28791-82-4Relevant articles and documents
Niobium complexes containing a new chiral heteroscorpionate ligand and the reactivity of such a complex with O2 to give the first gem-diolate niobium complex
Otero,Fernandez-Baeza,Antinolo,Tejeda,Lara-Sanchez,Sanchez-Barba,Exposito,Rodriguez
, p. 1614 - 1619 (2007/10/03)
The synthesis of a novel unsymmetrical bis(pyrazol-1-yl) ligand, (3,5-diphenylpyrazol-1-yl-3′,5′-dimethylpyrazol-1-yl)methane (dpmpzm), 1, has been studied. Deprotonation at the methylene group of 1 with BunLi, followed by reaction with carbon dioxide yielded a racemic mixture of [{Li(dpmpza)(H2O)}4], 2 [dpmpza = (3,5-diphenylpyrazol-1-yl-3′,5′-dimethylpyrazol-1-yl)acetate], which is a novel chiral monoanionic NNO tripod ligand. This compound is an excellent precursor for the introduction of this scorpionate ligand into transition metal complexes. The complexes [NbCl3(dme)(RC≡CR′)] (dme = 1,2-dimethoxyethane) reacted with 2, to give the corresponding [NbCl 2(dpmpza)(RC≡CR′)] complexes (R = R′ = Me 3; R = R′ = SiMe3, 4; R = Ph, R′ = Me, 5; R = Ph, R′ = Et, 6). The structures of these complexes have been determined by spectroscopic methods. Variable-temperature NMR studies of these complexes were carried out in order to study their dynamic behaviour in solution. The barriers to alkyne rotation have also been calculated. The reactivity of [NbCl2(dpmpza) (Me3SiOC≡CSiMe3)], 4, toward molecular oxygen is particularly noteworthy since it led to the formation of the first gem-diolate niobium species, [(NbCl2O)2(μ-η1O, O′tpzpdo)], 7 [tpzpdo = 1,3-bis(3,5-diphenylpyrazol-1-yl)-1,3- bis(3′,5′-dimethylpyrazol-1-yl)-2,2′-propanediolate], in a process that has no precedent in the literature. The molecular structure of this gem-diolate has been determined crystallographically. The Royal Society of Chemistry 2003.
Organotransition-metal complexes of multidentate ligands XV. Chelate-assisted synthesis of molybdenum(II) carbonyl complexes; crystal structure of 2-dppm)(η1-dppm)(CO)2Br2> (dppm = bis(diphenylphosphino)methane)
Shiu, Kom-Bei,Yih, Kuang-Hway,Wang, Sue-Lein,Liao, Fen-Ling
, p. 165 - 176 (2007/10/02)
The bis(3,5-dimethylpyrazol-1-yl)methane (H2CPz'2) of the air-stable compounds, and 3-allyl)Br>, is easily removed in the course of reaction with phosphorus donors whose core angles are less than or equal to 125 deg to give, respectively, (L = PMe3 or P(OMe)3, n = 3: L = dppm or dppe, n = 2) and 3-allyl)Br> (L = PMe3 or P(OMe)3, n = 2: L = dppm or dppe, n = 1).This demonstrates that a variety of molybdenum(II) carbonyl complexes can be obtained readily from through the chelate assistance of the nitrogen bidentate ligand, H2CPz'2, where dppm is bis(diphenylphosphino)methane and dppe is 1,2-bis(diphenylphosphino)ethane.The structure of has been determined by X-ray crystallography supporting the conclusion that both and include one bidentate and one unidentate dppm of dppe ligands respectively, space group P1, a = 12.999(4), b = 13.917(4), c = 14.592(5) Angstroem, α = 78.85(3), β = 71.63(3), γ = 73.02(3) deg, V = 2381.1(13) Angstroem, Z = 2, Dcalc = 1.507 g/cm3, R = 0.032 and Rw = 0.031 on 5542 reflections with I > 3.0?(I).
