IP Library › Granted Patent US 11,964,264
Granted Patent B1
US 11,964,264 · App. 18/218,365 · Granted Apr 23, 2024

Method of forming metal oxide nanostructures on a TiO2-ZnO-buffered substrate

Inventors: Mohamed Shaker Sayed Adam (Al-Ahsa, SA); Amel Musa Taha (Al-Ahsa, SA); Mohamed M. Makhlouf (Al-Ahsa, SA)
Assignee: KING FAISAL UNIVERSITY
B01J31/2217B01J21/063B01J23/06B01J31/38B01J35/0013B01J37/0221B01J37/0228B01J37/0244B01J37/035B01J37/04B01J37/343C07C45/29C07C51/295B01J2231/40B01J2231/763B01J2531/004B01J2531/16
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Quick Facts
Patent No.
US 11,964,264
App. No.
18/218,365
Granted
Apr 23, 2024
Kind
B1
Abstract

A method of forming TiO 2 —ZnO nanoparticles coated by a copper (II) complex includes forming a mononuclear copper complex by treating a ligand with Cu 2+ ions; and immobilizing the mononuclear copper complex on TiO 2 —ZnO nanoparticles to obtain the TiO 2 —ZnO nanoparticle coated by the copper (II) complex. The TiO 2 —ZnO nanoparticles coated by a copper (II) complex thus produced have improved catalytic effectiveness and increased efficiency by reducing catalytic reaction time and temperature, particularly in methods of catalyzing oxidation of an alcohol or of catalyzing decarboxylative bromination of an acid.

Claims (44)

1. A method of catalyzing oxidation of an alcohol, the method comprising:

contacting a TiO 2 —ZnO nanoparticle coated with a copper (II) complex with the alcohol in the presence of aqueous H 2 O 2 or tBuOOH; and

obtaining a corresponding aldehyde and acid;

wherein the TiO 2 —ZnO nanoparticle coated with a copper (II) complex is prepared by a method comprising:

forming a mononuclear copper complex by treating a ligand with Cu 2+ ions; and

immobilizing the mononuclear copper complex on TiO 2 —ZnO nanoparticles to obtain the TiO 2 —ZnO nanoparticle coated with the copper (II) complex;

wherein the ligand is 2-((4-hydroxybenzylidene)amino)phenol.

2. The method according to claim 1 , wherein the alcohol is benzyl alcohol, the aldehyde is benzaldehyde, and the acid is benzoic acid, wherein a yield of the benzaldehyde of at least 90% is obtained.

3. The method according to claim 2 , wherein the yield of the benzaldehyde is about 92% to about 94%.

4. The method according to claim 1 , wherein the ligand and the Cu 2+ ions are present in a 2:1 stoichiometric ratio.

5. The method according to claim 1 , wherein the ligand is prepared by condensing 4-hydroxy benzaldehyde with 2-aminophenol in ethanol.

6. The method according to claim 1 , wherein the Cu 2+ ions are obtained by providing copper (II) acetate monohydrate in water.

7. The method according to claim 1 , wherein the copper (II) acetate monohydrate in water is poured into an ethanolic solution containing the ligand at room temperature, followed by refluxing.

8. The method according to claim 1 , wherein the TiO 2 —ZnO nanoparticles are prepared according to a method comprising:

preparing a ZnO nanoparticle solution of Saussurea costus and Zn(NO 3 ) 2 ·6H 2 O;

adjusting pH of the ZnO nanoparticle solution to about 10 by adding KOH;

preparing a TiO 2 solution by ultrasonication of TiO 2 in ethanol;

adding the TiO 2 solution to the ZnO nanoparticle solution to obtain a mixture; and

obtaining the TiO 2 —ZnO nanoparticles as a precipitate from the mixture.

9. The method according to claim 1 , wherein the immobilizing step comprises:

refluxing the mononuclear copper complex in acetonitrile with the TiO 2 —ZnO nanoparticles in acetonitrile in an ultrasonic bath at about 80° C. for about 24 hours; and

obtaining immobilized mononuclear copper complex on TiO 2 —ZnO nanoparticles by filtration.

10. A method of catalyzing decarboxylative bromination of an acid, the method comprising:

contacting a TiO 2 —ZnO nanoparticle coated with a copper (II) complex with the acid and a bromide in the presence of aqueous H 2 O 2 or tBuOOH; and

obtaining a corresponding decarboxylated acid;

wherein the TiO 2 —ZnO nanoparticle coated with a copper (H) complex is prepared by a method comprising:

forming a mononuclear copper complex by treating a ligand with Cu 2+ ions; and

immobilizing the mononuclear copper complex on TiO 2 —ZnO nanoparticles to obtain the TiO 2 —ZnO nanoparticle coated with the copper (II) complex;

wherein the ligand is 2-((4-hydroxybenzylidene)amino)phenol.

11. The method according to claim 10 , wherein the acid is α,β-cinnamic acid, the bromide is potassium bromide, and the corresponding decarboxylate acid is 2-bromovinyl benzene, wherein a yield of the 2-bromovinyl benzene of at least 90% is obtained.

12. The method according to claim 11 , wherein the yield of the 2-bromovinyl benzene is about 94% to about 95%.

13. The method according to claim 10 , wherein the ligand and the Cu 2+ ions are present in a 2:1 stoichiometric ratio.

14. The method according to claim 10 , wherein the ligand is prepared by condensing 4-hydroxy benzaldehyde with 2-aminophenol in ethanol.

15. The method according to claim 10 , wherein the Cu 2+ ions are obtained by providing copper (II) acetate monohydrate in water.

16. The method according to claim 10 , wherein the copper (II) acetate monohydrate in water is poured into an ethanolic solution containing the ligand at room temperature, followed by refluxing.

17. The method according to claim 10 , wherein the TiO 2 —ZnO nanoparticles are prepared according to a method comprising:

preparing a ZnO nanoparticle solution of Saussurea costus and Zn(NO 3 ) 2 ·6H 2 O;

adjusting pH of the ZnO nanoparticle solution to about 10 by adding KOH;

preparing a TiO 2 solution by ultrasonication of TiO 2 in ethanol;

adding the TiO 2 solution to the ZnO nanoparticle solution to obtain a mixture; and

obtaining the TiO 2 —ZnO nanoparticles as a precipitate from the mixture.

18. The method according to claim 10 , wherein the immobilizing step comprises:

refluxing the mononuclear copper complex in acetonitrile with the TiO 2 —ZnO nanoparticles in acetonitrile in an ultrasonic bath at about 80° C. for about 24 hours; and

obtaining immobilized mononuclear copper complex on TiO 2 —ZnO nanoparticles by filtration.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2023
From: ADAM, MOHAMED SHAKER SAYED; TAHA, AMEL MUSA; MAKHLOUF, MOHAMED M.
To: KING FAISAL UNIVERSITY
Reel/Frame 064171/0751 →
Continuity (1)
Division 18110525 · Feb 16, 2023