Replacement of the m-phenylene moiety of m-benziporphyrins
with the 2,7-naphthalenyl subunit yielded 28-hetero-2,7-naphthiporphyrinsmacrocycles
that can be considered as expanded carbaporphyrinoids. This group
retains some features of parent m-benziporphyrins,
but due to larger size and different shape of the macrocyclic cavity,
their coordination properties are different. Upon reduction and conformational
rearrangement the 28-thia- and 28-selena-2,7-naphthiporphyrin form
organophosphorus(V) complexes.
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