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一种发光的铂铁自旋交叉配合物。

A luminescent PtFe spin crossover complex.

作者信息

Schäfer Bernhard, Bauer Thomas, Faus Isabelle, Wolny Juliusz A, Dahms Fabian, Fuhr Olaf, Lebedkin Sergei, Wille Hans-Christian, Schlage Kai, Chevalier Katharina, Rupp Fabian, Diller Rolf, Schünemann Volker, Kappes Manfred M, Ruben Mario

机构信息

Institut für Nanotechnologie, Karlsruher Institut für Technologie (KIT), Campus Nord, Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany.

Fachbereich Physik, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. 46, 67663 Kaiserslautern, Germany.

出版信息

Dalton Trans. 2017 Feb 14;46(7):2289-2302. doi: 10.1039/c6dt04360g.

Abstract

A heterotrinuclear [PtFe] spin crossover (SCO) complex was developed and synthesized employing a ditopic bridging bpp-alkynyl ligand L and alkynyl coordinated Pt terpy units: Fe(L-Pt) (1). We identified two different types of crystals of 1 which differ in their molecular packing and the number of co-crystallized solvent molecules: 1H (1·3.5CHCl in P1[combining macron]) and 1L (1·10CHCl in C2/c); while 1L shows a reversible SCO with a transition temperature of 268 K, the analogous compound 1H does not show any SCO and remains blocked in the HS state. The temperature-dependent magnetic properties of 1H and 1L were complementarily studied by Mössbauer spectroscopy. It has been shown that 1L performs thermal spin crossover and that 1L can be excited to a LIESST state. The vibrational properties of 1 were investigated by experimental nuclear resonance vibrational spectroscopy. The experimentally determined partial density of vibrational states (pDOS) was compared to a DFT-based simulation of the pDOS. The vibrational modes of the different components were assigned and visualized. In addition, the photophysical properties of 1 and L-Pt were investigated in the solid state and in solution. The ultrafast transient absorption spectroscopy of 1 in solution was carried out to study the PL quenching channel via energy transfer from photoexcited Pt terpy units to the Fe-moiety.

摘要

利用双齿桥联bpp-炔基配体L和炔基配位的Pt三联吡啶单元,合成了一种异核[PtFe]自旋交叉(SCO)配合物:Fe(L-Pt)(1)。我们鉴定出1的两种不同类型晶体,它们在分子堆积和共结晶溶剂分子数量上有所不同:1H(在P1[组合宏]中为1·3.5CHCl)和1L(在C2/c中为1·10CHCl);虽然1L显示出可逆的SCO,转变温度为268 K,但类似的化合物1H没有显示出任何SCO,并且保持在高自旋(HS)状态。通过穆斯堡尔光谱对1H和1L的温度依赖性磁性进行了补充研究。结果表明,1L表现出热自旋交叉,并且1L可以被激发到光诱导激发自旋态(LIESST)。通过实验性核共振振动光谱研究了1的振动性质。将实验测定的振动态部分密度(pDOS)与基于密度泛函理论(DFT)的pDOS模拟进行了比较。对不同组分的振动模式进行了归属和可视化。此外,还研究了1和L-Pt在固态和溶液中的光物理性质。对1在溶液中的超快瞬态吸收光谱进行了研究,以通过从光激发的Pt三联吡啶单元到Fe部分的能量转移来研究光致发光(PL)猝灭通道。

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