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Volumn 60, Issue 1-2, 2008, Pages 115-122

X-ray crystal structure of a p-hydroxycalix[6]arene derivative

Author keywords

1,2,3 alternate conformation; Calixarenes; Calixhydroquinones; Solvent channel; X ray crystal structure

Indexed keywords


EID: 38349128188     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-007-9359-3     Document Type: Article
Times cited : (7)

References (32)
  • 2
    • 0004287470 scopus 로고    scopus 로고
    • Asfari, Z., Böhmer, V., Harrowfield, J., Vicens J.: (eds.) Kluwer, Dordrecht
    • (b) Asfari, Z., Böhmer, V., Harrowfield, J., Vicens J.: (eds.) Calixarenes 2001, Kluwer, Dordrecht (2001)
    • (2001) Calixarenes 2001
  • 3
    • 0041717105 scopus 로고
    • An improved preparation of phenolic [ 1.1.1.1] metacyclophanes
    • (a) Patrick, T.B., Egan, P.A.: An improved preparation of phenolic [ 1.1.1.1] metacyclophanes. J. Org. Chem. 42, 382-383 (1977)
    • (1977) J. Org. Chem. , vol.42 , pp. 382-383
    • Patrick, T.B.1    Egan, P.A.2
  • 6
    • 0001282566 scopus 로고
    • Syntheses and NMR behavior of calix[4]quinone and calix[4] hydroquinone
    • (d) Morita, Y., Agawa, T.: Syntheses and NMR behavior of calix[4]quinone and calix[4] hydroquinone. J. Org. Chem. 57, 3658-3662 (1992)
    • (1992) J. Org. Chem. , vol.57 , pp. 3658-3662
    • Morita, Y.1    Agawa, T.2
  • 7
    • 0028826501 scopus 로고
    • Conformational restriction of calixarenes by 'meta' substitution
    • (e) Mascal, M., Naven, R.T., Warmuth, R.: Conformational restriction of calixarenes by 'meta' substitution. Tetrahedron Lett. 51, 9361-9364 (1995)
    • (1995) Tetrahedron Lett. , vol.51 , pp. 9361-9364
    • Mascal, M.1    Naven, R.T.2    Warmuth, R.3
  • 8
    • 0001100306 scopus 로고    scopus 로고
    • P-(Benzyloxy)calix[8]arene: One-pot synthesis and functionalization
    • (f) Casnati, A., Ferdani, R., Pochini, A., Ungaro, R.: p-(Benzyloxy)calix[8]arene: One-pot synthesis and functionalization J. Org. Chem. 62, 6236-6239 (1997).
    • (1997) J. Org. Chem. , vol.62 , pp. 6236-6239
    • Casnati, A.1    Ferdani, R.2    Pochini, A.3    Ungaro, R.4
  • 9
    • 0034340808 scopus 로고    scopus 로고
    • Synthesis and inclusion properties of a upper-rim-connected biscalix[4]arene
    • (g) Araki, K., Hayashida, H.: Synthesis and inclusion properties of a upper-rim-connected biscalix[4]arene. Chem. Lett. 20-21 (2000)
    • (2000) Chem. Lett. , pp. 20-21
    • Araki, K.1    Hayashida, H.2
  • 11
    • 33745394944 scopus 로고
    • Supramolecular synthons in crystal engineering - A new organic synthesis
    • (b) Desiraju, G.R.: Supramolecular synthons in crystal engineering - a new organic synthesis. Angew. Chem., Int. Ed. Engl. 34, 2311-2327 (1995)
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2311-2327
    • Desiraju, G.R.1
  • 15
    • 38349093629 scopus 로고    scopus 로고
    • Harrowfield, J., Vicens, J.: (eds.) chapt. 16 Springer, Netherlands
    • Gaeta, C., Tedesco, C., Neri, P.: In: Harrowfield, J., Vicens, J.: (eds.) Calixarenes in the Nanoworld, chapt. 16, pp. 335-354. Springer, Netherlands 2006
