Synthesis, electronic properties, and self-assembly on Au{111} of thiolated phenylethynyl phenothiazines

Thiolated phenylethynyl phenothiazines can be regarded as redox-active “alligator clips”. They are readily synthesized from ethynyl phenothiazines and show intense blue-green luminescence upon ultraviolet (UV) excitation. Cyclic voltammetry reveals reversible oxidation, also after the chemisorption...

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Bibliographic Details
Main Authors: Barkschat, Christa S. (Author) , Stoycheva, Svetlana (Author) , Himmelhaus, Michael (Author) , Müller, Thomas J. J. (Author)
Format: Article (Journal)
Language:English
Published: 2010
In: Chemistry of materials
Year: 2010, Volume: 22, Issue: 1, Pages: 52-63
ISSN:1520-5002
DOI:10.1021/cm901514t
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/cm901514t
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Author Notes:Christa S. Barkschat, Svetlana Stoycheva, Michael Himmelhaus, and Thomas J.J. Müller
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Summary:Thiolated phenylethynyl phenothiazines can be regarded as redox-active “alligator clips”. They are readily synthesized from ethynyl phenothiazines and show intense blue-green luminescence upon ultraviolet (UV) excitation. Cyclic voltammetry reveals reversible oxidation, also after the chemisorption of in situ liberated thiols on gold electrodes. The chemisorption on Au{111} was studied by ellipsometry, contact angle measurements, X-ray photoelectron spectroscopy, and infrared reflection absorption spectroscopy, and the obtained data support the formation of self-assembled monolayers, depending on the structure of the substrates. These findings classify them as promising candidates for molecular wires switchable by redox manipulation.
Item Description:Revised Manuscript Received November 20, 2009
Gesehen am 01.12.2022
Physical Description:Online Resource
ISSN:1520-5002
DOI:10.1021/cm901514t