Synthesis, electrochemical, in-situ spectroelectrochemical and in-situ electrocolorimetric characterization of new phthalocyanines containing macrocyclic moieties

Electrochemical and spectroelectrochemical properties of thiadiazole substituted metallo-phthalocyanines

“…CuPc complex has a redox inactive metal center thus voltammetric responses of the complex are completely different than those of TiOPc and FePc. CuPc just gives common Pc based electron transfer reactions [12,13]. As shown in Fig.…”

“…1 H NMR and 13 C NMR (for phthalonitrile compound) spectra were recorded on a Varian XL-200 NMR spectrophotometer in CDCl 3 and chemical shifts were reported (δ) relative to Me 4 Si as internal standard. FT-IR spectra were recorded on a Perkin-Elmer Spectrum one FT-IR Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 153 (2016) 71-78 spectrometer.…”

Synthesis, characterization, aggregation and electrochemical properties of peripheral octa-2-{[4-(2-benzylphenoxy]benzyl]thio} ethoxy group substituted cobalt(II) phthalocyanine

“…thio}ethoxy) phthalonitrile (2) synthesized according to literature. 26 The synthetic pathways for the preparation of 1-3 shown in Scheme 1.…”

Tunable properties based on regioselectivity of 1,2,3-triazole units in axially chiral 2,2′-linked 1,1′-binaphthyl-based copolymers for ions and acid responsiveness

“…[7,8] Further functionalization of the BINap derivatives by strategically positioned functional groups on the naphthyl rings has led to new generations of binaphthyl-based derivatives for applications in asymmetric catalysis, [9,10] chiral fluorescent sensors [11,12] and electro-optical switchable devices. [13][14][15] Functionalized chiral binaphthyls have been recently employed as enantioselective optical sensors for amino acids, with enhanced affinities towards only one of the enantiomers. [16,17] Due to the challenging functionalization of the BINap units, [18] most of the previous reports were focused on their incorporation through positions 3 and 3´ or 6 and 6´.…”