The synthesis and characterization of new metal-free and metallo phthalocyanines substituted with four dithiatetraoxa macrocyclic moieties

2007-01-01
Kantekin, Halit
Rakap, Murat
Misir, Mirac Nedim
Goek, Halil Zeki
Acar, Irfan
New metal-free phthalocyanine ( 7) fused symmetrically in peripheral positions with four dithiatetraoxa macrocycles, has been synthesized by cyclotetramerization of the isoindoline-diimine derivative of macrocyclic 6. Metallophthalocyanine ( 8) was synthesized by reaction of phthalonitrile derivative ( 5) with anhydrous nickel( II) chloride. The new compounds were characterized by elemental analysis, H-1 and C-13-NMR, IR UV-Vis and mass spectroscopies.
JOURNAL OF COORDINATION CHEMISTRY

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Citation Formats
H. Kantekin, M. Rakap, M. N. Misir, H. Z. Goek, and I. Acar, “The synthesis and characterization of new metal-free and metallo phthalocyanines substituted with four dithiatetraoxa macrocyclic moieties,” JOURNAL OF COORDINATION CHEMISTRY, pp. 1965–1972, 2007, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/68134.