2003
DOI: 10.1070/mc2003v013n01abeh001704
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Unusual catalytic effect of halide anions in the protolytic dissociation of indium(III) octaphenyltetraazaporphyrins

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Cited by 5 publications
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“…Meanwhile, the use of TMSBr for hydrolysis of In-1b led to the complete removal of metal atoms from the porphyrin macrocycle, as was observed previously for tetraazaporphyrins, , and the partial hydrolysis of one ethyl group to give the free monoester of the meso -porphyrinylphosphonic acid 2H-2b . Nevertheless, the addition of triethylamine to the reaction mixture prevents C–P bond cleavage, and the formation of triethylammonium salts of Ga-4a – Ga-4c and In-4a – In-4c after the addition of MeOH occurs in quantitative yields.…”
Section: Resultsmentioning
confidence: 60%
“…Meanwhile, the use of TMSBr for hydrolysis of In-1b led to the complete removal of metal atoms from the porphyrin macrocycle, as was observed previously for tetraazaporphyrins, , and the partial hydrolysis of one ethyl group to give the free monoester of the meso -porphyrinylphosphonic acid 2H-2b . Nevertheless, the addition of triethylamine to the reaction mixture prevents C–P bond cleavage, and the formation of triethylammonium salts of Ga-4a – Ga-4c and In-4a – In-4c after the addition of MeOH occurs in quantitative yields.…”
Section: Resultsmentioning
confidence: 60%