The reaction of an amino-functionalized DPP with acrolein
Tetrahedron Letters, ISSN: 0040-4039, Vol: 100, Page: 153853
2022
- 1Citations
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.
Metrics Details
- Citations1
- Citation Indexes1
- CrossRef1
Article Description
An aminophenyl-functionalized diketopyrrolopyrrole (DPP) was designed and synthesized to react with acrolein. The cyclization reaction between acrolein and the aminophenyl group resulted in an increase in fluorescence at 612 nm in the emission spectrum, along with an 18 nm blue-shift from 630 to 612 nm. This phenomenon occurred because the formation of a quinolyl group led to the disturbance of photoinduced electron transfer from the electron-rich amine group to the electron-poor DPP core.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0040403922002726; http://dx.doi.org/10.1016/j.tetlet.2022.153853; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85130330737&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0040403922002726; https://dx.doi.org/10.1016/j.tetlet.2022.153853
Elsevier BV
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know