Leveraging Metal Complexes for Optical Read-out of Magnetic Fields

Optical detection of magnetic phenomena offers a compelling pathway toward the development of highly sensitive and versatile molecular sensors. This thesis investigates the design of metal complexes tailored for magnetic field read-out through light–matter interactions, focusing on two strategies. The first section explores magnetochiral dichroism (MChD), an optical effect that emerges from the interplay between molecular chirality and magnetism. By systematically varying the metal centers within a series of chiral lanthanide complexes—specifically, Tb³⁺ and Dy³⁺—we examine how differences in magnetic moment modulate the MChD response. This comparative study reveals fundamental chemical design principles for enhancing MChD intensity and deepens our understanding of how structural and electronic factors jointly shape this directional optical effect. The second section addresses the challenge of engineering optically addressable molecular qubits based on Ni²⁺ complexes. Realizing effective spin-state read-out in these systems requires precise control over both magnetic and photophysical properties. To this end, we investigate ligand modification strategies aimed at enhancing luminescence while preserving an S = 1 ground state suitable for quantum applications. Collectively, we hope these studies contribute to a better understanding of the design space for spin–photon coupled molecular systems, offering new tools for magnetooptical sensing.

Name thesis:degree_name

Doctoral

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Chemistry

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2025

Author dc:creator

• Yi, Seungyeon

Advisor dc:contributor.advisor

• Freedman, Danna E.

Statement dc:rights

• Attribution-ShareAlike 4.0 International (CC BY-SA 4.0)
• Copyright retained by author(s)

Licence dc:rights.uri

• https://creativecommons.org/licenses/by-sa/4.0/

Handle dc:identifier.uri

https://hdl.handle.net/1721.1/162332

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/162332