Please use this identifier to cite or link to this item: https://doi.org/10.3762/bjoc.13.141
DC FieldValue
dc.titleMechanochemical synthesis of graphene oxide-supported transition metal catalysts for the oxidation of isoeugenol to vanillin
dc.contributor.authorFranco, A
dc.contributor.authorDe, S
dc.contributor.authorBalu, A.M
dc.contributor.authorGarcia, A
dc.contributor.authorLuque, R
dc.date.accessioned2020-10-23T04:42:24Z
dc.date.available2020-10-23T04:42:24Z
dc.date.issued2017
dc.identifier.citationFranco, A, De, S, Balu, A.M, Garcia, A, Luque, R (2017). Mechanochemical synthesis of graphene oxide-supported transition metal catalysts for the oxidation of isoeugenol to vanillin. Beilstein Journal of Organic Chemistry 13 : 1439-1445. ScholarBank@NUS Repository. https://doi.org/10.3762/bjoc.13.141
dc.identifier.issn18605397
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179472
dc.description.abstractVanillin is one of the most commonly used natural products, which can also be produced from lignm-derived feedstocks. The chemical synthesis of vanillin is well-established in large-scale production from petrochemical-based starting materials. To overcome this problem, lignin-derived monomers (such as eugenol, isoeugenol, feruhc acid etc.) have been effectively used n the past few years. However, selective and efficient production of vanillin from these feedstocks still remains an issue to replace the existing process. In this work, new transition metal-based catalysts were proposed to investigate their efficiency in vanillin production. Reduced graphene oxide supported Fe and Co catalysts showed high conversion of isoeugenol under mild reaction conditions using H2O2 as oxidizing agent. Fe catalysts were more selective as compared to Co catalysts, providing a 63% vanillin selectivity at 61% conversion in 2 h. The mechanochemical process was demonstrated as an effective approach to prepare supported metal catalysts that exhibited high activity for the production of vanillin from isoeugenol. @ 2017 Franco et al.; licensee Beilstein-Institut. License and terms: see end of document.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.3762/bjoc.13.141
dc.description.sourcetitleBeilstein Journal of Organic Chemistry
dc.description.volume13
dc.description.page1439-1445
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_3762_bjoc_13_141.pdf1.05 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons