Department of Chemistry and Materials Science, Tokyo Institute of Technology , Meguro-ku, Tokyo 152-8551, Japan.
J Am Chem Soc. 2014 Jun 25;136(25):9158-64. doi: 10.1021/ja503652c. Epub 2014 Jun 11.
Trans-cis photoisomerization in an azo compound containing azobenzene chromophores and long alkyl chains leads to a photoinduced crystal-melt transition (PCMT). X-ray structure analysis of this crystal clarifies the characteristic coexistence of the structurally ordered chromophores through their π···π interactions and disordered alkyl chains around room temperature. These structural features reveal that the PCMT starts near the surface of the crystal and propagates into the depth, sacrificing the π···π interactions. A temporal change of the powder X-ray diffraction pattern under light irradiation and a two-component phase diagram allow qualitative analysis of the PCMT and the following reconstructive crystallization of the cis isomer as a function of product accumulation. This is the first structural characterization of a compound showing the PCMT, overcoming the low periodicity that makes X-ray crystal structure analysis difficult.
含有偶氮苯发色团和长烷基链的偶氮化合物的顺反光致异构化导致光致晶-熔转变(PCMT)。该晶体的 X 射线结构分析阐明了在室温下结构有序发色团通过π···π 相互作用和无序烷基链的特征共存。这些结构特征表明,PCMT 从晶体表面附近开始,并向深度传播,牺牲了π···π 相互作用。在光照下粉末 X 射线衍射图谱的时变和双组分相图允许对 PCMT 进行定性分析,并随着产物积累对顺式异构体的重建结晶进行分析。这是首例对表现出 PCMT 的化合物的结构特征进行的描述,克服了使 X 射线晶体结构分析变得困难的低周期性。