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Advantageous Microwave-Assisted Suzuki Polycondensation for the Synthesis of Aniline-Fluorene Alternate Copolymers as Molecular Model with Solvent Sensing Properties

机译:有利的微波辅助铃木缩聚,用于合成苯胺 - 芴替换共聚物作为溶剂感应性能的分子模型

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摘要

Polymerization via Suzuki coupling under microwave (µW) irradiation has been studied for the synthesis of poly{1,4-(2/3-aminobenzene)-alt-2,7-(9,9-dihexylfluorene)} (PAF), chosen as molecular model. Briefly, µW-assisted procedures accelerated by two orders of magnitude the time required when using classical polymerization processes, and the production yield was increased (>95%). In contrast, although the sizes of the polymers that were obtained by non-conventional heating reactions were reproducible and adequate for most applications, with this methodology the molecular weight of final polymers were not increased with respect to conventional heating. Asymmetric orientation of the amine group within the monomer and the assignments of each dyad or regioregularity, whose values ranged from 38% to 95% with this molecule, were analysed using common NMR spectroscopic data. Additionally, the synthesis of a new cationic polyelectrolyte, poly{1,4-(2/3-aminobenzene)-co-alt-2,7-[9,9´-bis(6’’-N,N,N-trimethylammonium-hexyl)fluorene]} dibromide (PAFAm), from poly{1,4-(2/3-aminobenzene)-co-alt-2,7-[9,9´-bis(6’’-bromohexyl)fluorene]} (PAFBr) by using previously optimized conditions for µW-assisted heating procedures was reported. Finally, the characterization of the final products from these batches showed unkown interesting solvatochromic properties of the PAF molecule. The study of the solvatochromism phenomena, which was investigated as a function of the polarity of the solvents, showed a well-defined Lippert correlation, indicating that the emission shift observed in PAF might be due to its interaction with surrounding environment. Proven high sensitivity to changes of its environment makes PAF a promising candidate of sensing applications.
机译:通过铃木聚合下微波耦合(μW)照射已经研究了合成聚{1,4-(三分之二氨基苯)-alt-2,7-(9,9-二己基)}(PAF),选择作为分子模型。简言之,μW辅助手术加速由两个数量级使用经典聚合方法时所需要的时间,生产产量增加(> 95%)。相反,尽管通过非常规加热反应获得的聚合物的尺寸是大多数应用的可再现和足够的,但是通过该方法,最终聚合物的分子量不增加常规加热。使用常见的NMR光谱数据分析单体内单体内的胺基的不对称和每个二元或再生性的分配,其值与该分子的值范围为38%至95%。此外,一个新的阳离子型聚电解质,聚{1,4-(三分之二氨基苯) - 共 - 交替-2,7- [9,9'-双(6“”的合成 - N,N,N-三甲基铵己基)芴]}二溴化物(PAFAm),从聚{1,4-(三分之二氨基苯) - 共 - 交替-2,7- [9,9'-双(6“” - 溴己基)芴报道]通过使用用于μW辅助加热程序先前优化的条件}(PAFBr)。最后,来自这些批次的最终产物的表征显示了PAF分子的不概述有趣的溶解度。的溶致变色现象,这是研究作为溶剂的极性的功能的研究中,显示出良好定义的利珀特相关性,这表明PAF在所观察到的发射偏移可能是由于其与周围环境的相互作用。证明对环境变化的高度敏感性使PAF成为传感应用的有希望的候选者。

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