β-1,3-glucan polysaccharide (schizophyllan) acting as a one-dimensional host for creating supramolecular dye assemblies

Organic Letters

Volumn 8, Issue 24, 2006, Pages 5533-5536

  Numata, Munenori ^a   Tamesue, Shingo ^a   Fujisawa, Tomohisa ^a   Haraguchi, Shuichi ^a   Hasegawa, Teruaki ^a   Bae, Ah Hyun ^a   Li, Chun ^a,c   Sakurai, Kazuo ^b   Shinkai, Seiji ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b UNIVERSITY OF KITAKYUSHU   (Japan)

^c TSINGHUA UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33846018029     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol062229a     Document Type: Article

References (23)

1. (a) Würthner, F.; Yao, S.; Beginn, U. Angew. Chem., Int. Ed. 2003, 42, 3247.
2. (b) Parins, L. J.; Thalacker, C.; Würthner, F.; Timmerman, P.; Reinhoudt, D. N. Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 10042.
3. (c) Jones, R. M.; Lu, L.; Helgeson, R.; Bergstedt, T. S.; McBranch, D. W.; Whitten, D. G. Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 14769.
4. (d) Yao, S.; Beginn, U.; Gress, T.; Lysetska, M.; Würthner, F. J. Am. Chem. Soc. 2004, 126, 8336.
5. (e) Morikawa, M.-a.; Yoshihara, M.; Endo, T.; Kimizuka, N. J. Am. Chem. Soc. 2005, 127, 1358.
6. (a) Hannah, K. C.; Armitage, B. A. Acc. Chem. Res. 2004, 37, 845 and references cited therein.
7. (b) Amylose has been utilized as an effective template for a dye assembly formation: Heuer, W. B.; Kim, O.-K. Chem. Commun. 1998, 2649.
8. (c) Clays, K.; Olbrechts, G.; Munters, T.; Persoons, A.; Kim, O.-K.; Choi, L.-S. Chem. Phys. Lett. 1998, 293, 337.
9. Yanaki, T.; Norisue, T.; Fujita, M. Macromolecules 1980, 13, 1462.
10. (a) Numata, M.; Asai, M.; Kaneko, K.; Hasegawa, T.; Fujita, N.; Kitada, Y.; Sakurai, K.; Shikai, S. Chem. Lett. 2004, 33, 232.
11. (b) Numata, M.; Asai, M.; Kaneko, K.; Bae, A.-H.; Hasegawa, T.; Sakurai, K.; Shinkai, S. J. Am. Chem. Soc. 2005, 127, 5875.
12. (c) Numata, M.; Hasegawa, T.; Fujisawa, T.; Sakurai, K.; Shinkai, S. Org. Lett. 2004, 6, 4447.
13. (d) Bae, A.-B.; Numata, M.; Hasegawa, T.; Li, C.; Sakurai, K.; Shinkai, S. Angew. Chem., Int. Ed. 2005, 44, 2030.
14. (e) Li, C.; Numata, M.; Bae, A.-H.; Sakurai, K.; Shinkai, S. J. Am. Chem. Soc. 2005, 127, 4548.
15. (f) Hasegawa, T.; Haraguchi, S.; Numata, M.; Fujisawa, T.; Li, C.; Kaneko, K.; Sakurai, K.; Shinkai, S. Chem. Lett. 2005, 34, 40.
16. (g) Sakurai, K.; Uezu, K.; Numata, M.; Hasegawa, T.; Li, C.; Kenji, K.; Shinkai, S. Chem. Commun. 2005, 4383.
17. Similar molecular designs have already been reported: (a) Aoki, K.; Nakagawa, M.; Ichimura, K. J. Am. Chem. Soc. 2000, 122, 10997.
18. (b) Aoki, K.; Nakagawa, M.; Seki, T.; Ichimura, K. Chem. Lett. 2002, 378.
19. (c) Nakagawa, M.; Ishii, D.; Aoki, K.; Seki, T.; Iyoda, T. Adv. Mater. 2005, 17, 200.
20. -1). From an LB plot at 446 nm, it is confirmed that no aggregate is formed at the concentration range used.
21. -1. For related papers, see: Tanaka, S.; Shirakawa, M.; Kaneko, K.; Takeuchi, M.; Shinkai, S. Langmuir 2005, 21, 2163 and references cited therein.
22. Similar morphologies were confirmed in TEM images (Supporting Information, Figure S4).
23. 1c