltd.) p. 537.

  13. Xu Z, Chen X, Kim H N and Yoon J 2010 Chem. Soc. Rev. 39 127

  14. Maity S B and Bharadwaj P K 2013 Inorg. Chem. 52 1161

  15. (a) Khalifa M E and Hafez M A H 1998 Talanta 47 547; (b) Hensley A L and Barney J E II 1960 Anal. Chem. 32 828; (c) Brownley F I Jr. and Howle C W Jr. 1960 Anal. Chem. 32 1330

  16. (a) Zaporozhets O A and Tsyukalo L Y 2007 Anal. Chim. Acta 597 171; (b) Rohit, Kanwar L and Rao K K 2010 Sens. Actuators B 149 245; (b) Devine R F and Partington G L 1975 Environ. Sci. Technol. 9 678

  17. (a) Datta B K, Kar C, Basu A and Das G 2013 Tetrahedron Lett. 54 771; (b) Dey S K and Das G 2011 Chem. Commun. 47 4983; (c) Pramanik A and Das G 2009 Tetrahedron. 65 2196; (d) Kar C, Basu A and Das G 2012 Tetrahedron Lett. 53 4754; (e) Basu A and Das G 2011 Dalton Trans. 40 2837; (f) Kar C, Adhikari M D, Ramesh A and Das G 2012 RSC Adv. 2 9201; (g) Kar C and Das G 2013 J. Photochem. Photobiol., A. 251 128; (h) Basu A and Das G 2012 Inorg. Chem. 51 882; (i) Kar C, Adhikari M D, Ramesh A and Das G 2013 Inorg. Chem. 52 743; (j) Datta B K, Mukherjee S, Kar C, Ramesh A and Das G 2013 Anal. Chem. 85 8369; (k) Kar C, Adhikari M D, Datta B K, Ramesh A and Das G 2013 Sens. Actuators B 188 1132

Download references

Acknowledgements

GD thanks CSIR (01/2727/13/EMR-II) and Science & Engineering Research Board (SR/S1/OC-62/2011) New Delhi, India for financial support and CIF of IITG for providing instrument facilities. BKD and CK thank IIT Guwahati for fellowship.

Author information

Authors and Affiliations

  1. Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati, 781 039, India

    BARUN KUMAR DATTA, CHIRANTAN KAR & GOPAL DAS

Authors
  1. BARUN KUMAR DATTA
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. CHIRANTAN KAR
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. GOPAL DAS
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to GOPAL DAS.

Additional information

Supplementary Information

The supplementary information can be seen in www.ias.ac.in/chemsci.

Electronic supplementary material

Below is the link to the electronic supplementary material.

(PDF 1.42 MB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

DATTA, B.K., KAR, C. & DAS, G. Fluorescent naphthalene-based benzene tripod for selective recognition of fluoride in physiological condition. J Chem Sci 127, 337–342 (2015). https://doi.org/10.1007/s12039-015-0779-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12039-015-0779-0

Keywords

Search

Navigation