Direct UV-induced functionalization of surface hydroxy groups by thiol-ol chemistry

Angewandte Chemie - International Edition

Volumn 53, Issue 15, 2014, Pages 3835-3839

  Li, Linxian ^a,b   Li, Junsheng ^a,b   Du, Xin ^a,b   Welle, Alexander ^a   Grunze, Michael ^a,b   Trapp, Oliver ^b   Levkin, Pavel A ^a,b  

^a KARLSRUHE INSTITUTE OF TECHNOLOGY   (Germany)

^b UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

alcohols; photochemistry; photopatterning; surface chemistry; thiols

Indexed keywords

ALCOHOLS; AMINO ACIDS; ETHYLENE; MOLECULES; PHOTOCHEMICAL REACTIONS; POLYETHYLENE GLYCOLS; SURFACE CHEMISTRY;

CYSTEINE-CONTAINING PEPTIDES; DOUBLE PATTERNING; FUNCTIONAL MOLECULES; FUNCTIONALIZATIONS; PHOTO PATTERNING; PHOTOCHEMICAL MODIFICATIONS; SURFACE MODIFICATION METHODS; THIOLS;

FUNCTIONAL GROUPS;

EID: 84898059643     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201310692     Document Type: Article

References (57)

1. J. S. Li, E. Ueda, A. Nallapaneni, L. X. Li, P. A. Levkin, Langmuir 2012, 28, 8286-8291
2. H. S. Lim, D. Kwak, D. Y. Lee, S. G. Lee, K. Cho, J. Am. Chem. Soc. 2007, 129, 4128-4129
3. T. Sun, G. Wang, L. Feng, B. Liu, Y. Ma, L. Jiang, D. Zhu, Angew. Chem. 2004, 116, 361-364
4. Angew. Chem. Int. Ed. 2004, 43, 357-360.
5. X. P. Deng, C. Friedmann, J. Lahann, Angew. Chem. 2011, 123, 6652-6656
6. Angew. Chem. Int. Ed. 2011, 50, 6522-6526
7. A. M. Ross, D. Zhang, X. P. Deng, S. L. Chang, J. Lahann, Anal. Chem. 2011, 83, 874-880
8. H. Y. Chen, J. H. Lai, X. W. Jiang, J. Lahann, Adv. Mater. 2008, 20, 3474-3480.
9. D. Meinhold, R. Schweiss, S. Zschoche, A. Janke, A. Baier, F. Simon, H. Dorschner, C. Werner, Langmuir 2004, 20, 396-401
10. R. A. M. Hikmet, R. Thomassen, Adv. Mater. 2003, 15, 115-117.
11. B. V. Di Carlo, A. C. Habert, J. Mater. Sci. 2013, 48, 1457-1464
12. D. V. Bax, Y. W. Wang, Z. Li, P. K. M. Maitz, D. R. McKenzie, M. M. M. Bilek, A. S. Weiss, Biomaterials 2011, 32, 5100-5111
13. D. V. Bax, D. R. McKenzie, A. S. Weiss, M. M. M. Bilek, Biomaterials 2010, 31, 2526-2534
14. C. Satriano, M. Edvardsson, G. Ohlsson, G. Wang, S. Svedhem, B. Kasemo, Langmuir 2010, 26, 5715-5725.
15. D. Zahner, J. Abagat, F. Svec, J. M. J. Fréchet, P. A. Levkin, Adv. Mater. 2011, 23, 3030-3034
16. M. Bouriga, M. M. Chehimi, C. Combellas, P. Decorse, F. Kanoufi, A. Deronzier, J. Pinson, Chem. Mater. 2013, 25, 90-97
17. J. Balart, V. Fombuena, T. Boronat, M. J. Reig, R. Balart, J. Mater. Sci. 2012, 47, 2375-2383
18. A. Berisha, C. Combellas, G. Hallais, F. Kanoufi, J. Pinson, F. I. Podvorica, Chem. Mater. 2011, 23, 3449-3459
19. M. Källrot, U. Edlund, A. C. Albertsson, Biomaterials 2006, 27, 1788-1796
20. Y. L. Wang, H. H. Lai, M. Bachman, C. E. Sims, G. P. Li, N. L. Allbritton, Anal. Chem. 2005, 77, 7539-7546
21. B. Ranby, Macromol. Symp. 1992, 63, 55
22. T. Rohr, E. F. Hilder, J. J. Donovan, F. Svec, J. M. J. Frechet, Macromolecules 2003, 36, 1677-1684
23. F. L. Geyer, E. Ueda, U. Liebel, N. Grau, P. A. Levkin, Angew. Chem. 2011, 123, 8575-8578
