The structures of some nitrosubstituted meso-tetraarylporphyrins were determined by a simple comparison of their 1H NMRspectra, and confirmed by NOE experiments. On the basis of these investigations it was found that in the meso-tetraphenylporphyrin (meso-TPP) and its 3-methoxy, 3-methyl, and 3-chloro-substituted derivatives (in the meso-aryl rings), the electrophilic nitration occurred in position 4-.
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