Both alcohol and halogenated solvents soluble soft-metal sensor functional phthalocyanines: synthesis, electrochemistry, spectroelectrochemistry

KANDAZ M., YARAŞIR M. N., Guney T., KOCA A.

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, cilt.13, sa.6, ss.712-721, 2009 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 13 Sayı: 6
  • Basım Tarihi: 2009
  • Doi Numarası: 10.1142/s108842460900084x
  • Dergi Adı: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.712-721
  • Anahtar Kelimeler: phthalocyanine, silver, palladium, metal sensor, job method, MALDI-TOF, electrochemistry, spectroelectrochemistry, ION BINDING, SUBSTITUTED COBALT, COMPLEXES, REDUCTION, METALLOPHTHALOCYANINES, PORPHYRAZINES, SPECTROSCOPY, OXIDATION, OXYGEN, FILMS
  • Marmara Üniversitesi Adresli: Evet

Özet

In this study, we report a novel both alcohol and haloganated solvent soluble selective ionophore functional ligand and its beta-substituted 2(3),9(10),16(17),23(24)-tetrakis(1-hydroxyhexan-3-ylthio)- phthalocyanines, M{Pc[S-CH(CH(2)CH(2)CH(3))(CH(2)CH(2)OH)](4)}, (Pc: Phthalocyanine) (M = Zn, Cu, Co), where -OH indicates peripheral functionality. Pcs exhibiting both hydrophobic and hydrophilic character were characterized spectroscopically (FT-IR, (1)H and (13)C NMR, MS (MALDI-TOF) and UV-vis), electrochemically and spectroelectrochemically. The complexes were soluble in both polar solvents, such as MeOH and EtOH, and non-polar solvents such as CHCl(3), CH(2)Cl(2), benzene, toluene, and even hexane. Absorption spectral changes of the functional MPcs during addition of Ag(I) and Pd(II) soft-metal ions are evaluated by monomer-oligomer and even polymer formations technique and monitored for in situ monitoring technique in the UV-vis spectroscopy. The binding process results in considerable blue-shift in the absorption spectra of MPcs. According to continuous variation method, the ligand: metal ratio was found ca. 1:1 and 1.5:1 for total concentration of 1.0 x 10(-5) M and 7.5 x 10(-5) M, respectively. Their electrochemical and spectroelectrochemical studies show that the complexes exhibited stable monoanionic M{Pc[S-CH(CH(2)CH(2)CH(3))(CH(2)CH(2)OH)](4)}(1-), dianionic M{Pc[S-CH(CH(2)CH(2)CH(3)) (CH(2)CH(2)OH)](4)}(2-) and monocationic M{Pc[S-CH(CH(2)CH(2)CH(3))(CH(2)CH(2)OH)](4)}(1+) species during reduction and oxidation processes.