Cooperative switching events in azobenzene foldamer denaturation

Chemistry - A European Journal

Volumn 18, Issue 34, 2012, Pages 10519-10524

  Yu, Zhilin ^a   Hecht, Stefan ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

azobenzenes; cooperativity; foldamers; photochromism

Indexed keywords

COOPERATIVITY; FOLDAMERS; PHOTO-SWITCHABLE;

AMPHIPHILES; PHOTOCHROMISM;

AZOBENZENE;

EID: 84865012469     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201201624     Document Type: Article

References (42)

1. Organic Photochromes (Ed.:, A. V. El'tsov,), Consultants Bureau, New York, 1990
2. Photochromism: Molecules and Systems (Eds.:, H. Dürr, H. Bouas-Laurent,), Elsevier, 2003
3. Molecular Switches, 2nd ed., (Ed.: B. L. Feringa,), Wiley-VCH: Weinheim, 2011
4. S. Hecht, Small 2004, 1, 26-29
5. M.-M. Russew, S. Hecht, Adv. Mater. 2010, 22, 3348-3360
6. R. S. Stoll, S. Hecht, Angew. Chem. 2010, 122, 5176-5200
7. Angew. Chem. Int. Ed. 2010, 49, 5054-5075.
8. V. Ferri, M. Elbing, G. Pace, M. Dickey, M. Zharnikov, P. Samorì, M. Mayor, M. Rampi, Angew. Chem. 2008, 120, 3455-3457
9. Angew. Chem. Int. Ed. 2008, 47, 3407-3409
10. M. Yamada, M. Kondo, J.-I. Mamiya, Y. Yu, M. Kinoshita, C. Barrett, T. Ikeda, Angew. Chem. 2008, 120, 5064-5066
11. Angew. Chem. Int. Ed. 2008, 47, 4986-4988.
12. R. Siewertsen, H. Neumann, B. Buchheim-Stehn, R. Herges, C. Näther, F. Renth, F. Temps, J. Am. Chem. Soc. 2009, 131, 15594-15595
13. M. Böckmann, N. L. Doltsinis, D. Marx, Angew. Chem. 2010, 122, 3454-3456
14. Angew. Chem. Int. Ed. 2010, 49, 3382-3384
15. A. A. Beharry, O. Sadovski, G. A. Woolley, J. Am. Chem. Soc. 2011, 133, 19684-19687.
16. D. Bléger, J. Dokić, M. Peters, L. Grubert, P. Saalfrank, S. Hecht, J. Phys. Chem. B 2011, 115, 9930-9940
17. D. Bléger, T. Liebig, R. Thiermann, M. Maskos, J. P. Rabe, S. Hecht, Angew. Chem. 2011, 123, 12767-12771
18. Angew. Chem. Int. Ed. 2011, 50, 12559-12563.
19. A. Khan, C. Kaiser, S. Hecht, Angew. Chem. 2006, 118, 1912-1915
20. Angew. Chem. Int. Ed. 2006, 45, 1878-1881
21. A. Khan, S. Hecht, Chem. Eur. J. 2006, 12, 4764-4774
22. Z. Yu, S. Hecht, Angew. Chem. 2011, 123, 1678-1681
23. Angew. Chem. Int. Ed. 2011, 50, 1640-1643.
24. C. Tie, J. C. Gallucci, J. R. Parquette, J. Am. Chem. Soc. 2006, 128, 1162-1171
25. E. D. King, P. Tao, T. T. Sanan, C. M. Hadad, J. R. Parquette, Org. Lett. 2008, 10, 1671-1674
26. Y. Hua, A. H. Flood, J. Am. Chem. Soc. 2010, 132, 12838-12840.
27. D. J. Hill, M. J. Mio, R. B. Prince, T. S. Hughes, J. S. Moore, Chem. Rev. 2001, 101, 3893-4012.
28. R. B. Prince, J. G. Saven, P. G. Wolynes, J. S. Moore, J. Am. Chem. Soc. 1999, 121, 3114-3121.
29. S. Lahiri, J. L. Thompson, J. S. Moore, J. Am. Chem. Soc. 2000, 122, 11315-11319.
30. R. B. Prince, L. Brunsveld, E. W. Meijer, J. S. Moore, Angew. Chem. 2000, 112, 234-236
31. Angew. Chem. Int. Ed. 2000, 39, 228-230
32. R. B. Prince, J. S. Moore, L. Brunsveld, E. W. Meijer, Chem. Eur. J. 2001, 7, 4150-4154.
33. L. Brunsveld, E. W. Meijer, R. B. Prince, J. S. Moore, J. Am. Chem. Soc. 2001, 123, 7978-7984
34. 2O aqueous acetonitrile solution was determined to be >4 μ M; see
35. M. T. Stone, J. M. Heemstra, J. S. Moore, Acc. Chem. Res. 2006, 39, 11-20.
36. R. B. Prince, S. A. Barnes, J. S. Moore, J. Am. Chem. Soc. 2000, 122, 2758-2762.
37. J. D. Badjić, A. Nelson, S. J. Cantrill, W. B. Turnbull, J. F. Stoddart, Acc. Chem. Res. 2005, 38, 723-732
38. C. A. Hunter, H. L. Anderson, Angew. Chem. 2009, 121, 7624-7636
39. Angew. Chem. Int. Ed. 2009, 48, 7488-7499.
40. For related observations, see:, L.-X. Liao, F. Stellacci, D. V. McGrath, J. Am. Chem. Soc. 2004, 126, 2181-2185.
41. R. A. Mathies, S. W. Lin, J. B. Ames, W. T. Pollard, Annu. Rev. Biophys. Biophys. Chem. 1991, 20, 491-518.
42. D. Bléger, Z. Yu, S. Hecht, Chem. Commun. 2011, 47, 12260-12266.