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2/HCl(c)). The resulting porphyrin dications were stable until neutralization whereupon the starting N-alkylated tetra-oxocyclohexadienylidene porphyrinogens were obtained.14
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41
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4344625434
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note
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Structure figures of the unsubstituted parent, 2, were generated from a CIF file obtained from the Cambridge Crystallographic Data Centre, 12 Union Rd., Cambridge, CB2 1EZ, UK. E-mail: data_request@ccdc.cam.ac.uk or fax: +44 1223 336033.
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