Synthetic strategies and porphyrin building blocks for unsymmetrical multichromophores

Tetrahedron Letters

Volumn 49, Issue 14, 2008, Pages 2236-2239

  Fazekas, Marijana ^a   Pintea, Monica ^a   Senge, Mathias O ^a,b   Zawadzka, Monika ^a  

^a TRINITY COLLEGE DUBLIN   (Ireland)

^b Dublin Molecular Medicine Centre   (Ireland)

Author keywords

Halogenation; Nonlinear optical limiting; Pd catalyzed coupling; Porphyrins; Tetrapyrroles

Indexed keywords

ARGON; DIMER; PORPHYRIN DERIVATIVE;

ARTICLE; BIOMEDICINE; CHROMATOPHORE; DIMERIZATION; HALOGENATION; OLIGOMERIZATION; OPTICS; SONOGASHIRA REACTION; SUZUKI REACTION;

EID: 40249105771     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.02.029     Document Type: Article

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29. -1. The beam was spatially filtered to remove the higher order modes and tightly focused with a 9 cm focal length lens as described in Ref. 11.