Нековалентная стабилизация водорастворимого фталоцианината цинка в гидрозоле оксида графена
- Авторы: Нугманова А.Г.1, Горшкова А.И.2, Ягодин А.В.1, Аверин А.А.1, Калинина М.А.1
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Учреждения:
- Институт физической химии и электрохимии им. А.Н. Фрумкина РАН
- Московский государственный университет им. М.В. Ломоносова
- Выпуск: Том 85, № 6 (2023)
- Страницы: 781-794
- Раздел: Статьи
- URL: https://journals.rcsi.science/0023-2912/article/view/231814
- DOI: https://doi.org/10.31857/S0023291223600700
- EDN: https://elibrary.ru/XTLVXB
- ID: 231814
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Аннотация
В данной работе была изучена возможность стабилизации 2,3,9,10,16,17,23,24-окта[(3,5-бискарбоксилат натрия)фенокси]фталоцианината цинка(II) (ZnPc16) путем его гибридизации с поверхностью листов оксида графена (ОГ) за счет дисперсионных или координационных взаимодействий с фрагментами углеродного каркаса в объеме гидрозолей ОГ. С помощью сочетания физико-химических методов анализа (СЭМ, флуоресцентная микроскопия, рентгеновская порошковая дифракция, КР-спектроскопия) была подтверждена интеграция ZnPc16 с нанолистами ОГ и изучены морфология и структура полученных гибридных материалов. С помощью спектроскопии электронного поглощения установлено, что, независимо от метода гибридизации, связывание макроцикла с неорганической частицей приводит к увеличению устойчивости ZnPc16 в водной среде под действием видимого света. На основе анализа данных спектральных кинетических исследований показано, что, в отличие от системы, полученной путем прямой интеграции ZnPc16 и ОГ, гибридный материал, сформированный за счет координационных связей между компонентами с использованием ацетата цинка (Zn(OAc)2) в качестве связующего металлокластера, способен проявлять фотокаталитические свойства в окислительной фотодеструкции ряда модельных органических субстратов-поллютантов (родамина 6G, 1,5-дигидроксинафталина, 1,4-нитрофенола). Предложенный коллоидно-химический подход к стабилизации фотоактивных водорастворимых фталоцианинатов потенциально позволяет увеличивать их устойчивость к фотоиндуцированному самоокислению и может быть адаптирован для различных производных тетрапиррольных соединений, обладающих фотосенсибилизирующими свойствами.
Ключевые слова
Об авторах
А. Г. Нугманова
Институт физической химии и электрохимии им. А.Н. Фрумкина РАН
Email: kalinina@phyche.ac.ru
Россия, 119071, Москва, Ленинский просп. 31, корп. 4
А. И. Горшкова
Московский государственный университет им. М.В. Ломоносова
Email: kalinina@phyche.ac.ru
Россия, 119991, Москва,
Ленинские Горы 1, стр. 73, факультет наук о материалах
А. В. Ягодин
Институт физической химии и электрохимии им. А.Н. Фрумкина РАН
Email: kalinina@phyche.ac.ru
Россия, 119071, Москва, Ленинский просп. 31, корп. 4
А. А. Аверин
Институт физической химии и электрохимии им. А.Н. Фрумкина РАН
Email: kalinina@phyche.ac.ru
Россия, 119071, Москва, Ленинский просп. 31, корп. 4
М. А. Калинина
Институт физической химии и электрохимии им. А.Н. Фрумкина РАН
Автор, ответственный за переписку.
Email: kalinina@phyche.ac.ru
Россия, 119071, Москва, Ленинский просп. 31, корп. 4
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