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Light-Induced Spin Crossover in an Intermediate-Spin Penta-Coordinated Iron(III) Complex
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    Light-Induced Spin Crossover in an Intermediate-Spin Penta-Coordinated Iron(III) Complex
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    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 2019, 123, 46, 9883–9892
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    https://doi.org/10.1021/acs.jpca.9b06490
    Published October 30, 2019
    Copyright © 2019 American Chemical Society

    Abstract

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    (PMe3)2FeCl3 is an Fe(III) complex that exists in the intermediate-spin ground state in a distorted trigonal bipyramidal geometry. An electronic state with high-spin configuration lies in close vicinity to the ground state, making it a potential spin crossover candidate. A mechanistic account of the spin crossover from the lowest quartet state (Q0) to the lowest sextet state (S1) of this complex is provided by exploring both thermal and light-induced pathways. The presence of a large barrier between the two spin states suggests a possible thermal spin crossover at a rather high temperature. The light-induced spin crossover is investigated by employing complete active space self-consistent field calculations together with dynamic correlation and spin–orbit coupling for the lowest seven quartet and lowest five sextet states. The system in the Q0 state upon light absorption is excited to the optically bright Q4 LMCT state. By following minimum energy pathways along the electronic states, two light-induced pathways for spin crossover are identified. From the Q4 state, the system can photo-regenerate the ground intermediate-spin state (Q0) through an internal conversion of Q4/Q3 followed by Q3/S1 and S1/Q0 intersystem crossings. In an alternate route, through Q4/S2 intersystem crossing followed by S2/S1 internal conversion, the system can complete the spin crossover from the Q0 to S1 state.

    Copyright © 2019 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.jpca.9b06490.

    • SA-CASSCF/CASPT2 computed energies of the lowest seven quartet states and the lowest five sextet states; configuration state functions and CI coefficients contributing to the quartet and sextet states; and composition of the spin-orbit eigenstates in terms of the scalar-relativistic quartet and sextet states at different geometries (PDF)

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    This article is cited by 4 publications.

    1. M. C. Vázquez, J. W. Reid, Y. Avila, M. González, L. Sánchez, L. Martínez-dlCruz, J. Rodríguez-Hernández, B. D. Moreno, E. Reguera. Fe(L)2[M(CN)4] with L = 4-Ethyl Isonicotinate and M = Ni, Pd, Pt.─A Series of Hofmann-Type Frameworks with Spin Crossover: The Dominant Role of the Fe–NC Coordination Bond. The Journal of Physical Chemistry C 2024, 128 (22) , 9353-9363. https://doi.org/10.1021/acs.jpcc.4c01838
    2. Sakshi Nain, Aritra Mukhopadhyaya, Md. Ehesan Ali. Unravelling the Highest Magnetic Anisotropy Among all the nd-Shells in [WCp2]0 Metallocene. Inorganic Chemistry 2024, 63 (16) , 7401-7411. https://doi.org/10.1021/acs.inorgchem.4c00437
    3. Kishan Kumar Dakua, Karunamoy Rajak, Sabyashachi Mishra. Spin–vibronic coupling in the quantum dynamics of a Fe(III) trigonal-bipyramidal complex. The Journal of Chemical Physics 2022, 156 (13) https://doi.org/10.1063/5.0080611
    4. Manabu Nakaya, Ryo Ohtani, Leonard F. Lindoy, Shinya Hayami. Light-induced excited spin state trapping in iron( iii ) complexes. Inorganic Chemistry Frontiers 2021, 8 (2) , 484-498. https://doi.org/10.1039/D0QI01188F

    The Journal of Physical Chemistry A

    Cite this: J. Phys. Chem. A 2019, 123, 46, 9883–9892
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.jpca.9b06490
    Published October 30, 2019
    Copyright © 2019 American Chemical Society

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