@prefix _13: <info:fedora/uuid:>.
@prefix _14: <info:fedora/fedora-system:>.
@prefix _15: <info:fedora/ora:>.
@prefix _16: <info:fedora/uuid:e5e50d36-579d-4d32-9de5-470bea1277d8/>.
@prefix _17: <info:fedora/type:>.
@prefix dc: <http://purl.org/dc/elements/1.1/>.
@prefix model: <info:fedora/fedora-system:def/model#>.
@prefix ore: <http://www.openarchives.org/ore/terms/>.
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#>.
@prefix rdfs1: <http://www.w3.org/2001/01/rdf-schema#>.
@prefix rel: <info:fedora/fedora-system:def/relations-external#>.
@prefix view: <info:fedora/fedora-system:def/view#>.

 _13:e5e50d36-579d-4d32-9de5-470bea1277d8 a model:FedoraObject;
     dc:creator "Goicoechea, Jose",
         "Zhou, Binbin";
     dc:date "2012";
     dc:description "<p>The group 14 Zintl clusters [E₉]⁴⁻ (E = Ge, Sn, Pb) have been reacted with organometallic reagents in solution in the presence of alkali metal cation sequestering agents. The synthesis, characterisation and reactivity studies of the resultant complexes are reported herein.</p><p>These negatively charged clusters reductively cleave one of the M–C bonds in the group 12 homoleptic organometallic reagents MR₂ (M = Zn, Cd; R = Ph, mes, ⁱPr) to yield η⁴-coordinated functionalised clusters closo-[E₉MR]³⁻. They can also activate both of the M–C bonds in Cd(mes)₂ to form metal-bridged dimers [Ge₉CdGe₉]⁶⁻ and [Pb₉CdCdPb₉]⁶⁻. Investigating the reactivity of the functionalised cluster [E₉CdPh]³⁻ (E = Sn, Pb) towards HSn(ⁿBu)₃ results in the synthesis of the novel closo-clusters [E₉CdSn(ⁿBu)₃]³⁻.</p><p>The reaction of K₄Ge₉ with the heteroleptic organometallic reagent Fe(COT)(CO)₃ yields the metalated cluster anion [Ge₈Fe(CO)₃]³⁻, in which the nuclearity of the Zintl anion is altered upon coordination of the [Fe(CO)₃] moiety. Two side products have also been isolated as [K(2,2,2-crypt)]⁺ salts of [Fe(η³-C₈H₈)(CO)₃]⁻ and [Fe₂(η³, η′³-C<sub<16</sub<H<sub>16</sub>)(CO)₆]²⁻.</p><p>In the presence of highly reduced Zintl anions, all the M–C bonds in homoleptic mid-row transition metal organometallic reagents can also be cleaved. These ‘naked’ metal atoms have templated the formation of the endohedral clusters [Fe@Ge<sub>10</sub>]³⁻, [Fe@Sn<sub>10</sub>]³⁻ and [Mn@Pb<sub>12</sub>]³⁻. These clusters adopt very different geometries and the electronic origin of their structures has been investigated in-depth by DFT calculations. Structural characterisation of some side products is also reported for: [E₉(mes)]³⁻ (E = Ge, Sn) and [Ge₉Mn(mes)]³⁻.</p>",
         "This thesis is not currently available via ORA.";
     dc:format "born digital";
     dc:identifier "ora:6497",
         "urn:uuid:e5e50d36-579d-4d32-9de5-470bea1277d8";
     dc:language "en";
     dc:subject "Crystallography",
         "Inorganic chemistry",
         "Organometallic Chemistry",
         "Zintl anions",
         "metal clusters",
         "organometallic reagents";
     dc:title "Solution reactivity studies of group 14 zintyl clusters towards organometallic reagents";
     dc:type "mixed material",
         "thesis";
     rdfs1:isDefinedBy <http://ora.ox.ac.uk/objects/uuid:e5e50d36-579d-4d32-9de5-470bea1277d8/aggregation.xml>;
     model:createdDate "2012-10-05T13:05:03.249Z"^^<http://www.w3.org/2001/XMLSchema#dateTime>;
     model:hasContentModel _14:DefaultContentModel-1;
     model:label "ora:6497";
     model:ownerId "fedoraAdmin";
     model:state model:Active;
     rel:isMemberOf _17:thesis;
     rel:isMemberOfCollection _15:thesis;
     view:disseminates _16:CITATION,
         _16:DC,
         _16:EVENT,
         _16:MARC21,
         _16:MODS,
         _16:RELS-EXT;
     view:lastModifiedDate "2012-10-05T13:05:08.384Z"^^<http://www.w3.org/2001/XMLSchema#dateTime>. 

 <http://ora.ox.ac.uk/objects/uuid:e5e50d36-579d-4d32-9de5-470bea1277d8/aggregation.xml> a ore:resourceMap.