Journal
ORGANOMETALLICS
Volume 40, Issue 7, Pages 838-842Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.organomet.1c00086
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Funding
- National Institutes of Health [GM-59426]
- University of California at Riverside
- National Science Foundation [CHE 1919677]
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The molybdenum and tungsten oxo 2-adamantylidene complexes were prepared by adding 2-methylene- or 2-ethylideneadamantane to neophylidene or neopentylidene complexes. The tungsten complex 2(w) is a thermally stable dimer with unsymmetrically bridging oxo ligands, while the molybdenum complex 2(Mo) is a stable monomer. These complexes are reactive olefin metathesis initiators with dimers 5(Mo) and 5(w) being relatively poor initiators.
Molybdenum and tungsten oxo 2-adamantylidene (Adene) complexes that contain two nonafluoro-tert-butoxide (ORF9) ligands have been prepared through addition of 2-methylene- or 2-ethylideneadamantane to neophylidene or neopentylidene complexes. The isolated oxo complexes include W(O)(Adene)(ORF9)(2)(PPh2Me) (1(w)), W(O)(Adene)(ORF9)(2) (2(w)), W(O)Adene)(2,5-dimethylpyrrolide)(2) (3(w)), W(O)(Adene)(2,5-dimethylpyrrolide)-(2,6-dimesitylphenoxide) (4(w)), Mo(O)(Adene)(ORF9)(2) (PPhMe2) (1(Mo)), and Mo(O)(Adene)(ORF9)(2) (2(Mo)). Compound 2(w) is a dimer that contains unsymmetrically bridging oxo ligands; it dissociates readily and reversibly into monomers, especially in the presence of a donor such as THF. In contrast, 2(Mo) is a monomer. Both 2(w) and 2(Mo) are remarkably stable thermally. The pale-blue complexes Mo(Adene)(ORF9)(2)Cl-2 (5(Mo)) and W(Adene)(ORF9)(2)Cl-2 (5(w)) are formed upon addition of PCl5 to 2(Mo) and 2(w), respectively. The oxo complexes are reactive olefin metathesis initiators, while 5(Mo) and 5(w) are relatively poor initiators. We ascribe the thermal stability of 2(Mo) and 2 w to resistance of the 2-adamantylidene ligands to couple bimolecularly, to the absence of an alpha-hydrogen in the alkylidene, or both.
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