    • (2006) Calixarenes in the Nanoworld , pp. 335-354
    • Gaeta, C.1    Tedesco, C.2    Neri, P.3
  • 16
    • 0035850853 scopus 로고    scopus 로고
    • Ultrathin single-crystalline silver nanowire arrays formed in an ambient solution phase
    • (a) Hong, B.H., Bae, S.C., Lee, C.-W., Jeong, S., Kim K.S.: Ultrathin single-crystalline silver nanowire arrays formed in an ambient solution phase. Science 294, 348-351 (2001)
    • (2001) Science , vol.294 , pp. 348-351
    • Hong, B.H.1    Bae, S.C.2    Lee, C.-W.3    Jeong, S.4    Kim, K.S.5
  • 17
    • 0035980399 scopus 로고    scopus 로고
    • Self-assembled arrays of organic nanotubes with infinitely long onedimensional H-bond chains
    • (b) Hong, B.H., Lee, J.Y., Lee, C.-W. Kim, J.C. Bae, S.C. Kim, K.S.: Self-assembled arrays of organic nanotubes with infinitely long onedimensional H-bond chains. J. Am. Chem. Soc. 123, 10748-10749 (2001).
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 10748-10749
    • Hong, B.H.1    Lee, J.Y.2    Lee, C.-W.3    Kim, J.C.4    Bae, S.C.5    Kim, K.S.6
  • 18
    • 1242297018 scopus 로고    scopus 로고
    • Nature of One-dimensional short hydrogen bonding: Bond distances, bond energies, and solvent effects
    • (c) Suh, S.B., Kim, J.C., Choi, Y.C., Yun, S., Kim, K.S.: Nature of One-dimensional short hydrogen bonding: Bond distances, bond energies, and solvent effects. J. Am. Chem. Soc. 126, 2186-2193 (2004)
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2186-2193
    • Suh, S.B.1    Kim, J.C.2    Choi, Y.C.3    Yun, S.4    Kim, K.S.5
  • 19
    • 25844473220 scopus 로고    scopus 로고
    • Interconnected water channels and isolated hydrophobic cavities in a calixarene-based, nanoporous supramolecular architecture
    • (a) Tedesco, C., Immediata, I., Gregoli, L., Vitagliano, L., Immirzi, A., Neri, P.: Interconnected water channels and isolated hydrophobic cavities in a calixarene-based, nanoporous supramolecular architecture. Cryst. Eng. Comm. 7, 449-453 (2005).
    • (2005) Cryst. Eng. Comm. , vol.7 , pp. 449-453
    • Tedesco, C.1    Immediata, I.2    Gregoli, L.3    Vitagliano, L.4    Immirzi, A.5    Neri, P.6
  • 21
    • 0034147434 scopus 로고    scopus 로고
    • Octa(p-hydroxy)octakis(propyloxy)calix[8]arene: The first crystal structure of a p-hydroxy calixarene
    • Leverd, P.C., Huc, V., Palacin, S., Nierlich, M.: Octa(p-hydroxy) octakis(propyloxy)calix[8]arene: the first crystal structure of a p-hydroxy calixarene. J. Inclus. Phenom. Macrocyclic Chem. 36, 259-266 (2000)
    • (2000) J. Inclus. Phenom. Macrocyclic Chem. , vol.36 , pp. 259-266
    • Leverd, P.C.1    Huc, V.2    Palacin, S.3    Nierlich, M.4
  • 22
    • 0001282086 scopus 로고
    • Versatility in inclusion hosts: Unusual conformation in the crystal structure of the p-tert-butylcalix[8]arene: Pyridine (1:8) clathrate
    • (a) Czugler, M., Tisza, S., Speier, G.: Versatility in inclusion hosts: unusual conformation in the crystal structure of the p-tert-butylcalix[8]arene: pyridine (1:8) clathrate. J. Incl. Phenom. Mol. Recognit. Chem. 11, 323-331 (1991).
    • (1991) J. Incl. Phenom. Mol. Recognit. Chem. , vol.11 , pp. 323-331
