Electron spin polarization in the triplet state of methoxy-substituted phosphorus(V) tetraphenyl porphyrins

D. Panariti , B.J. Bayard , A. Barbon , Y.E. Kandrashkin , P.K. Poddutoori , A. van der Est , M. Di Valentin
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Abstract

Photoexcited triplet states of porphyrins are of great relevance in various applications due to their high yield, long lifetime, and strong electron spin polarization. This study delves into properties and spin dynamics of the triplet state of a series of hypervalent phosphorus(V) porphyrins. Transient Electron Paramagnetic Resonance (TrEPR) measurements, supported by quantum chemical calculations as well as by optical absorption/luminescence experiments, reveal that, unlike singlet states, the lowest triplet state does not exhibit charge-transfer (CT) character upon photoexcitation. However, the presence of excited CT singlet states alters the intersystem crossing in phosphorus(V) porphyrins, leading to a sign change in the initial multiplet polarization of the photoexcited triplet state. TrEPR results further demonstrate that significant net polarization develops in the triplet states of the phosphorus(V) porphyrins due to the dynamic Jahn-Teller effect. Yet, this effect remains largely unaffected by differences in their molecular structures.

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甲氧基取代磷(V)四苯基卟啉三重态的电子自旋极化
卟啉的光激发三重态具有产量高、寿命长、电子自旋极化强等特点,因此在各种应用中具有重要意义。本研究深入探讨了一系列高价磷(V)卟啉的三重态特性和自旋动力学。在量子化学计算以及光吸收/发光实验的支持下,瞬态电子顺磁共振(TrEPR)测量结果表明,与单重态不同,最低三重态在光激发时并不表现出电荷转移(CT)特性。然而,激发 CT 单重态的存在会改变磷(V)卟啉的系统间交叉,导致光激发三重态的初始多极化发生符号变化。TrEPR 结果进一步证明,由于动态贾恩-泰勒效应,磷(V)卟啉的三重态会出现显著的净极化。然而,这种效应基本上不受它们分子结构差异的影响。
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