201140-18-3Relevant academic research and scientific papers
In vitro photodynamic activity of lipid vesicles with zinc phthalocyanine derivative against Enterococcus faecalis
Sobotta, Lukasz,Dlugaszewska, Jolanta,Kasprzycki, Piotr,Lijewski, Sebastian,Teubert, Anna,Mielcarek, Jadwiga,Gdaniec, Maria,Goslinski, Tomasz,Fita, Piotr,Tykarska, Ewa
, p. 111 - 118 (2018)
Zinc(II) phthalocyanine bearing eight non-peripheral 2-propoxy substituents was subjected to physicochemical study and, after incorporation in lipid vesicles, assessed as a potential photosensitizer for antibacterial photodynamic therapy. The phthalocyani
Synthesis and structural characterization of 2,3,7,8,12,13,17,18- octakis(propyl), N, N, N′, N′-tetramethylaminoporphyrazines and 2,3,9,10,16,17,23,24-octa substituted phthalocyanine and the kinetic studies of their Co(II) and Cu(II) metalated complexes
Isabirye, David A.,Mtunzi, Fanyana M.,Aiyelabola, Temitayo O.
, p. 214 - 222 (2014)
Three tetrapyrrole macrocyclic compounds 2,3,7,8,12,13,17,18- octakis(propyl)porphyrazine, N, N, N′, N′-tetramethylamino porphyrazine hybrid and 2,3,9,10,16,17,23,24-octa substituted phthalocyanine were synthesized and characterized using elemental analys
A facile and regioselective synthesis of trans-heterofunctionalized porphyrazine derivatives
Forsyth, Timothy P.,Bradley G Williams,Montalban, Antonio Garrido,Stern, Charlotte L.,Barrett, Anthony G. M.,Hoffman, Brian M.
, p. 331 - 336 (2007/10/03)
New methodology was developed for the selective synthesis of regiochemically defined porphyrazines of the form M[pz(A2;B2)] (shown in Chart 1) where A and B represent peripheral functionalization attached to the β-positions of the pyrroles. Specifically, phthalonitriles or derivatives thereof with sterically bulky groups in positions 3 and 6, in particular 4,7- bis(isopropyloxy)-1,3-diiminoisoindoline (3) act as a 'trans director' when macrocyclized with heteroatom-appended maleonitriles under Linstead conditions, the result being preferential formation of the trans- M[pz(A2;B2)] pigment where A = SR, NMe2, OR, as well as R (shown in Chart 2). Linstead crossover macrocyclization of 3 with 4, 11, 15, and 18 gave pigments 10, 14, 17, and 19, respectively. These pigments were characterized by 1H NMR, 13C NMR, UV-visible spectroscopy, mass spectrometry, microanalysis, and 17 was characterized by single-crystal X-ray analysis.
