Octakis(dodecyl)phthalocyanines: Influence of Peripheral versus Non-Peripheral Substitution on Synthetic Routes, Spectroscopy and Electrochemical Behaviour.

ABSTRACT: Non-peripherally octakis-substituted phthalocyanines (npPc's), MPc(C12H25)8 with M = 2H (3) or Zn (4), as well as peripherally octakis-substituted phthalocyanines (pPc's) with M = Zn (6), Mg (7) and 2H (8), were synthesized by cyclotetramerization of 3,6- (2) or 4,5-bis(dodecyl)phthalonitrile (5), template cyclotetramerization of precursor phthalonitriles in the presence of Zn or Mg, metal insertion into metal-free phthalocyanines, and removal of Mg or Zn from the phthalocyaninato coordination cavity. The more effective synthetic route towards pPc 8 was demetalation of 7. npPc's were more soluble than pPc's. The Q-band λmax of npPc's was red-shifted with ca. 18 nm, compared to that of pPc's. X-ray photoelectron spectroscopy (XPS) differentiated between N-H, Nmeso and Ncore nitrogen atoms f

SUBMITTER: Swart G 

PROVIDER: S-EPMC8911678 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature