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Volumn 103, Issue 43, 1999, Pages 9356-9365

Chain length dependence of intramolecular excimer formation with 1,n-bis(1-pyrenylcarboxy)alkanes for n = 1-16, 22, and 32

Author keywords

[No Author keywords available]

Indexed keywords


EID: 21944443735     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp991611k     Document Type: Article
Times cited : (82)

References (60)
  • 16
    • 21944431953 scopus 로고    scopus 로고
    • note
    • The concept "ground-state dimer" implies that the dimers are preformed within the experimental time resolution.
  • 19
    • 21944443762 scopus 로고    scopus 로고
    • note
    • The synthesis of bis(1-pyrenylcarboxy)methane 1PC(1)1PC was carried out by J. Teles at the Centro de Quimica Estrutural in Lisbon.
  • 27
    • 21944457279 scopus 로고
    • Ph.D. Thesis, University Göttingen, Germany
    • Reynders, P. Ph.D. Thesis, University Göttingen, Germany, 1988.
    • (1988)
    • Reynders, P.1
  • 37
    • 21944445537 scopus 로고    scopus 로고
    • note
    • The solvent viscosities at 20 °C are (ref 25): 0.731 cP (methylcyclohexane) and 3.451 cP (n-hexadecane). For liquid-paraffin at 20 °C a viscosity of 125 cP was measured, see Experimental Section.
  • 39
    • 21944446202 scopus 로고    scopus 로고
    • note
    • o′ has an amplitude zero in the monomer decay. The excimer decay is double-exponential under all conditions when one excimer is present, see ref 21.
  • 40
    • 85086352921 scopus 로고    scopus 로고
    • note
    • -1) is much smaller relative to 1/τ (eq 3) than for 1PC(1).
  • 42
    • 85086353069 scopus 로고    scopus 로고
    • note
    • o′ (eq 1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.