Hydroquinone–pyrrole dyads with varied linkers
A series of pyrroles functionalized in the 3-position with p-dimethoxybenzene via various linkers (CH2, CH2CH2, CH=CH, C≡C) has been synthesized. Their electronic properties have been deduced from 1H NMR, 13C NMR, and UV–vis spectra to detect possible interactions between the two aromatic subunits....
Main Authors: | , , , , |
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Format: | Online |
Language: | English |
Published: |
Beilstein-Institut
2016
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734300/ |