
Chemistry Letters p. 833 - 834 (1997)
Update date:2022-08-05
Topics:
Mikami, Shinji
Sugiura, Ken-Ichi
Sakata, Yoshiteru
A series of oligo-para-phenylene (OPP) substituted new porphyrins was prepared by the combinations of aryl coupling reactions and Lindsey's pyrrole condensation reactions. Low field shifts of OPP protons in 1H-NMR spectra became larger when the protons locate closer to the center of the molecule.
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