Preparation of vinyl allenes from 1-lithio-1,3-dienyl phosphine oxides and aldehydes by the Wittig-Horner reaction

[reaction: see text] Vinyl allenes were prepared in high yields by the Wittig-Horner reaction of 1-lithio-1,3-dienyl phosphine oxides with aldehydes. 1-Lithio-1,3-dienyl phosphine oxides were generated in situ from lithiation of 1-iodo-1,3-dienyl phosphine oxides, which were obtained by iodination of alpha-phosphinozirconacyclopentadienes. As a whole, a vinyl allene is synthesized from two different alkynes and one aldehyde.     

Sulfur-containing polymers. X. Aromatic poly(sulfenyl thiocarbonates)

Aromatic poly(sulfenyl thiocarbonates) have been synthesized by the interfacial polycondensation of bis(dithiocarbonyl chlorides) with bisphenols. Bisphenols having the hydroxyl groups on separate rings gave polymers in high yields. The inherent viscosities of the polymers ranged from 0.22 to 0.51. In general, they were soluble in chloroform, sym-tetrachloroethane, hexamethylphosphoramide, m-cresol, and dimethylformamide and formed transparent tough films on evaporation of chloroform solutions. Almost all of the polymers were amorphous and gave melt-spun fibers. The polymer films decomposed upon ultraviolet irradiation with liberation of carbonyl sulfide.     

Selective vinyl cationic polymerization of monomers with two cationically polymerizable groups. III. 2-vinyloxyethyl glycidyl ether: An epoxy-functionalized vinyl ether

Cationic polymerization of 2-vinyloxyethyl glycidyl ether (VEGE), a vinyl ether with an epoxy group, was conducted with various initiators in CH₂Cl₂ in the temperature range from +15 to ?78°C, and the possibility of its selective vinyl polymerization was investigated. BF₃OEt₂ polymerized both vinyl and epoxy groups of VEGE to yield polymers partially insoluble in organic solvents. HI/I₂, iodine, and CF₃SO₃H gave soluble, low-molecular-weight oligomers with epoxy pendants. ¹H-NMR structural analysis of the oligomeric products showed that the epoxy/vinyl ratio of the pendants decreases in the order: 100% epoxy ～ CF₃SO₃H > HI/I₂ ～ I₂ ? BF₃OEt₂. Although HI/I₂ or iodine mainly polymerized the vinyl group, the reaction of the vinyl ether-type growing end with an epoxy group of VEGE took place during the polymerization, so that the monomer conversion leveled off at about 40%.     

Nanoscale soldering of metal nanoparticles for construction of higher-order structures

We demonstrated that platinum nanoparticles dispersed in pure water were "soldered" by gold into higher-order structures such as "nanowebs". In practice, gold nanoparticles in water containing the platinum nanoparticles were melted by irradiation of a pulsed 532-nm laser, which excites selectively the surface plasmon band of the gold nanoparticles, and the melted gold nanoparticles solder the platinum nanoparticles together into the nanowebs. Optical absorption spectroscopy and electron microscopy together with electron probe microanalysis were employed to observe the structure of the nanowebs and to elucidate their formation dynamics.     

Transport coefficients and orientational distributions of rodlike particles with magnetic moment normal to the particle axis under circumstances of a simple shear flow

