1982
DOI: 10.1021/ja00384a052
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Characterization of novel rhodium(II) dimers with N-phenylacetamido bridging ligands

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Cited by 28 publications
(17 citation statements)
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“…The axial coordination with chloride anions (Table 2) resulted in a significant shift towards lower potentials, when compared to the literature data (Table 1). These observations agree with the literature data, that show that redox processes are favored by axial coordination which stabilizes the intermediate species or makes the oxidation process easier by increasing the electron density [17][18][19] . Furthermore, in the presence of higher Cl -levels a decrease in ∆E or about 100 mV for E m1 and 50 mV for E m2 was observed (scan rate of 25 mV s -1 ).…”
Section: Cyclic Voltammetry Behavior Of Soluble [Rh 2 (O 2 Cch 3 ) 4 supporting
confidence: 83%
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“…The axial coordination with chloride anions (Table 2) resulted in a significant shift towards lower potentials, when compared to the literature data (Table 1). These observations agree with the literature data, that show that redox processes are favored by axial coordination which stabilizes the intermediate species or makes the oxidation process easier by increasing the electron density [17][18][19] . Furthermore, in the presence of higher Cl -levels a decrease in ∆E or about 100 mV for E m1 and 50 mV for E m2 was observed (scan rate of 25 mV s -1 ).…”
Section: Cyclic Voltammetry Behavior Of Soluble [Rh 2 (O 2 Cch 3 ) 4 supporting
confidence: 83%
“…Indeed, for each equatorial group exchanged, a decrease of 225 mV in its midpoint potential E m [where: E m =(E a +E c )/2] is observed 18 . Less intense effects are also observed upon changing ligangs in the axial positions [17][18][19] . Table 1 shows the values for both midpoint potentials (E m1 and E m2 ) obtained for rhodium acetamidates under the same conditions in different solvents.…”
Section: Cyclic Voltammetry Behavior Of Soluble [Rh 2 (O 2 Cch 3 ) 4 mentioning
confidence: 80%
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“…A síntese do Rh 2 (tfc)4 foi feita através da fusão do Rh 2 (ac)4 com excesso de trifluoroacetamida [19], método pelo qual também são obtidos outros tetra-amidatos de ródio (11) [35][36][37][38][39][40] e onde também são necessárias condições mais drásticas como a fusão, para facilitar a troca de ligantes carboxilatos pelos amidatos. A trifluoroacetamida, além de ligante, comporta-se também como solvente, facilitando a dissolução do Rh 2 (ac)4 após se atingir o seu ponto de fusão.…”
Section: Resultados E Discussõesunclassified