Becker Patrick M, Förster Christoph, Carrella Luca M, Boden Pit, Hunger David, van Slageren Joris, Gerhards Markus, Rentschler Eva, Heinze Katja
Department of Chemistry, Johannes Gutenberg University of Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
Department of Chemistry and Research Center Optimas, University Kaiserslautern, Erwin-Schrödinger-Straße, 67663, Kaiserslautern, Germany.
Chemistry. 2020 Jun 5;26(32):7199-7204. doi: 10.1002/chem.202001237. Epub 2020 May 20.
The chromium(III) complex [Cr (ddpd) ] (molecular ruby; ddpd=N,N'-dimethyl-N,N'-dipyridine-2-yl-pyridine-2,6-diamine) is reduced to the genuine chromium(II) complex [Cr (ddpd) ] with d electron configuration. This reduced molecular ruby represents one of the very few chromium(II) complexes showing spin crossover (SCO). The reversible SCO is gradual with T around room temperature. The low-spin and high-spin chromium(II) isomers exhibit distinct spectroscopic and structural properties (UV/Vis/NIR, IR, EPR spectroscopies, single-crystal XRD). Excitation of [Cr (ddpd) ] with UV light at 20 and 290 K generates electronically excited states with microsecond lifetimes. This initial study on the unique reduced molecular ruby paves the way for thermally and photochemically switchable magnetic systems based on chromium complexes complementing the well-established iron(II) SCO systems.
铬(III)配合物[Cr(ddpd)](分子红宝石;ddpd = N,N'-二甲基-N,N'-二吡啶-2-基吡啶-2,6-二胺)被还原为具有d电子构型的真正铬(II)配合物[Cr(ddpd)]。这种还原后的分子红宝石是极少数表现出自旋交叉(SCO)的铬(II)配合物之一。在室温附近,其可逆的自旋交叉是渐进的。低自旋和高自旋的铬(II)异构体表现出不同的光谱和结构性质(紫外/可见/近红外光谱、红外光谱、电子顺磁共振光谱、单晶X射线衍射)。在20和290 K下用紫外光激发[Cr(ddpd)]会产生具有微秒级寿命的电子激发态。对这种独特的还原分子红宝石的初步研究为基于铬配合物的热和光化学可切换磁性系统铺平了道路,补充了成熟的铁(II)自旋交叉系统。