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Peripherally tetra-4-carboxyethylphenoxy substituted oxotitanium (IV), cobalt(II), zinc(II) and metal free phthalocyanines were synthesized to research the sensitizing abilities of these dye molecules in standard dye sensitized solar cells (DSSCs). All the synthesized phthalocyanine complexes have been characterized by using elemental analyses, UV-Vis, FT-IR, H-1 NMR and MALDI-TOF MS spectroscopic techniques. Electrochemistry of metallo phthalocyanines (MPcs) were studied with electrochemical and in-situ spectroelectrochemical measurements. H2Pc (7) and ZnPc (5) illustrated similar Pc based electron transfer reactions. Differently, CoPc (6) and TiOPc (4) illustrated metal based redox reactions, which enhanced the redox functionality of these complexes. Metal based reductions for CoPc (6) and TiOPc (4) were recorded in addition to the Pc based one. In-situ spectroelectrochemical measurements supported the proposed voltametric mechanism. Moreover, the color and spectra of the electrogenerated species were determined with the in-situ spectroelectrochemical analyses to predict possible optoelectrochemical application of the complexes. Pronounced optical and color changes during the electrolysis of the complexes indicated electrooptical and possible solid state electrochemical functionality of the complexes. TiO2 semiconductor on the fluoride doped indium tin oxide coated glass electrode (FTO) was decorated with H2Pc (7) and TiOPc (4) bearing four carboxyl anchoring groups and they were first of all tested as possible dye for the DSSC. H2Pc (7), TiOPc (4), CoPc (6) and ZnPc (5) dyes used in DSSCs showed 2.9%, 3.3%, 1.02% and 2.2% of power conversion efficiencies respectively.

In this study, a new Donor-Acceptor-Donor (D-A-D) electroactive molecules (HCQM1 and HCQM2) containing 9H-carbazole and 9-phenyl-9H-carbazole as donor along with quinoxaline (HQ) as acceptor were synthesized and then coated on Indium Tin Oxide/Glass (ITO/Glass) surface by the electrochemical oxidation process. The HOMO-LUMO band gap values obtained by electrochemical oxidation and reduction onsets were calculated as 2.64 and 2.68 eV, respectively. On the other hand, UV-Vis absorption measurements showed that the charge transfer band of HCQM1 was detected at 500 nm with 50 nm red shift upon compared with the HCQM2. According to AFM results, it is seen that the roughness of the poly(HCQM2) film is higher than the poly(HCQM1) film. Finally, the polymer film of HCQM2 showed multi-electrochromic color change (yellow, green, and dark blue) upon the oxidation process. When the electrochromic performance of the HCQM1 and HCQM2 polymer films was compared, it was discovered that the HCQM2 with phenylene spacer unit has better stability and a higher percentage transmittance change (& UDelta;T%) between neutral and oxidized states.

In this study, metal and metal-free novel phthalocyanines containing peripheral and non-peripheral tetra 2-ben-zylphenoxy groups were synthesized. The compounds were characterized by UV-Vis, FT-IR, H-1 NMR, and MALDI-TOF mass spectrometry as well as elemental analysis. These new phthalocyanines exhibited excellent solubility in most organic solvents, and their redox behavior was investigated in different solvents such as dimethyl sulfoxide (DMSO) and dichloromethane (DCM). The redox behavior of the peripheral and non-peripheral phthalocyanine compounds 1a -c and 2a -c was determined by cyclic voltammetry and in situ spec-troelectrochemistry. According to organic field-effect transistors (OFETs) measurements, the peripheral and non-peripheral phthalocyanine-cobalt complexes which have higher mobility than others were utilized top-gate bottom-contact OFETs fabrication. The output characteristics of the device show that its mobility is approximately 5 x 10(-2) cm(2)/Vs with p-type accumulation.