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2 protocols using 5 formyl 2 thienylboronic acid

1

Synthesis and Characterization of Thiophene-Pyrrole Dyes

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2,4-Dimethylpyrrole
(≥ 97.0, Sigma-Aldrich), 4-bromobenzaldehyde (≥ 99.0,
Sigma-Aldrich), trifluoroacetic acid (≥ 99.0, Sigma-Aldrich),
DDQ (≥ 98.0, Sigma-Aldrich), boron trifluoride diethyl etherate
(≥ 98.0, TCI), 5-formyl-2-thienylboronic acid (≥ 95.0,
Sigma-Aldrich), bis(triphenylphosphine)palladium(II) dichloride (≥
98.0, Sigma-Aldrich), n-hexane (HPLC grade, ≥ 99.0, Sigma-Aldrich),
dichloromethane (anhydrous, ≥ 99.9, Sigma-Aldrich), acetonitrile
(anhydrous, ≥ 99.9, Sigma-Aldrich), ethanol (≥ 99.8,
Sigma-Aldrich), chloroform (≥ 99.8, Sigma-Aldrich), and ethyl
acetate (anhydrous, ≥ 99.8, Sigma-Aldrich) were used. All metal
salts were used as their water-soluble sulfate, nitrate, or chloride
salts, purchased from Sigma-Aldrich (≥ 95). A Varian VNMRJ
600 nuclear magnetic resonance spectrometer was used for 1H NMR and 13C NMR measurements. Mass analysis was conducted
with a Thermo Q-Exactive Orbitrap device. Ultraviolet–visible
(UV–vis) absorption spectra were obtained with a spectrophotometer
(Shimadzu 1900i). Fluorescence emission measurements were obtained
using a Varian Cary Eclipse fluorescence spectrophotometer. Quantum
yield measurements were conducted with a Hamamatsu Quantaurus-QY absolute
PL quantum yield spectrometer.
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2

Synthesis of Thiophene-based Compounds

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Spectroscopic grade acetonitrile and 5-dimethylthiophene-2-carbaldehyde (95%), 5-(dimethylamino)thiophene-2-carbaldehyde (95%), 5-formyl-2-thienylboronic acid (95%) and 1-bromonaphthalene (95%) were purchased from Sigma Aldrich and used as received. 1-Bromo-4-dimethylaminonaphthalene (95%) was purchased from Alfa Aesar and used as received. Tetrakis(triphenylphosphine)palladium was purchased from Strem Chemicals and used as received. ACS reagent grade toluene, tetrahydrofuran, dichloromethane and hexane for synthesis were purchased from Pharmco Aaper. 1, 2, DMA-2, DMA-3, 4 and DMA-4 have been previously reported (30 (link), 37 , 43 , 44 (link)). 3, 5 and DMA-5 were prepared using a previously reported standard procedure (30 (link)) from the commercially available 5-dimethylamino-thiophene-2-carbaldehyde, and the prepared 5-ald and DMA-5-ald, respectively.
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