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TripletState Delocalization in a Conjugated PorphyrinDimer Probed by Transient Electron Paramagnetic Resonance Techniques

机译:三胞胎共轭卟啉中的状态离域瞬态电子顺磁共振技术探测二聚体

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摘要

The delocalization of the photoexcited triplet state in a linear butadiyne-linked porphyrin dimer is investigated by time-resolved and pulse electron paramagnetic resonance (EPR) with laser excitation. The transient EPR spectra of the photoexcited triplet states of the porphyrin monomer and dimer are characterized by significantly different spin polarizations and an increase of the zero-field splitting parameter D from monomer to dimer. The proton and nitrogen hyperfine couplings, determined using electron nuclear double resonance (ENDOR) and X- and Q-band HYSCORE, are reduced to about half in the porphyrin dimer. These data unequivocally prove the delocalization of the triplet state over both porphyrin units, in contrast to the conclusions from previous studies on the triplet states of closely related porphyrin dimers. The results presented here demonstrate that the most accurate estimate of the extent of triplet state delocalization can be obtained from the hyperfine couplings, while interpretation of the zero-field splitting parameter D can lead to underestimation of the delocalization length, unless combined with quantum chemicalcalculations. Furthermore, orientation-selective ENDOR and HYSCOREresults, in combination with the results of density functional theory(DFT) calculations, allowed determination of the orientations of thezero-field splitting tensors with respect to the molecular frame inboth porphyrin monomer and dimer. The results provide evidence fora reorientation of the zero-field splitting tensor and a change inthe sign of the zero-field splitting D value. Thedirection of maximum dipolar coupling shifts from the out-of-planedirection in the porphyrin monomer to the vector connecting the twoporphyrin units in the dimer. This reorientation, leading to an alignmentof the principal optical transition moment and the axis of maximumdipolar coupling, is also confirmed by magnetophotoselection experiments.
机译:线性丁二炔连接的卟啉二聚体中的光激发三重态的离域是通过时间分辨和脉冲电子顺磁共振(EPR)和激光激发来研究的。卟啉单体和二聚体的光激发三重态的瞬态EPR光谱的特征是自旋极化明显不同,零场分裂参数D从单体到二聚体的增加。使用电子核双共振(ENDOR)以及X和Q波段HYSCORE测得的质子和氮超精细偶联在卟啉二聚体中减少到一半左右。这些数据明确地证明了在两个卟啉单元上三重态的离域化,这与先前有关紧密相关的卟啉二聚体的三重态的研究结论相反。此处给出的结果表明,可以从超精细偶合获得最准确的三重态离域程度的估计,而零场分裂参数D的解释可能导致离域长度的低估,除非与量子化学结合使用计算。此外,方向选择ENDOR和HYSCORE结果,结合密度泛函理论的结果(DFT)计算,可以确定关于分子框架中的零场分裂张量卟啉单体和二聚体。结果为零场分裂张量的重新定向和零场分裂D值的符号。的最大偶极耦合方向从平面外偏移卟啉单体的方向是连接两者的载体二聚体中的卟啉单元。重新定位,导致对齐光学跃迁矩和最大轴的关系磁光选择实验也证实了偶极耦合。

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