Abstract
Spins in molecules are particularly attractive targets for next-generation quantum
technologies, enabling chemically programmable qubits and potential for scale-up
via self-assembly. Here, we demonstrate chemical control of the degree of s-orbital
mixing into the spin-bearing d-orbital associated with a series of spin-½ La(II) and
Lu(II) molecules. Increased s-orbital character reduces spin-orbit coupling and
enhances the electron-nuclear Fermi contact interaction. Both outcomes are
beneficial for quantum applications: the former reduces spin-lattice relaxation,
while the latter gives rise to a record molecular hyperfine interaction for Lu(II) that,
in turn, generates a massive 9 GHz hyperfine clock transition and an order of
magnitude increase in phase memory time. These findings suggest new strategies
for development of molecular quantum technologies, akin to trapped ion systems.