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. 2016 May 11;120(22):12149–12156. doi: 10.1021/acs.jpcc.6b04484

Figure 5.

Figure 5

SABRE studies with the water-soluble CODDA/Ir SABRE catalyst (13/15) in 100% D2O. (a) Thermally polarized reference 1H NMR scan from the solution following activation with pH2 in the presence of excess substrate (py); the spectrum is vertically scaled 5-fold compared to panel b, which shows two spectra exhibiting successful observation of SABRE enhancement after bubbling with 1 atm of pH2 at ∼10 mT [total bubbling times of 210 s (30 s immediately prior to acquisition, green dashed curve) and 240 s (30 s immediately prior to acquisition, red solid curve) for the spectra, respectively], then transfer to 9.39 T for high-field acquisition (note that the green curve is shown horizontally offset by a fraction of a ppm to show the enhancement compared to the red curve). Corresponding peak enhancements were ∼25-fold and ∼32-fold for py in water with only 1 atm of pH2 bubbling in the two spectra, using a catalyst concentration of 0.3 mM. The inset shows the corresponding hydride region. A separate experiment where SABRE was attempted using the standard Ir/IMes catalyst in deuterated water exhibited no SABRE enhancement (c). (Vertical scale for panel c is different from that of panels a and b.)