Molecular Engineeringof Emissive Molecular QubitsBased on Spin-Correlated Radical Pairs

Spin chemistry of photogenerated spin-correlated radical pairs (SCRPs) offers a practical approach to control chemical reactions and molecular emissions by using weak magnetic fields. This capability to harness magnetic field effects (MFEs) paves the way for developing SCRPs-based molecular qubits. Here, we introduce a new series of donor–chiral bridge–acceptor (D−χ–A) molecules that demonstrate significant MFEs on fluorescence intensity and lifetime in solution at room temperaturecritical for quantum sensing. By precisely tuning the donor site through torsional locking, distance extension, and planarization, we achieved remarkable control over key quantum properties, including field-response range and line width. In the most responsive systems, emission lifetimes increased by over 200%, and the total emission intensity was modulated by up to 30%. This level of tunability shows the power of synthetic spin chemistry. The rational design principle of optically addressable SCRP-based molecular systems, presented in this work, represents a major leap toward functional synthetic molecular qubits, advancing the field of molecular quantum technologies.

Publication Details

Journal
Figshare
Published
2025-03-19
DOI
https://doi.org/10.1021/jacs.4c16164.s001
Primary Topic
Magnetism in coordination complexes
Type
article
Field-Weighted Citation Impact
0.00
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Molecular Engineeringof Emissive Molecular QubitsBased on Spin-Correlated Radical Pairs

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Magnetism in coordination complexes
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Molecular Engineeringof Emissive Molecular QubitsBased on Spin-Correlated Radical Pairs

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Abstract

Spin chemistry of photogenerated spin-correlated radical pairs (SCRPs) offers a practical approach to control chemical reactions and molecular emissions by using weak magnetic fields. This capability to harness magnetic field effects (MFEs) paves the way for developing SCRPs-based molecular qubits. Here, we introduce a new series of donor–chiral bridge–acceptor (D−χ–A) molecules that demonstrate significant MFEs on fluorescence intensity and lifetime in solution at room temperaturecritical for quantum sensing. By precisely tuning the donor site through torsional locking, distance extension, and planarization, we achieved remarkable control over key quantum properties, including field-response range and line width. In the most responsive systems, emission lifetimes increased by over 200%, and the total emission intensity was modulated by up to 30%. This level of tunability shows the power of synthetic spin chemistry. The rational design principle of optically addressable SCRP-based molecular systems, presented in this work, represents a major leap toward functional synthetic molecular qubits, advancing the field of molecular quantum technologies.

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Openalex Percentile: Top 67%
Magnetism in coordination complexes
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Molecular Engineeringof Emissive Molecular QubitsBased on Spin-Correlated Radical Pairs · Figshare (2025) | TGRS Research Map | TGRS