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首页> 外文期刊>Journal of porphyrins and phthalocyanines >Discotic liquid crystals of transition metal complexes, 54(+): Rapid microwave-assisted synthesis and homeotropic alignment of phthalocyanine-based liquid crystals
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Discotic liquid crystals of transition metal complexes, 54(+): Rapid microwave-assisted synthesis and homeotropic alignment of phthalocyanine-based liquid crystals

机译:过渡金属配合物的盘状液晶,54(+):磷酸酞菁的液晶的快速微波辅助合成和垂直对齐

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摘要

The most difficult problem on syntheses of the phthalocyanine-based liquid crystals is the long reaction time. In order to shorten the reaction time, we have developed novel Methods A, B and D, for the syntheses of phthalocyanine-based liquid crystals by using microwave heating and/or adding a phase transfer catalysis of Aliquat 336. A series of phthalocyanine derivatives CnPcZn(1) (n = 10, 12, 14, 16 and 18: a, b, c and e) could be successfully synthesized in a dramatically short reaction time of 30-60 min using Methods A and B by microwave heating. On the other hand, anothor series of the derivatives C-n(OH) PcZn (2a-2e) could not be synthesized by microwave heating. Therefore, all these derivatives were synthesized using conventional Method C by oil bath heating, but the reaction took a very long time (22.5-88 h). To shorten the reaction time, we have developed Method D by oil bath heating with adding a phase transfer catalyst of Aliquat 336. In this method, we successfully shortened the reaction time from 88 h to 3 h for the synthesis of the derivative 2a. Thus, the reaction time for oil bath heating can be also greatly shortened by adding the phase transfer catalyst of Aliquat 336. Furthermore, we have established from POM, DSC and temperature-dependent X-ray diffraction measurements that the derivative C10PcZn (1a) shows a very rare pseudohexagonal columnar (Col(hr)) phase, and that the derivatives CnPcZn (1b-1e) and C-n(OH) PcZn (2b-2e) exhibit spontaneous perfect homeotropic alignment in a large area between two glass plates in their Col(tet) phases.
机译:基于酞菁的液晶合成的最困难的问题是长反应时间。为了缩短反应时间,我们通过使用微波加热和/或加入Aliquat 336的相转移催化来开发新的方法A,B和D.对于基于酞菁的液晶的合成。一系列酞菁衍生物CNPCZN (1)(n = 10,12,14,16和18:a,b,c和e)可以在通过微波加热的方法a和b的30-60分钟的短时间内反应时间成功地合成。另一方面,通过微波加热不能合成衍生物C-N(OH)PCZN(2A-2E)的Anothor系列。因此,所有这些衍生物都是通过油浴加热使用常规方法C合成的,但反应花了很长时间(22.5-88小时)。为了缩短反应时间,我们通过加入Aliquat 336的相转移催化剂进行了方法D.在该方法中,我们成功地将反应时间从88小时从88小时缩短,以合成衍生物2a。因此,通过添加Aliquat 336的相转移催化剂,还可以大大缩短油浴加热的反应时间。此外,我们已经从POM,DSC和温度依赖性X射线衍射测量中建立,即衍生物C10PCZN(1A)显示一个非常罕见的假胶柱柱状柱(COL(HR))相,并且衍生物CNPCZN(1B-1E)和CN(OH)PCZN(2B-2E)在其COL的两个玻璃板之间的大面积中表现出自发的完美垂直对齐(Tet)阶段。

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