A new type of tungsten(VI) phenylimido alkylidene complex and its triorganotungsten precursor with an O,N-chelating ligand; molecular structures of [W(CH2SiMe3)3(![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif) NPh){OCPh2(2-py)}] and [W{
NPh){OCPh2(2-py)}] and [W{![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif) CHSiMe3(CH2SiMe3)(
CHSiMe3(CH2SiMe3)(![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif) NPh){OCPh2(2-py)}](py = pyridine)
NPh){OCPh2(2-py)}](py = pyridine)                                                    
                    Abstract
A new type of tungsten(VI) alkylidene complex has been prepared with [OCPh2(2-py)], a potentially bidentate O,N-chelating monoanionic ligand, and the corresponding triorganotungsten phenylimido alkoxide precursor complexes have been isolated; the new tungsten(VI) alkylidene complex [W(![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif) CHSiMe3)(CH2SiMe3)(
CHSiMe3)(CH2SiMe3)(![[double bond, length half m-dash]](https://www.rsc.org/images/entities/char_e006.gif) NPh)-{OCPh2(2-py)}]3 reacts with norbornene (70 °C) to provide selectively the cis-polymer in a ring-opening metathesis polymerization reaction.
NPh)-{OCPh2(2-py)}]3 reacts with norbornene (70 °C) to provide selectively the cis-polymer in a ring-opening metathesis polymerization reaction.
 
                



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        ![[double bond, length half m-dash]](https://www.rsc.org/images/entities/h2_char_e006.gif) NPh){OCPh2(2-py)}] and [W{
NPh){OCPh2(2-py)}] and [W{