Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101688
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorHaque, Aen_US
dc.creatorAlenezi, KMen_US
dc.creatorMoll, HEen_US
dc.creatorKhan, MSen_US
dc.creatorWong, WYen_US
dc.date.accessioned2023-09-18T07:41:24Z-
dc.date.available2023-09-18T07:41:24Z-
dc.identifier.issn1420-3049en_US
dc.identifier.urihttp://hdl.handle.net/10397/101688-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Haque, A., Alenezi, K. M., Moll, H. E., Khan, M. S., & Wong, W. Y. (2022). Synthesis of Mixed Arylalkyl Tertiary Phosphines via the Grignard Approach. Molecules, 27(13), 4253 is available at https://doi.org/10.3390/molecules27134253.en_US
dc.subjectCross-couplingen_US
dc.subjectGrignard reactionen_US
dc.subjectOrganophosphorus chemistryen_US
dc.subjectPhosphinesen_US
dc.subjectTrivalent phosphorusen_US
dc.titleSynthesis of mixed arylalkyl tertiary phosphines via the grignard approachen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume27en_US
dc.identifier.issue13en_US
dc.identifier.doi10.3390/molecules27134253en_US
dcterms.abstractTrialkyl and triaryl phosphines are important classes of ligands in the field of catalysis and materials research. The wide usability of these low-valent phosphines has led to the design and development of new synthesis routes for a variety of phosphines. In the present work, we report the synthesis and characterization of some mixed arylalkyl tertiary phosphines via the Grignard approach. A new asymmetric phosphine is characterized extensively by multi-spectroscopic techniques. IR and UV–Vis spectra of some selected compounds are also compared and discussed. Density functional theory (DFT)-calculated results support the formation of the new compounds.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecules, July 2022, v. 27, no. 13, 4253en_US
dcterms.isPartOfMoleculesen_US
dcterms.issued2022-07-
dc.identifier.scopus2-s2.0-85133465292-
dc.identifier.pmid35807497-
dc.identifier.artn4253en_US
dc.description.validate202309 bcvc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextDeputy for Research & Innovation, Ministry of Education in Saudi Arabiaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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