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大分子何时从聚合物链转变为纳米颗粒?

When does a macromolecule transition from a polymer chain to a nanoparticle?

作者信息

Fischer Jacob, Han Lu, Saito Tomonori, Dadmun Mark

机构信息

Department of Chemistry, University of Tennessee Knoxville Tennessee USA

Chemical Sciences Division, Oak Ridge National Lab Oak Ridge Tennessee USA.

出版信息

Nanoscale Adv. 2022 Nov 8;4(23):5164-5177. doi: 10.1039/d2na00617k. eCollection 2022 Nov 22.

Abstract

Frequently, the defining characteristic of a nanoparticle is simply its size, where objects that are 1-100 nm are characterized as nanoparticles. However, synthetic and biological macromolecules, in particular high molecular weight chains, can satisfy this size requirement without providing the same phenomena as one would expect from a nanoparticle. At the same time, soft polymer nanoparticles are important in a broad range of fields, including understanding protein folding, drug delivery, vitrimers, catalysis and nanomedicine. Moreover, the recent flourish of all polymer nanocomposites has led to the synthesis of soft all-polymer nanoparticles, which emerge from internal crosslinking of a macromolecule. Thus, there exists a transition of an internally crosslinked macromolecule from a polymer chain to a nanoparticle as the amount of internal crosslinks increases, where the polymer chain exhibits different behavior than the nanoparticle. Yet, this transition is not well understood. In this work, we seek to address this knowledge gap and determine the transition of a macromolecule from a polymer chain to a nanoparticle as internal crosslinking increases. In this work, small angle neutron scattering (SANS) offers insight into the structure of polystyrene and poly(ethyl hexyl methacrylate) nanostructures in dilute solutions, with crosslinking densities that vary from 0.1 to 10.7%. Analyses of the SANS data provides structural characteristics to classify a nanostructure as chain-like or particle-like and identify a crosslinking dependent transition between the two morphologies. It was found that for both types of polymeric nanostructures, a crosslinking density of 0.81% (∼ a crosslink for every 1 in 125 monomers) or higher exhibit clear particle-like behavior. Lower crosslinking density nanostructures showed amounts of collapse similar to that of a star polymer (0.1% XL) or a random walk polymer chain (0.4% XL). Thus, the transition of an internally crosslinked macromolecule from a polymer chain to a nanoparticle is not an abrupt transition but occurs the gradual contraction of the chain with incorporated crosslinks.

摘要

通常,纳米颗粒的定义特征仅仅是其尺寸,即尺寸在1至100纳米的物体被视为纳米颗粒。然而,合成和生物大分子,特别是高分子量链,虽然能满足这一尺寸要求,但却不会表现出纳米颗粒所预期的相同现象。同时,软质聚合物纳米颗粒在广泛的领域中都很重要,包括理解蛋白质折叠、药物递送、玻璃态高聚物、催化和纳米医学。此外,最近所有聚合物纳米复合材料的蓬勃发展导致了软质全聚合物纳米颗粒的合成,这些纳米颗粒是由大分子的内部交联形成的。因此,随着内部交联量的增加,存在一种从聚合物链到纳米颗粒的内部交联大分子的转变,其中聚合物链表现出与纳米颗粒不同的行为。然而,这种转变尚未得到很好的理解。在这项工作中,我们试图填补这一知识空白,并确定随着内部交联增加,大分子从聚合物链到纳米颗粒的转变。在这项工作中,小角中子散射(SANS)为稀溶液中聚苯乙烯和聚(甲基丙烯酸乙己酯)纳米结构的结构提供了深入了解,其交联密度在0.1%至10.7%之间变化。对SANS数据的分析提供了结构特征,以将纳米结构分类为链状或颗粒状,并识别两种形态之间的交联依赖性转变。结果发现,对于这两种类型的聚合物纳米结构,交联密度为0.81%(约每125个单体中有1个交联)或更高时表现出明显的颗粒状行为。较低交联密度的纳米结构显示出与星型聚合物(0.1%交联)或无规行走聚合物链(0.4%交联)相似的塌陷量。因此,内部交联大分子从聚合物链到纳米颗粒的转变不是突然的转变,而是随着交联的引入,链逐渐收缩而发生的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a1/9680937/ae9dd01c320d/d2na00617k-f1.jpg

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