Premium
A Rare Carbon Skeletal Oxidative Rearrangement of Camphene Catalyzed by Al‐Exchanged Keggin Heteropolyacid Salts
Author(s) -
da Silva Márcio J.,
de Andrade Leles Lorena C.,
Ferreira Sukarno O.,
da Silva Rene C.,
de V. Viveiros Kennedy,
Chaves Diego M.,
Pinheiro Patricia F.
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201901025
Subject(s) - catalysis , chemistry , camphene , hydrogen peroxide , keggin structure , salt (chemistry) , inorganic chemistry , nuclear chemistry , medicinal chemistry , organic chemistry , chromatography , essential oil
In this work, aluminum‐exchanged Keggin heteropolyacid salts (i. e., AlPW 12 O 40 , AlPMo 12 O 40 , and Al 4/3 SiW 12 O 40 ) were synthesized and evaluated as catalysts on the camphene oxidation with hydrogen peroxide. The aluminum silicotungstate salt (i. e., Al 4/3 SiW 12 O 40 ) was the most active and selective toward formation of borneol and two novel products; 1‐(3‐(2‐hydroxypropan‐2‐yl) cyclopentyl) ethan‐1‐one, and 3‐(3‐hydroxycyclopentyl)‐3‐methylbutan‐2‐one), which were spectroscopically characterized (FT‐IR, 13 C and 1 H NMR analyses). All the catalysts were characterized by FT‐IR/ ATR spectroscopy, BET, XRD, EDS/SEM, and TG/DSC analyses. After the characterization of the HPA salts, it was possible to link their structural properties to their catalytic activity. The effects of the main reaction variables were assessed. The aluminum cation as well as the silicotungstic anion showed to be essential to formation of three goal‐products.