Literature DB >> 30505212

Titanium Imido Complexes via Displacement of -SiMe3 and C-H Bond Activation in a Ti(III) Amido Complex, Promoted by a Cyclic (Alkyl)(Amino) Carbene (cAAC).

Qing Ye1,2, Micah S Ziegler1, K V Lakshmi1,3, T Don Tilley1.   

Abstract

A strong σ-donating cyclic (alkyl)(amino) carbene (cAAC) triggers rearrangement of the silyl(aryl) amido ligand -N(SiMe3)Dipp (Dipp = 2,6-diisopropylphenyl) in the coordination sphere of titanium(III) to afford a novel zwitterionic titanium imido complex with a TiCH2SiMe2[cAAC] linkage. Reduction of this species produces a new DippN=Ti imido complex containing a cAAC-centered radical species, characterized by single crystal diffraction analysis and electron paramagnetic resonance spectroscopy.

Entities:  

Keywords:  cAAC; imido; radical; silyl; titanium

Year:  2017        PMID: 30505212      PMCID: PMC6261457          DOI: 10.1002/ejic.201700295

Source DB:  PubMed          Journal:  Eur J Inorg Chem        ISSN: 1434-1948            Impact factor:   2.524


  31 in total

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10.  1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group.

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