寄稿論文 ナノスケールの孤独空間を有する包接化合物 ～カプセル分子～ | 東京化成工業
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1 2
2 Gutsche Cone 3
3 ebek, Jr. Cone upper rim 6a 6b Donor - AcceptorFET Fluorescence esonance Energy Transfer 4
4 Pd(II) Pt(II) Stang Pd(II) Pt(II) 5
5
6 12 M Pd(II) Pt(II) 14 Dalcanale 7
7 2+ 2+ C C C C Ph 2 P PPh 2 Pd 2CF 3 S - 3 LM = Pd Ph 2 P P Ph 2 or Ph 2 P PPh 2 Pt 2CF 3 S - 3 or Pt Ph 2 P P Ph 2 C C C C LM LM ML ML C C C C AFM 8
8 DA DA 9
9 PVP DA PVP DA PVP 13 DA dyad triad triad 10
10 Lehn Stang Pd(II) Pt(II) Pd(II) Pd(II) 15 16b Pd(II) 11
11 12
12 Fe(II) Fe(II) Fe II Ph 2 Ph C Ph 2 FeII Ph C Ph Ph ai KI I - I - Zn KI
13 C4 einhoudt 23 upper-rim Zn(II) Zn 26 14
14 15
15 1) D. J. Cram, J. M. Cram, Container Molecules and Their Guests, Monographs in Supramolecular Chemistry. 2) C. D. Gutsche, Acc. Chem. es., 16, 161 (1983). 3) A. Ikeda, S. Shinkai, Chem. ev., 97, 1713 (1997). 4) F. Hof, S. L. Craig, C. uckolls, J. ebeck, Jr., Angew. Chem. Int. Ed., 41, 1488 (2002). 5) K. Koh, K. Araki, S. Shinkai, Tetrahedron Lett., 44, 8255 (1994). 6) a) A. Arduini, M. Fabbi, M. Mantovani, L. Mirone, A. Pochini, A. Secchi,. Ungaro, J. rg. Chem., 60, 1454 (1995). b) A. Arduini, L. Domiano, L. gliosi, A. Pochini, A. Secchi,. Ungaro, J. rg. Chem., 62, 1454 (1997). c). Struck, W. Verboom, W. J. Smeets, A. J. Spek, D.. einhoudt, J. Chem. Soc., Perkin Trans. 2, 1997, ) a) K. D. Shimizu, J. ebek, Jr., Proc. atl. Acad. Sci. U. S. A., 92, (1995). b) B. C. Hamman, K. D. Shimizu, J. ebek, Jr., Angew. Chem. Int. Ed. Engl., 35, 1326, (1996). c). K. Castellano, D. M. udkevich, J. ebek, Jr., Proc. atl. Acad. Sci. U. S. A., 94, 7132 (1997). d). K. Castellano, J. ebek, Jr., J. Am. Chem. Soc., 120, 3657 (1998). e). K. Castellano, C. uckolls, S. H. Eichhorn, M.. Wood, A. J. Lovinger, J. ebek, Jr., Angew. Chem. Int. Ed. Engl., 38, 2603 (1999). 8). K. Castellano, S. L. Craig, C. uckolls, J. ebek, Jr., J. Am. Chem. Soc., 122, 7876 (2000). 9) a) M. Fujita, Chem. Soc. ev., 27, 417 (1998). b). Takeda, K. Umemoto, K. Yamaguchi, M. Fujita, ature, 398, 794 (1999). c) M. Fujita, S. agao, K. gura, J. Am. Chem. Soc., 117, 1649 (1995). d) S. Leininger, B. lenyuk, Stang, P. J., Chem. ev., 100, 853 (2000). 10) a) Z. L. Zhong, A. Ikeda, M. Ayabe, S. Shinkai, S. Sakamoto, K. Yamaguchi, J. rg. Chem., 66, 1002 (2001). b) Z. L. Zhong, A. Ikeda, S. Shinkai, S. Sakamoto, K. Yamaguchi., rg. Lett., 3, 1085 (2001). 11) A. Ikeda, M. Yoshimura, F. Tani, Y. aruta, S. Shinkai, Chem. Lett., 1998, ) A. Ikeda, M. Yoshimura, H. Udzu, C. Fukuhara, S. Shinkai, J. Am. Chem. Soc., 121, 4296 (1999). 13) A. Ikeda, M. Yoshimura, H. Udzu, S. Shinkai, Tetrahedron, 56, 1825 (2000). 14) a) K. Kobayashi, T. Shirasaka, K. Yamaguchi, S. Sakamoto, E. Horn,. Furukawa, Chem. Commun., 2000, 41. b). G. Chapman, J. C. Sherman, J. Am. Chem. Soc., 120, 9818 (1998). c) A. Shivanyuk, E. F. Paulus, V. Bohmer, Angew. Chem. Int. Ed., 38, 2906 (1999). 