TY - JOUR
T1 - Oxidation of para‐ and meta‐ Cresols by C‐ Meso‐5,7,7,12,14,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane‐Nickel (III), to the Corresponding Aldehydes in Aqueous Media
AU - Uzan, Y.
AU - Meyerstein, D.
PY - 1986
Y1 - 1986
N2 - The tervalent nickel complex with C‐meso‐ 5,7,7,12,14,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane, Ni‐(III)L, as its disulphate form, Ni(III)L(SO4)2, oxidizes cresols in aqueous solutions. The major products after two electron equivalents are consumed are the corresponding hydroxybenzyl alcohols. The products after four electron equivalents are consumed are the corresponding hydroxybenzaldehydes. Excess tervalent nickel does not lead to the formation of the corresponding hydroxybenzoic acids. The results indicate that the oxidation reactions observed occur via the outer sphere mechanism. The use of NiL2+ as a catalyst for the oxidation of cresols is discussed.
AB - The tervalent nickel complex with C‐meso‐ 5,7,7,12,14,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane, Ni‐(III)L, as its disulphate form, Ni(III)L(SO4)2, oxidizes cresols in aqueous solutions. The major products after two electron equivalents are consumed are the corresponding hydroxybenzyl alcohols. The products after four electron equivalents are consumed are the corresponding hydroxybenzaldehydes. Excess tervalent nickel does not lead to the formation of the corresponding hydroxybenzoic acids. The results indicate that the oxidation reactions observed occur via the outer sphere mechanism. The use of NiL2+ as a catalyst for the oxidation of cresols is discussed.
UR - http://www.scopus.com/inward/record.url?scp=85005623170&partnerID=8YFLogxK
U2 - 10.1002/ijch.198600042
DO - 10.1002/ijch.198600042
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AN - SCOPUS:85005623170
SN - 0021-2148
VL - 27
SP - 280
EP - 283
JO - Israel Journal of Chemistry
JF - Israel Journal of Chemistry
IS - 3
ER -