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疏水末端调制的基于氨基酸的中性水凝胶剂:碳纳米材料的结构特异性包合

Hydrophobic End-Modulated Amino-Acid-Based Neutral Hydrogelators: Structure-Specific Inclusion of Carbon Nanomaterials.

作者信息

Choudhury Pritam, Mandal Deep, Brahmachari Sayanti, Das Prasanta Kumar

机构信息

Department of Biological Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, 700032, India.

出版信息

Chemistry. 2016 Apr 4;22(15):5160-72. doi: 10.1002/chem.201504888. Epub 2016 Feb 24.

DOI:10.1002/chem.201504888
PMID:26916229
Abstract

Hydrophobic end-modulated l-phenylalanine-containing triethylene glycol monomethyl ether tagged neutral hydrogelators (1-4) are developed. Investigations determine the gelators' structure-dependent inclusion of carbon nanomaterials (CNMs) in the self-assembled fibrillar network (SAFIN). The gelators (1, 3, and 4) can immobilize water and aqueous buffer (pH 3-7) with a minimum gelator concentration of 10-15 mg mL(-1). The hydrophobic parts of the gelators are varied from a long chain (C-16) to an extended aromatic pyrenyl moiety, and their abilities to integrate 1 D and 2 D allotropes of carbon (i.e., single-walled carbon nanotubes (SWNTs) and graphene oxide (GO), respectively) within the gel are investigated. Gelator 1, containing a long alkyl chain (C-16), can include SWNTs, whereas the pyrene-containing 4 can include both SWNTs and GO. Gelator 3 fails to incorporate SWNTs or GO owing to its slow rate of gelation and possibly a mismatch between the aggregated structure and CNMs. The involvement of various forces in self-aggregated gelation and physicochemical changes occurring through CNM inclusion are examined by spectroscopic and microscopic techniques. The distinctive pattern of self-assembly of gelators 1 and 4 through J- and H-type aggregation might facilitate the structure-specific CNM inclusion. Inclusion of SWNTs/GO within the hydrogel matrix results in a reinforcement in mechanical stiffness of the composites compared with that of the native hydrogels.

摘要

开发了含疏水性末端修饰的 l - 苯丙氨酸的三甘醇单甲醚标记的中性水凝胶剂(1 - 4)。研究确定了这些凝胶剂在自组装纤维网络(SAFIN)中对碳纳米材料(CNM)的结构依赖性包合。凝胶剂(1、3 和 4)能固定水和水性缓冲液(pH 3 - 7),最低凝胶剂浓度为 10 - 15 mg mL⁻¹。凝胶剂的疏水部分从长链(C - 16)变化到扩展的芘基部分,并研究了它们在凝胶中整合一维和二维碳同素异形体(即分别为单壁碳纳米管(SWNTs)和氧化石墨烯(GO))的能力。含长烷基链(C - 16)的凝胶剂 1 能包含 SWNTs,而含芘的凝胶剂 4 能同时包含 SWNTs 和 GO。凝胶剂 3 由于其凝胶化速率慢且可能聚集结构与 CNM 不匹配,未能掺入 SWNTs 或 GO。通过光谱和显微镜技术研究了各种力在自聚集凝胶化中的作用以及通过包含 CNM 发生的物理化学变化。凝胶剂 1 和 4 通过 J 型和 H 型聚集形成的独特自组装模式可能有助于结构特异性的 CNM 包合。与天然水凝胶相比,在水凝胶基质中包含 SWNTs/GO 会导致复合材料的机械刚度增强。

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