88915-85-9

Upstream product

• 110024-05-0 Ta(2,6-diisopropylphenoxide)3Cl₂ 
• 1822-00-0 trimethylsilylmethyllithium 
• 72727-49-2 lithium 2,6-diisopropylphenolate 
• 41924-30-5 Ta(CH₂SiMe₃)₃Cl₂ 

Downstream Products

• 110024-01-6 bis(2,6-di-isopropylphenoxo)(trimethylsilylmethyl)(trimethylsilylmethylene)tantalum(V) 
• 134388-22-0 Ta(H)3(P(CH₃)2C₆H₅)2(OC₆H₃(CH(CH₃)2)2)2 
• 166330-64-9 Ta(H)3(P(CH₃)3)2(OC₆H₃(CH(CH₃)2)2)2 
• 134388-22-0 {Ta(OC₆H₃(CH(CH₃)2)2)2(H)3(P(CH₃)2C₆H₅)2} 

Relevant academic research and scientific papers

The Synthesis and Structure of Group 5 Metal Alkyl and Alkylidene Complexes containing 2,6-Dialkylphenoxide Ligands: X-Ray Crystal Structures of , , and t2-2,6)2(=CHSiMe3)(CH2SiMe3)>

A number of alkyl and alkylidene complexes of niobium and primarily tantalum containing 2,6-dialkylphenoxide ligation, OC6H3R2-2,6 (R = Me, Pri, or But) have been synthesized and characterized.For the sterically less demanding 2,6-dimethyl- and 2,6-di-isopropyl-phenoxides a series of compounds (R' = H, SiMe3, or Ph) can be readily obtained by alkylation of the corresponding mixed chloro-aryloxide.The remaining two aryloxides are more resistant to further substitution.Spectroscopic evidence supports the ?-bonded compounds adopting a trigonal-bipyramidal structure with trans-axial aryloxide ligands.This structure was confirmed by a single-crystal X-ray diffaction study on .The di- and mono-alkyls and have also been isolated and the latter shown to adopt a square-pyramidal structure in the solid state with an axial methyl group.In contrast the reaction of t2-2,6)2Cl3> with Li(CH2SiMe3) or Mg(CH2Ph)2 leads to the mixed alkyl-alkylidene complexes t2-2,6)2(=CHR')(CH2R')> (R' = SiMe3 or Ph).The presence of the alkylidene functional group was confirmed both spectroscopically and by a single-crystal X-ray diffraction study on the trimethylsilyl derivative.A related complex, i2-2,6)2(=CHSiMe3)(CH2SiMe3)>, was obtained by photolysis of i2-2,6)2(CH2SiMe3)3>.