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A series of H2O and/or EtOH soluble, self-assembling quaternary ammonium salts containing a dansyl (DNS) fluorescent moiety suitable for attachment to both porous ([DNS–NH–(CH2)3–NMe2–R+][X] (2; R = –Si(OMe)3, X = Cl) and non-porous (3a; R = –PO(OEt)2, 3b; –PO(Oi-Pr)2, 3c; –(PO(OH)2, X = Br), 4; ([DNS–NH–(CH2)3–NMe2–(CH2)3–NH(CH2PO(OEt)2)2+][Br], 5; R = –((CH2)3SCOCH3, X = Cl), 6a; (R = –(CH2)nO(C6H4)CO(C6H5), n = 3, X = Br, 6b; n = 3, X = Cl, 6c; n = 3, X = I, 6d; n = 4, X = Br, 6e; n = 4, X = I, 6f; n = 6, X = Br, 6g; n = 6, X = Cl, 6h; n = 6, X = I), 7; (R = –CH2–CH[double bond, length as m-dash]CH2, X = Br) surfaces were prepared from the precursor dansyl amine (1; DNS–NH–(CH2)3–NMe2). Compounds 1–7 were characterized by NMR (1H, 13C, 29Si (2), 31P (3a–c, 4)) spectroscopy, HRMS, UV-Vis and fluorescence spectroscopy. Additional characterization of compounds 1 and 7 were carried out by X-ray structure determinations. Physical attachment of compound 2 to cotton surfaces after immersion in solutions containing fluorescent dyes was verified by exposure to UV light and by complexation with bromo-phenol blue that rendered the surfaces visibly blue in colour. Phosphorus containing dansyl fluorescent dye, 3c, was attached to a stainless steel surface by exposure to an aqueous solution containing this dye, resulting in the formation of a self-assembled fluorescent monolayer. UV cure of plastic surfaces (polypropylene, silicon medical tubing) coated with compound 6a resulted in the covalent attachment of the dyes.

Graphical abstract: Synthesis, structures and properties of self-assembling quaternary ammonium dansyl fluorescent tags for porous and non-porous surfaces

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