Department of Chemistry and Materials Science Program, University of New Hampshire, Durham, New Hampshire, 03824, USA.
Alan G. MacDiarmid Institute, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Macromol Rapid Commun. 2014 Jan;35(2):249-253. doi: 10.1002/marc.201300677. Epub 2013 Oct 30.
An efficient route to architecturally defined, sub-20 nm soft nanoparticles fabricated from single polymer chains via intramolecular photodimerization of pendant anthracene units is presented. Photodimerization is confirmed by the disappearance of the characteristic anthracene π-π* absorption peak at ≈ 360 nm measured by UV-vis spectroscopy. Size exclusion chromatography (SEC) with UV, multi-angle light scattering (MALS), and viscometric detection confirms that as photodimers form, the chains fold to form nanoparticles, demonstrated by shifts in the SEC traces to longer retention times as a function of increased irradiation time. These shifts indicate a reduction in hydrodynamic radius, corroborated and quantified by viscometric data. MALS detector traces reveal the presence of a small amount of chain-chain coupling during this process, but confirm that this is primarily a single-chain phenomenon. Electron microscopy provides visual confirmation of nanoparticle formation.
本文提出了一种通过分子内光二聚化修饰侧基芘单元来制备具有特定结构且尺寸小于 20nm 的软纳 米粒子的有效途径。通过紫外-可见光谱(UV-vis)测量发现特征的芘π-π*吸收峰在 ≈ 360nm 处消失,证实了光二聚化的发生。采用带有紫外、多角度光散射(MALS)和粘度检测的凝胶渗透色谱(SEC)证实,随着光二聚体的形成,分子链折叠形成纳米粒子,这可以通过 SEC 谱图随辐照时间的增加向更长保留时间的移动来证明。这些移动表明流体力学半径减小,这与粘度数据相符并可定量计算。MALS 检测器谱图显示在此过程中存在少量的链-链偶联,但证实这主要是单链现象。电子显微镜为纳米粒子的形成提供了直观的证据。