反键分子轨道
旋转交叉
化学
自旋态
离域电子
激发态
俘获
人口
旋转
原子轨道
电子
原子物理学
分子物理学
凝聚态物理
物理
结晶学
无机化学
量子力学
人口学
有机化学
社会学
生态学
生物
作者
Shiladitya Karmakar,Pradip Chakraborty,Tanusri Saha‐Dasgupta
摘要
A computational study of the light-induced excited spin-state trapping (LIESST) in a number of Fe(II) spin crossover complexes, coordinated by monodentate, bidentate and multidentate ligands is carried out, with the goal to uncover the trend in the low temperature relaxation rate. A nine order of magnitude change in low temperature relaxation rate is observed among the complexes. The trend is rationalized in terms of the change in metal-ligand covalency, numerically estimated by the crystal orbital Hamiltonian population, thus influencing the back donation or delocalization of the electrons from the low-lying Fe(II)-centered molecular orbital to the empty low-lying ligand-centered π* antibonding molecular orbitals.
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