Hydrolysis of (Me3SiCH2)PhSnCl2. Isomerisation of the dimeric tetraorganodistannoxane [(Me3SiCH2)Ph(Cl)SnOSn(Cl)-Ph(CH2SiMe3)]2
Data(s) |
01/01/2003
|
---|---|
Resumo |
The hydrolysis of (Me<sub>3</sub>SiCH<sub>2</sub>)PhSnCl<sub>2</sub>(<b> 1</b>) was studied under two different reaction conditions (<i>i</i>) by using an excess of aqueous NaOH in toluene at reflux temperature and (<i>ii</i>) by using small amounts of NEt<sub>3</sub> and water in CH<sub>2</sub>Cl<sub>2</sub> at room temperature. For (<i>i</i>) the products (Me<sub>3</sub>SiCH<sub>2</sub>)Ph<sub>2</sub>SnOSnPh<sub>2</sub>(CH<sub>2</sub>SiMe<sub>3</sub>)( <b>2</b>) and [(Me<sub>3</sub>SiCH<sub>2</sub>Sn)<sub>12</sub>O<sub>14</sub>(OH)<sub>6</sub>](OH)<sub>2</sub>(<b> 3</b>) were isolated indicating that a phenyl group migration took place. For (<i>ii</i>) the dimeric tetraorganodistannoxane [(Me<sub>3</sub>SiCH<sub>2</sub>)Ph(Cl)SnOSn(Cl)Ph(CH<sub>2</sub>SiMe<sub>3</sub>)]<sub>2</sub>( <b>4</b>) was obtained. In solution, <b>4</b> exists as an equilibrium mixture of all five possible isomers <b>4a–4e</b>; in the solid state two of these isomers <b>4d</b> and <b>4e</b> co-crystallized in the same crystal modification. The observation of interconvertible isomers of <b>4</b> was attributed to the kinetic lability of the ladder-like Sn4O2Cl4 structural motif. Compounds<b> 1</b> and <b>4</b> were investigated by X-ray crystallography.<br /> |
Identificador | |
Idioma(s) |
eng |
Publicador |
RSC Publishing |
Relação |
http://dro.deakin.edu.au/eserv/DU:30002073/duthie-hydrolysisof-2003.pdf http://dx.doi.org/10.1039/b211070a |
Direitos |
2003, The Royal Society of Chemistry |
Tipo |
Journal Article |