15) P. Jacopozzi, E. Dalcanale, Angew. Chem. Int. Ed. Engl., 36, 613 (1997). 16) F. Fochi, P. Jacopozzi, E. Wegelius, K. issanen, P. Cozzini, E. Marastoni, E. Fisicaro, P. Manini,. Fokkens, E. Dalcanale, J. Am. Chem. Soc., 123, 7539 (2001). 17) S. A. Levi, P. Guatteri, F. C. J. M. van Veggel, G. J. Vancso, E. Dalcanale, D.. einhoudt., Angew. Chem. Int. Ed., 40, 1892 (2001). 18) S. D. M. Islam, M. Fujitsuka,. Ito, A. Ikeda, T. Hatano, S. Shinkai, Chem. Lett., 2000, ) A. Ikeda, T. Hatano, M. Kawaguchi, H. Suenaga, S. Shinkai, Chem. Commun., 1999, ) T. Hatano, A. Ikeda, T. Akiyama, S. Yamada, M. Sano, Y. Kanekiyo, S. Shinkai, J. Chem. Soc., Perkin Trans. 2, 2000, ) A. Ikeda, T. Hatano, S. Shinkai, T. Akiyama, S. Yamada, J. Am. Chem. Soc., 123, 4855 (2001). 16
16 22) a) K. Uosaki, T. Kondo, X. Q. Zhang, M. Yanagida, J. Am. Chem. Soc., 119, 8367 (1997). b) H. Imahori, H. Yamada, S. zawa, K. Ushida, Y. Sakata, Chem. Commun., 1999, c) H. Imahori, H. Yamada, Y. ishimura, I. Yamazaki, Y. Sakata, J. Phys. Chem. B, 104, 2099 (2000). d) A. omoto, Y. Kobuke, Chem. Commun., 2002, ) a) K. Tashiro, T. Aida, J.-Y. Zheng, K. Kinbara, K. Saigo, S. Sakamoto, K. Yamaguchi, J. Am. Chem. Soc., 121, 9477 (1999). b) T. ishioka, K. Tashiro, T. Aida, J.-Y. Zheng, K. Kinbara, K. Saigo, S. Sakamoto, K. Yamaguchi, Macromolecules, 33, 9182, (2000). c) M. Ayabe, A. Ikeda, Y. Kubo, M. Takeuchi, S. Shinkai, Angew. Chem. Int. Ed., 41, 2790, (2002). d) M. Ayabe, A. Ikeda, S. Shinkai, S. Sakamoto, K. Yamaguchi, Chem. Commun., 2002, ) a) S. Tamaru, M. akamura, M. Takeuchi, S. Shinkai, rg. Lett., 3, 3631 (2001). b) S. Tamaru, S. Uchino, M. Takeuchi, M. Ikeda, T. Hatano, S. Shinkai, Tetrahedron Lett., 43, 3751 (2002). 25) a) C. M. Drain, J. M. Lehn, J. Chem. Soc., Chem. Commun., 1994, b) P. J. Stang, J. Fan, B. lenyuk, Chem. Commun., 1997, c) J. Fan, J. A. Whiteford, B. lenyuk, M. D. Levin, P. J. Stang, E. B. Fleischer, J. Am. Chem. Soc., 121, 2741, (1999). 26) A. Ikeda, M. Ayabe, S. Shinkai, S. Sakamoto, K. Yamaguchi, rg. Lett., 2, 3707 (2000). 27) A. Ikeda, M. Ayabe, S. Shinkai, Chem. Lett., 2001, ). Kobayashi, K. Mizuno, T. sa, Inorg. Chim. Acta, 1, 224 (1994). 29) T. agasaki, H. Fujishima, M. Takeuchi, S. Shinkai, J. Chem. Soc., Perkin Trans. 1, 1995, ). Fiammengo, P. Timmerman, F. De Jong, D.. einhoudt, Chem. Commun., 2000, ) A. Ikeda, K. Sonoda, S. Shinkai, Chem. Lett., 2000, EAT ICP SST Izatt-Christensen Backer Lecture Vielberth Lectureship 17
4) H. Takayama et al.: J. Med. Chem., 45, 1949 (2002). 5) H. Takayama et al.: J. Am. Chem. Soc., 112, 8635 (2000). 6) H. Takayama et al.: Tetrahedron Lett., 42, 2995 (2001). 9) M. Kitajima et al: Chem.
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