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Synthesis and characterization of novel metal-free and metallophthalocyanines peripherally fused to four 24-membered tetraoxatetraaza macrocycles

✍ Scribed by S. Zeki̇ Yildiz; Hali̇t Kanteki̇n; Yaşar Gök


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
180 KB
Volume
05
Category
Article
ISSN
1088-4246

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✦ Synopsis


New metal-free 5 and metallophthalocyanines 6-11( M = Cu , Ni , Co , Pb , Zn ) fused in peripheral positions with four 24-membered tetraoxatetraaza macrocycles were prepared by cyclotetramerization of 24,25-dicyano-4,10,13,17-tetra(toluene-p-sulfonyl)-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22-didicontinehydrobenzo[y][3,9,12,18]tetraaza[1,7,16,22]tetraoxatetradicontine in the presence of the corresponding metal salt or a strong organic base. While the N-tosylated derivatives of the phthalocyanines are soluble in common organic solvents, the detosylated derivative of copper phthalocyaninate is soluble in water. The aggregation properties of the phthalocyanines were also investigated as a function of concentration, solvent and oxidative medium. The new compounds are characterized by a combination of elemental analysis and ^1^ H NMR, ^13^ C NMR, IR, UV-vis and MS spectral data.


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The new metal-free phthalocyanine 5 and phthalocyaninatometals &8 (M=Co, Ni, or Zn) fused in peripheral positions with four 13-membered tetrathiamacrocycles were prepared by cyclotetramerization of 2,3,6,7,9,10-hexdhydro-SH-[1,4,8,1 l]benzotetrathiacyclotridecine-13,14-dicarbonitrile in the presence