Tungstene cyclobutane

The active species responsible for metathesis polymerization of cyclic alkanes has also been identified by NMR spectroscopy. These species (tungsten carbenes and tungsten cyclobutane derivatives) can form simultaneously (equation 9). The equilibria conditions involving these species have not yet been established. The living, ring-opening polymerization of norbornene with bis(cyclopentadienyl)titanacyclobutane derivatives was also followed by NMR spectroscopy. ... 

When alkenes are allowed to react with certain catalysts (mostly tungsten and molybdenum complexes), they are converted to other alkenes in a reaction in which the substituents on the alkenes formally interchange. This interconversion is called metathesis 126>. For some time its mechanism was believed to involve a cyclobutane intermediate (Eq. (16)). Although this has since been proven wrong and found that the catalytic metathesis rather proceeds via metal carbene complexes and metallo-cyclobutanes as discrete intermediates, reactions of olefins forming cyclobutanes,... 

Reactions of Cjq with metal carbene complexes also yield the [6,6] methano-fullerenes [392]. These adducts are probably not formed via a carbene addition, but via a formal [2-1-2] cycloaddition under formation of a metalla cyclobutane intermediate. The Fischer carbene complex [mefhyl(methoxymethylene)]pentacarbonyl chromium can be utilized to prepare l,2-mefhyl(methoxymethano)-fullerene in 20% yield [392]. A tungsten carbene complex was primarily used to initiate the formation of a polyacetylene polymer, but it was discovered that addition of to the complex-polymer-mixture improves the polymerization and dramatically increases the catalytic activity of the carbene complex [393]. can be integrated into the polymer via carbene addition. 

It has been speculated (5) that the olefin metathesis reaction mech-nism involves a four-centered quasi-cyclobutane transition state. The three basic steps postulated for the reaction, namely, formation of a bis-olefin-tungsten complex, transalkylidenation and olefin exchange, may account, in general, for the initiation and propagation steps in the ringopening polymerization of cycloolefins. Several modes of termination have been considered, but suitable data to test these are not yet available. 

Chromium and tungsten carbene complexes containing an alkynyl or alkenyl substituent afford moderate to high yields of cyclobutene or cyclobutane complexes respectively via formal [2 - - 2]cycloaddition with... 

The disproportionation of propylene on supported tungsten oxide catalysts is thought to proceed via a cyclobutane intermediate as follows. 

Four different stereoisomers are possible for polymer XLII, poly (cyclobutane-1,2-diyl) (Sec. 8-lf). Cis and trans isomers are possible for pol3mier XLin, poly (but-1-ene-1,4-diyl). (XLni is the same polymer obtained by the l,4-pol3fmerization of 1,3-butadiene— Sec. 8.10). Traditional Ziegler-Natta initiators based on vanadium and metallocene initiators yield polymerizations almost exclusively through the double bond. Titanium, tungsten, and ruthenium initiators yield predominantly ROMP with varying amounts of cis and trans placements. 

Subsequently, other Ti-cyclobutane species were shown to be the reaction products of the Tebbe complex with olefins the analogous reaction with acetylenes gives metallacyclobutenes." Utilization of Ti-metaUacycles as initiators in metathesis provides the first example of a living metathesis polymerization system. Clear evidence of the intervention of metaUacarbenes and metallacyclobutanes in olefin metathesis was later furnished by Kress et al. through minute nuclear magnetic resonance (NMR) studies on norbomene polymerization with tungsten alkylidenes. 

---