Mixed cyclisations giving phthalocyanine-naphthalocyanine hybrids

Tetrahedron Letters

Volumn 50, Issue 25, 2009, Pages 3013-3016

  Cammidge, Andrew N ^a   Goddard, Victoria H M ^a,b   Will, Geoffrey ^b   Arnold, Dennis P ^b   Cook, Michael J ^a  

^a UNIVERSITY OF EAST ANGLIA   (United Kingdom)

^b QUEENSLAND UNIVERSITY OF TECHNOLOGY   (Australia)

Author keywords

Cyclisation; Dyes; Naphthalocyanines; Phthalocyanines

Indexed keywords

PHTHALOCYANINE;

ARTICLE; CHEMICAL REACTION; COLUMN CHROMATOGRAPHY; CYCLIZATION; ESTERIFICATION; NUCLEAR MAGNETIC RESONANCE;

EID: 65449168264     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.03.193     Document Type: Article

References (20)

1. McKeown N.B. Phthalocyanine Materials: Synthesis. Structure and Function (1998), CUP, Cambridge
2. de la Torre G., Claessens C.G., and Torres T. Chem. Commun. (2007) 2000-2015
3. Eichhorn H. J. Porphyrins Phthalocyanines 4 (2000) 88-102
4. Piechocki C., Simon J., Skoulios A., Guillon D., and Weber P. J. Am. Chem. Soc. 104 (1982) 5245-5247
5. Cammidge, A. N.; Bushby, R. J. In Handbook of Liquid Crystals Demus, D., Goodby, J. W., Gray, G. W., Spiess, H. -W., Vill, V., Eds., Wiley-VCH: Weinheim, Vol. II, p693.
6. Sergeyev S., Pisula W., and Geerts Y.H. Chem. Soc. Rev. 36 (2007) 1902-1929
7. Laschat S., Baro A., Steinke N., Giesselmann F., Hagle C., Scalia G., Judele R., Kapatsina E., Sauer S., Schreivogel A., and Tosoni M. Angew. Chem., Int. Ed. 46 (2007) 4832-4887
8. Chandrasekhar S., Sadashiva B.K., and Suresh K.A. Pramana 9 (1977) 471-480
9. See for example:. Cammidge A.N., Chambrier I., Cook M.J., Garland A.D., Heeney M.J., and Welford K. J. Porphyrins Phthalocyanines 1 (1997) 77-86
10. Mohr B., Wegner G., and Ohta K. J. Chem. Soc., Chem. Commun. (1995) 995-996
11. Msayib K., Makhseed S., and McKeown N.B. J. Mater. Chem. 11 (2001) 2784-2789
12. Bedworth P.V., Perry J.W., and Marder S.R. Chem. Commun. (1997) 1353-1354
13. Rodriguez-Morgade M.S., Torres T., Atienza-Castellanos C., and Guldi D.M. J. Am. Chem. Soc. 128 (2006) 15145-15154
14. O'Regan B.C., Lopez-Duarte I., Martinez-Diaz M.V., Forneli A., Albero J., Morandeira A., Palomares E., Torres T., and Durrant J.R. J. Am. Chem. Soc. 130 (2008) 2906-2907
15. Cammidge A.N., Berber G., Chambrier I., Hough P.W., and Cook M.J. Tetrahedron 61 (2005) 4067-4074
16. Berber G., Cammidge A.N., Chambrier I., Cook M.J., and Hough P.W. Tetrahedron Lett. 44 (2003) 5527-5529
17. Kobayashi N., and Konami H. In: Leznoff C.C., and Lever A.B.P. (Eds). Phthalocyanines: Properties and Applications Vol. 4 (1996), VCH, Weinheim 349
18. max 721 (log ε = 5.15) nm.
19. Cook M.J., Daniel M.F., Harrison K.J., McKeown N.B., and Thomson A.J. J. Chem. Soc., Chem. Commun. (1987) 1086-1088
20. Tomoda H., Saito S., Ogawa S., and Shiraishi S. Chem. Lett. (1980) 1277-1280