메뉴 건너뛰기




Volumn 122, Issue 7, 2000, Pages 1486-1491

Synthesis and alkali metal ion binding properties of two rigid sterochemical isomers of calix[6]arene bis-crown-4

Author keywords

[No Author keywords available]

Indexed keywords

ALKALI METAL; CALIXARENE; CESIUM ION;

EID: 0033996051     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja991810h     Document Type: Article
Times cited : (93)

References (44)
  • 1
    • 0000580063 scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1994) Supramol. Sci. , vol.1 , pp. 103-110
    • Asfari, Z.1    Wenger, S.2    Vicens, J.3
  • 2
    • 54249141414 scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1995) Pure Appl. Chem. , vol.67 , pp. 1037-1043
    • Asfari, Z.1    Wenger, S.2    Vicens, J.3
  • 3
    • 0028906278 scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2767-2777
    • Casnati, A.1    Pochini, A.2    Ungaro, R.3    Ugozzoli, F.4    Arnaud, F.5    Fanni, S.6    Schwing, M.-J.7    Egberink, R.J.M.8    De Jong, F.9    Reinhoudt, D.N.10
  • 4
    • 0031562381 scopus 로고    scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1997) Tetrahedron , vol.53 , pp. 3767-3776
    • Arduini, A.1    Domiano, L.2    Pochini, A.3    Secchi, A.4    Ungarro, R.5    Ugozzoli, F.6    Struck, O.7    Verboom, W.8    Reinhoudt, D.N.9
  • 5
    • 0030014135 scopus 로고    scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3907-3910
    • Pappalardo, S.1    Petringa, A.2    Parisi, M.F.3    Ferguson, G.4
  • 6
    • 0002503801 scopus 로고    scopus 로고
    • (a) For reviews and references on calix[4]crowns, see: Asfari, Z.; Wenger, S.; and Vicens, J. Supramol. Sci. 1994, 1, 103-110. (b) Asfari, Z.; Wenger, S.; and Vicens, J. Pure Appl. Chem. 1995, 67, 1037-1043. (c) Casnati, A.; Pochini, A.; Ungaro, R.; Ugozzoli, F.; Arnaud, F.; Fanni, S.; Schwing, M.-J.; Egberink, R. J. M.; de Jong, F.; Reinhoudt, D. N. J. Am. Chem. Soc. 1995, 117, 2767-2777. For references on 1,2-alternate calixcrowns, see: (d) Arduini, A.; Domiano, L.; Pochini, A.; Secchi, A.; Ungarro, R.; Ugozzoli, F.; Struck, O.; Verboom, W.; Reinhoudt, D. N. Tetrahedron 1997, 53, 3767-3776. (e) Pappalardo, S.; Petringa, A.; Parisi, M. F.; Ferguson, G. Tetrahedron Lett. 1996, 37, 3907-3910. For refernces on calix[8]crowns, see: (f) Geraci, C.; Chessari, G.; Piattelli, M.; Neri, P. J. Chem. Soc., Chem. Commun. 1997, 921-922.
    • (1997) J. Chem. Soc., Chem. Commun. , pp. 921-922
    • Geraci, C.1    Chessari, G.2    Piattelli, M.3    Neri, P.4
  • 27
    • 0000033877 scopus 로고
    • Calixarenes
    • Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge
    • 2Ar carbons. The other aryl rings in the cyclic array are then designated by proceeding around the ring. Departures from true up/down orientations are handled by additional "o" or "i" notation. For example, rings that project outward may be described as uo or do for "up out" and "down out". (a) Gutsche, C. D. Calixarenes; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry; The Royal Society of Chemistry: Cambridge, 1989. (b) Gutsche, C. D. Calixarenes Revisited; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry; The Royal Society of Chemistry: Cambridge, 1998.
    • (1989) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 28
    • 0003277099 scopus 로고    scopus 로고
    • Calixarenes Revisited
    • Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge
    • 2Ar carbons. The other aryl rings in the cyclic array are then designated by proceeding around the ring. Departures from true up/down orientations are handled by additional "o" or "i" notation. For example, rings that project outward may be described as uo or do for "up out" and "down out". (a) Gutsche, C. D. Calixarenes; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry; The Royal Society of Chemistry: Cambridge, 1989. (b) Gutsche, C. D. Calixarenes Revisited; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry; The Royal Society of Chemistry: Cambridge, 1998.
    • (1998) Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 30
    • 0343185450 scopus 로고    scopus 로고
    • note
    • The X-ray crystal structure for the 1,2,3-alternate conformer 3 was solved, but the R value was only 13%. Even though this is not ideal, it is still sufficient to determine the conformation.
  • 31
    • 0004187703 scopus 로고
    • Wiley & Sons: New York
    • Connors, K. A. Binding Constants; Wiley & Sons: New York, 1987; pp 24-28.
    • (1987) Binding Constants , pp. 24-28
    • Connors, K.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.