Department of Physics, University of California at Berkeley, Berkeley, California 94720, USA.
Phys Rev Lett. 2010 Apr 30;104(17):178301. doi: 10.1103/PhysRevLett.104.178301. Epub 2010 Apr 28.
Single-molecule-resolved scanning tunneling microscopy of tetra-tert-butyl azobenzene (TTB-AB) molecules adsorbed onto Au(111) reveals chirality selection rules in their photoswitching behavior. This observation is enabled by the fact that trans-TTB-AB molecules self-assemble into homochiral domains. Cis-TTB-AB molecules produced via photoisomerization are found in two distinct conformations with final state chirality determined by the initial trans isomer chirality. Based on these observations and ab initio calculations, we propose a new inversion-based dynamical photoswitching mechanism for azobenzene molecules at a surface.
利用单分子分辨扫描隧道显微镜研究了吸附在 Au(111)表面上的四叔丁基偶氮苯(TTB-AB)分子的光致异构化行为,揭示了其光开关行为中的手性选择规则。这一观察结果是由于以下事实:反式 TTB-AB 分子自组装成手性相同的区域。通过光异构化产生的顺式 TTB-AB 分子存在两种不同的构象,最终的手性由初始反式异构体的手性决定。基于这些观察结果和从头算计算,我们提出了一种新的基于反转的表面偶氮苯分子动态光开关机制。