Hassan Hammed Ham, Elhusseiny Amel F, Elkony Yasmeen Ma, Mansour El-Sayed Me
Chemistry Department, Faculty of Science, Alexandria University, P,O, Box 426-Ibrahimia, Alexandria 21321, Egypt.
Chem Cent J. 2013 Jan 23;7(1):13. doi: 10.1186/1752-153X-7-13.
The introduction of pendent bulky groups along the polymer backbone results in a less ordered polymer matrix and increases the solubility characteristics without affecting thermal properties. The inclusion of chromogenic chemical moieties in the chains can give rise to the luminescent converter material which permits the preparation of materials with potential applications. Aromatic polymers containing heterocyclic rings in the main chain are known for their high thermal resistance, good hydrolytic stability, low dielectric and tough mechanical properties. There is currently much research directed towards the discovery of new blue light-emitting polymers, with characteristics of high efficiency and high reliability. Herein, we describe the preparation of aromatic polyamides and poly (1,3,4-oxadiazole-amide)s nanoparticles with pendant structures comprised of m- and p-acetoxybenzamide groups, where the acetoxybenzamide groups act as signaling units due to their fluorescent and chromogenic characteristics.
Aromatic polyamides and poly(1,3,4-oxadiazole-amide)s nanoparticles with pendant structures comprised of m- and p-acetoxybenzamide groups were successfully prepared and characterized using different analytical methods. Most polyamides were obtained as well-separated spherical nanoparticles while aramide containing pyridine produced aggregated particles attributed to the molecular self assembly via H-bond directed organization of molecular precursors. The thermal behavior of all polymers exhibited two major thermal decompositions due to the subsequent breakage of the acetoxy group in the lateral chain and cleavage of the main amide bonds. Photoluminescence studies revealed that the blue emissions for the polyamide derived from benzidine were blue-shifted (shifted to a lower wavelength) compared to that of polyamides containing flexible linkages.
We report the synthesis of aromatic polyamides and poly(1,3,4-oxadiazole-amide)s nanoparticles with pendant structures comprised of m- and p-acetoxybenzamide groups. The thermal behavior of all polymers exhibited two major decompositions due to breakage of the acetoxy group in the lateral chain and cleavage of the main amide bonds. Structure- photoluminescence correlation demonstrated an interesting connection between structural modification and optical properties. The blue emissions for the polyamide derived from benzidine, attributed to the highly conjugation system, was blue shifted with the introduction of flexible linkages. The prepared polymers dissolved in warm polar aprotic solvents. Further investigations to obtain films with reasonably good mechanical properties for different applications are in progress.
沿着聚合物主链引入悬垂的庞大基团会导致聚合物基体的有序度降低,并在不影响热性能的情况下提高溶解性。在链中引入发色化学基团可产生发光转换材料,从而能够制备具有潜在应用价值的材料。主链中含有杂环的芳香族聚合物以其高耐热性、良好的水解稳定性、低介电常数和坚韧的机械性能而闻名。目前,有许多研究致力于发现具有高效率和高可靠性特征的新型蓝色发光聚合物。在此,我们描述了具有由间位和对位乙酰氧基苯甲酰胺基团组成的悬垂结构的芳香族聚酰胺和聚(1,3,4-恶二唑-酰胺)纳米颗粒的制备,其中乙酰氧基苯甲酰胺基团因其荧光和发色特性而充当信号单元。
成功制备了具有由间位和对位乙酰氧基苯甲酰胺基团组成的悬垂结构的芳香族聚酰胺和聚(1,3,4-恶二唑-酰胺)纳米颗粒,并使用不同的分析方法对其进行了表征。大多数聚酰胺以分离良好的球形纳米颗粒形式获得,而含吡啶的芳酰胺产生聚集颗粒,这归因于分子前体通过氢键定向组织的分子自组装。所有聚合物的热行为均表现出两个主要的热分解过程,这是由于侧链中乙酰氧基的后续断裂和主酰胺键的裂解所致。光致发光研究表明,与含有柔性链段的聚酰胺相比,由联苯胺衍生的聚酰胺的蓝色发射发生了蓝移(移至较低波长)。
我们报道了具有由间位和对位乙酰氧基苯甲酰胺基团组成的悬垂结构的芳香族聚酰胺和聚(1,3,4-恶二唑-酰胺)纳米颗粒的合成。由于侧链中乙酰氧基的断裂和主酰胺键的裂解,所有聚合物的热行为均表现出两个主要分解过程。结构-光致发光相关性证明了结构修饰与光学性质之间存在有趣的联系。归因于高度共轭体系,由联苯胺衍生的聚酰胺的蓝色发射随着柔性链段的引入而发生蓝移。所制备的聚合物可溶于温热的极性非质子溶剂中。目前正在进行进一步的研究,以获得具有合理良好机械性能的薄膜用于不同应用。