双金属片
材料科学
炔烃
试剂
纳米线
选择性
模板
点击化学
DNA
纳米技术
膜
组合化学
化学工程
金属
化学
高分子化学
有机化学
催化作用
冶金
工程类
生物化学
作者
Monika Fischler,Ulrich Simon,Hadar Nir,Yoav Eichen,Glenn A. Burley,Johannes Gierlich,Philipp M. E. Gramlich,Thomas Carell
出处
期刊:Small
[Wiley]
日期:2007-02-19
卷期号:3 (6): 1049-1055
被引量:109
标识
DOI:10.1002/smll.200600534
摘要
Abstract Uniform bimetallic nanowires, tunable in size, have been grown on artificial DNA templates via a two‐step metallization process. Alkyne‐modified cytosines were incorporated into 900‐base‐pair polymerase‐chain‐reaction fragments. The alkyne modifications serve as addressable metal‐binding sites after conversion to a sugar triazole derivative via click chemistry. Reaction of the Tollens reagent with these sugar‐coated DNA duplexes generates Ag 0 metallization centers around the sugar modification sites of the DNA. After a subsequent enhancement step using gold, nanowires ≤10 nm in diameter with a homogeneous surface profile were obtained. Furthermore, the advantage of this two‐step procedure lies in the high selectivity of the process, due to the exact spatial control of modified DNA base incorporation and hence the confinement of metallization centers at addressable sites. Besides experiments on a membrane as a proof for the selectivity of the method, atomic force microscopy (AFM) studies of the wires produced on Si–SiO 2 surfaces are discussed. Furthermore, we demonstrate time‐dependent metallization experiments, monitored by AFM.
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