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. Author manuscript; available in PMC: 2017 Jan 4.
Published in final edited form as: Chem Commun (Camb). 2016 Jan 4;52(1):167–170. doi: 10.1039/c5cc07956j

Fig. 2.

Fig. 2

a) UV-vis spectral changes upon addition of HBArF (0–2 equiv) to 2 in CH2Cl2. Inset: spectral titration at 723 nm showing maximal formation of product at 1 equiv HBArF. b) Comparison of 1H NMR spectra (400 MHz) near the aryl region of 2 (black) and 3 (red) in CD2Cl2 at 23 °C.