Wegeberg Christina, Wenger Oliver S
Department of Chemistry, University of Basel, St. Johanns-Ring 19, 4056 Basel, Switzerland.
Dalton Trans. 2022 Jan 25;51(4):1297-1302. doi: 10.1039/d1dt03763c.
In this Frontier article, recently discovered chromium(0) and manganese(I) complexes emitting from metal-to-ligand charge transfer (MLCT) excited states are highlighted. Chelating isocyanide ligands give access to this new class of 3d emitters with MLCT lifetimes in (or close to) the nanosecond regime in solution at room temperature. Although the so far achievable luminescence quantum yields in these open-shell complexes are yet comparatively low, the photophysical properties of the new chromium(0) and manganese(I) isocyanides are reminiscent of those of well-known ruthenium(II) polypyridines. Our findings provide insight into how undesired nonradiative MLCT deactivation in 3d complexes can be counteracted, and they seem therefore relevant for the further development of new luminescent first-row transition metal complexes based on iron(II) and cobalt(III) in addition to chromium(0) and manganese(I).
在这篇前沿文章中,重点介绍了最近发现的从金属到配体电荷转移(MLCT)激发态发射的零价铬和一价锰配合物。螯合异腈配体可产生这类新型的3d发射体,其在室温下于溶液中的MLCT寿命处于(或接近)纳秒范围。尽管到目前为止,这些开壳配合物中可实现的发光量子产率相对较低,但新型零价铬和一价锰异腈的光物理性质让人联想到著名的钌(II)多吡啶配合物。我们的研究结果深入探讨了如何抵消3d配合物中不期望的非辐射MLCT失活,因此,除了零价铬和一价锰之外,它们似乎与基于二价铁和三价钴的新型发光第一排过渡金属配合物的进一步发展相关。