Synthesis of porphyrazines bearing thioalkylthiol tethers: Useful building blocks for supramolecular chemistry

Tetrahedron Letters

Volumn 52, Issue 10, 2011, Pages 1105-1107

  Pietrangeli, Daniela ^a   Ricciardi, Giampaolo ^a  

^a UNIVERSITY OF BASILICATA   (Italy)

Author keywords

Alkanethiol tetrapyrroles; S Acetyl protected thiol alkylthio porphyrazines; Supramolecular chemistry; Template cyclotetramerization; Thioalkylthiol tethers

Indexed keywords

2,3,7,8,12,13,17,18 OCTAKIS 6 ACETYLTHIOHEXYLTHIO 5,10,15,20 (21H,23H)PORPHYRAZINE; 2,3,7,8,12,13,17,18 OCTAKIS 6 BROMOHEXYLTHIO 5,10,15,20 (21H,23H)PORPHYRAZINE; ETHER DERIVATIVE; PORPHYRAZINE DERIVATIVE; PORPHYRIN DERIVATIVE; THIOL; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; SUPRAMOLECULAR CHEMISTRY; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 79551687031     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.12.103     Document Type: Article

References (22)

1. D.C. Hone, P.I. Walker, R. Evans-Gowing, S. FitzGerald, A. Beeby, I. Chambrier, M.J. Cook, and D.A. Russel Langmuir 18 2002 2985 2987
2. M.C.G. Vior, D. Cobice, L.E. Dicelio, and J. Awruch Tetrahedron Lett. 50 2009 2467 2469
3. L. Wei, H. Tiznado, G. Liu, K. Padmaja, J.S. Lindsey, F. Zaera, and D.F. Bocian J. Phys. Chem. B 109 2005 23963 23971
4. M.E. Wieder, D.C. Hone, A.H. Cook, M.M. Handsley, J. Gavrilovic, and D.A. Russel Photochem. Photobiol. Sci. 5 2006 727 734
5. A. Kotiahoa, R. Lahtinena, A. Efimova, H. Lehtivioria, N.V. Tkachenkoa, T. Kanervab, and H. Lemmetyinena J. Photochem. Photobiol. A: Chem. 212 2010 129 134
6. M. Kanehara, H. Takahashi, and T. Teranishi Angew. Chem., Int. Ed. 47 2008 307 310
7. S. Ristori, G. Ricciardi, D. Pietrangeli, A. Rosa, and A. Feis J. Phys. Chem. C 113 2009 8537 8540
8. H. Akkus, and A. Gul Transition Met. Chem. 26 2001 689 694
9. O. Saglam, and A. Gul Polyhedron 20 2001 269 275
10. R.Z. Uslu, and A. Gul C. R. Acad. Sci. Paris. Serie IIC/Chim. 2000 643 648
11. P. Sun, H. Zong, K. Salaita, J.B. Ketter, A.G.M. Barrett, B.M. Hoffman, and C.A. Mirkin J. Phys. Chem. B 110 2006 18151 18153
12. H. Zong, P. Sun, C.A. Mirkin, A.G.M. Barrett, and B.M. Hoffman J. Phys. Chem. B 113 2009 14892 14903
13. S. Ristori, A. Salvati, G. Martini, O. Spalla, D. Pietrangeli, A. Rosa, and G. Ricciardi J. Am. Chem. Soc. 129 2007 2728 2729
14. A. Salvati, S. Ristori, D. Pietrangeli, J. Oberdisse, L. Calamai, G. Martini, and G. Ricciardi Biophys. Chem. 131 2007 43 51
15. C.J. Schramm, and B.M. Hoffman Inorg. Chem. 19 1980 383 385
16. C.S. Velazquez, W.E. Broderick, M. Sabat, A.G.M. Barrett, and B.M. Hoffman J. Am. Chem. Soc. 112 1990 7408 7410
17. I.V. Koval Russ. J. Org. Chem. 41 2005 631 648
18. X. Zhou, J.M. El Khoury, L. Qu, L. Dai, and Q. Li J. Colloid Interface Sci. 308 2007 381 384
19. 3): δ = 117.4, 108.4, 31.2, 30.1, 28.7, 25.9, 23.8, 23.7.
20. max, nm (log ): 379 (4.20), 675 (4.10).
21. max, nm (log ): 362 (4.67), 526 (4.18), 641 (4.60), 713 (4.18).
22. 3: C, 49.73; H, 6.34; N, 5.73; S, 26.23. Found: C, 49.75; H, 6.83; N, 5.87; S, 26.61.