2014
DOI: 10.6060/mhc140511k
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Substituted Tetraphenylporphyrins as Promising Molecular Systems with High Antioxidant Activity

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Cited by 14 publications
(4 citation statements)
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“…In [39] this method was successfully applied to study of substituted tetraphenyporphyrines antioxidant activity. group in order to regulate the solubility and transport function of complexes [41].…”
Section: Introductionmentioning
confidence: 98%
“…In [39] this method was successfully applied to study of substituted tetraphenyporphyrines antioxidant activity. group in order to regulate the solubility and transport function of complexes [41].…”
Section: Introductionmentioning
confidence: 98%
“…Particular features of porphyrin compounds, such as the high thermal and chemical stability of macrocycles, possibility of formation of stable complexes with different metals, possibility of variation of the oxidation state of the central metal atom, outstanding chromophoric properties of the π-conjugated macrocycle system, diverse supramolecular behavior, high biocompatibility etc., make this class of compounds attractive for solution to many applied problems. In particular, high biocompatibility of porphyrins allows considering tetraphenylporphyrins as promising drugs for photodynamic treatment of cancer [6,7] and as possible antioxidant agents [8][9][10][11][12][13]. Development of the methods of formation of polyfunctional porphyrin-based film materials [14] is important for development of catalysts [15], sensors [16], electromagnetic radiation converters [17], electronic devices [18], etc.…”
Section: Introductionmentioning
confidence: 99%
“…[2] Исследуются антиоксидантные свойства мезо-замещенных синтетических тетраарилпорфиринов, которые благодаря легкости синтеза и модификации, устойчивости, особым физико-химическим свойствам, широко применяются в технике [3,4] и медицине. [5] Данные соединения препятствуют окислительному гемолизу эритроцитов, [6] обладают антирадикальной активностью. Так, установлена способность мезо-замещенного порфи-рина с фрагментами 2,6-ди-трет-бутилфенола (R 4 PH 2 ) утилизировать супероксид анион-радикал.…”
Section: Introductionunclassified