化学
对映体药物
偶极子
圆二色性
磁偶极子
镧系元素
手性(物理)
电偶极子跃迁
过渡金属
二色性
光谱学
结晶学
离子
对映选择合成
有机化学
光学
对称性破坏
物理
催化作用
量子力学
生物化学
手征对称破缺
Nambu–Jona Lasinio模型
作者
Chong-Yang Li,Langit Cahya Adi,Kévin Paillot,Ivan Breslavetz,La‐Sheng Long,Lan‐Sun Zheng,G. L. J. A. Rikken,Cyrille Train,Xiang‐Jian Kong,Matteo Atzori
摘要
Here we report on the strong magneto-chiral dichroism (MChD) detected through visible and near-infrared light absorption up to 5.0 T on {Er5Ni6} metal clusters obtained by reaction of enantiopure chiral ligands and NiII and ErIII precursors. Single-crystal diffraction analysis reveals that these compounds are 3d-4f heterometallic clusters, showing helical chirality. MChD spectroscopy reveals a high gMChD dissymmetry factor of ca. 0.24 T-1 (T = 4.0 K, B = 1.0 T) for the 4I13/2 ← 4I15/2 magnetic-dipole allowed electronic transition of the ErIII centers. This record value is 1 or 2 orders of magnitude higher than that of the d-d electronic transitions of the NiII ions and the others f-f electric-dipole induced transitions of the ErIII centers. These findings clearly show the key role that magnetic-dipole allowed transitions have in the rational design of chiral lanthanide systems showing strong MChD.
科研通智能强力驱动
Strongly Powered by AbleSci AI