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模型阴离子嵌段共聚物囊泡为方解石内高效纳米颗粒包裹提供了重要的设计规则。

Model Anionic Block Copolymer Vesicles Provide Important Design Rules for Efficient Nanoparticle Occlusion within Calcite.

机构信息

Department of Chemistry , University of Sheffield , Brook Hill, Sheffield , South Yorkshire S3 7HF , U.K.

School of Chemistry , University of Leeds , Woodhouse Lane , Leeds , LS2 9JT , U.K.

出版信息

J Am Chem Soc. 2019 Feb 13;141(6):2557-2567. doi: 10.1021/jacs.8b12507. Epub 2019 Jan 29.

Abstract

Nanoparticle occlusion within growing crystals is of considerable interest because (i) it can enhance our understanding of biomineralization and (ii) it offers a straightforward route for the preparation of novel nanocomposites. However, robust design rules for efficient occlusion remain elusive. Herein, we report the rational synthesis of a series of silica-loaded poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacrylate)-poly(ethylene glycol dimethacrylate)-poly(methacrylic acid) tetrablock copolymer vesicles using polymerization-induced self-assembly. The overall vesicle dimensions remain essentially constant for this series; hence systematic variation of the mean degree of polymerization (DP) of the anionic poly(methacrylic acid) steric stabilizer chains provides an unprecedented opportunity to investigate the design rules for efficient nanoparticle occlusion within host inorganic crystals such as calcite. Indeed, the stabilizer DP plays a decisive role in dictating both the extent of occlusion and the calcite crystal morphology: sufficiently long stabilizer chains are required to achieve extents of vesicle occlusion of up to 41 vol %, but overly long stabilizer chains merely lead to significant changes in the crystal morphology, rather than promoting further occlusion. Furthermore, steric stabilizer chains comprising anionic carboxylate groups lead to superior occlusion performance compared to those composed of phosphate, sulfate, or sulfonate groups. Moreover, occluded vesicles are subjected to substantial deformation forces, as shown by the significant change in shape after their occlusion. It is also demonstrated that such vesicles can act as "Trojan horses", enabling the occlusion of non-functional silica nanoparticles within calcite. In summary, this study provides important new physical insights regarding the efficient incorporation of guest nanoparticles within host inorganic crystals.

摘要

纳米颗粒在生长晶体中的阻塞引起了相当大的关注,因为 (i) 它可以增强我们对生物矿化的理解,(ii) 它为制备新型纳米复合材料提供了一种直接的途径。然而,高效阻塞的稳健设计规则仍然难以捉摸。在此,我们报告了使用聚合诱导自组装合理合成一系列负载有二氧化硅的聚(甘油单甲基丙烯酸酯)-聚(2-羟丙基甲基丙烯酸酯)-聚(乙二醇二甲基丙烯酸酯)-聚(甲基丙烯酸)四嵌段共聚物囊泡。对于这个系列,囊泡的整体尺寸基本保持不变;因此,阴离子聚(甲基丙烯酸)位阻稳定剂链的平均聚合度 (DP) 的系统变化为研究高效纳米颗粒在方解石等宿主无机晶体中的阻塞设计规则提供了前所未有的机会。事实上,稳定剂 DP 在决定阻塞程度和方解石晶体形态方面起着决定性的作用:需要足够长的稳定剂链才能达到高达 41 体积%的囊泡阻塞程度,但过长的稳定剂链只会导致晶体形态发生显著变化,而不会促进进一步的阻塞。此外,由阴离子羧酸酯组成的位阻稳定剂链比由磷酸盐、硫酸盐或磺酸盐组成的链具有更好的阻塞性能。此外,如阻塞后形状发生显著变化所示,被阻塞的囊泡受到相当大的变形力。还证明了这些囊泡可以作为“特洛伊木马”,使非功能性二氧化硅纳米颗粒能够被阻塞在方解石中。总之,本研究为高效地将客体纳米颗粒嵌入宿主无机晶体提供了重要的新物理见解。

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