1996
DOI: 10.1016/1381-1169(96)00030-1
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Factors which affect the catalytic activity of iron(III) meso tetrakis(2,6-dichlorophenyl) porphyrin chloride in homogeneous system

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Cited by 52 publications
(16 citation statements)
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“…1). The latter four ligands were selected because they are more resistant to degradation and, the three electron-deficient ligands [H 2 (TFPP), H 2 (T2NPCl 8 P) and H 2 (T2TFMPP)] result in more reactive metalloporphyrin species than the parent ligand, 5,10,15,20-tetraphenylporphyrin [H 2 (TPP)] [10][11][12]. The aim was to identify the most reactive sites of PZQ and to determine conditions that lead to selective oxidation of some sites.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…1). The latter four ligands were selected because they are more resistant to degradation and, the three electron-deficient ligands [H 2 (TFPP), H 2 (T2NPCl 8 P) and H 2 (T2TFMPP)] result in more reactive metalloporphyrin species than the parent ligand, 5,10,15,20-tetraphenylporphyrin [H 2 (TPP)] [10][11][12]. The aim was to identify the most reactive sites of PZQ and to determine conditions that lead to selective oxidation of some sites.…”
Section: Introductionmentioning
confidence: 99%
“…MeP have been thoroughly studied as catalysts for the oxidation of simple compounds such as alkanes and alkenes [7][8][9][10][11][12][13], but there are relatively few reported studies of drug oxidation: some examples include lidocaine, odapipam, ABT-200; ABT-418, aminopyrine [2], acetaminophen [4,14] and others [5,15].…”
Section: Introductionmentioning
confidence: 99%
“…Therefore we concluded that ImH should have been oxidized in a competitive reaction at higher concentrations, although, the possibility of the formation of catalytically inactive six-coordinate manganese complex, [Mn(TPFPP)(ImH) 2 ] ? , cannot be ruled out [36][37][38][39][40]. n-Bu 4 NOAc clearly showed better co-catalytic activity than ImH at all co-catalyst/Mn(TPFPP)Cl molar ratios considering both conversion % and selectivity %.…”
Section: Comparison Of Co-catalytic Effects Of Imh and Tetrabutylammomentioning
confidence: 83%
“…[23,24] При окислении стирола NaIO 4 в присутствии пор-фиринов металлов (1-2, 1а-2а) основными продуктами являются 2-фенилоксиран и фенилацетальдегид. Образование данных продуктов окисления определяли методом газовой хроматографии с масс-спектрометрией (ГХ-МС) с использованием внутреннего стандарта (ацетофенона).…”
Section: обсуждение результатовunclassified