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脲嘧啶嘧啶酮接枝簇的有机阳离子调节组装行为。

Organic-Cation Modulated Assembly Behaviors of a Ureidopyrimidone-Grafting Cluster.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China.

出版信息

Molecules. 2023 Apr 24;28(9):3677. doi: 10.3390/molecules28093677.

Abstract

Ureidopyrimidone (UPy) is an important building block for constructing functional supramolecular polymers and soft materials based on their characteristic quadruple hydrogen bonds. While the evidence from the single-crystal X-ray diffraction data for the existence of linear hydrogen bonding has still been absent up to now. To obtain the crystals of UPy-containing molecules with high quality, enhanced rigidity and crystallinity are expected. Herein, an inorganic Anderson-Evans type cluster [Mn(OHMoO], which can provide suitable stiffness and charge, is used as a linker to covalently anchor two UPy units. The prepared organic-inorganic polyanion with three negative charges has a linear architecture, which is prone to form an infinite one-dimensional structure based on the supramolecular forces. The results indicate that the combination models of UPy units can be conveniently modulated by organic counter cations with different sizes, and therefore three unreported models are observed under various conditions. The present study gives a unique understanding of the intermolecular interactions in UPy-based supramolecular polymers and also provides a simple tuning method, which benefits the construction of functional materials and the adjustment of their properties.

摘要

尿嘧啶并嘧啶酮(UPy)是构建基于其特征四重氢键的功能超分子聚合物和软材料的重要构建块。尽管到目前为止,单晶 X 射线衍射数据仍缺乏线性氢键存在的证据。为了获得具有高质量、增强刚性和结晶度的 UPy 含分子晶体,期望使用无机 Anderson-Evans 型簇 [Mn(OHMoO]作为连接物,将两个 UPy 单元共价连接。所制备的具有三个负电荷的有机-无机聚阴离子具有线性结构,易于基于超分子力形成无限一维结构。结果表明,UPy 单元的组合模型可以通过具有不同大小的有机抗衡阳离子方便地调节,因此在各种条件下观察到三种未报道的模型。本研究对 UPy 基超分子聚合物中的分子间相互作用提供了独特的理解,并且还提供了一种简单的调节方法,这有利于功能材料的构建和其性能的调整。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd01/10180284/050e1366840f/molecules-28-03677-sch001.jpg

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