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Design synthesis and structure of novel G-2 melamine-based dendrimers incorporating 4-(n-octyloxy)aniline as a peripheral unit

机译:以4-(正辛氧基)苯胺为外围单元的新型G-2三聚氰胺基树枝状聚合物的设计合成和结构

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>Background: 4-(n-Octyloxy)aniline is a known component in the elaboration of organic materials with mesogenic properties such as N-substituted Schiff bases, perylene bisimide assemblies with a number of 2-amino-4,6-bis[4-(n-octyloxy)phenylamino]-s-triazines, amphiphilic azobenzene-containing linear-dendritic block copolymers and G-0 monomeric or dimeric dendritic liquid crystals with photochromic azobenzene mesogens. The present ab initio study explores a previously unknown use of 4-(n-octyloxy)aniline in the synthesis, structure and supramolecular behaviour of new dendritic melamines. >Results: Starting from 4-(n-octyloxy)aniline, seven G-2 melamine-based dendrimers were obtained in 29–79% overall yields. Their iterative convergent- and chemoselective synthesis consisted of SN2-Ar aminations of cyanuric chloride and final triple N-acylations and Williamson etherifications (→ G-2 covalent trimers) or stoichiometric carboxyl/amino 1:3 neutralisations (→ G-2 ionic trimers). These transformations connected G-1 chloro- and amino-termini dendrons to m-trivalent cores (triazin-2,4,6-triyl and benzene-1,3,5-triyl units) or tripodands (central building blocks), such as N-substituted melamines with 4-hydroxyphenyl or phenyl-4-oxyalkanoic motifs. Owing to the diversity of cores and central building blocks, the structural assortment of the dendritic series was disclosed by solvation effects (affecting reactivity), rotational stereodynamism and self-organisation phenomena (determining a vaulted and/or propeller macromolecular shape in solution). DFT calculations (in solution), (VT) NMR and IR (KBr) spectroscopy supported these assignments. TEM analysis revealed the ability of the title compounds towards self-assembling into homogeneously packed spherical nano-aggregates. >Conclusions: The (non)covalent synthesis and step-by-step structural elucidation of novel G-2 melamine dendrimers based on 4-(n-octyloxy)aniline are reported. Our study demonstrates the crucial influence of the nature (covalent vs ionic) of the dendritic construction in tandem with that of its central building blocks on the aptitude of dendrimers to self-organise in solution and to self-assembly in the solid state.
机译:>背景:4-(正辛基氧基)苯胺是具有介晶性质的有机材料(例如N-取代的席夫碱,带有多个2-氨基-4的per双酰亚胺化合物)的已知组分,6-双[4-(正辛氧基氧基)苯基氨基]-三嗪,两亲性含偶氮苯的线性树状嵌段共聚物和具有光致变色偶氮苯介晶的G-0单体或二聚体树枝状液晶。目前的从头开始研究探索了4-(n-辛基氧基)苯胺在新的树枝状三聚氰胺的合成,结构和超分子行为中的先前未知用途。 >结果:从4-(正辛氧基)苯胺开始,获得了7种基于G-2三聚氰胺的树枝状聚合物,总产率为29-79%。他们的迭代收敛和化学选择性合成由氰尿酰氯的SN2-Ar胺化和最终的三重N-酰化和Williamson醚化(→G-2共价三聚体)或化学计量的羧基/氨基1:3中和(→G-2离子三聚体)组成。这些转化将G-1氯和氨基末端树突连接至间三价核心(三嗪2,4,6-三基和苯-1,3,5-三基单元)或三脚架(中央结构单元),例如具有4-羟基苯基或苯基-4-氧基链烷酸基团的N-取代的三聚氰胺。由于核心和中心结构单元的多样性,通过溶剂化效应(影响反应性),旋转立体动力学和自组织现象(确定溶液中的拱形和/或螺旋桨大分子形状)公开了树突系列的结构分类。 DFT计算(在溶液中),(VT)NMR和IR(KBr)光谱支持这些分配。 TEM分析表明标题化合物具有自组装成均匀堆积的球形纳米聚集体的能力。 >结论:报告了基于4-(正辛氧基)苯胺的新型G-2三聚氰胺树枝状聚合物的(非)共价合成和分步结构解析。我们的研究表明,树枝状结构及其中心结构的本质(共价与离子性)串联对树枝状聚合物在溶液中自组织和固态自组装的适应性至关重要。

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