메뉴 건너뛰기




Volumn , Issue 3, 1997, Pages 575-579

Cation complexation by chemically modified calixarenes. Part 10. Thioamide derivatives of p-tert-butylcalix[4]-, [5]- And [6]-arenes with selectivity for copper, silver, cadmium and lead. X-Ray molecular structures of calix[4]arene thioamide-lead(II) and calix[4]arene amide-copper(II) complexes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001721877     PISSN: 03009580     EISSN: None     Source Type: Journal    
DOI: 10.1039/a605417j     Document Type: Article
Times cited : (21)

References (41)
  • 1
    • 0000033877 scopus 로고
    • Calixarenes
    • ed. J. F. Stoddart, Royal Society of Chemistry, Cambridge
    • C. D. Gutsche, Calixarenes, vol. 1 in 'Monographs in Supramolecular Chemistry', ed. J. F. Stoddart, Royal Society of Chemistry, Cambridge, 1989.
    • (1989) Monographs in Supramolecular Chemistry , vol.1
    • Gutsche, C.D.1
  • 5
  • 19
    • 0347799219 scopus 로고    scopus 로고
    • ref. 2
    • R. Ungaro and A. Pochini, ref. 2, pp. 127-147; C. Alfieri, E. Dradi, A. Pochini, R. Ungaro and G. D. Andreetti, J. Chem. Soc., Chem. Commun., 1983, 1075; E. Ghidini, F. Ugozzoli, R. Ungaro, S. Harkema, A. Abu El-Fadl and D. N. Reinhoudt, J. Am. Chem. Soc., 1990, 112, 6979.
    • Ungaro, R.1    Pochini, A.2
  • 24
    • 0001547159 scopus 로고
    • D. Diamond, G. Svehla, E. Seaward and M. A. McKervey. Anal. Chim. Acta, 1988, 204, 223; K. Kumura, M. Matsuo and T. Shona, Chem. Lett., 1988, 615.
    • (1988) Chem. Lett. , pp. 615
    • Kumura, K.1    Matsuo, M.2    Shona, T.3
  • 27
    • 84986946891 scopus 로고
    • For a preliminary report of this work, excluding the X-ray crystal structures, see F. Arnaud-Neu, M. A. McKervey and M.-J. Schwing-Weill, J. Phys. Org. Chem., 1992, 5, 496. Shortly after this report, the use of calixarene derivatives, including thioamides as ionophores in ESFET devices, was described by P. L. H. M. Cobben, R. J. M. Egberink, J. G. Bomer, P. Bergveld, W. Verboom and D. N. Reinhoudt, J. Am. Chem. Soc., 1992, 114, 10573.
    • (1992) J. Phys. Org. Chem. , vol.5 , pp. 496
    • Arnaud-Neu, F.1    McKervey, M.A.2    Schwing-Weill, M.-J.3
  • 28
    • 0000784569 scopus 로고
    • For a preliminary report of this work, excluding the X-ray crystal structures, see F. Arnaud-Neu, M. A. McKervey and M.-J. Schwing- Weill, J. Phys. Org. Chem., 1992, 5, 496. Shortly after this report, the use of calixarene derivatives, including thioamides as ionophores in ESFET devices, was described by P. L. H. M. Cobben, R. J. M. Egberink, J. G. Bomer, P. Bergveld, W. Verboom and D. N. Reinhoudt, J. Am. Chem. Soc., 1992, 114, 10573.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10573
    • Cobben, P.L.H.M.1    Egberink, R.J.M.2    Bomer, J.G.3    Bergveld, P.4    Verboom, W.5    Reinhoudt, D.N.6
  • 34
    • 85088670671 scopus 로고
    • P. Guilbaud, A. Varnek and G. Wipff, J. Am. Chem. Soc., 1993, 115, 8289; A. Varnek and G. Wipff, J. Phys. Chem., 1993, 97, 10840.
    • (1993) J. Phys. Chem. , vol.97 , pp. 10840
    • Varnek, A.1    Wipff, G.2
  • 38
    • 0001647167 scopus 로고
    • G. M. Sheldrick, C. Kruger and R. Goddard, Oxford University Press, London
    • G. M. Sheldrick, SHELXS86, Crystallographic Computing 3, G. M. Sheldrick, C. Kruger and R. Goddard, Oxford University Press, London, 1986, pp 175-189.
    • (1986) SHELXS86, Crystallographic Computing , vol.3 , pp. 175-189
    • Sheldrick, G.M.1
  • 40
    • 0345907893 scopus 로고
    • ORTEPII. Report ORNL-5138. Oak Ridge National Laboratory, Tennessee, USA
    • C. K. Johnson, ORTEPII. Report ORNL-5138. Oak Ridge National Laboratory, Tennessee, USA 1976.
    • (1976)
    • Johnson, C.K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.