Destruction Features of Tetra(4-iodo-5-tert-butyl)phthalocyanine Under the Action of n-Butylamine in Benzene–DMSO Media

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Аннотация

The properties of the newly synthesized tetra(4-iodo-5-tert-butyl)phthalocyanine were studied in the presence of n-butylamine in a benzene–dimethyl sulfoxide media. It was shown that the molecular form of tetra(4-iodo-5-tert-butyl)phthalocyanine and its proton transfer complex undergo degradation under the action of n-butylamine, which is described by various kinetic equations. The influence of the polarity and basicity of the media on the speed and activation parameters of the process was established and destruction schemes were proposed.

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Авторлар туралы

О. Petrov

Ivanovo State University of Chemical Technology

Хат алмасуға жауапты Автор.
Email: poa@isuct.ru
ORCID iD: 0000-0003-3424-7135
Ресей, Ivanovo, 153000

Е. Shagalov

Ivanovo State University of Chemical Technology

Email: poa@isuct.ru
ORCID iD: 0000-0002-9628-2692
Ресей, Ivanovo, 153000

А. Kiselev

Krestov Institute of Solution Chemistry of the Russian Academy of Sciences

Email: poa@isuct.ru
ORCID iD: 0000-0002-6664-6221
Ресей, Ivanovo, 153045

V. Maizlish

Ivanovo State University of Chemical Technology

Email: poa@isuct.ru
ORCID iD: 0000-0001-5423-3297
Ресей, Ivanovo, 153000

Әдебиет тізімі

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1. JATS XML
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2. Scheme 1.

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3. Fig. 1. Electronic absorption spectrum of H2Pc(I)4(t-Bu)4 in benzene and benzene-DMSO medium at 298 K.

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4. Fig. 2. Variation of the electronic absorption spectrum of H2Pc(I)4(t-Bu)4 in the presence of BuNH2 in benzene-5% DMSO medium for 278 min at c0BuNH2 = 4.58 mol/L at 323 K.

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5. Fig. 3. Variation of the electronic absorption spectrum of H2Pc(I)4(t-Bu)4 in the presence of BuNH2 in benzene-10% DMSO medium for 176 min at c0BuNH2 = 4.58 mol/L at 323 K.

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6. Fig. 4. Time dependence of ln(c0/c) for the degradation of H2Pc(I)4(t-Bu)4 (1) and H2Pc(I)4(t-Bu)4∙2BuNH2 (2) in the presence of BuNH2 in benzene-5% DMSO medium at 333 K and [BuNH2] = 4.58 mol/L.

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7. Fig. 5. Dependence of lgkH on lgc0BuNH2 of the degradation reaction of H2Pc(I)4(t-Bu)4 (1) and H2Pc(I)4(t-Bu)4∙2BuNH2 (2) in the presence of BuNH2 in benzene-5% DMSO (1) and benzene-20% DMSO (2) at 333 K.

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8. Fig. 6. Electronic absorption spectrum of H2Pc(I)4(t-Bu)4 in benzene (1) and benzene-DMSO medium (2) at c0BuNH2 = 4.58 mol/L at 298 K.

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9. Fig. 7. Variation of the electronic absorption spectrum of H2Pc(I)4(t-Bu)4 ∙ 2BuNH2 in benzene-20% DMSO medium for 135 min at c0BuNH2 = 4.58 mol/L at 323 K.

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10. Fig. 8. Variation of the electronic absorption spectrum of H2Pc(I)4(t-Bu)4 ∙ 2BuNH2 in benzene-40% DMSO medium for 117 min at c0BuNH2 = 4.58 mol/L at 333 K.

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