Dye-sensitized photoelectric conversion device
A photoelectric conversion and device technology, applied in the fields of photovoltaic power generation, electrical components, semiconductor devices, etc., can solve the problems of lack of practicality, low durability, and high cost of pigments
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Embodiment 1
[0132] 1 part of the following compound (532) and 0.45 parts of methyl cyanoacetate were dissolved in 10 parts of ethanol, and 0.05 parts of anhydrous piperazine was added to the solution. After performing the reflux reaction for 2 hours, the solid obtained by cooling was filtered, washed, and dried. The solid was refluxed in 20 parts ethanol in the presence of 1 part potassium hydroxide for 2 hours. After adding 50 parts of water to the reaction solution, it was neutralized with hydrochloric acid, and the precipitated orange crystals were filtered, washed with water, and recrystallized with ethanol to obtain 0.71 parts of Compound (197) as orange-brown crystals.
[0133] λmax (EtOH: 435nm)
[0134] 1H-NMR (PPM: d6-DMSO): 2.97 (s.CH 3 .6H), 6.77(d.arom.2H), 7.42(d.thio.1H), 7.56(d.arom.2H), 7.66(d.thio.1H), 8.08(s.-CH=.1H)
[0135]
Embodiment 2
[0137] Except that 1 part of compound (532) was replaced with 1.6 parts of the following compound (533), the same treatment as in Example 1 was carried out to obtain 0.98 parts of compound (205) as orange-brown crystals.
[0138] λmax (EtOH: 431)
[0139] 1H-NMR (PPM: d6-DMSO): 6.98 (d.arom.2H), 7.12 (m.arom.6H), 7.37 (m.arom.4H), 7.64 (d.thio.1H), 7.69 (d .arom.2H), 8.00(d.thio.1H), 8.47(s.-CH=.1H)
[0140]
Embodiment 3
[0142]Except that 1 part of compound (532) was replaced with 1.7 parts of the following compound (534), the same treatment as in Example 1 was carried out to obtain 1.23 parts of compound (523) as brown crystals.
[0143] λmax (EtOH: 457nm)
[0144] 1H-NMR (PPM:d6-DMSO): 6.98(d.arom.2H), 7.01-7.20(m.(arom.6H+-CH=.1H)), 7.27-7.44(m.(arom.4H+-CH =.1H)), 7.64(d.thio.1H), 7.68(d.arom.2H), 7.99(d.thio.1H), 8.47(s.-CH=.1H)
[0145]
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