首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >Synthesis and optical properties of new 5-aryl-substituted 25-bis(3-decyl-22-bithiophen-5-yl)-134-oxadiazoles
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Synthesis and optical properties of new 5-aryl-substituted 25-bis(3-decyl-22-bithiophen-5-yl)-134-oxadiazoles

机译:新型5-芳基取代的25-双(3-癸基-22-联噻吩-5-基)-134-恶二唑的合成及光学性质

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摘要

New photoluminescent donor–acceptor–donor (DAD) molecules, namely 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles were prepared by palladium-catalyzed coupling from readily available compounds such as ethyl 3-decyl-2,2'-bithiophene-5-carboxylate and aryl halides. The obtained compounds feature increasing bathochromic shifts in their emission spectra with increasing aryl-substituent size yielding blue to bluish-green emissions. At the same time, their absorption spectra are almost independent from the identity of the terminal substituent with λmax values ranging from 395 to 405 nm. The observed trends are perfectly predicted by quantum chemical DFT/TDDFT calculations carried out for these new molecules.
机译:制备了新的光致发光供体-受体-供体(DAD)分子,即5'-芳基取代的2,5-双(3-癸基-2,2'-联噻吩-5-基)-1,3,4-恶二唑通过钯催化的偶合反应,可从容易获得的化合物(例如3-癸基-2,2'-联噻吩-5-羧酸乙酯和芳基卤化物)中进行偶联。所获得的化合物的特征在于其发射光谱中的红移增加,而芳基取代基的大小增加,从而产生蓝色至蓝绿色的发射。同时,它们的吸收光谱几乎与末端取代基的身份无关,λmax值在395至405 nm范围内。通过对这些新分子进行的量子化学DFT / TDDFT计算,可以完美地预测观察到的趋势。

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