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

被引:1
作者
Panariti, D. [1 ]
Bayard, B. J. [2 ]
Barbon, A. [1 ]
Kandrashkin, Y. E. [3 ]
Poddutoori, P. K. [2 ]
van der Est, A. [4 ]
Di Valentin, M. [1 ]
机构
[1] Univ Padua, Dept Chem Sci, Marzolo 1, I-35131 Padua, Italy
[2] Univ Minnesota Duluth, Dept Chem & Biochem, Duluth, MN 55812 USA
[3] FRC Kazan Sci Ctr RAS, Zavoisky Phys Tech Inst, Sibirsky Tract 10-7, Kazan 420029, Russia
[4] Brock Univ, Dept Chem, 1812 Sir Isaac Brock Way, St Catharines, ON L2S 3A1, Canada
来源
JOURNAL OF MAGNETIC RESONANCE OPEN | 2024年 / 21卷
关键词
EPR; Triplet state; Phosphorus porphyrins; Electron spin polarization; Radical hyperpolarization; Intersystem crossing; ENERGY-TRANSFER; RESONANCE; EPR; MAGNETOPHOTOSELECTION; DELOCALIZATION; DYNAMICS; VALENCE; TREPR;
D O I
10.1016/j.jmro.2024.100169
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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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页数:9
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