Unsymmetrical Zirconacyclopentadienes from Isolated Zirconacyclopropenes with 1-Alkynylphosphine Ligands

The reaction of one equiv of 1-alkynylphosphines, R2PC CR' (R = E-t Pr-i, or Ph and R' = Ph or Mes), with Cp2Zr(pyr)(eta(2)-Me3SiC CSiMe3) resulted in formation of monoalkyne complexes. In the case where R = Et, Pr-i, or Ph and R' = Ph, a "ligand free" zirconacyclopropene complex is produced. These complexes are stabilized by intermolecular donation of the phosphorus lone-pair in the dimeric complexes [Cp2Zr(eta(2)-R2PC CPh)](2) (R = Et, Pr-i, or Ph). However, with R = Ph and R' = Mes, the zirconocyclopropene-pyridine comples Cp2Zr(pyr)(eta(2)-Ph2PC CMeS) is formed. Homocoupling of the 1-alkynylphosphines was demonstrated by reaction of a second equiv of Ph2PC CPh with [Cp2Zr(eta(2)-PhPC CPh)](2) to give the diphosphinozirconacyclopentadiene Cp2Zr[2,5-(Ph2P)(2)-3,4-Ph2C4] with high regioselectivity (77%). The zirconacyclopropene complexes also react with one equiv of PhC CPh or EtC CEt to give zirconacyclopentadienes in which the phosphino substituent preferentially adopts the 2-position (alpha) of the zirconacyclopentadiene ring. These unsymmetrical zirconacyclopentadienes undergo substitution of the R2PCCR' moiety with the less bulky alkynes PhC CPh or EtC CEt. The substituents on the 1-alkynylphosphines significantly influence the rates of alkyne substitution such that sterically more demanding substituents in either the alpha- (-(PPr2)-Pr-i) or beta- (-Mes) position of the zirconacycle lead to faster exchange. The alpha-phosphinozirconacyclopentadienes were readily converted to 1-phosphinobutadienes via reaction with benzoic acid. The zirconacyclopentadiene Cp2Zr[2-Ph2P-3,4,5-Ph3C4] was converted to the corresponding thiophene oxide by the oxo-transfer reaction with sulfur dioxide. In the case of ((1Z,3E)-3-ethyl-2-phenylhexa-1,3-dienyl)diphenylphosphine and (3,4,5-triphenylthiophen-2-yl oxide)diphenylphosphine, the molecules were isolated as their phosphine oxides. Reactions of the zirconacyclopropene complexes [Cp2Zr(eta(2)-Ph2PC CPh)](2) and Cp2Zr(pyr)(eta(2)-Ph2PC CMes) with the diyne (F5C6)C C-1,4-(C6H4-C C(C6F5) gave bis(zirconacycle)s terminated with phosphino groups. These bis(zirconacycle)s were converted to the corresponding phosphino-terminated oligomers by protonolysis with hydrochloric acid. In addition, the Ph,PCCMes moiety Of [Cp2Zr(2-Ph2P-3-Mes-4-(C6F5)C-4]-1,4-C6H4-Cp2Zr[2-Ph2P-3-Mes-4-(C6F5)C-4] was exchanged with PhC=CPh to give the phenylene(zirconacyclopentadiene) Cp2Zr[2,3-Ph-2-4-(C6F5)C-4]-1,4-C6H4-Cp2Zr[2,3-Ph-2-4-(C6F5)C-4].