Tethered Alkylidenes for REMP from Carbon Disulfide Cleavage.

Reactions between tungsten alkylidyne [ t BuOCO]W≡C t Bu(THF) 2 1 and sulfur containing small molecules are reported. Complex 1 reacts with CS 2 to produce intermediate η 2 bound CS 2 complex [O 2 C( t BuC═)W(η 2 -( S , C )-CS 2 )(THF)] 8 . Heating complex 8 provides a mixture of a monomeric tungsten sulfido complex 9 and a dimeric complex 10 in a 4:1 ratio, respectively. Heating the mixture does not perturb the ratio. Addition of excess THF in a solution of 9 and 10 (4:1) converts 10 to 9 (>96%) with concomitant loss of (CS) x . Both 9 and 10 can be selectively crystallized from the mixture. An alternative synthesis of exclusively monomeric 9 involves the reaction between 1 and PhNCS. Demonstrating ring expansion metathesis polymerization (REMP), tethered tungsten alkylidene 8 polymerizes norbornene to produce cis -selective syndiotactic cyclic polynorbornene ( c -poly(NBE)).