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Abstract:
Two α-substituted vanadium-oxo phthalocyanines, [(OC 6H3(t-Bu)2)4Pc]VO and [(OC 8H17)4Pc]VO, where OC6H 3(t-Bu)2 is 2,4-di-tert-butylphenoxy and OC 8H17 is 2,2,4-tri-methyl-3-pentoxy, were synthesized and characterized by elemental analysis, mass spectrometry, UV-visible, IR, ESR spectroscopy and electrochemistry. Both complexes have good solubility and do not aggregate in polar or non-polar solvents. Three reductions and two oxidations can be observed in DMF containing 0.2 M TBAP. A HOMO-LUMO gap of ∼ 1.4 V is seen for both complexes. The first two one-electron reductions and first oxidation are reversible diffusion controlled electrode processes under the given experimental conditions. The effects of solvent and phthalocyanine macrocycle substituents on the Q bands of the electronic absorption spectra are discussed. Copyright © 2005 Society of Porphyrins & Phthalocyanines.
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Journal of Porphyrins and Phthalocyanines
ISSN: 1088-4246
Year: 2005
Issue: 5
Volume: 9
Page: 352-360
1 . 3 3 9
JCR@2005
0 . 9 0 0
JCR@2023
ESI Discipline: CHEMISTRY;
JCR Journal Grade:2
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ESI Highly Cited Papers on the List: 0 Unfold All
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