η-Allylpentacarbonylvanadium

The preparation of η-C₃H₅V(CO)₅ from allyl chloride and sodium hexacarbonylvanadate (–I) is reported. Composition, IR and NMR spectra are in accordance with a π-bonded C₃H₅-moiety; the preparation has been extended to give complexes with substituted allyl groups. Furthermore (1-3-η-2-butenyl)pentacarbonylvanadium can be obtained by the addition of butadiene to HV (CO)₆.     

Allyl complexes of dicyclopentadienyl-niobium(III) and -tantalum(III)

The synthesis and the properties of the complexes Cp₂TaCl₂, Cp₂M(allyl), Cp₂M(1-methylallyl) and Cp₂M(2-methylallyl) with M  Nb, Ta are described. The complex Cp₂TaCl₂ has one unpaired electron per tantalum atom, while the allyl complexes are diamagnetic. The IR and PMR spectra indicate that the allyl group is π-bonded to the metal. The mass spectra of the complexes are discussed; the thermal stability of the Cp₂Nb- and Cp₂Ta-(allyl) complexes was investigated by differential thermal analysis. The properties of the niobium and tantalum complexes are compared with those of the corresponding titanium complexes.     

Reaction des lithiens avec les organophosphores. Reaction d'addition du t-butyllithium sur le noyau benzenique des sels de phenylphosphoniums

A new reaction of organolithium compounds with phosphonium salts is described; reaction of t-butyllithium with dibenzylaminophosphonium or tetraphenylphosphonium bromides takes place through addition of the t-butyl group on a benzene ring at the position para to the phosphorus atom, the ylid formed reacts in a characteristic Wittig reaction with p-tolylaldehyde.     

Hydrogen abstraction and dimerisation reactions of some organo-transition metal free radicals

The 17-electron species [M(CO)_5χL_χ] (M  Mn, Re, χ  0; M  Mn, Re; L  Ph₃P, χ  1, 2; M  Mn, Re; L  (o-MeC₆H₄O)₃P, χ  2; M  Mn; L  (p-ClC₆H₄O)₃P, (PhO)₃P, χ  2; M  Mn; L  P(OMe)₃, χ  3) have been generated by one electron oxidation of the corresponding anions and show typical radical reactivity, undergoing dimerisation or hydride abstraction in reactions controlled by steric effects. Evidence is presented for the source of the hydrogen atom. The 19-electron species [M(CO)₃(η⁷-C₇H₇)]^? (M  Cr, Mo) and [Fe(CO)₃(η⁵-C₆H₇)]^?, generated by reduction of the corresponding cations, undergo dimerisation at the organic ligand. Similar treatment of [Fe(CO)₂-L(η-cp)]⁺ (L  CO, PPh₃, P(OPh)₃, Me₂CO) yields [Fe₂(CO)₄(η-cp)₂] and these reduction reactions are rationalised in terms of the nature of the HOMO in the intermediate radical. Similar reduction of [Rh(diphos)₂]⁺ yield the 17-electron intermediate [Rh(diphos)₂] and this also undergoes hydrogen abstraction.     

Stabilization of platinum(II) hydrides by tri-t-butylarsine; facile syntheses of stable trans-PtH2[As(t-Bu)3]2 and trans-PtHX[As(t-Bu)3]2 complexes

trans-PtH₂[As(t-Bu)₃]₂ was prepared in very good yield by afacile reaction of K₂PtC1₄ with As(t-Bu)₃ in alkaline ethanol. Treatment of trans-PtH₂[As(t-Bu)₃]₂ with CF₃CO₂H or HCI afforded trans-PtH(O₂CCF₃)[As(t-Bu)₃]₂ or trans-PtHCl[As(t-Bu)₃]₂. respectively, in almost quantitative yield.     

Solvent effects on the syn-anti isomerization rates of hydrazones of acetone

The coalescence temperature for the C-methyl peaks in the NMR spectra of hydrazones of acetone are above 200°, indicating an energy barrier for syn-anti isomerization greater than 28 kcal mole^?1. the presence of halogenated compounds decreases the energy barrier, due to the formation of a charge transfer complex between the hydrazone acting as a donor and the halogenated compound acting as the electron acceptor.     

The reaction of amines with phthalimide derivatives a convenient synthesis of isoxazolidine

The reaction of tert-butylamine, isoxazolidine and hydrazine with N-[(3-chloropropyl)oxy]phthalimide is investigated. A convenient synthesis of oxazolidine is described.     

The phase diagram for the binary system K2CrO4CaCrO4

The phase diagram for the binary system K₂CrO₄CaCrO₄ has been determined for CaCrO₄ concentrations up to 60 mole%, using the techniques of differential thermal analysis, X-ray diffraction, and drop calorimetry. Essential features of the phase diagram are: the solid-solid phase transition for pure K₂CrO₄ at 670°C, β-K₂CrO₄ ? α-K₂CrO₄; a eutectoid reaction at 14 mole% CaCrO₄ and 548°C, β-K₂CrO₄ ? α-K₂CrO₄ + K₂CrO₄ · CaCrO₄; a peritectoid event at 50 mole% CaCrO₄ and 640°C, β-K₂CrO₄ + CaCrO₄ ? K₂CrO₄ · CaCrO₄; and a eutectic reaction at 51 mole% CaCrO₄ and 678°C, L ? β-K₂CrO₄ + CaCrO₄. X-ray diffraction studies lead to the determination of the unit cell dimensions for the K₂CrO₄ · CaCrO₄ double salt, a C-centered monoclinic form with a₀ = 7.615(6) Å, b₀ = 22.797(15) Å, c₀ = 9.777(9) Å, β = 115.45(5)°.     

Enantiomers of polarized alkenes: chromatographic enrichment and thermal interconversion

(+)- and (?)-$\text{1}$ as well as (+)- and (?)-$\text{2}$ were partially separated by liquid chromatography on triacetylcellulose; racemizations resulted in the barriers (Table 2) to rotation via planarized transition states.     

The crystal structure of CuVo3(II), a high-pressure ilmenite phase

The crystal structure of a second high-pressure copper vanadate phase, CuVO₃(II), has been determined and refined by full-matrix least-squares procedures using automatic diffractometer data to a residual R = 0.042 (R_w = 0.051). The space group is rhombohedral, $\text{R}\text{3}$, with hexagonal unit cell a = 4.966(2) and c = 14.084(5) Å [a_R = 5.501(2) Å and α = 53.66(3)°]. The structure is the fully ordered ilmenite-type and, on the basis of published magnetic data and the interatomic distances, the valence distribution Cu⁺V⁵⁺O₃ is proposed. This represents a unique example of Cu⁺ in an octahedral environment.