Abstract:
A hitherto unknown meso-tetrakis(3,5-dihydroxyphenyl)N-confused
porphyrin (NCPH) was synthesized and characterized. The
typical 3H and 2H tautomeric existence of the N-confused
derivative was controlled exclusively by protic and aprotic
solvents rather than the established polar and non-polar driving
forces. An unprecedented morphological change controlled by
two tautomeric forms of NCPH during aggregation was investigated.