2 research outputs found

    Reactions of Tungsten Acetylide–Silylene Complexes with Pyridines: Direct Observation of Silylene/Silyl Migration in Tungsten Acetylide and Carbyne/Vinylidene Frameworks

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    Reaction of acetylide–silylene complex Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>)­(CC<sup><i>t</i></sup>Bu) (<b>1a</b>) with 4-(dimethylamino)­pyridine (DMAP) gave an equilibrium mixture of DMAP-stabilized silylene acetylide complexes <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·DMAP)­(CC<sup><i>t</i></sup>Bu) (<i><b>trans</b></i><b>-4</b> and <i><b>cis</b></i><b>-4</b>). The corresponding reaction using Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>)­(CCSiMe<sub>3</sub>) (<b>2</b>) produced the novel DMAP-coordinated silenylcarbyne/silylvinylidene complex Cp*­(CO)<sub>2</sub>W­[CC­(SiPh<sub>2</sub>·DMAP)­(SiMe<sub>3</sub>)] (<b>6a</b>) as a major product, which was equilibrated with <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·DMAP)­(CCSiMe<sub>3</sub>) (<i><b>trans</b></i><b>-5a</b> and <i><b>cis</b></i><b>-5a</b>) via silylene/silyl migration. The novel structures of <i><b>cis</b></i><b>-4</b> and <b>6a</b> were revealed by X-ray crystallography. A mixture of <b>2</b> and pyridine exhibited interesting temperature-dependent NMR spectral changes, indicating the formation of <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·py)­(CCSiMe<sub>3</sub>) (<i><b>trans</b></i><b>-5b</b> and <i><b>cis</b></i><b>-5b</b>) and Cp*­(CO)<sub>2</sub>W­[CC­(SiPh<sub>2</sub>·py)­(SiMe<sub>3</sub>)] (<b>6b</b>) at low temperature, while a mixture of <b>1a</b> and pyridine showed no such spectral changes

    Reactions of Tungsten Acetylide–Silylene Complexes with Pyridines: Direct Observation of Silylene/Silyl Migration in Tungsten Acetylide and Carbyne/Vinylidene Frameworks

    No full text
    Reaction of acetylide–silylene complex Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>)­(CC<sup><i>t</i></sup>Bu) (<b>1a</b>) with 4-(dimethylamino)­pyridine (DMAP) gave an equilibrium mixture of DMAP-stabilized silylene acetylide complexes <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·DMAP)­(CC<sup><i>t</i></sup>Bu) (<i><b>trans</b></i><b>-4</b> and <i><b>cis</b></i><b>-4</b>). The corresponding reaction using Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>)­(CCSiMe<sub>3</sub>) (<b>2</b>) produced the novel DMAP-coordinated silenylcarbyne/silylvinylidene complex Cp*­(CO)<sub>2</sub>W­[CC­(SiPh<sub>2</sub>·DMAP)­(SiMe<sub>3</sub>)] (<b>6a</b>) as a major product, which was equilibrated with <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·DMAP)­(CCSiMe<sub>3</sub>) (<i><b>trans</b></i><b>-5a</b> and <i><b>cis</b></i><b>-5a</b>) via silylene/silyl migration. The novel structures of <i><b>cis</b></i><b>-4</b> and <b>6a</b> were revealed by X-ray crystallography. A mixture of <b>2</b> and pyridine exhibited interesting temperature-dependent NMR spectral changes, indicating the formation of <i>trans-</i> and <i>cis</i>-Cp*­(CO)<sub>2</sub>W­(SiPh<sub>2</sub>·py)­(CCSiMe<sub>3</sub>) (<i><b>trans</b></i><b>-5b</b> and <i><b>cis</b></i><b>-5b</b>) and Cp*­(CO)<sub>2</sub>W­[CC­(SiPh<sub>2</sub>·py)­(SiMe<sub>3</sub>)] (<b>6b</b>) at low temperature, while a mixture of <b>1a</b> and pyridine showed no such spectral changes
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