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芳香族聚(甲亚胺)的液相合成、其物理化学性质以及造粒粉末样品的电导率测量

Liquid phase synthesis of aromatic poly(azomethine)s, their physicochemical properties, and measurement of electrical conductivity of pelletized powdered samples.

作者信息

Hafeez Abdul, Akhter Zareen, Gallagher John F, Siddiqui Humaira M

机构信息

Department of Chemistry, Quaid-i-Azam University, Islamabad, Pakistan.

School of Chemical Sciences, Dublin City University, Dublin, Ireland.

出版信息

Des Monomers Polym. 2016 Sep 23;20(1):74-88. doi: 10.1080/15685551.2016.1231042. eCollection 2017.

Abstract

Aromatic -aldehydes have been used as building blocks in the synthesis of polyazomethines (a class of conjugated Schiff bases) and their physicochemical properties have been studied. Six dialdehydes have been synthesized, , via etherification reaction between aromatic diols () and 4-fluorobenzaldehyde () (see Scheme 1), and then polymerized with 1,4-phenylenediamine () and 4,4'-oxydianiline () (see Scheme 2). The chemical structures of the -aldehydes were elucidated by FTIR, H NMR and C NMR spectroscopic studies, elemental analysis and single crystal whereas the polymers were studied by FTIR and NMR spectroscopy. Their physicochemical properties were examined by their inherent viscosity, organosolubility, differential scanning calorimetry, X-ray powder diffraction, thermogravimetric analysis, solvatochromism, and photoluminescence. We report the electrical conductivity of each polymer measured by the four probe method. The results indicate that the electrical conductivity of polymers lies in range 0.019-0.051 mScm which is reasonably higher than any reported value.

摘要

芳香醛已被用作合成聚甲亚胺(一类共轭席夫碱)的基础原料,并且对其物理化学性质进行了研究。通过芳族二醇()与4-氟苯甲醛()之间的醚化反应合成了六种二醛(见方案1),然后使其与1,4-苯二胺()和4,4'-二氨基二苯醚()聚合(见方案2)。通过傅里叶变换红外光谱(FTIR)、氢核磁共振(¹H NMR)和碳核磁共振(¹³C NMR)光谱研究、元素分析和单晶对二醛的化学结构进行了阐明,而通过FTIR和核磁共振光谱对聚合物进行了研究。通过它们的特性粘度、有机溶剂溶解性、差示扫描量热法、X射线粉末衍射、热重分析、溶剂化显色和光致发光对其物理化学性质进行了研究。我们报告了通过四探针法测量的每种聚合物的电导率。结果表明,聚合物的电导率在0.019 - 0.051 mS/cm范围内,这比任何已报道的值都要高得多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e02a/5812128/ed4511d6175f/TDMP_A_1231042_F0001_OC.jpg

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