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Carbonylative Suzuki‐Miyaura Cross‐Coupling Over Pd NPs/Rice‐Husk Carbon‐Silica Solid Catalyst: Effect Of 1,4‐Dioxane Solvent
Author(s) -
Ketike Thirupathaiah,
Velpula Venkata Ramana Kumar,
Madduluri Venkata Rao,
Kamaraju Seetha Rama Rao,
Burri David Raju
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201801100
Subject(s) - phenylboronic acid , catalysis , chemistry , selectivity , solvent , palladium , ketone , organic chemistry , iodobenzene , polymer chemistry , nuclear chemistry
With the aim of investigating the role of solvent in directing the product selectivity in carbonylative Suzuki‐Miyaura cross‐coupling (CSMC), Rice‐Husk (RH) derived carbon‐silica supported palladium nanoparticle (PdNPs/C‐SiO 2 ) catalysts were prepared and characterized by various techniques. The structural and textural properties of these catalysts have been determined by XRD, BET, SEM, TEM, FT‐IR and XPS. In CSMC over Pd NPs/C‐SiO 2 catalysts solvents are playing a critical role in directing the product selectivity particularly with 1, 4‐dioxane solvent biaryl ketone alone formed from iodobenzene, carbon monoxide and phenylboronic acid, addressing the in‐situ formation of phenylboronate ester from 1, 4‐dioxane solvent and phenyl boronic acid and subsequent biaryl ketone formation with 100% selectivity and appealing catalytic activity ( Extreamly high TON= 3,61,650).