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巯基化(寡)苯并噻嗪在金{111}表面的自组装及其电子性能。

Synthesis, electronic properties and self-assembly on Au{111} of thiolated (oligo)phenothiazines.

机构信息

Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität Düsseldorf, Universitätsstr. 1, D-40225 Düsseldorf, Germany.

出版信息

Beilstein J Org Chem. 2010 Jul 2;6:72. doi: 10.3762/bjoc.6.72.

DOI:10.3762/bjoc.6.72
PMID:20703376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2919263/
Abstract

(Oligo)phenothiazinyl thioacetates, synthesized by a one-pot sequence, are electrochemically oxidizable and highly fluorescent. SAMs can be readily formed from thiols prepared by in situ deprotection of the thioacetates in the presence of a gold-coated silicon wafer. Monolayer formation is confirmed by ellipsometry and the results compared to those obtained by force field and DFT calculations.

摘要

(寡)苯并噻嗪基硫代乙酸酯,通过一锅法序列合成,可电化学氧化且具有强荧光性。在金覆盖的硅片存在的情况下,通过对硫代乙酸酯的现场脱保护作用,很容易从巯基制备 SAMs。通过椭圆测量法确认单层形成,并将结果与通过力场和 DFT 计算获得的结果进行比较。

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本文引用的文献

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