Thiophene derivative and application thereof
A technology of thiophene derivatives and heterocycles, which is applied in the field of thiophene derivatives, can solve the problems of reducing the relative quantum yield and application efficiency, and achieve the effects of excellent relative quantum yield, improved solubility, and easy use
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Embodiment 1
[0054] Thiophene derivatives of formula (12) were prepared in a 2 (in excess to 2.1):1 molar ratio feed according to the following procedure:
[0055]
[0056] Among them, the molecular weight of the obtained compound is 242, and its hydrogen spectrum identification position is given by 1 H NMR (solvent CDCl, 400MHz, ppm) chemical shift (δ) 7.63 (s, Ar-H 4H), 7.36-7.35 (d, Ar-H 2H), 7.31-7.30 (d, Ar-H 2H) , 7.12-7.09 (m, Ar-H 2H).
Embodiment 2
[0058] Thiophene derivatives of formula (13) were prepared in a 2 (in excess to 2.1):1 molar ratio feed according to the following procedure:
[0059]
[0060] Among them, the molecular weight of the obtained compound is 342, and its hydrogen spectrum identification position is given by 1 H NMR records (solvent CDCl 3 , 400MHz, ppm) chemical shift (δ): 7.90-7.87 (m, Ar-H 4H), 7.65-7.63 (m, Ar-H 2H), 7.43-7.41 (m, Ar-H 4H), 7.35-7.32 (m, Ar-H2H), 7.24-7.23 (m, Ar-H2H).
Embodiment 3
[0062] Thiophene derivatives of formula (14) were prepared in a 2 (in excess to 2.1):1 molar ratio feed according to the following procedure:
[0063]
[0064] Formula (14)
[0065] Among them, the molecular weight of the obtained compound is 270, and its hydrogen spectrum identification position is given by 1 H NMR records (solvent CDCl 3 , 400MHz, ppm) chemical shift (δ) 7.52 (s, Ar-H 4H), 7.24-7.23 (d, Ar-H 2H), 6.96-6.95 (d, Ar-H 2H), 2.38 (s, -CH 3 6H).
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Abstract
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