1,3-Di-amidoquinoline conjugate of calix[4]arene (L) as a ratiometric and colorimetric sensor for Zn 2+: Spectroscopy, microscopy and computational studies

Dalton Transactions

Volumn 41, Issue 6, 2012, Pages 1671-1674

  Mummidivarapu, V V Sreenivasu ^a   Tabbasum, Khatija ^a   Chinta, Jugun Prakash ^a   Rao, Chebrolu P ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AFM; BLUE-GREEN EMISSIONS; CALIX[4]ARENES; COLORIMETRIC SENSORS; COMPUTATIONAL STUDIES; DFT METHOD; FLUORESCENCE SENSORS; RATIOMETRIC; SINGLE CRYSTAL XRD;

FEATURE EXTRACTION; SENSORS;

ZINC;

AMIDE; CALIX(4)ARENE; CALIXARENE; NANOMATERIAL; PHENOL DERIVATIVE; QUINOLINE DERIVATIVE; ZINC;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; COLORIMETRY; EVALUATION; METHODOLOGY; SENSITIVITY AND SPECIFICITY; SPECTROFLUOROMETRY; ULTRASTRUCTURE; X RAY CRYSTALLOGRAPHY;

AMIDES; CALIXARENES; COLORIMETRY; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; NANOSTRUCTURES; PHENOLS; QUINOLINES; SENSITIVITY AND SPECIFICITY; SPECTROMETRY, FLUORESCENCE; ZINC;

EID: 84856756595     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/c2dt11900e     Document Type: Article

References (28)

1. B. E. Golden in Zinc in Human Biology (Ed.:, C. F. Mills,), Springer-Verlag, London, 1989, pp. 119-128
2. W. J. Bettger B. L. O'Dell Life Sci. 1981 28 1425
3. R. J. P. Williams in Zinc in Human Biology (Ed.:, C. F. Mills,), Springer-Verlag, London, 1989, pp. 15-31
4. C. J. Frederickson Int. Rev. Neurobiol. 1989 31 145
5. Y. Q. Pei I Koyama Epilepsia 1986 27 183
6. A. I. Bush W. H. Pettingel M. D. Paradis R. E. Tanzi J. Biol. Chem. 1994 269 12152
7. P. A. E. Sillevis-Smitt T. P. J. Mulder H. W. Verspaget H. G. T. Blaauwgeers D. Troost J. M. B. Vianney de Jong Biol. Signals 1994 3 193
8. J. S. Kim D. T. Quang Chem. Rev. 2007 107 3780
9. I. A. Bagatin E. S. De Souza A. S. Ito H. E. Toma Inorg. Chem. Commun. 2003 6 288
10. S. Y. Park J. H. Yoon C. S. Hong R. Souane J. S. Kim S. E. Matthews J. Vicens J. Org. Chem. 2008 73 8212
11. I. Leray B. Valeur Eur. J. Inorg. Chem. 2009 3525
12. M. Kumar R. Kumar V. Bhalla Chem. Commun. 2009 7384
13. N. M. Buie V. S. Talanov R. J. Butcher G. G. Talanova Inorg. Chem. 2008 47 3549
14. A. Senthilvelan I.-T. Ho K.-C. Chang G.-H. Lee Y.-H. Liu W.-S. Chung Chem.-Eur. J. 2009 15 6152
15. E. Tamanini A. Katewa L. M. Sedger M. H. Todd M. Watkinson Inorg. Chem. 2009 48 319
16. J. F. Zhang S. Bhuniya Y. H. Lee C. Bae J. H. Lee J. S. Kim Tetrahedron Lett. 2010 51 3719
17. J. Dessingou R. Joseph C. P. Rao Tetrahedron Lett. 2005 46 7967
18. R. Joseph B. Ramanujam H. Pal C. P. Rao Tetrahedron Lett. 2008 49 6257
19. R. K. Pathak S. M. Ibrahim C. P. Rao Tetrahedron Lett. 2009 50 2730
20. R. Joseph P. C. Jugun C. P. Rao J. Org. Chem. 2010 75 3387
21. R. K. Pathak A. G. Dikundwar T. N. Guru Row C. P. Rao Chem. Commun. 2010 4345
22. R. Joseph B. Ramanujam A. Acharya C. P. Rao J. Org. Chem. 2010 74 8181
23. R. Joseph B. Ramanujam A. Acharya C. P. Rao Tetrahedron Lett 2009 50 2735
24. Y. Zhang X. Guo W. Si L. Jia X Qian Org. Lett 2008 10 473
25. J. Jiang H. Jiang X. Tang L. Yang W. Dou W. Liu R. Fang W. Liu Dalton. Trans. 2011 40 6367
26. J. A. Pople and coworkers, Gaussian 03, revision C.02, Gaussian, Inc., Wallingford, CT, 2004 (total reference is given in S16 ESI†)
27. J. Fang M. Saunders Y. L. Guo C. L. Raston K. S. Iyer Chem. Commun. 2010 46 3037
28. G. M. Sheldrick Acta Cryst. 2008 A64 112