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石墨上离散嵌段分子的超分子环缝:萘二亚胺封端的聚二甲基硅氧烷实现的可调疏水性

Supramolecular Loop Stitches of Discrete Block Molecules on Graphite: Tunable Hydrophobicity by Naphthalenediimide End-Capped Oligodimethylsiloxane.

作者信息

Berrocal José Augusto, Teyssandier Joan, Goor Olga J G M, De Feyter Steven, Meijer E W

机构信息

Institute for Complex Molecular Systems and Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands.

Division of Molecular Imaging and Photonics, Department of Chemistry, KU Leuven-University of Leuven, Celestijnenlaan 200 F, B-3001 Leuven, Belgium.

出版信息

Chem Mater. 2018 May 22;30(10):3372-3378. doi: 10.1021/acs.chemmater.8b00820. Epub 2018 May 1.

DOI:10.1021/acs.chemmater.8b00820
PMID:29861547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5973779/
Abstract

The noncovalent functionalization of surfaces has gained widespread interest in the scientific community, and it is progressively becoming an extremely productive research field offering brand new directions for both supramolecular and materials chemistry. As the end-groups often play a dominant role in the surface properties obtained, creating loops with end-groups only at the surface will lead to unexpected architectures and hence properties. Here we report the self-assembly of discrete block molecules-structures in-between block copolymers and liquid crystals-featuring oligodimethylsiloxanes (ODMS) end-capped with naphthalenediimides (NDIs) at the 1-phenyloctane/highly oriented pyrolytic graphite (1-PO/HOPG) interface. These structures produce unprecedented vertically nanophase-separated monolayers featuring NDI moieties that regularly arrange on the HOPG surface, while the highly dynamic ODMS segments form loops above them. Such arrangement is preserved upon drying and generates hydrophobic HOPG substrates in which the ODMS block length tunes the hydrophobicity. Thus, the exact structural fidelity of the discrete macromolecules allows for the correlation of nanoscopic organization with macroscopic properties of the self-assembled materials. We present a general strategy for tunable hydrophobic coatings on graphite based on molecularly combining crystalline aromatic moieties and immiscible oligodimethylsiloxanes.

摘要

表面的非共价功能化已在科学界引起广泛关注,并逐渐成为一个极具生产力的研究领域,为超分子化学和材料化学都提供了全新的方向。由于端基通常在所得表面性质中起主导作用,仅在表面形成带有端基的环会导致意想不到的结构,进而产生意想不到的性质。在此,我们报道了离散嵌段分子(介于嵌段共聚物和液晶之间的结构)在1-苯基辛烷/高度取向热解石墨(1-PO/HOPG)界面的自组装,其特征是萘二亚酰胺(NDIs)封端的低聚二甲基硅氧烷(ODMS)。这些结构产生了前所未有的垂直纳米相分离单层,其中NDI部分规则排列在HOPG表面,而高度动态的ODMS链段在其上方形成环。这种排列在干燥后得以保留,并产生疏水性HOPG基底,其中ODMS嵌段长度可调节疏水性。因此,离散大分子精确的结构保真度使得纳米级组织与自组装材料的宏观性质之间具有相关性。我们提出了一种基于分子结合结晶芳香部分和不混溶的低聚二甲基硅氧烷在石墨上制备可调谐疏水涂层的通用策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/6d6bbc90852f/cm-2018-00820x_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/4172ef55439b/cm-2018-00820x_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/28339c63777f/cm-2018-00820x_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/a78b24527696/cm-2018-00820x_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/3f7e17ccc9e1/cm-2018-00820x_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/6d6bbc90852f/cm-2018-00820x_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/4172ef55439b/cm-2018-00820x_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/28339c63777f/cm-2018-00820x_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/a78b24527696/cm-2018-00820x_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/3f7e17ccc9e1/cm-2018-00820x_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5edb/5973779/6d6bbc90852f/cm-2018-00820x_0005.jpg

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