Kruglova Olga, Mendes Eduardo, Yildirim Zeynep, Wübbenhorst Michael, Mulder Fokko M, Stride John A, Picken Stephen J, Kearley Gordon J
Department of Radiation, Radionuclides & Reactors, Faculty of Applied Sciences, Delft University of Technology, Mekelweg 15, 2629 JB Delft, The Netherlands.
Chemphyschem. 2007 Jun 25;8(9):1338-44. doi: 10.1002/cphc.200700134.
The structure of the charge-transfer complex hexakis(n-hexyloxy)triphenylene-2,4,7-trinitro-9-fluorenone (HAT6-TNF) has been characterized by neutron scattering, X-ray diffraction (XRD), optical microscopy, and dielectric relaxation spectroscopy (DRS). On the basis of these data and the 1:1 stoichiometry, a consistent structure for the complex is proposed. This structure differs markedly from structures previously proposed for similar materials, because the TNF molecules are found to be situated between the discotic columns rather than sandwiched between the discotic molecules of a given column. The addition of TNF to HAT6 is found to stiffen the structure, and quasi-elastic neutron scattering shows that the local dynamics of the discotic molecules in HAT6-TNF is slowed by the presence of the TNF molecules. This scenario is consistent with the observation of two VFT-type (VFT=Vogel-Fulcher-Tamman) dielectric relaxation processes that relate to the columnar glass transition and a polyethylene-like hindered glass transition originating from the nano-phase-separated fraction of the aliphatic tails.
电荷转移复合物六(正己氧基)三亚苯 - 2,4,7 - 三硝基 - 9 - 芴酮(HAT6 - TNF)的结构已通过中子散射、X射线衍射(XRD)、光学显微镜和介电弛豫光谱(DRS)进行了表征。基于这些数据和1:1的化学计量比,提出了该复合物的一致结构。这种结构与先前针对类似材料提出的结构有显著不同,因为发现TNF分子位于盘状柱之间,而不是夹在给定柱的盘状分子之间。发现向HAT6中添加TNF会使结构变硬,并且准弹性中子散射表明,TNF分子的存在减缓了HAT6 - TNF中盘状分子的局部动力学。这种情况与观察到的两个与柱状玻璃化转变以及源自脂肪族尾部纳米相分离部分的类似聚乙烯的受阻玻璃化转变相关的VFT型(VFT = 沃格尔 - 富尔彻 - 塔曼)介电弛豫过程一致。