1988
DOI: 10.1039/p29880000071
|View full text |Cite
|
Sign up to set email alerts
|

Facile aerial oxidation of a porphyrin. Part 3. Some metal complexes of meso-tetrakis-(3,5-di-t-butyl-4-hydroxyphenyl)porphyrin

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

3
20
0
2

Year Published

1988
1988
2017
2017

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 42 publications
(25 citation statements)
references
References 0 publications
3
20
0
2
Order By: Relevance
“…The free base porphyrins meso-tetraphenylporphyrin and meso-tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)porphyrin were synthesized as described previously by the known procedures [25][26][27][28], purified by silica gel column chromatography using CHCl 3 , 80% CHCl 3 , and 20% hexane as the eluting solvents and identified by UV-Vis and IR spectroscopy. UVVis spectra were recorded on a Varian 100S spectrophotometer in CH 2 Cl 2 , benzene, CHCl 3 , and oleic acid.…”
Section: Methodsmentioning
confidence: 99%
“…The free base porphyrins meso-tetraphenylporphyrin and meso-tetrakis(3,5-di-tert-butyl-4-hydroxyphenyl)porphyrin were synthesized as described previously by the known procedures [25][26][27][28], purified by silica gel column chromatography using CHCl 3 , 80% CHCl 3 , and 20% hexane as the eluting solvents and identified by UV-Vis and IR spectroscopy. UVVis spectra were recorded on a Varian 100S spectrophotometer in CH 2 Cl 2 , benzene, CHCl 3 , and oleic acid.…”
Section: Methodsmentioning
confidence: 99%
“…Oxidation of porphyrins 1a-f and 2a-f to the corresponding radicals 1a Å -f Å and 2a Å -f Å Porphyrins 1a-f and 2a-f were oxidized in anhydrous toluene by the tenfold excess of PbO 2 at 293 K using diphenylpicrylhydrazyl as a standard in the determination of gfactor. The experimental X-band EPR spectra of radicals 1a Å -f Å and 2a Å -f Å show triplets typical for organic phenoxyl radicals [31,32] characterizing interaction of a spin of the unpaired electron with two equivalent meta-protons in phenoxyl residue (Fig. 2).…”
Section: Synthesismentioning
confidence: 99%
“…[13][14][15][16][17][18] Получены серии порфиринов, содержащих фенольные (1-2) или фенильные (1а-2а) заместители.…”
Section: экспериментальная частьunclassified