期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2007, 期 24, 页码 4032-4037出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.200700044
关键词
surface chemistry; monolayers; peptides; DNA; helicene
A feasible method of grafting complex amine structures (methyl ester of glycine, Rho-Lys-Arg-NH2, amine-terminated oligonucleotide and 7,8,11,12-tetrahydro-5-hexahelicenamine) onto a silicon wafer surface is described. The two step process comprises (1) anchoring 10-isocyanatodecyl-trichlorosilane to a 1.8-2-nm thin silica layer on a single silicon wafer crystal (100) and (2) the attachment of amine substrates through a urea linkage by reacting those with isocyanate groups on the wafer surface. Both steps can be monitored by ATR FTIR showing the appearance/disappearance of the isocyanate band. Measuring the contact angles along with the AFM imaging of the surfaces indicated the formation of the monolayers. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim Germany, 2007).
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