Photoexcitation to the S1 state in fluoropyridine enhances N-site chemical shift sensitivity to ring vibrations through charge redistribution, unlike the F site.
Vibrational structure in inner shell photoionization of molecules
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Photoinduced enhancement of chemical shift sensitivity to local vibrations
Photoexcitation to the S1 state in fluoropyridine enhances N-site chemical shift sensitivity to ring vibrations through charge redistribution, unlike the F site.