TY - JOUR
T1 - Measuring the Electric Fields of Ions Captured in Crown Ethers
AU - Maitra, Anwesha
AU - Lake, William R.
AU - Mohamed, Ahmed
AU - Edington, Sean C.
AU - Das, Pratyusha
AU - Thompson, Barry C.
AU - Hammes-Schiffer, Sharon
AU - Johnson, Mark
AU - Dawlaty, Jahan M.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/25
Y1 - 2024/7/25
N2 - Controlling reactivity with electric fields is a persistent challenge in chemistry. One approach is to tether ions at well-defined locations near a reactive center. To quantify fields arising from ions, we report crown ethers that capture metal cations as field sources and a covalently bound vibrational Stark shift probe as a field sensor. We use experiments and computations in both the gas and liquid phases to quantify the vibrational frequencies of the probe and estimate the electric fields from the captured ions. Cations, in general, blue shift the probe frequency, with effective fields estimated to vary in the range of ∼0.2-3 V/nm in the liquid phase. Comparison of the gas and liquid phase data provides insight into the effects of mutual polarization of the molecule and solvent and screening of the ion’s field. These findings reveal the roles of charge, local screening, and geometry in the design of tailored electric fields.
AB - Controlling reactivity with electric fields is a persistent challenge in chemistry. One approach is to tether ions at well-defined locations near a reactive center. To quantify fields arising from ions, we report crown ethers that capture metal cations as field sources and a covalently bound vibrational Stark shift probe as a field sensor. We use experiments and computations in both the gas and liquid phases to quantify the vibrational frequencies of the probe and estimate the electric fields from the captured ions. Cations, in general, blue shift the probe frequency, with effective fields estimated to vary in the range of ∼0.2-3 V/nm in the liquid phase. Comparison of the gas and liquid phase data provides insight into the effects of mutual polarization of the molecule and solvent and screening of the ion’s field. These findings reveal the roles of charge, local screening, and geometry in the design of tailored electric fields.
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U2 - 10.1021/acs.jpclett.4c01303
DO - 10.1021/acs.jpclett.4c01303
M3 - Article
C2 - 39008844
AN - SCOPUS:85199068210
SN - 1948-7185
VL - 15
SP - 7458
EP - 7465
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 29
ER -