dc.contributor.authorTay, Madelyn Qin Yi
dc.date.accessioned2016-02-29T02:05:41Z
dc.date.accessioned2017-07-23T08:44:41Z
dc.date.available2016-02-29T02:05:41Z
dc.date.available2017-07-23T08:44:41Z
dc.date.issued2016
dc.identifier.citationTay, M. Q. Y. (2016). Building a lewis acidic phosphorus. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/66010
dc.description.abstractThis work involves the synthesis and characterization of phosphenium cations whose stability reflects the σ- and π- donating properties of carbone ligands. A coordinatively unsaturated P(III)-containing dication, [iPr2NPC(PPh3)2]2+, has been synthesized and fully characterized by single crystal X-ray diffraction and theoretical calculations. Its reactivity towards DMAP, PMe3, H2O, MeOH, and CoCp2 is presented; no reactions were observed with 2-butyne, dimethylbutadiene and anisole. Two other putative Ph- and Cl-substituted dications [XPC(PPh3)2]2+ were targeted. These could not be observed directly, but evidence for their formation has been obtained through trapping with alkynes and 1,3-dienes to form dicationic species containing phosphirene and phospholene rings, respectively. Reduction of [Me2C2PClC(PPh3)2]2+ with elemental magnesium resulted in the formation of [Me2C2PC(PPh3)2]+, while the dehydrohalogenation of [Me2C4H4PClC(PPh3)2]2+ by 2-methylpyridine resulted in the formation of a phosphole. Preliminary studies on the hydrolysis of the Cl-substituted phosphirenium salt, [Me2C2PClC(PPh3)2]2+ shows a possible formation of a stable phosphirene oxide.en_US
dc.format.extent184 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organometallic compoundsen_US
dc.titleBuilding a lewis acidic phosphorusen_US
dc.typeThesis
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.contributor.supervisorDragoslav Vidovicen_US
dc.description.degreeCHEMISTRY and BIOLOGICAL CHEMISTRYen_US
dc.identifier.doihttps://doi.org/10.32657/10356/66010


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