2012
DOI: 10.6060/mhc2012.111149z
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Regularities of Coordination Reaction between Cobalt(III) 5,15-Diphenyl­octaalkylporphyrin and Organic Bases

Abstract: The process of molecular interaction of cobalt (III)

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Cited by 8 publications
(6 citation statements)
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“…The rigidly spatially ori ented lone electron pair of the N (3) pyridine nitrogen atom can participate in protonation (logB 1 lies within a range of 7-7.7, where B 1 is the imidazole protona tion constant) and in coordination of metal ions. 2 Methylimidazole, a substituted imidazole forms less stable complexes in comparison with imida zole due to the steric hindrances created by the substit uent [19]. Thermal, thermogravimetric, and elemental analy ses, potentiometry, photometry, spectrophotometry, and IR spectroscopy were used to analyze the synthe sized salts, to study their properties, and to establish the composition and stability of mixed ligand com plexes in solution.…”
Section: Hooc Coohmentioning
confidence: 99%
“…The rigidly spatially ori ented lone electron pair of the N (3) pyridine nitrogen atom can participate in protonation (logB 1 lies within a range of 7-7.7, where B 1 is the imidazole protona tion constant) and in coordination of metal ions. 2 Methylimidazole, a substituted imidazole forms less stable complexes in comparison with imida zole due to the steric hindrances created by the substit uent [19]. Thermal, thermogravimetric, and elemental analy ses, potentiometry, photometry, spectrophotometry, and IR spectroscopy were used to analyze the synthe sized salts, to study their properties, and to establish the composition and stability of mixed ligand com plexes in solution.…”
Section: Hooc Coohmentioning
confidence: 99%
“…The latter forms salts of another composition and less stable complexes in solution as compared with imidazole due to the presence of substituent in molecule [13].…”
Section: Methodsmentioning
confidence: 99%
“…The nitrogen N(3) atom with an unshared electron pair is capable of protonation (lgB1 has values in the range of 7-7.7; B1 is the constant of imidazole protonization) and the coordination of metal ions. The compound 2-methylimidazole C4H6N2 forms less stable complexes than imidazole because of emerging steric hindrances owing to a substituent [24].…”
Section: Himmentioning
confidence: 99%