Optically transparent hydrogels from an auxin-amino-acid conjugate super hydrogelator and its interactions with an entrapped dye

Chemistry - A European Journal

Volumn 18, Issue 24, 2012, Pages 7575-7581

  Reddy, Amarendar ^a   Sharma, Aashish ^a   Srivastava, Aasheesh ^a  

^a INDIAN INSTITUTE OF SCIENCE EDUCATION AND RESEARCH BHOPAL   (India)

Author keywords

amino acids; dyes; gels; hormones; hydrogen bonds

Indexed keywords

AROMATIC RESIDUES; CARBOXYLATE GROUPS; DENSE NETWORK; FTIR SPECTROSCOPY; GEL-MELTING TEMPERATURES; GELATORS; H NMR SPECTROSCOPY; H-BONDING; HIGH ASPECT RATIO; HYDROGELATORS; J AGGREGATES; L-PHENYLALANINE; LARGE SHIFTS; LOW MOLECULAR WEIGHT; PH VALUE; SHEET-LIKE; SOFT MATERIAL; TRANSPARENT GELS; VARIABLE TEMPERATURE; WATER-SOLUBLE DYE; ZERO ORDER KINETICS;

AGGREGATES; AMINO ACIDS; ASPECT RATIO; CARBOXYLATION; DYES; FOURIER TRANSFORM INFRARED SPECTROSCOPY; GELS; HORMONES; MOLECULES; NAPHTHALENE; PH; STEREOCHEMISTRY; XEROGELS;

HYDROGEN BONDS;

AMINO ACID; FLUORESCENT DYE; NAPHTHALENE 1 ACETAMIDE, L PHENYLALANINE; NAPHTHALENE DERIVATIVE; NAPHTHALENE-1-ACETAMIDE, L-PHENYLALANINE; PHENYLALANINE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGEL; HYDROGEN BOND; MOLECULAR WEIGHT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS;

AMINO ACIDS; FLUORESCENT DYES; HYDROGELS; HYDROGEN BONDING; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MOLECULAR WEIGHT; NAPHTHALENES; PHENYLALANINE;

EID: 84861831820     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201103757     Document Type: Article

References (40)

