Laboratory of Physics, Lappeenranta University of Technology, Box 20, 53851 Lappeenranta, Finland.
J Phys Chem B. 2010 Apr 1;114(12):4159-65. doi: 10.1021/jp909658v.
The 4-generation carbosilane dendrimer with terminal cyanobiphenyl mesogenic groups in dilute solution of CDCl(3) was investigated using (1)H NMR technique. The spectrum was obtained and the relaxation time, T(1), was measured in the temperature range 320-225 K. For the first time, the extrema of T(1) values were achieved for majority of the dendrimer functional groups. The values of activation energies of the dendrimer functional groups were obtained. The relaxation data for outer and inner methyl groups show that the dendrimer investigated has dense corona and hollow core. This structure is formed because the mesogenic groups do not allow terminal segments to penetrate into the dendrimer, that is, the backfolding effect is absent. The NMR spectral and relaxation data give evidence for changing conformation of the dendrimer internal segments with decreasing temperature. This reorganization is most likely connected with a change of dendrimer size. We suppose that our experimental results will provide additional information for understanding principles of dendrimer nanocontainer operation. NMR can possibly be a tool for indicating the encapsulation effect as well as the dendrimer effective size.
在 CDCl(3) 的稀溶液中,用 (1)H NMR 技术研究了具有末端氰基联苯介晶基团的四代碳硅烷树状大分子。获得了光谱,并在 320-225 K 的温度范围内测量了弛豫时间 T(1)。首次为大多数树状大分子官能团达到 T(1)值的极值。获得了树状大分子官能团的活化能值。外甲基和内甲基的弛豫数据表明,所研究的树状大分子具有致密的冠和空心核。这种结构的形成是因为介晶基团不允许末端片段渗透到树状大分子中,也就是说,不存在反向折叠效应。NMR 光谱和弛豫数据表明,随着温度的降低,树状大分子内部片段的构象发生变化。这种重排很可能与树状大分子尺寸的变化有关。我们假设,我们的实验结果将为理解树状纳米容器操作原理提供额外的信息。NMR 可能是一种工具,可以指示包封效应以及树状大分子的有效尺寸。