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(E)-4-甲基-N-((喹啉-2-基)亚乙基)苯胺作为IIB超分子配合物的配体:合成、结构、聚集诱导发光增强及其在聚甲基丙烯酸甲酯掺杂杂化材料中的应用

(E)-4-Methyl-N-((quinolin-2-yl)ethylidene)aniline as ligand for IIB supramolecular complexes: synthesis, structure, aggregation-induced emission enhancement and application in PMMA-doped hybrid material.

作者信息

Wang Ani, Fan Ruiqing, Dong Yuwei, Chen Wei, Song Yang, Wang Ping, Hao Sue, Liu Zhigang, Yang Yulin

机构信息

MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, P. R. China.

出版信息

Dalton Trans. 2016 Dec 20;46(1):71-85. doi: 10.1039/c6dt03853k.

DOI:10.1039/c6dt03853k
PMID:27897300
Abstract

Judicious structural design employing 2-quinolinecarboxaldehyde and 4-methylaniline was used to generate the Schiff base ligand (E)-4-methyl-N-((quinolin-2-yl)ethylidene)aniline (L). Five IIB complexes, namely, [ZnLCl] (1), [ZnL(NO)] (2), [ZnL(OAc)] (3), [CdL(OAc)] (4), and [HgLCl] (5) have been synthesized based on L. Single-crystal X-ray diffraction analysis indicates that complexes 1, 3 and 4 exhibit 3D networks, whereas 2 and 5 form 2D layers and 1D chains, respectively. TD-DFT calculations show a good correlation with the UV-vis absorption assigned to π → π* intraligand transitions. Furthermore, complexes 1-5 displayed strong greenish luminescent emissions (518-524 nm) in the aggregate state but weak emissions in solution (aggregation-induced emission enhancement), which may be due to the existence of C-HCl/O hydrogen bonding and ππ stacking interactions, resulting in restriction of intramolecular rotation (RIR). Variable-concentration H NMR studies suggested that the aggregates undergo intramolecular changes in conformation due to intermolecular interactions. Moreover, the emission intensity and lifetime exhibited obvious increases induced by mechanical grinding and temperature reduction, which were also attributed to AIEE properties. Subsequently, complex 1 was incorporated into poly(methyl methacrylate) (PMMA), whereby 1-PMMA exhibited enhanced emission intensity (20-fold increase in comparison with that of 1), which offers opportunities for use in plastic greenhouses to increase leaf photosynthesis.

摘要

采用2-喹啉甲醛和4-甲基苯胺进行合理的结构设计,以生成席夫碱配体(E)-4-甲基-N-((喹啉-2-基)亚乙基)苯胺(L)。基于L合成了五种IIB族配合物,即[ZnLCl] (1)、[ZnL(NO)] (2)、[ZnL(OAc)] (3)、[CdL(OAc)] (4)和[HgLCl] (5)。单晶X射线衍射分析表明,配合物1、3和4呈现三维网络结构,而配合物2和5分别形成二维层状和一维链状结构。TD-DFT计算结果与归属于配体内π→π*跃迁的紫外可见吸收具有良好的相关性。此外,配合物1-5在聚集态下表现出强烈的绿色发光发射(518-524 nm),但在溶液中发射较弱(聚集诱导发光增强),这可能是由于存在C-HCl/O氢键和π-π堆积相互作用,导致分子内旋转受限(RIR)。可变浓度1H NMR研究表明,聚集体由于分子间相互作用而发生分子内构象变化。此外,机械研磨和降温导致发射强度和寿命明显增加,这也归因于聚集诱导发光增强特性。随后,将配合物1掺入聚甲基丙烯酸甲酯(PMMA)中,由此1-PMMA表现出增强的发射强度(与1相比增加了20倍),这为在塑料温室中用于增强叶片光合作用提供了机会。

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