## Abstract The assembly of alternating DNA and positively charged poly‐(dimethyldiallylammonium chloride) (PDDA) multilayer films by electrostatic layer‐by‐layer adsorption has been studied. Real time surface plasmon resonance (BIAcore) technique was used to characterize and monitor the formation
Multilayer Films Fabricated from Oppositely Charged Polyphenylene Dendrimers by Electrostatic Layer-by-Layer Assembly
✍ Scribed by Dong Ha Kim; Jose Luis Hernandez-Lopez; Jianyun Liu; George Mihov; Linjie Zhi; Roland E. Bauer; Dörte Grebel-Köhler; Markus Klapper; Tanja Weil; Klaus Müllen; Silvia Mittler; Wolfgang Knoll
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 269 KB
- Volume
- 206
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Summary: Assemblies of oppositely charged L‐lysine/carboxylic acid functionalized polyphenylene dendrimers and hybrid multilayers of L‐lysine dendrimers/colloidal gold nanocrystals were fabricated as alternate multilayers on 3‐mercaptopropionic acid coated gold surfaces via layer‐by‐layer deposition. The fabrication of the multilayer films was monitored by kinetic and scan mode surface plasmon resonance spectroscopy. The permeability properties of the dendritic polyelectrolyte layers were characterized by electrochemistry in the presence of [Fe(CN)~6~]^3−/4−^ as the redox couple. A high interfacial charge‐transfer resistance, originating from the electrostatic repulsion of the negatively charged redox couple against the negatively charged interface was observed and the charge‐transfer resistance found to increase with increasing number of layers.
3D‐structure of the investigated polyphenylene dendrimers: a) G~2~(L‐lysine)~8~ and b) G~2~(COOH)~16~.
magnified image3D‐structure of the investigated polyphenylene dendrimers: a) G~2~(L‐lysine)~8~ and b) G~2~(COOH)~16~.
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