We
introduce a new family of highly efficient polarizing agents
for dynamic nuclear polarization (DNP)-enhanced nuclear magnetic resonance
(NMR) applications, composed of asymmetric bis-nitroxides, in which
a piperidine-based radical and a pyrrolinoxyl or a proxyl radical
are linked together. The design of the AsymPol family was guided by
the use of advanced simulations that allow computation of the impact
of the radical structure on DNP efficiency. These simulations suggested
the use of a relatively short linker with the intention to generate
a sizable intramolecular electron dipolar coupling/J-exchange interaction, while avoiding parallel nitroxide orientations.
The characteristics of AsymPol were further tuned, for instance with
the addition of a conjugated carbon–carbon double bond in the
5-membered ring to improve the rigidity and provide a favorable relative
orientation, the replacement of methyls by spirocyclohexanolyl groups
to slow the electron spin relaxation, and the introduction of phosphate
groups to yield highly water-soluble dopants. An in-depth experimental
and theoretical study for two members of the family, AsymPol and AsymPolPOK,
is presented here. We report substantial sensitivity gains at both
9.4 and 18.8 T. The robust efficiency of this new family is further
demonstrated through high-resolution surface characterization of an
important industrial catalyst using fast sample spinning at 18.8 T.
This work highlights a new direction for polarizing agent design and
the critical importance of computations in this process.