24. Angew. Chem. Int. Ed. 2011, 50, 8424-8427
25. J. E. Poelma, B. P. Fors, G. F. Meyers, J. W. Kramer, C. J. Hawker, Angew. Chem. 2013, 125, 6982-6986
26. Angew. Chem. Int. Ed. 2013, 52, 6844-6848.
27. R. M. Hensarling, V. A. Doughty, J. W. Chan, D. L. Patton, J. Am. Chem. Soc. 2009, 131, 14673-14675
28. C. Wendeln, S. Rinnen, C. Schulz, H. F. Arlinghaus, B. J. Ravoo, Langmuir 2010, 26, 15966-15971
29. J. T. Wu, C. H. Huang, W. C. Liang, Y. L. Wu, J. S. Yu, H. Y. Chen, Macromol. Rapid Commun. 2012, 33, 922-927.
30. M. Glassner, K. K. Oehlenschlaeger, A. Welle, M. Bruns, C. Barner-Kowollik, Chem. Commun. 2013, 49, 633-635.
31. M. Dietrich, G. Delaittre, J. P. Blinco, A. J. Inglis, M. Bruns, C. Barner-Kowollik, Adv. Funct. Mater. 2012, 22, 304-312.
32. T. Gong, B. J. Adzima, N. H. Baker, C. N. Bowman, Adv. Mater. 2013, 25, 2024-2028
33. B. J. Adzima, Y. H. Tao, C. J. Kloxin, C. A. DeForest, K. S. Anseth, C. N. Bowman, Nat. Chem. 2011, 3, 256-259.
34. T. Pauloehrl, G. Delaittre, M. Bruns, M. Meissler, H. G. Borner, M. Bastmeyer, C. Barner-Kowollik, Angew. Chem. 2012, 124, 9316-9319
35. Angew. Chem. Int. Ed. 2012, 51, 9181-9184.
36. M. P. Stewart, J. M. Buriak, J. Am. Chem. Soc. 2001, 123, 7821-7830
37. M. P. Stewart, J. M. Buriak, Angew. Chem. 1998, 110, 3447-3450
38. Angew. Chem. Int. Ed. 1998, 37, 3257-3260.
39. S. J. Pastine, D. Okawa, B. Kessler, M. Rolandi, M. Llorente, A. Zettl, J. M. J. Frechet, J. Am. Chem. Soc. 2008, 130, 4238-4239.
40. B. S. Chiou, S. A. Khan, Macromolecules 1997, 30, 7322-7328
41. O. Okay, S. K. Reddy, C. N. Bowman, Macromolecules 2005, 38, 4501-4511
42. T. Y. Lee, T. M. Roper, E. S. Jonsson, C. A. Guymon, C. E. Hoyle, Macromolecules 2004, 37, 3606-3613
43. N. B. Cramer, T. Davies, A. K. O'Brien, C. N. Bowman, Macromolecules 2003, 36, 4631-4636
44. V. S. Khire, A. W. Harant, A. W. Watkins, K. S. Anseth, C. N. Bowman, Macromolecules 2006, 39, 5081-5086
45. A. W. Harant, V. S. Khire, M. S. Thibodaux, C. N. Bowman, Macromolecules 2006, 39, 1461-1466.
46. B. D. Fairbanks, T. F. Scott, C. J. Kloxin, K. S. Anseth, C. N. Bowman, Macromolecules 2009, 42, 211-217
47. G. J. Chen, J. Kumar, A. Gregory, M. H. Stenzel, Chem. Commun. 2009, 6291-6293
48. C. E. Hoyle, A. B. Lowe, C. N. Bowman, Chem. Soc. Rev. 2010, 39, 1355-1387
49. R. Hoogenboom, Angew. Chem. 2010, 122, 3489-3491
50. Angew. Chem. Int. Ed. 2010, 49, 3415-3417
51. A. B. Lowe, C. E. Hoyle, C. N. Bowman, J. Mater. Chem. 2010, 20, 4745-4750
52. D. Konkolewicz, A. Gray-Weale, S. Perrier, J. Am. Chem. Soc. 2009, 131, 18075-18077.
53. E. Robert-Banchereau, S. Lacombe, J. Ollivier, Tetrahedron 1997, 53, 2087-2102
54. E. Robert-Banchereau, S. Lacombe, J. Ollivier, J. C. Micheau, D. Lavabre, Int. J. Chem. Kinet. 1997, 29, 825-834.
55. A. N. Efremov, E. Stanganello, A. Welle, S. Scholpp, P. A. Levkin, Biomaterials 2013, 34, 1757-1763
56. E. Ueda, F. L. Geyer, V. Nedashkivska, P. A. Levkin, Lab Chip 2012, 12, 5218-5224.
57. S. Lacombe, H. Cardy, M. Simon, A. Khoukh, J. P. Soumillion, M. Ayadim, Photochem. Photobiol. Sci. 2002, 1, 347-354.