Solvation of molybdenum(O)-diimine-tetracarbonyl complexes

Summary Solubilities of molybdenum(O)-diimine-tetracarbonyl complexes containing pyridyl-primary amine Schiff base or substituted 1,4-diazabutadiene ligands are reported, for a variety of non-aqueous solvents, and for toluene + heptane, toluene + methanol, and methanol-rich methanol + water mixed solvents. Enthalpies and entropies of solution for several of these complexes in a selection of solvents have been derived from temperature variation of solubilities. These results, together with new data on solvent effects on infrared and n.m.r. (¹H, ¹³C, ⁹⁵Mo) spectra and published data on solvatochromism of this family of compounds, are discussed in relation to solvation of these complexes in pure and mixed solvents.     

Synthesis and characterization of novel fluoride‐releasing monomers. II. Dimethacrylates containing bis(aminodiacetic acid) and their ternary zirconium fluoride complexes

Novel dimethacrylate monomers containing bis(aminodiacetic acid) chelating ligands with or without additional hydroxyl groups were synthesized, starting from 2,2‐bis(4‐hydroxy‐3‐methylphenyl)propane. The structures of the monomers were characterized by electrospray mass spectrometry (ESMS), ¹H NMR, and ¹³C NMR. The structures and relative stability of fluoride‐releasing monomers containing one or more ternary zirconium fluoride complex moieties were studied by ESMS. The most stable ternary zirconium fluoride complex was in the form of [LZrF]^?, where H₄L is the monomer containing bis(aminodiacetic acid) without additional hydroxyl groups. The synthesized monomer was photopolymerized with camphorquinone and 1‐phenyl‐1,2‐propane‐dione as initiators and N,N‐dimethylaminoethyl methacrylate as the accelerator. The fluoride release, fluoride recharge, compressive strength, and flexure strength were tested on the experimental dental composite containing 13.7 wt % synthesized monomer and three commercial flowable dental composites. The results showed that the experimental composite has significantly higher fluoride release and recharge capabilities than the commercial flowable composites. The compressive strength was comparable to that of the commercial materials. The water sorption and solubility met the requirement of the ISO Specification 4049. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3153–3166, 2005     

Kinetics of substitution at ternary titanium(IV)–cyclopentadienyl,pyronato or pyridinato–halide or alkoxide complexes

Rate laws and kinetic parameters are reported for substitution at titanium(IV) complexes Ti(LL)₂X₂, where LLH=cyclopentadiene, the 4-pyrone ethylmaltol, several 4-pyridinones, and related ligands, and X=halide or alkoxide, in acetonitrile solution at 298.2 K. Reactivities are discussed in terms of the nature of the leaving group, the entering group and the non-leaving ligand LL^?. Activation volumes of ?15 and ?12 cm³ mol^?1 have been determined for thiocyanate attack at Ti(cp)₂Cl₂ and Ti(etmalt)₂Cl₂ respectively. Substitution mechanisms are discussed in the light of the kinetic parameters obtained.     

The determination of electron density profiles from refraction measurements obtained using holographic interferometry

The angles a fourth-harmonic holographic interferometer probing beam is refracted upon passing through a neodymium laser-produced plasma have been measured by varying the focus during reconstruction of the hologram. A method (not requiring the numerical inversion of an integral equation) for using such refraction measurements to give the plasma electron density profile is shown to produce a profile in agreement with that obtained from the phase information on the reconstructed in-focus interferogram.     

相对论性核碰撞中φ介子增强

用强子和弦级联模型LUCIAE系统地研究了相对论性p+p和Pb+Pb碰撞中φ介子产生.在模型框架内实验测得的158AGeV/cPb+Pb碰撞中φ介子产额相对于同能量p+p碰撞的增强现象,依赖于弦发射胶子的集体效应和奇异夸克压低约化两机制,在一定程度内能得到解释.     

在RHIC的极限碎裂和Ф介子产生(英文)

利用强子和串级联模型LUCIAE研究了PHOBOS的极限碎裂等以及在PHIC进行的Au +Au碰撞中带电粒子多重性的经验标度规律 .对介子的产生机制也通过与带电粒子多重性的比较进行类似的研究 .结果似乎表明在串级碎裂模型中带电粒子和介子有共同的产生机制 .还讨论了PHOBOS经验标度规律的模型依赖性 .     

Partial molal volumes for iron(II)-diimine complexes in water and in aqueous methanol

Summary Partial molal volumes of the perchlorate or chloride salts of several tris-diimine-iron(II) cations have been determined in aqueous and methanol-water solutions by vibrating-tube densimetry. Partial molal volumes of the cations at infinite dilution have been estimated for aqueous solution, and compared with values for related cations. Trends of limiting partial molal volumes for perchlorate salts in methanol-water media are compared with trends in transfer chemical potentials for the respective cations; both are discussed in terms of ligand-dependent preferential solvation behaviour.     

Stereoselective hydrogenations of aryl-substituted dienes

The carbene complex can mediate hydrogenations of dienes with up to 20:1.0 diastereoselectivity and 99% ee; the scope and limitations of these reactions were investigated.