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Synthesis and Crystal Structures of the Ligand‐Stabilized Silver Chalcogenide Clusters [Ag<sub>154</sub>Se<sub>77</sub>(dppxy)<sub>18</sub>], [Ag<sub>320</sub>(S<i>t</i>Bu)<sub>60</sub>S<sub>130</sub>(dppp)<sub>12</sub>], [Ag<sub>352</sub>S<sub>128</sub>(S<i>t</i>C<sub>5</sub>H<sub>11</sub>)<sub>96</sub>], and [Ag<sub>490</sub>S<sub>188</sub>(S<i>t</i>C<sub>5</sub>H<sub>11</sub>)<sub>114</sub>]
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References
2008
Year
Materials ScienceInorganic ChemistryChemical EngineeringSilver ThiolatesEngineeringTransition Metal ChalcogenidesMetal NanoparticlesCoordination ComplexSurface ScienceCrystal StructuresCluster ChemistryLarge Cluster MoleculesMain Group ChemistryChemistryCrystallographyPhosphane LigandsInorganic Synthesis
The reaction of silver thiolates with Se(SiMe3)2 or S(SiMe3)2 in the presence of bidentate phosphanes leads to the formation of very large cluster molecules with distorted spherical metal–chalcogenide cores with diameters of 2–4 nm. The surfaces of these cores are protected by thiolate and phosphane ligands. Structural analyses show a higher degree of disorder with increasing number of Ag atoms. The compound with the highest silver content (see figure) has an idealized formulation [Ag490S188(StC5H11)114].
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