TY - JOUR
T1 - Water-assisted sonochemically-induced demethylenation of benzyl alcohol to phenol over a structurally stable cupric oxide catalyst
AU - Bahry, Teseer
AU - Jiang, Shang
AU - Jonnalagadda, Umesh
AU - Liu, Wen
AU - Teychene, Benoit
AU - Jerome, Francois
AU - Mushrif, Samir H.
AU - Amaniampong, Prince N.
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/4/17
Y1 - 2023/4/17
N2 - Novel catalytic chemistry of demethylenation of benzyl alcohol to phenol is presented here using the synergy between an earth-abundant transition metal oxide (CuO) catalyst and high frequency ultrasound (HFUS). This chemistry is achieved in water and at room temperature. Using a combination of catalyst characterization, chemical and acoustic analysis, isotope labelling and density functional theory computations, we reveal the molecular reaction mechanism, involving benzaldehyde as an intermediate. Water is not just a benign solvation medium, but it directly participates in the chemistry by getting dissociated due to sonolysis. The adsorption of the OH from water on the catalyst surface inhibits its recombination. The surface adsorbed OH from water also activates the C-H bond in benzyl alcohol to form benzaldehyde and later incorporates itself into the phenyl ring to form phenol.
AB - Novel catalytic chemistry of demethylenation of benzyl alcohol to phenol is presented here using the synergy between an earth-abundant transition metal oxide (CuO) catalyst and high frequency ultrasound (HFUS). This chemistry is achieved in water and at room temperature. Using a combination of catalyst characterization, chemical and acoustic analysis, isotope labelling and density functional theory computations, we reveal the molecular reaction mechanism, involving benzaldehyde as an intermediate. Water is not just a benign solvation medium, but it directly participates in the chemistry by getting dissociated due to sonolysis. The adsorption of the OH from water on the catalyst surface inhibits its recombination. The surface adsorbed OH from water also activates the C-H bond in benzyl alcohol to form benzaldehyde and later incorporates itself into the phenyl ring to form phenol.
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U2 - 10.1039/d3cy00100h
DO - 10.1039/d3cy00100h
M3 - Article
AN - SCOPUS:85153870422
SN - 2044-4753
VL - 13
SP - 2982
EP - 2993
JO - Catalysis Science and Technology
JF - Catalysis Science and Technology
IS - 10
ER -