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基于多面体低聚倍半硅氧烷(POSS)核的树枝状大分子的外围基团:构建高级超结构的关键因素。

Peripheral groups of polyhedral oligomeric silsesquioxane (POSS) core-based dendrimers: a crucial factor for higher-level supra-architecture building.

作者信息

He Huiwen, Zheng Hao, Ma Meng, Shi Yanqing, Gao Zengliang, Chen Si, Wang Xu

机构信息

College of Materials Science and Engineering, Zhejiang University of Technology, 18 Chaowang Road, Hangzhou 310014, China.

College of mechanical Engineering, Zhejiang University of Technology, 288 Liuhe Road, Hangzhou 310000, China.

出版信息

Nanoscale. 2020 Jun 11;12(22):12146-12153. doi: 10.1039/d0nr03216f.

DOI:10.1039/d0nr03216f
PMID:32490499
Abstract

The role of peripheral groups (PGs) on dendrimers in the spontaneous higher-level organization of hierarchically assembled nanofibers was investigated in a series of POSS-based dendritic gelators (POSS-Lys-X, X: -Boc, -Cbz, -Fmoc, etc.). We demonstrate that the PGs not only affect the gelation ability in solutions, but also the construction of orderly entangled fibrous supramolecular networks, e.g., "loofah-like" networks. Attributed to the PGs (especially the -Boc group) causing a lower cooperative assembly, the steady state with the lowest potential energy of gelators can be easily achieved by the higher ordering of nanofiber entanglement into superstructures. The -Boc group-containing dendrimers show low molar enthalpy and molar entropy of gelation, which help the construction of unique three-dimensional (3D) "loofah-like" superstructures. In contrast, the high cooperative assembly of the dendrimer (-Cbz as the PG) promotes the gelator into a higher enthalpy gelation process, with a constructed normal fibrous network. Hence, the PGs of POSS-based dendrimers act as the crucial factor in controlling the hierarchical self-assembly via a thermodynamics approach. This research presents new perspectives to explicate the relationships between PGs of dendrimers, supra-architectures and gel performances, which further guide the design of functional supramolecular materials via controllable self-assembly.

摘要

在一系列基于倍半硅氧烷的树枝状凝胶剂(POSS-Lys-X,X:-Boc、-Cbz、-Fmoc等)中,研究了树枝状大分子上的外围基团(PGs)在分层组装纳米纤维的自发高级组织中的作用。我们证明,PGs不仅影响溶液中的凝胶化能力,还影响有序缠结的纤维状超分子网络的构建,例如“丝瓜状”网络。由于PGs(尤其是-Boc基团)导致较低的协同组装,通过纳米纤维缠结形成超结构的更高有序排列,可以轻松实现凝胶剂具有最低势能的稳态。含-Boc基团的树枝状大分子表现出较低的凝胶化摩尔焓和摩尔熵,这有助于构建独特的三维(3D)“丝瓜状”超结构。相比之下,树枝状大分子(以-Cbz作为PG)的高协同组装促进凝胶剂进入更高焓的凝胶化过程,形成正常的纤维网络。因此,基于倍半硅氧烷的树枝状大分子的PGs通过热力学方法成为控制分层自组装的关键因素。这项研究为阐明树枝状大分子的PGs、超结构和凝胶性能之间的关系提供了新的视角,进一步指导通过可控自组装设计功能性超分子材料。

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