A Novel Mixed Ag–Pd Nanoparticles Supported on SBA Silica Through [DMAP-TMSP-DABCO]OH Basic Ionic Liquid for Suzuki Coupling Reaction

In present protocol, we have a developed a mixed metallic Ag–Pd nanoparticles (NPs) supported on sugarcane bagasse ash silica through immobilization of 1-[3-(dimethylamino) propyl] -3-(3-trimethoxysilylpropyl)-1,4-diazabicyclo [2.2.2] octan-1-ium hydroxide]ionic liquid Ag-PdNPs_(DMAP-DABCO)OH_SBAsil...

Full description

Saved in:
Bibliographic Details
Published inTopics in catalysis Vol. 68; no. 13; pp. 1287 - 1296
Main Authors Shaikh, Nilophar M., Adimule, Vinayak, Bagihalli, Gangadhar B., Keri, Rangappa S.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.07.2025
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In present protocol, we have a developed a mixed metallic Ag–Pd nanoparticles (NPs) supported on sugarcane bagasse ash silica through immobilization of 1-[3-(dimethylamino) propyl] -3-(3-trimethoxysilylpropyl)-1,4-diazabicyclo [2.2.2] octan-1-ium hydroxide]ionic liquid Ag-PdNPs_(DMAP-DABCO)OH_SBAsilica. Ag-PdNPs_(DMAP-TMSP-DABCO) OH_SBA silica catalytic system was prepared by the method of reduction using NaBH 4 as reducing agent at controlled feed rate. Further the obtained catalytic system was used as effective catalyst for ligand free Suzuki coupling reaction in ethanol solvent system at 80 °C. Synthesized catalytic system was characterized by using SEM–EDS, FT-IR, TGA–DSC and XRD analysis. The synthesized mixed metallic Ag-PdNPs catalytic system provides better catalytic activity than mono metallic nanoparticles. It is observed that, the ionic liquid and mixed metallic nanoparticles hybrid system supported on natural waste rice husk ash silica provides better stability with high efficiency and enhances the physicochemical properties through intermolecular interactions and also consequently provides ease in recyclability up to next seven turns without loss in catalytic efficiency.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:1022-5528
1572-9028
DOI:10.1007/s11244-022-01586-6