Thiophene based hyperbranched polymers with tunable branching using direct arylation methods
Polymer Chemistry, ISSN: 1759-9962, Vol: 4, Issue: 12, Page: 3499-3506
2013
- 84Citations
- 64Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
An efficient one-pot synthesis of branched poly(3-alkylthiophene)s (b-P3ATs) is achieved via a dehydrohalogenative polycondensation reaction. The structures of the b-P3ATs are assigned based on H NMR spectra by comparing them to a model dendritic polymer and oligo(3-hexylthiophene-2,4-diyl) . The palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-alkylthiophenes was found to provide P3AT with tunable degree of branching (DB = 0-0.42) and high molecular weights. Viscosity measurements of the different b-P3ATs indicate that they display a more globular morphology compared to regiorandom P3AT and regioregular P3AT in solution, thereby confirming the branched structure. © 2013 The Royal Society of Chemistry.
Bibliographic Details
Royal Society of Chemistry (RSC)
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know