Departamento de Química, Universidad de los Andes, Cra 1 No. 18A - 12, 111711 Bogotá, Colombia.
Departamento de Química Física, Universidad de Sevilla, c/Profesor García González, s/n 41012 Sevilla, Spain.
Dalton Trans. 2019 Sep 17;48(36):13789-13798. doi: 10.1039/c9dt03102b.
The BPY[Ni(dmit)2]2 molecular crystal synthesized by Naito and coworkers (J. Am. Chem. Soc., 2012, 134, 18656) was characterized as a photo-magnetic-conductor. This crystal is a nonmagnetic semiconductor in the dark and becomes a magnetic conductor after UV irradiation. This work analyzes the key ingredients of the observed photomagnetism and photoconduction by means of wavefunction-based calculations on selected fragments and periodic calculations on the whole crystal. Our results demonstrate that UV-Vis light induces charge transfer processes between the closest [Ni(dmit)2]- and BPY2+ units, that introduce unpaired electrons on the unoccupied orbitals of the BPY cations. Since the conduction bands present a strong mixing of BPY and Ni(dmit)2, the optically activated anion-cation charge transfer enhances the conductivity. The photoinduced (BPY2+)* radicals can indeed interact with the close Ni(dmit)2 units, with non-negligible spin-spin magnetic couplings, which are responsible for the changes induced by the irradiation on the temperature dependence of the magnetic susceptibility.
由 Naito 和同事合成的 BPY[Ni(dmit)2]2 分子晶体被描述为光磁导体。该晶体在黑暗中是无磁性半导体,在紫外线照射后变为磁性导体。这项工作通过对选定片段的基于波函数的计算和对整个晶体的周期性计算,分析了观察到的光致磁性和光电导的关键因素。我们的结果表明,紫外可见光诱导了最接近的[Ni(dmit)2]-和 BPY2+单元之间的电荷转移过程,在 BPY 阳离子的空轨道上引入了未配对电子。由于导带呈现出 BPY 和 Ni(dmit)2 的强烈混合,光激活的阴离子-阳离子电荷转移增强了导电性。光诱导的(BPY2+)*自由基确实可以与临近的 Ni(dmit)2 单元相互作用,具有不可忽略的自旋-自旋磁耦合,这解释了照射对磁化率温度依赖性的诱导变化。