کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1403079 | 1501777 | 2013 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Improvement of the redox stability of dithieno[3,2-b:2′,3′-d]thiophene derivatives by using bulky substituents Improvement of the redox stability of dithieno[3,2-b:2′,3′-d]thiophene derivatives by using bulky substituents](/preview/png/1403079.png)
With the goal of improving the long term redox stability of dithieno[3,2-b:2′,3′-d]thiophene (DTT), we synthesized derivatives with differently sized substituents. It is well known that substituents in the 2, 6 positions of DTT are active in this respect. We provide in this article more insight into mechanism. The present study provides the first support for a size effect. Large size substituents in the 2, 6 positions of the DTT are more effective than small size substituents. In these compounds, the DTT acts as a core of a molecule where the HOMO is located and the substituents work as a cage to protect the core from various attacks from the outside. This core-cage system is not only effective to prevent polymerization but also to increase the long term redox stability. The compounds with large size substituents, such as (1,1′:3′,1″-terphenyl)-2-yl and 4,4′-di-tert-butyl-(1,1′-biphenyl)-2-yl, showed excellent long term redox stability. The oxidation potential was maintained during repeated oxidation up to 17,000 and 20,000 times, respectively. The compounds with small size substituents, such as phenyl and mesityl, showed 1/10 or less of this durability. We show the substituent effects on repeated oxidation by investigating the electrochemical and photophysical properties.
Substituent effects of dithieno[3,2-b:2′,3′-d]thiophene (DTT) derivatives using bulky phenyl substitutions on its 2, 6 position were investigated. Dihedral angle between planes of the DTT and the phenyl affects strongly on photochemical and electrochemical properties. Especially, the molecule which has the DTT enfolded by the bulky substituent will be improved a long-term redox stability.Figure optionsDownload as PowerPoint slideHighlights
► Highly redox stable compounds were obtained using core-cage system.
► Bulky substituents on 2, 6 position of DTT revealed excellent redox stability.
► A large size substituent is more effective than a small size substituent.
► The core-cage system support electrochromicity and long stability at the same time.
► The photophysical and electrochemical properties were studied using various cages.
Journal: Journal of Molecular Structure - Volume 1037, 10 April 2013, Pages 256–263