Publication:
Catalytic dehydrogenation of natural terpenes via CuPd alloy nanoparticles generated on mesoporous graphitic carbon nitride

dc.contributor.coauthorMekkaoui, Ayoub Abdelkader
dc.contributor.coauthorEl Houssame, Soufiane
dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentGraduate School of Sciences and Engineering
dc.contributor.kuauthorMetin, Önder
dc.contributor.kuauthorÖzer, Melek Sermin
dc.contributor.kuauthorSündü, Buse
dc.contributor.kuauthorYalın, Ahsen Sare
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteGRADUATE SCHOOL OF SCIENCES AND ENGINEERING
dc.date.accessioned2024-11-10T00:01:54Z
dc.date.issued2023
dc.description.abstractA facile wet-chemical protocol for the synthesis of bimetallic CuPd alloy nanoparticles (NPs) anchored on mesoporous graphitic carbon nitride (m-gCN), serving as both stabilizer and support material, was presented herein. The presented protocol allowed to synthesize nearly monodisperse CuPd alloy NPs with an average particle size of 3.9 +/- 0.9 nm without use of any additional surfactants and to prepare CuPd/m-gCN nanocatalysts with different Cu/Pd compositions (Cu25Pd75/m-gCN, Cu35Pd65/m-gCN, Cu16Pd74/m-gCN, Cu32Pd68/m-gCN, Cu10Pd90/m-gCN, and Cu50Pd50/m-gCN). After the detailed characterization of CuPd/m-gCN nanocatalysts, they were utilized as catalysts in the dehydrogenation of terpenes. Among all tested nanocatalysts, Cu50Pd50/m-gCN showed the highest activity in terms of the product yields within the same reaction time. Various parameters influencing the catalytic activity of Cu50Pd50/m-gCN were studied using himachalene as a model substrate and the optimum conditions were determined. Under the optimized reaction conditions, the catalytic application of Cu50Pd50/m-gCN nanocatalysts was extended to nine different terpenes and the corresponding products were obtained in high conversion yields (>90%) under mild conditions. A reusability test showed that Cu50Pd50/m-gCN nanocatalysts can be re-used up to four cycles without significant loss in their initial activity.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue1
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [119Z199]
dc.description.sponsorshipMoroccan Centre National pour la Recherche Scientifique et Technique (CNRST) The authors thank to The Scientific and Technological Research Council of Turkey (TUBITAK, Grant No: 119Z199) and The Moroccan Centre National pour la Recherche Scientifique et Technique (CNRST) for the financial support in the framework of TUBITAK-CNRST bilateral cooperation.
dc.description.volume37
dc.identifier.doi10.1002/aoc.6943
dc.identifier.eissn1099-0739
dc.identifier.issn0268-2605
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85141508596
dc.identifier.urihttps://doi.org/10.1002/aoc.6943
dc.identifier.urihttps://hdl.handle.net/20.500.14288/16053
dc.identifier.wos879541000001
dc.keywordsBimetallic nanocatalysts
dc.keywordsCopper
dc.keywordsDehydrogenation of terpenes
dc.keywordsGraphitic carbon nitride
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofApplied Organometallic Chemistry
dc.subjectChemistry
dc.subjectChemistry, inorganic
dc.subjectNuclear chemistry
dc.titleCatalytic dehydrogenation of natural terpenes via CuPd alloy nanoparticles generated on mesoporous graphitic carbon nitride
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorYalın, Ahsen Sare
local.contributor.kuauthorSündü, Buse
local.contributor.kuauthorÖzer, Melek Sermin
local.contributor.kuauthorMetin, Önder
local.publication.orgunit1GRADUATE SCHOOL OF SCIENCES AND ENGINEERING
local.publication.orgunit1College of Engineering
local.publication.orgunit1College of Sciences
local.publication.orgunit2Department of Chemistry
local.publication.orgunit2Graduate School of Sciences and Engineering
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