Simoncelli Sabrina, Aramendía Pedro F
INQUIMAE and Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón 2, Ciudad Universitaria, 1428 Ciudad de Buenos Aires, Argentina; CIBION, Centro de Investigaciones en Bionanociencias "Elizabeth Jares-Erijman", Godoy Cruz 2390, 1425 Ciudad de Buenos Aires, Argentina.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 May 5;142:94-100. doi: 10.1016/j.saa.2015.01.072. Epub 2015 Feb 7.
In this work, we use the photoisomerization of azobenzenes, a phenanthrospirooxazine, and a fulgide in a twisted nematic liquid crystalline phase to change the chiral twisting power of the system. The changes are probed by the rotatory power of linearly polarized light. Time resolved and steady state experiments are carried out. The chiral change and the photoisomerization process have similar characteristic recovery times and activation energy, thus probing that the change is induced by the modification in the chemical composition of the photochromic dopant system. The amplitude of the light twisting power change correlates with the order change in the liquid crystal (LC) but not with the modification in the absorption characteristics of the system. This indicates that the driving force of the chiral change is the microscopic order modification in the LC phase that affects the helical pitch of the phase.
在这项工作中,我们利用扭曲向列相液晶相中偶氮苯、菲并螺恶嗪和俘精酸酐的光异构化来改变体系的手性扭曲能力。通过线偏振光的旋光能力来探测这些变化。进行了时间分辨和稳态实验。手性变化和光异构化过程具有相似的特征恢复时间和活化能,从而表明这种变化是由光致变色掺杂剂体系化学成分的改变所引起的。光扭曲能力变化的幅度与液晶(LC)中的有序变化相关,而与体系吸收特性的改变无关。这表明手性变化的驱动力是液晶相中影响相螺旋间距的微观有序变化。