“…The yield of the methyl ester of III, 5-[4-(((5-carbomethoxypentyl)amino)-Polymer-Linked Porphyrins 1899 carbonyl)phenyl]-10,15,20-tri-p-tolylporphyrin (IV), was 50% (117 mg). NMR (deuteriochloroform): 9.00-8.75 (m, 8 H, 0-pyrrole), 8.2-7.95 (AB quartet, 4 H, carbomethoxyphenyl-2,3,5,6 and d, 6 H, tolyl-2,6), 7.6-7.4 (d, 6 H, tolyl-3,5), 3.6 (s, 3 H, OCH3), 3.S-3.2 (m, 2 H, CCH2CO), 2.6 (s, 9 H, CH3), 2.5-2.1 (m, 2 H, CCH2NH, 1.7-1.2 (m, 6 H, CCH2C), -2.65 (s, 2 H, pyrrole NH).…”