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2O; 2:1, v/v) was added, followed by drying and acquisition of the mass spectrum on a Bruker REFLEX IV spectrometer in positive mode with delayed extraction at 20 kV total acceleration voltage. Equireactive acids give a peak pattern of 1:4:6:4:1 for the porphyrin products. Deviations from this ratio of peak intensities were used to calculate relative reactivities, as described earlier (ref.6).
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14644389861
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3 by exposure to air for 4 h. The solution was aspired and analyzed by MALDI-TOF mass spectrometry, as previously described (ref.6).
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34
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