1. L. A. Estroff, A. D. Hamilton, Chem. Rev. 2004, 104, 1201-1218.
2. A. Srivastava, S. Ghorai, A. Bhattacharjya, S. Bhattacharya, J. Org. Chem. 2005, 70, 6574-6582.
3. S. M. Park, Y. S. Lee, B. H. Kim, Chem. Commun. 2003, 2912-2913.
4. M. Ma, Y. Kuang, Y. Gao, Y. Zhang, P. Gao, B. Xu, J. Am. Chem. Soc. 2010, 132, 2719-2728.
5. X. J. Fu, S. Q. Cao, N. X. Wang, S. Z. Zhang, H. Wang, Y. J. Yang, Chin. Chem. Lett. 2007, 18, 1001-1004.
6. S. Sutton, N. L. Campbell, A. I. Cooper, M. Kirkland, W. J. Frith, D. J. Adams, Langmuir 2009, 25, 10285-10291.
7. P. K. Vemula, G. A. Cruikshank, J. M. Karp, G. John, Biomaterials 2009, 30, 383-393.
8. F. Zhao, M. L. Ma, B. Xu, Chem. Soc. Rev. 2009, 38, 883-891.
9. X. Li, J. Li, Y. Gao, Y. Kuang, J. Shi, B. Xu, J. Am. Chem. Soc. 2010, 132, 17707-17709.
10. A. R. Hirst, B. Escuder, J. F. Miravet, D. K. Smith, Angew. Chem. 2008, 120, 8122-8139
11. Angew. Chem. Int. Ed. 2008, 47, 8002-8018.
12. R. V. Ulijn, N. Bibi, V. Jayawarna, P. D. Thornton, S. J. Todd, R. J. Mart, A. M. Smith, J. E. Gough, Mater. Res. Materials Today 2007, 10, 40-48.
13. Y. Gao, Z. Yang, Y. Kuang, M.-L. Ma, J. Li, F. Zhao, B. Xu, Biopolymers 2010, 94, 19-31.
14. Z. Yang, G. Liang, B. Xu, Soft Matter 2007, 3, 515-520.
15. D. J. Adams, Macromol. Biosci. 2011, 11, 160-173.
16. B. Escuder, M. Lusar, J. F. Miravet, J. Org. Chem. 2006, 71, 7747-7752.
17. A. R. Hirst, I. A. Coates, T. R. Boucheteau, J. F. Miravet, B. Escuder, V. Castelletto, I. W. Hamley, D. K. Smith, J. Am. Chem. Soc. 2008, 130, 9113-9121.
18. F. Rodríguez-Llansola, J. F. Miravet, B. Escuder, Chem. Commun. 2009, 7303-7305.
19. M. Suzuki, K. Hanabusa, Chem. Soc. Rev. 2009, 38, 967-975.
20. A. Friggeri, B. L. Feringa, J. van Esch, J. Controlled Release 2004, 97, 241-248.
21. L. Milanesi, C. A. Hunter, N. Tzokova, J. P. Waltho, S. Tomas, Chem. Eur. J. 2011, 17, 9753-9761.
22. R. Orbach, L. Adler-Abramovich, S. Zigerson, I. Mironi-Harpaz, D. Seliktar, E. Gazit, Biomacromolecules 2009, 10, 2646-2651.
23. R. V. Ulijn, A. M. Smith, Chem. Soc. Rev. 2008, 37, 664-675.
24. M. Zhou, A. M. Smith, A. K. Das, N. W. Hodson, R. F. Collins, R. V. Ulijn, J. E. Gough, Biomaterials 2009, 30, 2523-2530.
25. A. Shome, S. Debnath, P. K. Das, Langmuir 2008, 24, 4280-4288.
26. S. Cao, X. Fu, N. Wang, H. Wang, Y. Yang, Int. J. Pharm. 2008, 357, 95-99.
27. L. Chen, S. Revel, K. Morris, L. C. Serpell, D. J. Adams, Langmuir 2010, 26, 13466-13471.
28. A. Pal, A. Srivastava, S. Bhattacharya, Chem. Eur. J. 2009, 15, 9169-9182.
29. P. Campanoni, P. Nick, Plant Physiol. 2005, 137, 939-948.
30. S. Roy, A. Banerjee, Soft Matter 2011, 7, 5300-5308.
31. J. Shi, Y. Gao, Z. Yang, B. Xu, Beilstein J. Org. Chem. 2011, 7, 167-172.
32. C. Tang, A. M. Smith, R. F. Collins, R. V. Ulijn, A. Saiani, Langmuir 2009, 25, 9447-9453.
33. Y. Zhang, P. S. Cremer, Curr. Opin. Chem. Biol. 2006, 10, 658-663.
34. J. H. Jung, S. Shinkai, T. Shimizu, Chem. Eur. J. 2002, 8, 2684-2690.
35. C. Yan, D. J. Pochan, Chem. Soc. Rev. 2010, 39, 3528-3540.
36. J. Raeburn, G. Pont, L. Chen, Y. Cesbron, R. Lévy, D. J. Adams, Soft Matter 2012, 8, 1168-1174.
37. B. Andreas, Biochim.Biophys.Acta (BBA)-Bioenergetics 2007, 1767, 1073-1101.
38. J. Huang, D. Stockwell, A. Boulesbaa, J. Guo, T. Lian, J. Phys. Chem. C 2008, 112, 5203-5212.
39. M. Wang, G. L. Silva, B. A. Armitage, J. Am. Chem. Soc. 2000, 122, 9977-9986.
40. F. Rodríguez-Llansola, B. Escuder, J. F. Miravet, D. Hermida-Merino, I. W. Hamley, C. J. Cardin, W. Hayes, Chem. Commun. 2010, 46, 7960-7962.