Rausch Andreas F, Thompson Mark E, Yersin Hartmut
Universitat Regensburg, Institut fur Physikalische and Theoretische Chemie, 93053 Regensburg, Germany.
Inorg Chem. 2009 Mar 2;48(5):1928-37. doi: 10.1021/ic801250g.
The sky-blue emitting compound Ir(4,6-dFppy)(2)(pic) (iridium(III)bis[2-(4',6'-difluorophenyl)pyridinato-N,C(2')]-picolinate), commonly referred to as FIrpic and representing a well-known emitter material for organic light emitting diodes (OLEDs), has been investigated in detail by optical spectroscopy. Studies at temperatures from T = 1.5 K to T = 300 K were carried out in CH(2)Cl(2) and tetrahydrofuran (THF). In CH(2)Cl(2), two discrete sites were observed at cryogenic temperatures and studied by site-selective, high-resolution spectroscopy. The investigations reveal that the molecules located at the two sites exhibit distinctly different photophysical properties. For example, the three substates I, II, and III of the emitting triplet state T(1) of the low-energy site A show a distinctly larger zero-field splitting (ZFS) and exhibit shorter individual decay times than observed for the high-energy site B. The vibrational satellite structures in the emission spectra of the substates I(A) and I(B) exhibit clear differences in the ranges of metal-ligand (M-L) vibrations. For the compound studied in a polycrystalline THF host, giving only strongly inhomogeneously broadened spectra, the ZFS parameters and substate decay times vary in a similar range as observed for the two discrete sites in the CH(2)Cl(2) matrix. Thus, the amount of ZFS, the emission decay times, and also the intensities of the M-L vibrational satellites are affected by the matrix cage, that is, the host environment of the emitting complex. These properties are discussed with respect to variations of spin-orbit coupling routes. In particular, changes of d-orbital admixtures, that is, differences of the metal-to-ligand charge transfer (MLCT) character in the emitting triplet, play an important role. The matrix effects are expected to be also of importance for FIrpic and other Ir(III) compounds when applied as emitters in amorphous OLED matrixes.
发射天蓝色光的化合物Ir(4,6 - dFppy)(2)(pic)(铱(III)双[2-(4',6'-二氟苯基)吡啶-N,C(2')]-吡啶甲酸酯),通常称为FIrpic,是有机发光二极管(OLED)中一种著名的发光材料,已通过光谱学进行了详细研究。在T = 1.5 K至T = 300 K的温度范围内,在二氯甲烷(CH(2)Cl(2))和四氢呋喃(THF)中进行了研究。在CH(2)Cl(2)中,在低温下观察到两个离散位点,并通过位点选择性高分辨率光谱进行了研究。研究表明,位于这两个位点的分子表现出明显不同的光物理性质。例如,低能位点A的发射三重态T(1)的三个亚态I、II和III显示出明显更大的零场分裂(ZFS),并且与高能位点B相比,其单个衰减时间更短。亚态I(A)和I(B)发射光谱中的振动卫星结构在金属-配体(M-L)振动范围内表现出明显差异。对于在多晶THF主体中研究的该化合物,其光谱仅表现出强烈的非均匀展宽,ZFS参数和亚态衰减时间在与CH(2)Cl(2)基质中两个离散位点观察到的类似范围内变化。因此,ZFS的量、发射衰减时间以及M-L振动卫星的强度都受到基质笼的影响,即发光配合物的主体环境。针对自旋-轨道耦合路径的变化对这些性质进行了讨论。特别是,d轨道混合的变化,即发射三重态中金属-配体电荷转移(MLCT)特征的差异,起着重要作用。当FIrpic和其他Ir(III)化合物用作非晶OLED基质中的发光体时,预计基质效应也很重要。