The ugi four-component reaction route to photoinducible electron-transfer systems

ChemPlusChem

Volumn 78, Issue 2, 2013, Pages 137-141

  Bay, Sarah ^a   Villnow, Torben ^a   Ryseck, Gerald ^a   Rai Constapel, Vidisha ^a   Gilch, Peter ^a   Müller, Thomas J J ^a  

^a HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

chromophores; cyclic voltammetry; electron transfer; femtosecond spectroscopy; fluorescence spectroscopy; multicomponent reactions

Indexed keywords

EID: 84874164345     PISSN: None     EISSN: 21926506     Source Type: Journal    
DOI: 10.1002/cplu.201200279     Document Type: Article

References (58)

1. Functional Organic Materials. Syntheses, Strategies, and Applications (Eds.:, T.J.J. Müller, U.H.F. Bunz,), Wiley-VCH, Weinheim, 2007.
2. Introduction to Molecular Electronics (Eds.:, M.C. Petty, M.R. Bryce, D. Bloor,), Oxford University Press, New York, 1995
3. V. Balzani, A. Credi, M. Venturi, Molecular Devices and Machines-A Journey into the Nano World, Wiley-VCH, Weinheim, 2003.
4. H. Hoppe, N. S. Sariciftci, J. Mater. Res. 2004, 19, 1924-1945
5. X. Sun, Y. Liu, X. Xu, C. Yang, G. Yu, S. Chen, Z. Zhao, W. Qiu, Y. Li, D. Zhu, J. Phys. Chem. B 2005, 109, 10786-10792
6. P. Sonar, J. P. F. Lim, K. L. Chan, Energy Environ. Sci. 2011, 4, 1558-1574
7. B. Walker, C. Kim, T.-Q. Nguyen, Chem. Mater. 2011, 23, 470-482
8. Y. Lin, Y. Lia, X. Zhan, Chem. Soc. Rev. 2012, 41, 4245-4272.
9. G. J. Kavarnos, Fundamentals of Photoinduced Electron Transfer, VCH Publishers Inc., New York, 1993
10. J. H. Alstrum-Acevedo, M. K. Brennaman, T. J. Meyer, Inorg. Chem. 2005, 44, 6802-6827
11. O. S. Wenger, Chem. Soc. Rev. 2011, 40, 3538-3550
12. H. Lemmetyinen, N. V. Tkachenko, A. Efimov, M. Niemi, Phys. Chem. Chem. Phys. 2011, 13, 397-412
13. E. Vauthey, ChemPhysChem 2012, 13, 2001-2011
14. A. B. Ricks, K. E. Brown, M. Wenninger, S. D. Karlen, Y. A. Berlin, D. T. Co, M. R. Wasielewski, J. Am. Chem. Soc. 2012, 134, 4581-4588.
15. L. F. Dössel, V. Kamm, I. A. Howard, F. Laquai, W. Pisula, X. Feng, C. Li, M. Takase, T. Kudernac, S. DeFeyter, K. Müllen, J. Am. Chem. Soc. 2012, 134, 5876-5886.
16. D. Wrõbel, A. Graja, Coord. Chem. Rev. 2011, 255, 2555-2577.
17. Y. Sasaki, Y. Araki, O. Ito, M. M. Alam, Photochem. Photobiol. Sci. 2007, 6, 560-565
18. C. V. Suneesh, K. R. Gopidas, J. Phys. Chem. C 2010, 114, 18725-18734
19. T. Miura, R. Carmieli, M. R. Wasielewski, J. Phys. Chem. A 2010, 114, 5769-5778
20. Z. Li, Q. Dong, Y. Li, B. Xu, M. Deng, J. Pei, J. Zhang, F. Chen, S. Wen, Y. Gao, W. Tian, J. Mater. Chem. 2011, 21, 2159-2168.
21. H. Imahori, Y. Mori, Y. Matano, J. Photochem. Photobiol. C 2003, 4, 51-83
22. M. S. Rodríguez-Morgade, M. E. Plonska-Brzezinska, A. J. Athans, E. Carbonell, G. deMiguel, D. M. Guldi, L. Echegoyen, T. Torres, J. Am. Chem. Soc. 2009, 131, 10484-10496
23. A. S. D. Sandanayaka, H. Sasabe, T. Takata, O. Ito, J. Photochem. Photobiol. C 2010, 11, 73-92.
24. M. R. Wasielewski, Chem. Rev. 1992, 92, 435-461
