Highly Conjugated PorphyrinArrays Enable OpticalResolution of Ferromagnetic and Antiferromagnetic Aligned States ofthe Triplet Exciton and an Incorporated Stable Radical

Well-defined photogenerated molecular spin systems have potential utility in spintronics and quantum information science (QIS). Because molecular magnetic, optical, and electronic properties can be controlled by design, diverse spin systems can be prepared at modest temperatures. Photogenerated molecular spin systems often involve states prepared from the interaction of excitons and charges. Resolving the nature of electron spin alignment in photogenerated spin states described by the coupling of a triplet exciton and a stable radical commonly relies on EPR spectroscopy. We describe ethyne-bridged (porphinato)­metal (<b>PM</b><sub><i><b>n</b></i></sub>) oligomers that incorporate a macrocycle-bound Cu­(II) radical center. Upon photoexcitation of such <b>PM</b><sub><i><b>n</b></i></sub> arrays, a singdoublet (<sup>2</sup>S<sub>1</sub>) state is formed; ultrafast internal conversion (IC) then produces a tripdoublet (<sup>2</sup>T<sub>1</sub>) state, which undergoes intersystem crossing (ISC) to produce a tripquartet (<sup>4</sup>T<sub>1</sub>) state, before relaxation to the ground state (<sup>2</sup>S<sub>0</sub>). These highly conjugated Cu­(II) radical-containing <b>PM</b><sub><i><b>n</b></i></sub> arrays enable direct observation of copper porphyrin <sup>2</sup>T<sub>1</sub> → <sup>4</sup>T<sub>1</sub> ISC dynamics from the biexponential decay of the near-infrared (NIR) <sup>2,4</sup>T<sub>1</sub> → <sup>2,4</sup>T<sub><i>n</i></sub> transient absorption manifold. Multireference <i>n</i>-electron valence perturbation theory (NEVPT2) computations illuminate how <b>PM</b><sub><i><b>n</b></i></sub> electronic structure controls the relaxation dynamics of these long-lived (>10 ns) electronically excited multiplet states. These studies show that highly conjugated and polarizable porphyrin arrays incorporating stable spin centers provide rare π-delocalized systems where the ferromagnetic and antiferromagnetic alignment between a triplet exciton and a stable radical are both spectrally resolved and addressable using transient optical spectroscopy at wavelengths exceeding 1 μm, providing new opportunities to QIS.

Publication Details

Journal
Figshare
Published
2025-07-23
DOI
https://doi.org/10.1021/jacs.5c07638.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
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article
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Highly Conjugated PorphyrinArrays Enable OpticalResolution of Ferromagnetic and Antiferromagnetic Aligned States ofthe Triplet Exciton and an Incorporated Stable Radical

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Mycorrhizal Fungi and Plant Interactions
article

Highly Conjugated PorphyrinArrays Enable OpticalResolution of Ferromagnetic and Antiferromagnetic Aligned States ofthe Triplet Exciton and an Incorporated Stable Radical

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Abstract

Well-defined photogenerated molecular spin systems have potential utility in spintronics and quantum information science (QIS). Because molecular magnetic, optical, and electronic properties can be controlled by design, diverse spin systems can be prepared at modest temperatures. Photogenerated molecular spin systems often involve states prepared from the interaction of excitons and charges. Resolving the nature of electron spin alignment in photogenerated spin states described by the coupling of a triplet exciton and a stable radical commonly relies on EPR spectroscopy. We describe ethyne-bridged (porphinato)­metal (<b>PM</b><sub><i><b>n</b></i></sub>) oligomers that incorporate a macrocycle-bound Cu­(II) radical center. Upon photoexcitation of such <b>PM</b><sub><i><b>n</b></i></sub> arrays, a singdoublet (<sup>2</sup>S<sub>1</sub>) state is formed; ultrafast internal conversion (IC) then produces a tripdoublet (<sup>2</sup>T<sub>1</sub>) state, which undergoes intersystem crossing (ISC) to produce a tripquartet (<sup>4</sup>T<sub>1</sub>) state, before relaxation to the ground state (<sup>2</sup>S<sub>0</sub>). These highly conjugated Cu­(II) radical-containing <b>PM</b><sub><i><b>n</b></i></sub> arrays enable direct observation of copper porphyrin <sup>2</sup>T<sub>1</sub> → <sup>4</sup>T<sub>1</sub> ISC dynamics from the biexponential decay of the near-infrared (NIR) <sup>2,4</sup>T<sub>1</sub> → <sup>2,4</sup>T<sub><i>n</i></sub> transient absorption manifold. Multireference <i>n</i>-electron valence perturbation theory (NEVPT2) computations illuminate how <b>PM</b><sub><i><b>n</b></i></sub> electronic structure controls the relaxation dynamics of these long-lived (>10 ns) electronically excited multiplet states. These studies show that highly conjugated and polarizable porphyrin arrays incorporating stable spin centers provide rare π-delocalized systems where the ferromagnetic and antiferromagnetic alignment between a triplet exciton and a stable radical are both spectrally resolved and addressable using transient optical spectroscopy at wavelengths exceeding 1 μm, providing new opportunities to QIS.

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Highly Conjugated PorphyrinArrays Enable OpticalResolution of Ferromagnetic and Antiferromagnetic Aligned States ofthe Triplet Exciton and an Incorporated Stable Radical · Figshare (2025) | TGRS Research Map | TGRS