Palladium catalysed oligomerization of 1-alkynes

dc.contributor.advisorBillings, W. E.en_US
dc.creatorHunt, Ann Louise Bealen_US
dc.date.accessioned2018-12-18T21:22:00Zen_US
dc.date.available2018-12-18T21:22:00Zen_US
dc.date.issued1975en_US
dc.description.abstractThe oligomerization of 1-pentyne using palladium acetyl acetonate catalyst with various solvents and ligands was investigated. An equimolar mixture of HOAc and Et N proved to be a superior solvent. The major product observed in most cases was the dimer, 6-methylene-nona-yne, although both cis and trans-dect-ene-6-yne were observed in most cases. Trimers were formed when phosphines were replaced with bldentate amines or phosphite ligands. A one to one mixture of PPh and (CH ) P gave the highest yield of oligomers with 6-methylene-nona-4-yne as the major product. No aromatics were formed with any of the reaction systems studied. The general mechanism proposed, by Meriwether and elaborated by Maitlis is in agreement with these results.en_US
dc.format.digitalOriginreformatted digitalen_US
dc.format.extent51 ppen_US
dc.identifier.callnoThesis Chem. 1975 Hunten_US
dc.identifier.citationHunt, Ann Louise Beal. "Palladium catalysed oligomerization of 1-alkynes." (1975) Master’s Thesis, Rice University. <a href="https://hdl.handle.net/1911/104379">https://hdl.handle.net/1911/104379</a>.en_US
dc.identifier.digitalRICE2012en_US
dc.identifier.urihttps://hdl.handle.net/1911/104379en_US
dc.language.isoengen_US
dc.rightsCopyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder.en_US
dc.titlePalladium catalysed oligomerization of 1-alkynesen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentChemistryen_US
thesis.degree.disciplineNatural Sciencesen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Artsen_US
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