2004
DOI: 10.1016/j.matchemphys.2004.03.007
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Synthesis and investigations of copper hexadecafluorophthalocyanine CuPcF16

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Cited by 51 publications
(26 citation statements)
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“…The absence of aggregation effects indicates monomer behavior of ZnPcF 16 in DCB. 8,11) And with the increase of the polarity of solvents, the ground state is more stable than the excited state in the π-π* transition system, so the transition energy gap increases, which will induce the Q band shift to a shorter wave length to some extent. The spectrum of ZnPcF 16 dissolved in THF differs from the spectrums of this compound in DCB solvents since it shows two strong absorption peaks at 644 and 674 nm.…”
Section: Methodsmentioning
confidence: 99%
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“…The absence of aggregation effects indicates monomer behavior of ZnPcF 16 in DCB. 8,11) And with the increase of the polarity of solvents, the ground state is more stable than the excited state in the π-π* transition system, so the transition energy gap increases, which will induce the Q band shift to a shorter wave length to some extent. The spectrum of ZnPcF 16 dissolved in THF differs from the spectrums of this compound in DCB solvents since it shows two strong absorption peaks at 644 and 674 nm.…”
Section: Methodsmentioning
confidence: 99%
“…It demonstrates that ZnPcF 16 aggregates in THF solvent according to reference literature. 8,11) Figure 4 shows the UV-vis absorption curves of different concentrations of ZnPcF 16 in DMF. In the low concentration region, there are two strong absorption peaks at 640 and 674 nm for Q band.…”
Section: Methodsmentioning
confidence: 99%
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