25. H. Kurreck, M. Huber, Angew. Chem. 1995, 107, 929-947
26. Angew. Chem. Int. Ed. Engl. 1995, 34, 849-866
27. A. Gouloumis, D. González-Rodrbox drawings light down and leftguez, P. Vázquez, T. Torres, S. Liu, L. Echegoyen, J. Ramey, G. L. Hug, D. M. Guldi, J. Am. Chem. Soc. 2006, 128, 12674-12684
28. J. Wan, A. Ferreira, W. Xia, C. H. Chow, K. Takechi, P. V. Kamat, G. Jones, V. I. Vullev, J. Photochem. Photobiol. A 2008, 197, 364-374
29. Y. K. Kang, P. M. Iovine, M. J. Therien, Coord. Chem. Rev. 2011, 255, 804-824
30. J. Hankache, O. S. Wenger, Phys. Chem. Chem. Phys. 2012, 14, 2685-2692.
31. 60-phenothiazine dyads, see for example
32. N. Bucci, T. J. J. Müller, Tetrahedron Lett. 2006, 47, 8329-8332
33. N. Bucci, T. J. J. Müller, Tetrahedron Lett. 2006, 47, 8323-8327.
34. D. G. McCafferty, B. M. Bishop, C. G. Wall, S. G. Hughes, S. M. Mecklenburg, T. J. Meyer, B. W. Erickson, Tetrahedron 1995, 51, 1093-1106
35. D. R. Striplin, S. Y. Reece, D. G. McCafferty, C. G. Wall, D. A. Friesen, B. W. Erickson, T. J. Meyer, J. Am. Chem. Soc. 2004, 126, 5282-5291
36. C. P. Myers, M. E. Williams, Coord. Chem. Rev. 2010, 254, 2416-2428.
37. W.-W. Zhang, W.-L. Mao, Y.-X. Hu, Z.-Q. Tian, Z.-L. Wang, Q.-J. Meng, J. Phys. Chem. A 2009, 113, 9997-10004.
38. A. Dömling, I. Ugi, Angew. Chem. 2000, 112, 3300-3344
39. Angew. Chem. Int. Ed. 2000, 39, 3168-3210
40. A. Dömling, Chem. Rev. 2006, 106, 17-89
41. J. E. Biggs-Houck, A. Younai, J. T. Shaw, Curr. Opin. Chem. Biol. 2010, 14, 371-382.
42. A. Dömling, W. Wang, K. Wang, Chem. Rev. 2012, 112, 3083-3135.
43. L. N. Mataranga-Popa, A. W. Franz, S. Bay, T. J. J. Müller, Lett. Org. Chem. 2012, 9, 211-217.
44. D. Rehm, A. Weller, Z. Phys. Chem. (Muenchen Ger.) 1970, 69, 183-200.
45. C. S. Krämer, T. J. J. Müller, Eur. J. Org. Chem. 2003, 3534-3548
46. M. Sailer, A. W. Franz, T. J. J. Müller, Chem. Eur. J. 2008, 14, 2602-2614.
47. J. Shirdel, A. Penzkofer, R. Procházka, Z. Shen, J. Daub, Chem. Phys. 2007, 336, 1-13.
48. S. Laimgruber, H. Schachenmayr, B. Schmidt, W. Zinth, P. Gilch, Appl. Phys. B 2006, 85, 557-564
49. T. Schmierer, G. Ryseck, T. Villnow, N. Regner, P. Gilch, Photochem. Photobiol. Sci. 2012, 11, 1313-1321.
50. R. G. Compton, B. A. Coles, M. B. G. Pilkington, D. J. Bethell, J. Chem. Soc. Faraday Trans. 1990, 86, 663-670
51. H. J. vanRamesdonk, B. H. Bakker, M. M. Groeneveld, J. W. Verhoeven, B. D. Allen, J. P. Rostron, A. Harriman, J. Phys. Chem. A 2006, 110, 13145-13150
52. R. Frank, G. Greiner, H. Rau, Phys. Chem. Chem. Phys. 1999, 1, 3481-3490.
53. A. Lauer, A. L. Dobryakov, S. A. Kovalenko, H. Fidder, K. Heyne, Phys. Chem. Chem. Phys. 2011, 13, 8723-8732.
54. U. E. Steiner, T. Ulrich, Chem. Rev. 1989, 89, 51-146.
55. G. A. Zalesskaya, S. I. Blinov, Sov. Phys. Dokl. 1985, 30, 297-299.
56. W. G. Herkstroeter, A. A. Lamola, G. S. Hammond, J. Am. Chem. Soc. 1964, 86, 4537-4540.
57. R. A. Marcus, Rev. Mod. Phys. 1993, 65, 599-610
58. A. Nitzan, Chemical Dynamics in Condensed Phases, Oxford University Press, Oxford, 2006.