Charge-transfer host complex with channel-like cavity using disubstituted-1,1′-bi-2-naphthol and benzylviologen

Tetrahedron Letters

Volumn 50, Issue 42, 2009, Pages 5786-5789

  Kinuta, Takafumi ^a   Kise, Yuko ^a   Kamon, Kensaku ^a   Tajima, Nobuo ^b   Sato, Tomohiro ^c   Kuroda, Reiko ^c,d   Matsubara, Yoshio ^a   Imai, Yoshitane ^a  

^a KINKI UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE FOR MATERIALS SCIENCE   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

1,1 Bi 2 naphthol; CT complex; Host guest; Supramolecular host complex; Viologen

Indexed keywords

2,2' DIHYDROXY 1,1' BINAPHTHYL; 3,3' DIHYDROXY 1,1' BI 2 NAPHTHOL; ALCOHOL; BENZYLVIOLOGEN; METHANOL; UNCLASSIFIED DRUG; VIOLOGEN;

ADSORPTION; ARTICLE; COLOR; COMPLEX FORMATION; CRYSTAL STRUCTURE; REACTION ANALYSIS; SUPRAMOLECULAR CHEMISTRY; SYNTHESIS; X RAY POWDER DIFFRACTION;

EID: 69449086687     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.07.090     Document Type: Article

References (21)

1. In: Atwood J.L., Davies J.E.D., and MacNicol D.D. (Eds). Inclusion Compounds Vols. 1-3 (1984), Academic Press, New York
2. Walba D.M., Clark N.A., Razavi H.A., and Parmar D.S. In: Atwood J.L. (Ed). Inclusion Phenomenon and Molecular Recognition (1990), Plenum Press, New York
3. Lehn J.-M. Supramolecular Chemistry (1995), Wiley-VCH
4. In: Lehn J.-M., Atwood J.L., Davies J.E.D., MacNicol D.D., and Vogtle F. (Eds). Comprehensive Supramolecular Chemistry Vols. 1-11 (1996), Pergamon Press, Oxford
5. In: Atwood J.L., and Steed J.W. (Eds). Encyclopedia of Supramolecular Chemistry (2004), Mercel Dekker, New York
6. In: Toda F., and Bishop R. (Eds). Perspectives in Supramolecular Chemistry Vol. 8 (2004), John Wiley & Sons, Chichester, UK
7. Choi H.J., and Suh M.P. J. Am. Chem. Soc. 126 (2004) 15844-15851
8. Ohmori O., Kawano M., and Fujita M. J. Am. Chem. Soc. 126 (2004) 16292-16293
9. Moon H.R., Kim J.H., and Suh M.P. Angew. Chem., Int. Ed. 44 (2005) 1261-1265
10. Suh M.P., Moon H.R., Lee E.Y., and Jang S.Y. J. Am. Chem. Soc. 128 (2006) 4170-4718
11. Shimomura S., Matsuda R., Tsujino T., Kawamura T., and Kitagawa S. J. Am. Chem. Soc. 126 (2006) 15844-15851
12. Kuroda R., Imai Y., and Sato T. Chirality 13 (2001) 588-594
13. Imai Y., Tajima N., Sato T., and Kuroda R. Chirality 14 (2002) 604-609
14. Toda F., Senzaki M., and Kuroda R. Chem. Commun. (2002) 1788-1789
15. Imai Y., Tajima N., Sato T., and Kuroda R. Org. Lett. 8 (2006) 2941-2944
16. Imai Y., Kamon K., Kinuta T., Tajima N., Sato T., Kuroda R., and Matsubara Y. Cryst. Growth Des. 8 (2008) 3493-3496
17. Imai Y., Kinuta T., Sato T., Tajima N., Kuroda R., Matsubara Y., and Yoshida Z.-i. Tetrahedron Lett. 47 (2006) 3603-3606
18. 2 (11 mg)] were deposited and collected. The weight of each type of crystal is the total crop of the crystals obtained in a single batch.
19. 2) = 0.0883 using 7400 reflections with I > 2.0σ(I), R(all data) = 0.1012, T = 115(2) K. CCDC 724938.
20. It is determined by PLATON geometry calculation.
21. 2) = 0.0776 using 5519 reflections with I > 2.0σ(I), R(all data) = 0.1257, T = 130(2) K. CCDC 724939. Crystallographic data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB21EZ, UK; fax: (+44)1223 336 033; deposit@ccdc.cam.ac.uk).