Thiourea functionalized micromolecular co-sensitizing adsorbent
A functional, small molecule technology, applied in the field of organic dyes, can solve the problems of intermolecular agglomeration, narrow light absorption range, low photoelectric conversion efficiency, etc., and achieve the effect of short transmission path, small molecular structure and simple configuration
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Embodiment 1
[0025] Synthesis of thiourea functionalized small molecule co-sensitive adsorbent Ⅰ, the specific synthesis route and method are as follows:
[0026]
[0027] 1. Preparation of compound b
[0028] Under nitrogen protection, 8.56g (20.0mmol) of compound a, 50mL of toluene, and 6.46g (16.0mmol) of Lawson's reagent were successively added to a 100mL three-necked flask with a thermometer, and the stirring was started, and the reaction was refluxed for 12 hours, and the reaction solution was lowered to After reaching room temperature, filter out the insoluble matter, evaporate the filtrate to remove the solvent, and then purify by column chromatography (the developing solvent is a mixture of petroleum ether and ethyl acetate with a volume ratio of 8:1, and the filler is 200-300 mesh silica gel ), to obtain compound b6.65g, the yield was 75.0%.
[0029] 2. Preparation of compound f
[0030] Under nitrogen protection, 1.56g (10.0mmol) compound e, 3g (6.8mmol) compound b, 0.66g (...
Embodiment 2
[0035] Synthesis of thiourea functionalized small molecule co-sensitive adsorbent II, the specific synthesis route and method are as follows:
[0036]
[0037] In step 2 of Example 1, the compound e used was replaced with an equimolar compound g, and the other steps were the same as in Example 1 to prepare co-sensitive adsorbent II.
[0038] The NMR data of the prepared co-sensitive adsorbent II are: 1 H NMR (300MHz, CDCl 3 ): δ (ppm) 8.38 (s, 1H), 7.81 (s, 1H), 7.65 (s, 1H), 7.47 (d, J=4.2Hz, 1H), 7.33 (s, 1H), 7.19 (d, J=4.2Hz, 1H), 4.31(t, J=3.9Hz, 2H), 4.28(t, J=3.9Hz, 2H), 1.87-1.79(m, 4H), 1.47-1.32(m, 12H), 0.89 (t, J=3.3Hz, 6H).
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