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具有三(2,2'-联吡啶)钌催化剂核的温敏核壳水凝胶微球中的别洛索夫-扎鲍廷斯基反应。

The Belousov-Zhabotinsky Reaction in Thermoresponsive Core-Shell Hydrogel Microspheres with a Tris(2,2'-bipyridyl)ruthenium Catalyst in the Core.

机构信息

Department of Materials Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.

出版信息

J Phys Chem B. 2020 May 7;124(18):3828-3835. doi: 10.1021/acs.jpcb.0c02238. Epub 2020 Apr 24.

DOI:10.1021/acs.jpcb.0c02238
PMID:32293889
Abstract

The Belousov-Zhabotinsky (BZ) reaction shows temporal or spatiotemporal structures such as redox oscillation of the catalyst, [ruthenium(II)tris(2,2'-bipyridine)][PF] ([Ru(bpy)][PF]). In this study, autonomously oscillating hydrogel microspheres (microgels) were investigated, which show swelling/deswelling oscillation induced by the redox oscillation of the BZ reaction inside the gel. Despite the periodically and autonomously induced oscillation that does not require an external stimulus, it has not been possible to perform any manipulation of the oscillatory behavior over time. The results of the present study show that it is possible to reversibly switch the microgel oscillations from an "on" active state of the BZ reaction to an "off" inactive state by changing the temperature in combination with thermoresponsive microgels. To realize on-demand switching, the construction of double-shell structures is crucial; the thermoresponsive first shell allows the microgels to modulate the diffusion of the substrates or intermediates in the BZ reaction, while the second shell maintains colloidal stability under high temperatures and high ion concentrations. The functionalized double-shell microgels were prepared via multistep seeded precipitation polymerization. The oscillatory switching behavior of the BZ reaction was observed directly and evaluated by ultraviolet-visible (UV-vis) spectroscopy. The central concept of this study, i.e., "on-off switching" can be expected to benefit the development of advanced bioinspired materials.

摘要

别洛乌索夫-扎鲍廷斯基(BZ)反应表现出时间或时空结构,例如催化剂的氧化还原振荡,[钌(II)三(2,2'-联吡啶)][PF]([Ru(bpy)][PF])。在这项研究中,研究了自主振荡水凝胶微球(微凝胶),其表现出由凝胶内 BZ 反应的氧化还原振荡引起的溶胀/去溶胀振荡。尽管周期性和自主诱导的振荡不需要外部刺激,但一直无法对随时间变化的振荡行为进行任何操作。本研究的结果表明,通过改变温度结合温敏微凝胶,有可能将微凝胶的振荡从 BZ 反应的“开”活跃状态可逆地切换到“关”非活跃状态。为了实现按需切换,构建双层结构至关重要;温敏第一层允许微凝胶调节 BZ 反应中的底物或中间物的扩散,而第二层在高温和高离子浓度下保持胶体稳定性。功能化双层微凝胶通过多步种子沉淀聚合制备。通过紫外可见(UV-vis)光谱直接观察和评估 BZ 反应的振荡切换行为。本研究的核心概念,即“开-关切换”,有望有益于先进仿生材料的发展。

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