A simple synthesis of pyridine-tethered porphyrins

Author:

Cammidge Andrew N,Lifsey Karen M

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. D'Souza, F.; Hsieh, Y.-Y.; Deviprasad, G. R. Inorg. Chem. 1996, 35, 5747–5749 and references therein.

2. Takahashi, K.; Terashima, T.; Komura, T.; Imanaga, H. Bull. Chem. Soc. Jpn. 1989, 62, 3069–3074.

3. Maiya, G. B.; Krishnan, V. J. Phys. Chem. 1985, 89, 5225–5235.

4. Selected characterisation data. Compound 4: m.p. 197–200°C; δH (300 MHz, CDCl3) 1.4–1.8 (8H, m), 2.40 (2H, d, J 6.3 Hz, pyridine-H2,6), 2.92 (2H, t, J 5.6 Hz), 3.49 (2H, s), 3.87 (2H, t, J 7.6 Hz), 5.48 (2H, d, J 6.3 Hz, pyridine-H3,5), 7.23 (1H, m), 7.55–7.75 (11H, m), 8.12–8.28 (7H, m), 8.8–8.9 (8H, m); acc. mass (FAB) found 884.3036 (M+H), C56H46N5O2Zn=884.2943. Compound 5: m.p. >290°C; δH (300 MHz, CDCl3) 3.98 (3H, s), 7.33 (1H, dd, J 8.2 Hz, 2.6 Hz), 7.64 (1H, t, J 7.4 Hz), 7.72–7.84 (11H, m), 8.20–8.26 (6H, m), 8.94–9.02 (8H, m); acc. mass (FAB) found 707.1812 (M+H), C45H31N4OZn=707.1789.

5. Whitten, D. G.; Lopp, I. G.; Wildes, P. D. J. Am. Chem. Soc. 1968, 90, 7196–7200.

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