Büldt Laura A, Wenger Oliver S
Department of Chemistry, University of Basel, St Johanns-Ring 19, 4056 Basel, Switzerland.
Dalton Trans. 2017 Nov 14;46(44):15175-15177. doi: 10.1039/c7dt03620e.
In this invited frontier article, recently discovered d and d complexes with long-lived metal-to-ligand charge transfer (MLCT) excited states are highlighted. Chelating diisocyanide ligands give access to emissive Mo(0) and Cr(0) complexes with d electron configuration exhibiting photophysical properties similar to those of Ru(ii) polypyridines or cyclometalated Ir(iii) complexes. With Ni(0), these ligands yield luminescent tetrahedral d complexes similar to isoelectronic Cu(i) bis(diimine) compounds.
在这篇特邀前沿文章中,重点介绍了最近发现的具有长寿命金属到配体电荷转移(MLCT)激发态的d和d配合物。螯合二异氰化物配体可得到具有d电子构型的发光Mo(0)和Cr(0)配合物,其光物理性质与Ru(ii)多吡啶或环金属化Ir(iii)配合物相似。对于Ni(0),这些配体产生类似于等电子Cu(i)双(二亚胺)化合物的发光四面体d配合物。