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Volumn 7, Issue 6, 2005, Pages 971-974

Synthesis of 2,3-substituted tetracenes and evaluation of their self-assembling properties in organic solvents

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBON; ORGANIC SOLVENT;

EID: 18244408507     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol047526z     Document Type: Article
Times cited : (72)

References (38)
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    • Rodd, E.H.1
  • 11
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    • Academic Press: London, Chapter 23
    • (c) Clar, E. Polycyclic Hydrocarbons; Academic Press: London, 1964; Volume 1, Chapter 23, pp 386-422.
    • (1964) Polycyclic Hydrocarbons , vol.1 , pp. 386-422
    • Clar, E.1
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    • Thieme: New York, Chapter 4
    • (e) Houben-Weyl Methoden der Organischen Chemie; Thieme: New York, 1981; Bd 5/2b, Chapter 4, pp 359-470.
    • (1981) Houben-Weyl Methoden der Organischen Chemie , vol.5 , Issue.2 B , pp. 359-470
  • 20
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    • note
    • 3 of solvent was added to a weighed amount of gelator in a septum-capped test tube (ca. 4 cm length and 0.7 cm diameter) in order to obtain the desired concentration. The mixture was warmed to the boiling point until the solid dissolved, and then the mixture was allowed to cool to room temperature. When a gel was formed (generally within several minutes), the sample did not flow when the test tube was inverted.
  • 21
    • 0036274287 scopus 로고    scopus 로고
    • A "supergelator" is considered to have a cc ≈ 0.3-2.5 mM at rt according to Shinkai (Gronwald, O.; Snip, E.; Shinkai, S. Curr. Opin. Colloid Int. Sci. 2002, 7, 148-156) and Menger (Menger, F. M.; Caran, K. L. J. Am. Chem. Soc. 2000, 122, 11679-11691).
    • (2002) Curr. Opin. Colloid Int. Sci. , vol.7 , pp. 148-156
    • Gronwald, O.1    Snip, E.2    Shinkai, S.3
  • 22
    • 0034731020 scopus 로고    scopus 로고
    • A "supergelator" is considered to have a cc ≈ 0.3-2.5 mM at rt according to Shinkai (Gronwald, O.; Snip, E.; Shinkai, S. Curr. Opin. Colloid Int. Sci. 2002, 7, 148-156) and Menger (Menger, F. M.; Caran, K. L. J. Am. Chem. Soc. 2000, 122, 11679-11691).
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 11679-11691
    • Menger, F.M.1    Caran, K.L.2
  • 25
    • 18244362935 scopus 로고    scopus 로고
    • note
    • 10
  • 29
    • 0001011847 scopus 로고    scopus 로고
    • Hypochromic effects have been also observed in gels by others: (a) Kobayashi, H.; Friggeri, A.; Koumoto, K.; Amaikee, M.; Shinkai, S. Org. Lett. 2002, 4, 1423-1426. (b) Tamaru, S.; Nakamura, M.; Takeuchi, M.; Shinkai, S. Org. Lett. 2001, 3, 3631-3634. (c) Tamaru, S.; Uchino, S.; Takeuchi, M.; Ideker, M.; Hatano, T.; Shinkai, S. Tetrahedron Lett. 2002, 43, 3751-3755.
    • (2002) Org. Lett. , vol.4 , pp. 1423-1426
    • Kobayashi, H.1    Friggeri, A.2    Koumoto, K.3    Amaikee, M.4    Shinkai, S.5
  • 30
    • 0000310793 scopus 로고    scopus 로고
    • Hypochromic effects have been also observed in gels by others: (a) Kobayashi, H.; Friggeri, A.; Koumoto, K.; Amaikee, M.; Shinkai, S. Org. Lett. 2002, 4, 1423-1426. (b) Tamaru, S.; Nakamura, M.; Takeuchi, M.; Shinkai, S. Org. Lett. 2001, 3, 3631-3634. (c) Tamaru, S.; Uchino, S.; Takeuchi, M.; Ideker, M.; Hatano, T.; Shinkai, S. Tetrahedron Lett. 2002, 43, 3751-3755.
    • (2001) Org. Lett. , vol.3 , pp. 3631-3634
    • Tamaru, S.1    Nakamura, M.2    Takeuchi, M.3    Shinkai, S.4
  • 31
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    • Hypochromic effects have been also observed in gels by others: (a) Kobayashi, H.; Friggeri, A.; Koumoto, K.; Amaikee, M.; Shinkai, S. Org. Lett. 2002, 4, 1423-1426. (b) Tamaru, S.; Nakamura, M.; Takeuchi, M.; Shinkai, S. Org. Lett. 2001, 3, 3631-3634. (c) Tamaru, S.; Uchino, S.; Takeuchi, M.; Ideker, M.; Hatano, T.; Shinkai, S. Tetrahedron Lett. 2002, 43, 3751-3755.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 3751-3755
    • Tamaru, S.1    Uchino, S.2    Takeuchi, M.3    Ideker, M.4    Hatano, T.5    Shinkai, S.6
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    • Wiley-Interscience: London
    • Birks, J. B. Photophysics of Aromatic Compounds; Wiley-Interscience: London, 1970. Excimers have no fine structure and are red-shifted, but their excitation spectra may have a fine structure, e.g., for pyrene.
    • (1970) Photophysics of Aromatic Compounds
    • Birks, J.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.