The effect of heteroatom conformation on optoelectronic properties of cyclopentadithiophene derivatives
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 12, Issue: 15, Page: 2474-2478
2014
- 15Citations
- 15Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations15
- Citation Indexes15
- CrossRef15
- 13
- Captures15
- Readers15
- 15
Article Description
Cyclopentadithiophene (CPDT) derivatives with different heteroatom conformations have been synthesized. The optical, electrochemical and charge transport properties of these molecules are reported. The CPDT-anti-ketone not only exhibits the lowest optical and electronic bandgaps, but also exhibits reasonable hole mobility, 3 × 10 cm (V s) . Changing the carbonyl conformation to the syn position or incorporating the imine functionality results in a blue-shift in the lower energy band of the absorption spectrum indicative of the increased bandgaps. © the Partner Organisations 2014.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84896455965&origin=inward; http://dx.doi.org/10.1039/c3ob41648h; http://www.ncbi.nlm.nih.gov/pubmed/24604281; http://xlink.rsc.org/?DOI=C3OB41648H; http://pubs.rsc.org/en/content/articlepdf/2014/OB/C3OB41648H; https://xlink.rsc.org/?DOI=C3OB41648H; https://dx.doi.org/10.1039/c3ob41648h; https://pubs.rsc.org/en/content/articlelanding/2014/ob/c3ob41648h
Royal Society of Chemistry (RSC)
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