Two-dimensional molecular imprinting: Binding of sugars to boronic acid functionalized, polymerized Langmuir-Blodgett films

Chemistry Letters

Volumn , Issue 12, 2000, Pages 1356-1357

  Miyahara, Takashi ^a   Kurihara, Kazue ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0034345653     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2000.1356     Document Type: Article

References (19)

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11. -4) to examine.
12. 6) δ 9.77 (1H, s), 7.99 (2H, s), 7.80 (1H, s), 7.70 (1H, d, J = 8.3 Hz), 7.43 (1H, d, J = 7.3 Hz), 7.22 (1H, t, J = 7.7 Hz), 2.26 (6H, m), 1.56 (2H, quintet, J = 6.4 Hz,), 1.42 (4H, m), 1.22 (26H, apparent two peaks), 0.83 (3H, t, J = 6.8 Hz).
13. L. Rosenfeld and Y. C. Lee, Carbohydr. Res., 46, 155 (1976).
14. D. Day and H. Ringsforf, J. Polym. Sci., Polym. Lett., 16, 205 (1978).
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16. It was confirmed that 4′-nitrophenyl α-D-mannopyranoside-2,3;4,6-di-O-(3″-aminophenylboronate) (4) was quantitatively prepared by the dehydration (azeotropic distillation) of the 1:2 mixture of 3 and 3-aminophenylboronic acid in dioxane.
17. The cyclic boronic acid ester 4 was rapidly decomposed to the starting materials in the presence of water.
18. The UV-visible spectrum recorded just before being immersed in the solution of 3 in 2-butanone was not the same as spectrum II because the DODA monolayer deposited on the back side was dissolved in 2-butanone. Therefore, the spectrum II was used as the blank.
19. 2], respectively.