Kaleta Jiří, Dron Paul I, Zhao Ke, Shen Yongqiang, Císařová Ivana, Rogers Charles T, Michl Josef
†Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Flemingovo nám. 2, 16610 Prague, Czech Republic.
§Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030, 12840 Prague, Czech Republic.
J Org Chem. 2015 Jun 19;80(12):6173-92. doi: 10.1021/acs.joc.5b00661. Epub 2015 Jun 5.
A new generation of rod-shaped dipolar molecular rotors designed for controlled insertion into channel arrays in the surface of hexagonal tris(o-phenylenedioxy)cyclotriphosphazene (TPP) has been designed and synthesized. Triptycene is used as a stopper intended to prevent complete insertion, forcing the formation of a surface inclusion. Two widely separated (13)C NMR markers are present in the shaft for monitoring the degree of insertion. The structure of the two-dimensional rotor arrays contained in these surface inclusions was examined by solid-state NMR and X-ray powder diffraction. The NMR markers and the triptycene stopper functioned as designed, but half of the guest molecules were not inserted as deeply into the TPP channels as the other half. As a result, the dipolar rotators were distributed equally in two planes parallel to the crystal surface instead of being located in a single plane as would be required for ferroelectricity. Dielectric spectroscopy revealed rotational barriers of ∼4 kcal/mol but no ferroelectric behavior.
已经设计并合成了新一代棒状偶极分子转子,其设计目的是可控地插入六(邻苯二氧基)环三磷腈(TPP)表面的通道阵列中。均三苯被用作阻挡剂,以防止完全插入,促使形成表面包合物。轴中存在两个相距很远的(13)C NMR标记物,用于监测插入程度。通过固态NMR和X射线粉末衍射研究了这些表面包合物中所含二维转子阵列的结构。NMR标记物和均三苯阻挡剂按设计发挥了作用,但一半客体分子没有像另一半那样深入插入TPP通道。结果,偶极转子均匀分布在与晶体表面平行的两个平面中,而不是像铁电所要求的那样位于单个平面中。介电谱显示旋转势垒约为4 kcal/mol,但没有铁电行为。