激发态
铬
发光
电荷(物理)
配体(生物化学)
金属
自旋(空气动力学)
原子物理学
自旋态
材料科学
化学
物理
光电子学
冶金
量子力学
热力学
受体
生物化学
作者
Mengwei Yue,Wai‐Pong To,Yifan Zhao,Qiushi Hu,Xiaoyong Chang,Xihan Chen,Xi‐ai Zhang,Xuebo Chen,Liangliang Wu,Wei Lu
标识
DOI:10.1002/anie.202509601
摘要
Two paramagnetic Cr(I) complexes with homoleptic fac-bis(triarylisocyanide) ligands were prepared by chemical oxidation of the Cr(0) precursors and emission spectra with peak maximum at respective 568 and 525 nm have been recorded with THF solutions of these two low-spin d5 metal complexes at 298 K. Structural, spectroscopic, and theoretical studies revealed that the emission of the Cr(I) complexes could be tentatively assigned to be spin-allowed 2MLCT excited states. Femtosecond-resolved transient absorption spectra confirmed that the lifetimes of the excited states were in the tens of picoseconds, which could be explained by the fast nonradiative decay of 2MLCT state through low-lying quartet metal-centered (4MC) states. The Cr(I) complexes with luminescent 2MLCT excited states were distinct from the previously reported d5 Fe(III) complexes with luminescent 2LMCT excited states, enriching the diversity of emissive excited states of earth-abundant 3d transition metal complexes.
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