    • Czugler, M.1    Tisza, S.2    Speier, G.3
  • 23
    • 21244481009 scopus 로고    scopus 로고
    • Synthesis and Solid-State Conformation of a Calix [8]arene 1,5-Diquinone Derivative
    • (b) Rossella, F., Tedesco, C., Gaeta, C., Neri, P.: Synthesis and Solid-State Conformation of a Calix [8]arene 1,5-Diquinone Derivative. J. Incl. Phenom. Macrocyclic Chem. 52, 85-91 (2005)
    • (2005) J. Incl. Phenom. Macrocyclic Chem. , vol.52 , pp. 85-91
    • Rossella, F.1    Tedesco, C.2    Gaeta, C.3    Neri, P.4
  • 24
    • 33749015900 scopus 로고
    • Calixarenes. 4. the synthesis, characterization, and properties of the calixarenes from p-tert-butylphenol
    • Gutsche, C.D., Dhawan, B., No, K.H., Muthukrishnan, R.: Calixarenes. 4. The synthesis, characterization, and properties of the calixarenes from p-tert-butylphenol. J. Am. Chem. Soc. 103, 3782-3792 (1981)
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3782-3792
    • Gutsche, C.D.1    Dhawan, B.2    No, K.H.3    Muthukrishnan, R.4
  • 25
    • 0039719476 scopus 로고
    • Molecular inclusion in functionalized macrocycles. Part 3. Synthesis, proton and carbon-13 NMR spectra, and conformational preference of open chain ligands on lipophilic macrocycles
    • Bocchi, V., Foina, D., Pochini, A., Ungaro, R., Andreetti, G.D.: Molecular inclusion in functionalized macrocycles. Part 3. Synthesis, proton and carbon-13 NMR spectra, and conformational preference of open chain ligands on lipophilic macrocycles. Tetrahedron. 38, 373-378 (1982)
    • (1982) Tetrahedron. , vol.38 , pp. 373-378
    • Bocchi, V.1    Fonia, D.2    Pochini, A.3    Ungaro, R.4    Andreetti, G.D.5
  • 30
    • 34249916770 scopus 로고
    • Molecular inclusion in calixarenes. XVIII. Crystal and molecular structure of the p-tertbutylcalix[7]arene 1:3 pyridine complex/clathrate
    • Andreetti, G.D., Ugozzoli, F., Nakamoto, Y., Ishida, S.-I.: Molecular inclusion in calixarenes. XVIII. Crystal and molecular structure of the p-tertbutylcalix[7]arene 1:3 pyridine complex/clathrate. J. Incl. Phenom. 10, 241-253 (1991)
    • (1991) J. Incl. Phenom. , vol.10 , pp. 241-253
    • Andreetti, G.D.1    Ugozzoli, F.2    Nakamoto, Y.3    Ishida, S.-I.4
  • 31
    • 34249833028 scopus 로고
    • Symbolic representation of the molecular conformation of calixarenes
    • Ugozzoli, F., Andreetti, G.D.: Symbolic representation of the molecular conformation of calixarenes. J. Incl. Phenom. 13, 337-348 (1992)
    • (1992) J. Incl. Phenom. , vol.13 , pp. 337-348
    • Ugozzoli, F.1    Andreetti, G.D.2
  • 32
    • 0002181089 scopus 로고
    • Molecular inclusion in functionalized macrocycles. Part 10: Crystal and molecular structure of a p-tert-butylcalix[6]arene hexapodand
    • Ungaro, R., Pochini, A., Andreetti, G.D., Domiano, P.: Molecular inclusion in functionalized macrocycles. Part 10: crystal and molecular structure of a p-tert-butylcalix[6]arene hexapodand. J. Incl. Phenom. 3, 35-42 (1985)
    • (1985) J. Incl. Phenom. , vol.3 , pp. 35-42
    • Ungaro, R.1    Pochini, A.2    Andreetti, G.D.3    Domiano, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.