化学
冠醚
钐
结晶学
激发态
复分解
乙醚
电子结构
从头算
基态
光化学
物理化学
离子
计算化学
无机化学
聚合
原子物理学
有机化学
聚合物
物理
作者
Frankie D. White,Cristian Celis‐Barros,Jillian Rankin,Eduardo Solís-Céspedes,David Dan,Alyssa Gaiser,Yan Zhou,Jasmine Colangelo,Dayán Páez‐Hernández,Ramiro Arratia‐Pérez,Thomas E. Albrecht‐Schmitt
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-02-21
卷期号:58 (5): 3457-3465
被引量:16
标识
DOI:10.1021/acs.inorgchem.8b03566
摘要
The reaction of SmI2 with dibenzo-30-crown-10 (DB30C10), followed by metathesis with [Bu4N][BPh4], allows for the isolation of [SmII(DB30C10)][BPh4]2 as bright-red crystals in good yield. Exposure of [Sm(DB30C10)]2+ to solvents containing trace water results in the conversion to the dinuclear SmIII complex, Sm2(DB30C10)(OH)2I4. Structural analysis of both complexes shows substantial rearrangement of the crown ether from a folded, Pac-Man form with SmII to a twisted conformation with SmIII. The optical properties of [SmII(DB30C10)][BPh4]2 exhibit a strong temperature dependence and change from broad-band absorption features indicative of domination by 5d states to fine features characteristic of 4f → 4f transitions at low temperatures. Examination of the electronic structure of these complexes via ab initio wave function calculations (SO-CASSCF) shows that the ground state of SmII in [SmII(DB30C10)]2+ is a 4f6 state with low-lying 4f55d1 states, where the latter states have been lowered in energy by ∼12 000 cm–1 with respect to the free ion. The decacoordination of the SmII cation by the crown ether is responsible for this alteration in the energies of the excited state and demonstrates the ability to tune the electronic structure of SmII.
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