<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-26T23:55:53Z</responseDate><request verb="GetRecord" identifier="oai:researchcommons.waikato.ac.nz:10289/16108" metadataPrefix="uketd_dc">https://researchcommons.waikato.ac.nz/server/oai/request</request><GetRecord><record><header><identifier>oai:researchcommons.waikato.ac.nz:10289/16108</identifier><datestamp>2023-11-01T21:25:07Z</datestamp><setSpec>com_10289_2222</setSpec><setSpec>col_10289_2223</setSpec></header><metadata><uketd_dc:uketddc xmlns:uketd_dc="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:uketdterms="http://naca.central.cranfield.ac.uk/ethos-oai/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://naca.central.cranfield.ac.uk/ethos-oai/2.0/ http://naca.central.cranfield.ac.uk/ethos-oai/2.0/uketd_dc.xsd">
   <dc:title>Germanium hydride derivatives of transition metal carbonyls</dc:title>
   <dc:creator>Christie, Judy A.</dc:creator>
   <uketdterms:advisor>Mackay, Kenneth M.</uketdterms:advisor>
   <dcterms:abstract>Compounds of the type Fe(CO)₄(GeR₃)₂ containing two different methylgermyl substituents have been prepared and characterised. The preparation was via the exchange reaction&#xd;
&#xd;
Fe(CO)₄(GeR₃)₂ + [Mn(CO)₅]⁻ → [Fe(CO)₄(GeR₃)]⁻ + Mn(CO)₅(GeR₃)&#xd;
&#xd;
[Fe(CO)₄(GeR₃)]⁻ + GeXR’₃ → Fe(CO)₄(GeR₃)(GeR’₃)&#xd;
&#xd;
&#xd;
The compounds characterised were Fe(CO)₄(GeMeH₂) (GeH₃) Fe(CO)₄(GeMe₂H) (GeH₃), Fe(CO)₄ (GeMe₂H) (GeMeH₂), Fe(CO)₄(GeMe₃) (GeH₃) Fe(CO)₄(GeMe₃)(GeMeH₂) and Fe(CO)₄(GeMe₃)(GeMe₂H). Of these, the species Fe(CO)₄(GeMeH₂) (GeH₃) were characterised fully by infrared, proton nmr and mass spectroscopic studies.&#xd;
&#xd;
&#xd;
The self-reaction &#xd;
&#xd;
2Fe(CO)₄(GeR₃)₂ → [Fe(CO)₄(GeR₂)]₂ + 2GeR₄&#xd;
&#xd;
has also been examined in some detail. The methylgermane was eliminated in preference to GeH₄ and species of the type [Fe(CO)₄(GeH₃)]₂-GeR₂ were also identified in two cases. &#xd;
&#xd;
Halogenation of Fe(CO)₄(GeMeH₃) (GeH₃) and Fe(CO)₄(GeMe₂H) (GeH3) was followed by ¹H nmr studies. CCℓ₄ results in the substitution of Ge-H, while HCℓ cleaves Fe-Ge bonds. &#xd;
&#xd;
While Fe(CO)₄(GeMe₂H) (GeMeH₂), Fe(CO)₄(GeMe₃) (GeMeH₂) and Fe(CO)₄(GeMe₃) (GeMe₂H) have been prepared, spectroscopic identification of these species is rather tenuous as these samples were found always to be contaminated with either the symmetrically substituted species Fe(CO)₄(GeR₃)₂ and/or products from the self-reaction. &#xd;
&#xd;
Mn(CO)₅(GeR₃) species obtained in the above syntheses react with Co₂(CO)₈ to yield the species [Co₃ (CO)₉][Mn(CO)₅]Ge, [Co₂(CO)₇[Mn(CO)₅]GeMe and possibly [Co(CO)₄][Mn(CO)₅]GeMe₂. &#xd;
&#xd;
These species were characterised by their infrared and mass spectroscopic properties.</dcterms:abstract>
   <uketdterms:institution>The University of Waikato</uketdterms:institution>
   <dcterms:issued>1981</dcterms:issued>
   <dc:type>Thesis</dc:type>
   <dc:language xsi:type="dcterms:ISO639-2">en</dc:language>
   <dcterms:isReferencedBy>https://hdl.handle.net/10289/16108</dcterms:isReferencedBy>
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