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Cooperative Supramolecular Block Copolymerization for the Synthesis of Functional Axial Organic Heterostructures

机译:合作超分子嵌段嵌段共聚,用于合成功能轴向有机异质结构

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摘要

Supramolecular block copolymerzation with optically or electronically complementary monomers provides an attractive bottom-up approach for the non-covalent synthesis of nascent axial organic heterostructures, which promises to deliver useful applications in energy conversion, optoelectronics, and catalysis. However, the synthesis of supramolecular block copolymers (BCPs) constitutes a significant challenge due to the exchange dynamics of non-covalently bound monomers and hence requires fine microstructure control. Furthermore, temporal stability of the segmented microstructure is a prerequisite to explore the applications of functional supramolecular BCPs. Herein, we report the cooperative supramolecular block copolymerization of fluorescent monomers in solution under thermodynamic control for the synthesis of axial organic heterostructures with light-harvesting properties. The fluorescent nature of the core-substituted naphthalene diimide (cNDI) monomers enables a detailed spectroscopic probing during the supramolecular block copolymerization process to unravel a nucleation-growth mechanism, similar to that of chain copolymerization for covalent block copolymers. Structured illumination microscopy (SIM) imaging of BCP chains characterizes the segmented microstructure and also allows size distribution analysis to reveal the narrow polydispersity (polydispersity index (PDI) ≈ 1.1) for the individual block segments. Spectrally resolved fluorescence microscopy on single block copolymerized organic heterostructures shows energy migration and light-harvesting across the interfaces of linearly connected segments. Molecular dynamics and metadynamics simulations provide useful mechanistic insights into the free energy of interaction between the monomers as well as into monomer exchange mechanisms and dynamics, which have a crucial impact on determining the copolymer microstructure. Our comprehensive spectroscopic, microscopic, and computational analyses provide an unambiguous structural, dynamic, and functional characterization of the supramolecular BCPs. The strategy presented here is expected to pave the way for the synthesis of multi-component organic heterostructures for various functions.
机译:具有光学或电子互补的单体的超分子嵌段共聚合提供了一种有吸引力的自下而上的方法,用于非共价合成新生的轴向有机异质结构,这有助于在能量转换,光电子和催化中提供有用的应用。然而,由于非共价结合单体的交换动态,因此超分子嵌段共聚物(BCPS)的合成构成了显着的挑战,因此需要细胞结构控制。此外,分段微结构的时间稳定性是探索功能性超分子BCP的应用的先决条件。在此,我们在热动力控制下报告荧光单体的协同超分子嵌段共聚,用于合成轴向有机异质结构,具有光收获性能。核 - 取代的萘二酰亚胺(CNDI)单体的荧光性质使得在超分子嵌段共聚过程中进行详细的光谱探测,以解开成核 - 生长机制,类似于共价嵌段共聚物的链共聚物的核心生长机制。 BCP链的结构照明显微镜(SIM)成像表征分段的微观结构,并且还允许尺寸分布分析来揭示各个块段的窄多分散性(多分散指数(PDI)≈1.1)。单嵌段共聚有机异质结构上的光谱解析的荧光显微镜显示出线性连接段的界面的能量迁移和光收获。分子动力学和元动力学模拟为单体和单体交换机制和动力学的自由能量提供了有用的机械洞察力,以及对确定共聚物微观结构的关键影响。我们的综合光谱,微观和计算分析提供了超分子BCP的明确结构,动态和功能性表征。这里提出的策略预计将为各种功能合成多组分有机异质结构的方法。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2020年第26期|11528-11539|共12页
  • 作者单位

    New Chemistry Unit and School of Advanced Materials (SAMat) Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) Jakkur Bangalore 560064 India;

    Department of Chemistry Indian Institute of Technology Bombay Powai Mumbai 400076 India;

    New Chemistry Unit and School of Advanced Materials (SAMat) Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) Jakkur Bangalore 560064 India;

    Department of Applied Science and Technology Politecnico di Torino 10129 Torino Italy;

    Department of Innovative Technologies University of Applied Sciences and Arts of Southern Switzerland CH-6928 Manno Switzerland;

    Department of Chemistry Indian Institute of Technology Bombay Powai Mumbai 400076 India;

    New Chemistry Unit and School of Advanced Materials (SAMat) jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) Jakkur Bangalore 560064 India;

    Department of Applied Science and Technology Politecnico di Torino 10129 Torino Italy Department of Innovative Technologies University of Applied Sciences and Arts of Southern Switzerland CH-6928 Manno Switzerland;

    Department of Chemistry Indian Institute of Technology Bombay Powai Mumbai 400076 India;

    New Chemistry Unit and School of Advanced Materials (SAMat) Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) Jakkur Bangalore 560064 India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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