Dvinskikh Sergey V, Yamamoto Kazutoshi, Scanu David, Deschenaux Robert, Ramamoorthy Ayyalusamy
Biophysics and Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA.
J Phys Chem B. 2008 Oct 2;112(39):12347-53. doi: 10.1021/jp803265z. Epub 2008 Sep 9.
Liquid-crystalline materials containing fullerenes are valuable in the development of supramolecular switches and in solar cell technology. In this study, we characterize the liquid-crystalline and dynamic properties of fullerene-containing thermotropic compounds using solid-state natural abundance (13)C NMR experiments under stationary and magic angle spinning sample conditions. Chemical shifts spectra were measured in isotropic, liquid-crystalline nematic and smectic A and crystalline phases using one-dimensional (13)C experiments, while two-dimensional separated local-field experiments were used to measure the (1)H- (13)C dipolar couplings in mesophases. Chemical shift and dipolar coupling parameters were used to characterize the structure and dynamics of the liquid-crystalline dyads. NMR data of fullerene-containing thermotropic liquid crystals are compared to that of basic mesogenic unit and mesomorphic promoter compounds. Our NMR results suggest that the fullerene-ferrocene dyads form highly dynamic liquid-crystalline phases in which molecules rotate fast around the symmetry axis on the characteristic NMR time scale of approximately 10 (-4) s.
含富勒烯的液晶材料在超分子开关的开发和太阳能电池技术中具有重要价值。在本研究中,我们使用稳态和魔角旋转样品条件下的固态天然丰度(13)C NMR实验,表征了含富勒烯热致化合物的液晶和动态性质。使用一维(13)C实验在各向同性、液晶向列相和近晶A相以及晶相中测量化学位移谱,而使用二维分离局部场实验测量中间相中的(1)H-(13)C偶极耦合。化学位移和偶极耦合参数用于表征液晶二元组的结构和动力学。将含富勒烯热致液晶的NMR数据与基本介晶单元和介晶促进剂化合物的数据进行比较。我们的NMR结果表明,富勒烯-二茂铁二元组形成了高度动态的液晶相,其中分子在约10(-4)s的特征NMR时间尺度上围绕对称轴快速旋转。