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Volumn 14, Issue 18, 1998, Pages 5164-5171

Molecular recognition between 2,4,6-triaminopyrimidine lipid monolayers and complementary barbituric molecules at the air/water interface: Effects of hydrophilic spacer, ionic strength, and pH

Author keywords

[No Author keywords available]

Indexed keywords

ATOMIC FORCE MICROSCOPY; ELECTROSTATICS; FLUORESCENCE; FOURIER TRANSFORM INFRARED SPECTROSCOPY; HYDROGEN BONDS; IONIC STRENGTH; ISOTHERMS; LANGMUIR BLODGETT FILMS; MONOLAYERS; NITROGEN COMPOUNDS; PH EFFECTS; X RAY PHOTOELECTRON SPECTROSCOPY;

EID: 0032166340     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la971192n     Document Type: Article
Times cited : (65)

References (45)
  • 29
    • 0003915035 scopus 로고
    • Methuen & Co.: London, and John Wiley & Sons, Inc.: New York
    • Perrin, D. D. In Dissociation constants of organic bases in aqueous solution; Butterworths: London, 1961. Albert, A.; Serjeant, E. P. In Ionization constants of acids and bases; Methuen & Co.: London, and John Wiley & Sons, Inc.: New York, 1962.
    • (1962) Ionization Constants of Acids and Bases
    • Albert, A.1    Serjeant, E.P.2
  • 35
    • 11744328409 scopus 로고    scopus 로고
    • note
    • The mean molecular area were determined from the slop of the x-A isotherm curve by extrapolating at a zero surface pressure.
  • 45
    • 85086292503 scopus 로고    scopus 로고
    • note
    • -1 = 0.308/√c (nm) where c is the 1:1 electrolyte concentration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.