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dc.contributor.advisorKilian, Petr
dc.contributor.advisorWoollins, J. D. (J. Derek)
dc.contributor.authorSurgenor, Brian A.
dc.coverage.spatialxvii, 314 p.en_US
dc.date.accessioned2013-11-12T15:56:11Z
dc.date.available2013-11-12T15:56:11Z
dc.date.issued2013-07-24
dc.identifieruk.bl.ethos.581849 
dc.identifier.urihttp://hdl.handle.net/10023/4187
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subjectTertiary phosphinesen_US
dc.subjectLow coordinate phosphorusen_US
dc.subjectPhosphanylidene-phosphoraneen_US
dc.subjectFerroceneen_US
dc.subjectPhosphinideneen_US
dc.subjectPrimary phosphinesen_US
dc.subjectDichloro phosphinesen_US
dc.subjectPreparative scale developmenten_US
dc.subject.lccQD406.S8
dc.subject.lcshOrganophosphorus compoundsen_US
dc.subject.lcshOrganophosphorus compounds--Synthesisen_US
dc.titleThe synthesis and reactivity of a sterically unhindered phosphanylidene-phosphorane & the reduction of 1,3,2,4-dithiadiphosphetane-2,4-disulfides to primary and tertiary phosphinesen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.rights.embargodate2021-10-10en_US
dc.rights.embargoreasonThesis restricted in accordance with University regulations. Print and electronic copy restricted until 10th October 2021en_US


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