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. Author manuscript; available in PMC: 2012 Apr 4.
Published in final edited form as: Dalton Trans. 2011 Jan 24;40(10):2234–2241. doi: 10.1039/c0dt01036g

Fig. 2.

Fig. 2

(a) UV-vis spectra of 1 (0.4 mM) (black line) and 2 (0.4 mM) (red line) in CH3CN/CH3OH (1:1) at 0 °C. (b) ESI-MS of 2-18O. Inset shows isotope distribution patterns for 2-18O (blue line) and 2-16O (red line). (c) Resonance Raman spectra of 2 (4 mM) obtained upon excitation at 407 nm in CH3CN/CH3OH (1:1) at −20 °C. Red/blue lines: samples prepared with H216O2/H218O2; green line: difference spectrum, (16O–18O). The peak marked with “s” is ascribed to the solvents. (d) X-band EPR spectrum of 2 recorded in CH3CN/CH3OH (1:1) at 4.3 K. Spectroscopic settings: frequency = 9.10 GHz, microwave power = 1 mW, modulation frequency = 100 kHz.