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Volumn 56, Issue 3-4, 2006, Pages 315-321

New calix[4]arene based hydroxystyryl cyanine dyes

Author keywords

Absorption spectra; Chromophoric calixarenes; Conformational transformations; Merocyanine dyes

Indexed keywords


EID: 33846411129     PISSN: 09230750     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10847-005-9044-3     Document Type: Article
Times cited : (10)

References (45)
  • 1
    • 0004268367 scopus 로고    scopus 로고
    • Royal Society of Chemistry, Cambridge
    • (a) C.D. Gutsche: Calixarenes Revisited, Royal Society of Chemistry, Cambridge (1998);
    • (1998) Calixarenes Revisited
    • Gutsche, C.D.1
  • 6
    • 0038688726 scopus 로고    scopus 로고
    • For review on chromogenic calixarenes see:, Z. Asfari, V. Boehmer, J. Harowfield, and J. Vicens eds, Kluwer Academic Publishers, Dodrecht
    • For review on chromogenic calixarenes see: R. Ludwig: In Z. Asfari, V. Boehmer, J. Harowfield, and J. Vicens (eds.), Calixarenes 2001, Kluwer Academic Publishers, Dodrecht, 598 (2001).
    • (2001) Calixarenes 2001 , pp. 598
    • Ludwig, R.1
  • 8
    • 33846436670 scopus 로고    scopus 로고
    • M.A. McKervey, M.J. Schiwing-Weill, and F. Arnaud-Neu: Comprehensive Supramolecular Chemistry, 1: Receptors for Cationic Guests, (Ed. G.W. Gokel), Pergamon Press, New York, Oxford, 537 (1996);
    • (b) M.A. McKervey, M.J. Schiwing-Weill, and F. Arnaud-Neu: Comprehensive Supramolecular Chemistry, Vol. 1: Receptors for Cationic Guests, (Vol. Ed. G.W. Gokel), Pergamon Press, New York, Oxford, 537 (1996);
  • 27
    • 0001882611 scopus 로고    scopus 로고
    • Z. Asfari, V. Boehmer, J. Harowfield, and J. Vicens eds, Kluwer Academic Publishers, Dodrecht
    • F. Cadogan, K. Nolan, and D. Diamond: In Z. Asfari, V. Boehmer, J. Harowfield, and J. Vicens (eds.), Calixarenes 2001, Kluwer Academic Publishers, Dodrecht, 627 (2001).
    • (2001) Calixarenes 2001 , pp. 627
    • Cadogan, F.1    Nolan, K.2    Diamond, D.3
  • 38
    • 33846424116 scopus 로고    scopus 로고
    • Absorption spectra of meroforms 8A-11A recorded for the samples synthesized by previously reported method [18] and generated in situ by the addition of DBU to solution of hydroxystyryls 8-11 are identical.
    • Absorption spectra of meroforms 8A-11A recorded for the samples synthesized by previously reported method [18] and generated in situ by the addition of DBU to solution of hydroxystyryls 8-11 are identical.
  • 39
    • 33846454576 scopus 로고    scopus 로고
    • Calix[4]arene based merocyanines 3A-7A were not isolated as individual compounds. Therefore, their absorption spectra were recorded for samples generated in situ by the addition of DBU to solution of hydroxystyryls 3-7.
    • Calix[4]arene based merocyanines 3A-7A were not isolated as individual compounds. Therefore, their absorption spectra were recorded for samples generated in situ by the addition of DBU to solution of hydroxystyryls 3-7.
  • 40
    • 33846454193 scopus 로고    scopus 로고
    • Expression of the splitting value through energetical parameters shows that the both maxima have nonvibrational nature 3A -998 cm-1, 4A, 1467 cm-1, 6A, 1543 cm-1, 7A, 1372 cm-1
    • -1).
  • 42
    • 33846412094 scopus 로고
    • K. Venkataraman ed, Academic press, New York, London
    • (a) S.F. Mason: In K. Venkataraman (ed.), The Chemistry of Synthethic Dyes, v. 3, Academic press, New York - London, 213 (1970);
    • (1970) The Chemistry of Synthethic Dyes , vol.3 , pp. 213
    • Mason, S.F.1
  • 43
    • 33846422207 scopus 로고    scopus 로고
    • A.I. Kiprianov: Uspekhi Khimii (Russ.) 40, 1283 (1971). Obviously, the intramolecular chromophores interaction takes place in bismerocyanine 5A, where two multielectron π-systems form H-aggregate-type dimer; its band is observed at 559 nm.
    • (b) A.I. Kiprianov: Uspekhi Khimii (Russ.) 40, 1283 (1971). Obviously, the intramolecular chromophores interaction takes place in bismerocyanine 5A, where two multielectron π-systems form H-aggregate-type dimer; its band is observed at 559 nm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.