We have investigated the influences of the magnetic field strength, shear rate, and random forces on transport coefficients such as viscosity and diffusion coefficient, and also on the orientational distributions of rodlike particles of a dilute colloidal dispersion. This dispersion is composed of ferromagnetic spheroidal particles with a magnetic moment normal to the particle axis. In the present analysis, these spheroidal particles are assumed to conduct the rotational Brownian motion in a simple shear flow as well as an external magnetic field. The basic equation of the orientational distribution function has been derived from the balance of the torques and solved numerically. The results obtained here are summarized as follows. For a very strong magnetic field, the rodlike particle is significantly restricted in the field direction, so that the particle points to a direction normal to the flow direction (and also to the magnetic field direction). However, the present particle does not exhibit a strong directional characteristic, which is one of the typical properties for the previous particle with a magnetic moment parallel to the particle axis. That is, the particle can rotate around the axis of the magnetic moment, although the magnetic moment nearly points to the field direction. The viscosity significantly increases with the field strength, as in the previous particle model. The particle of a larger aspect ratio leads to the larger increase in the viscosity, since such elongated particles induce larger resistance in a flow field. The diffusion coefficient under circumstances of an applied magnetic field is in reasonable agreement between theoretical and experimental results.     

A novel synthetic method for optically active terpenes by the ring-opening reaction of (R)-(+)-β-methyl-β-propiolactone

Optically active terpene such as (R)-(+)-citronellol, (R)-(+)-pulegone or (S)-ar-turmerone is prepared in high enantiomeric excess from an intermediate, (R)-(+)-citronellic acid or (S)-(+)-3-p-tolylbutyric acid, which is easily prepared by the Sn2 type of ring opening reaction of (R)-(+)-β-methyl-β-propiolactone with homoprenylmagnesium bromide in the presence of a copper(I) salt or di-p-tolylcuprate.     

Synthesis of o-benzoquinones derived from [2.2]- and [3.3]paracyclophanes

Oxidation of [2.2]- and [3.3]paracyclophanols with benzeneseleninic anhydride readily afforded the corresponding cyclophane-o-quinones which showed the intramolecular charge-transfer interactions.     

过渡金属促进的从三种不同的炔烃高效合成苯衍 生物的策略

报道利用过渡金属有机化合物(二茂锆和有机铜化合物),从三种不同的炔烃,如何实现了高选择性高产率并且一锅煮地合成苯衍生物。     

Living cationic polymerization of vinyl ethers with carboxylic acid/tin tetrahalide initiating systems. I. New initiating systems based on acetic acid and selection of Lewis acid and basic additive leading to living polymers with low polydispersity

Cationic polymerization of isobutyl vinyl ether (IBVE) with acetic acid (CH₃COOH)/tin tetrahalide (SnX₄: X = Cl, Br, I) initiating systems in toluene solvent at 0°C was investigated, and the reaction conditions for living polymerization of IBVE with the new initiating systems were established. Among these tin tetrahalides, SnBr₄ was found to be the most suitable Lewis acid to obtain living poly(IBVE) with a narrow molecular weight distribution (MWD). The polymerization with the CH₃COOH/SnBr₄ system, however, was accompanied with the formation of a small amount of another polymer fraction of very broad MWD, probably due to the occurrence of an uncontrolled initiation by SnBr₄ coupled with protonic impurity. Addition of 1,4-dioxane (1–1.25 vol %) or 2,6-di-tert-butylpyridine (0.1–0.6mM) to the polymerization mixture completely eliminated the uncontrolled polymer to give only the living polymer with very narrow MWD (M _w/M _n ≤ 1.1; M _w, weight-average molecular weight; M _n, number-average molecular weight). The M _n of the polymers increased in direct proportion to monomer conversion, continued to increase upon sequential addition of a fresh monomer feed, and was in good agreement with the calculated values assuming that one CH₃COOH molecule formed one polymer chain. Along with these results, kinetic study and direct ¹H-NMR observation of the living polymerization indicated that CH₃COOH and SnBr₄ act as so-called “initiator” and “activator”, respectively, and the living polymerization proceeds via an activation of the acetate dormant species. The basic additives such as 1,4-dioxane and 2,6-di-tert-butylpyridine would serve mainly as a “suppressor” of the uncontrolled initiation by SnBr₄. The polymers produced after quenching the living polymerization with methanol possessed the acetate dormant terminal and they induced living polymerization of IBVE in conjunction with SnBr₄ in the presence of 1,4-dioxane. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 3173–3185, 1998