Publication:
A facile synthesis of mesoporous graphitic carbon nitride supported palladium nanoparticles as highly effective and reusable catalysts for Stille coupling reactions under mild conditions

dc.contributor.coauthorN/A
dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentGraduate School of Sciences and Engineering
dc.contributor.departmentKUYTAM (Koç University Surface Science and Technology Center)
dc.contributor.kuauthorÇetin, Sultan
dc.contributor.kuauthorKalay, Erbay
dc.contributor.kuauthorKölemen, Safacan
dc.contributor.kuauthorMetin, Önder
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF SCIENCES AND ENGINEERING
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2024-11-09T23:22:14Z
dc.date.issued2020
dc.description.abstractThe development of a Stille coupling protocol that is operable under moderate conditions without using a base is highly required for the synthetic organic chemistry community, which requires an efficient nanocatalyst. In this respect, addressed herein is a facile one-pot synthesis of mesoporous graphitic carbon nitride (mpg-CN) supported Pd NPs, denoted as mpg-CN/Pd hereafter, and investigation of their catalytic activity in Stille cross-coupling reactions for the first time. It has been demonstrated that mpg-CN nanosheets can serve as not only a support material but also a stabilizer for the generation of 4.5 nm Pd NPs. The ecofriendly generated heterogeneous nanocatalyst was characterized by TEM, XRD, XPS, BET surface area and ICP-MS analysis. The mpg-CN/Pd nanocatalysts showed high activity in the Stille coupling reaction of a variety of electron-deficient and electron-rich aryl iodides/bromides and two different organostannanes with a wide substrate scope to afford the corresponding biaryls without using any bases and additional ligands under relatively mild conditions. The catalyst can be easily recovered from the reaction medium by centrifugation. It can be reused at least 5 times without any loss of activity.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue17
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipTurkish Academy of Sciences (TUBA)
dc.description.sponsorshipKoc University O . Metin thanks the Turkish Academy of Sciences (TUBA) for the financial support. S. Kolemen thanks Koc University for the financial support.
dc.description.volume44
dc.identifier.doi10.1039/d0nj00546k
dc.identifier.eissn1369-9261
dc.identifier.issn1144-0546
dc.identifier.scopus2-s2.0-85084508048
dc.identifier.urihttps://doi.org/10.1039/d0nj00546k
dc.identifier.urihttps://hdl.handle.net/20.500.14288/11037
dc.identifier.wos532252100060
dc.keywordsIn-situ synthesis
dc.keywordsMetal nanoparticles
dc.keywordsGraphene oxide
dc.keywordsC-C
dc.keywordsEfficient
dc.keywordsSuzuki
dc.keywordsARYL
dc.keywordsHalides
dc.keywordsComplexes
dc.keywordsLigands
dc.language.isoeng
dc.publisherRoyal Soc Chemistry
dc.relation.ispartofNew Journal of Chemistry
dc.subjectChemistry
dc.titleA facile synthesis of mesoporous graphitic carbon nitride supported palladium nanoparticles as highly effective and reusable catalysts for Stille coupling reactions under mild conditions
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKalay, Erbay
local.contributor.kuauthorÇetin, Sultan
local.contributor.kuauthorKölemen, Safacan
local.contributor.kuauthorMetin, Önder
local.publication.orgunit1College of Sciences
local.publication.orgunit1GRADUATE SCHOOL OF SCIENCES AND ENGINEERING
local.publication.orgunit1Research Center
local.publication.orgunit2Department of Chemistry
local.publication.orgunit2KUYTAM (Koç University Surface Science and Technology Center)
local.publication.orgunit2Graduate School of Sciences and Engineering
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