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Updated: Mar 31, 2026

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
Assembly and stabilization of {E(cyclo-P3)2} (E = Sn, Pb) as a bridging ligand spanning two triaryloxyniobium units
Alexandra Velian1, Brandi M Cossairt, Christopher C Cummins
1Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA. ccummins@mit.edu.
Abstract:
Complexes (THF)0-2E[P3Nb(ODipp)3]2 (E = Sn, Pb; Dipp = 2,6-(i)Pr2C6H3) were isolated (>90%) from the salt metathesis of [Na(THF)3][P3Nb(ODipp)3] with E(2+) salts. The reaction of (THF)Sn[P3Nb(ODipp)3]2 with pyridine-N-oxide was investigated as a method to deposit a new SnP6 phase. Additionally, the neutral complex P3Nb(ODipp)2(py)2 (py = pyridine) was prepared from [Na(THF)3][P3Nb(ODipp)3] in the presence of pyridine and salts of coordinating cations (Mg(II), Sn(II), Pb(II), Ge(II), Hg(II) and Ag(I)). P3Nb(ODipp)2(py)2 was found to successfully produce AsP3 upon treatment with AsCl3. The characterization of complexes (THF)0-1Sn[P3Nb(ODipp)3]2, (THF)2Pb[P3Nb(ODipp)3]2 and P3Nb(ODipp)2(py)2, including their solid state structures, is discussed.
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