Elmahdy Mahdy M, Dou Xi, Mondeshki Mihail, Floudas George, Butt Hans-Jürgen, Spiess Hans W, Müllen Klaus
Department of Physics, University of Ioannina, 451 10 Ioannina, Greece.
J Am Chem Soc. 2008 Apr 16;130(15):5311-9. doi: 10.1021/ja7113618. Epub 2008 Mar 7.
The self-assembly, the molecular dynamics, and the kinetics of structure formation are studied in dipole-functionalized hexabenzocoronene (HBC) derivatives. Dipole substitution destabilizes the columnar crystalline phase except for the dimethoxy- and monoethynyl-substituted HBCs that undergo a reversible transformation to the crystalline phase. The disk dynamics are studied by dielectric spectroscopy and site-specific NMR techniques that provide both the time-scale and geometry of motion. Application of pressure results in the thermodynamic phase diagram that shows increasing stability of the crystalline phase at elevated pressures. Long-lived metastability was found during the transformation between the two phases. These results suggest new thermodynamic and kinetic pathways that favor the phase with the highest charge carrier mobility.
研究了偶极官能化六苯并蔻(HBC)衍生物的自组装、分子动力学和结构形成动力学。偶极取代使柱状晶相不稳定,除了二甲氧基和单乙炔基取代的HBC,它们会发生可逆转变为晶相。通过介电谱和位点特异性核磁共振技术研究盘状动力学,这些技术提供了运动的时间尺度和几何结构。施加压力会得到热力学相图,该相图显示在高压下晶相的稳定性增加。在两相转变过程中发现了长寿命的亚稳性。这些结果表明了有利于具有最高电荷载流子迁移率相的新的热力学和动力学途径。