Properties of molten carboxylates part 6. A quantiative differential thermal analysis study of phase transitions in some zinc and cadmium carboxylates

Quantitative DTA results are presented for the phase changes in some cadmium and zinc n-alkanoates. Cadmium carboxylates form liquid crystal phases. The total entropy of the solid-to-liquid transition is small indicating a high degree of aggregation in the isotropic liquid. The phases previously reported by Skoulios are shown to be due to the presence of basic carboxylates. The zinc carboxylates have solid—solid transformations but do not form liquid crystal phases. The entropies of fusion are of the same order as those in the lead salts showing only a small degree of aggregation in the liquid.     

Acid-catalysed hydrolysis of S(IV)N bond in N-sulphonyl sulphilimines—I : Mechanism and substituent effect

The acid-catalysed hydrolysis of sulphilimines of XC₆H₄(Me)SNTs and MePhSNSO₂C₆H₄Y type has been studied by a kinetic method in moderately concentrated (1–6 M) aqueous H₂SO₄ and HClO₄ solutions. The rate law: rate = k_ψ[sulphilimine] is valid for hydrolysis leading to sulphoxides and sulphonamides. The dependence of k_ψ on acidity, temperature and substituents X and Y has been measured and interpreted, ?_X, ?_Y and ΔS^‡ data (+ 1·19, + 1·00 and −18·7- - 22·6 e.u., resp) show that the nucleophilic attack of water on the positively polarized S(IV) atom of protonated sulphilimines can be regarded as the rate-determining step of the hydrolysis. From φ parameters (0·94−1·5) calculated for the hydrolysis of MePhSNTs it follows that water participates in the reaction as a nucleophile and proton-transfer agent.     

Copper and iron interactions with angiotensin-converting enzyme inhibitors. A study by fast-atom bombardment tandem mass spectrometry

Fast atom bombardment, combined with high-energy collision-induced tandem mass spectrometry, has been used to investigate gas-phase metal-ion interactions with captopril, enalaprilat and lisinopril, all angiotensin-converting enzyme inhibitors.Suggestions for the location of metal-binding sites are presented. For captopril, metal binding occurs most likely at both the sulphur and the nitrogen atom. For enalaprilat and lisinopril, binding preferably occurs at the amine nitrogen. Copyright 1999 John Wiley & Sons, Ltd.     

Stöber silica particles as basis for redox modifications: particle shape, size, polydispersity, and porosity

The synthesis of Stöber silica particles as basis for redox modifications is optimized for desired properties, in particular diameter in a wide sub-micrometer range, spherical shape, monodispersity, the absence of porosity, and aggregation free isolability for characterization and later covalent modification. The materials are characterized by SEM, DLS, nitrogen sorption isotherms, helium as well as Gay-Lussac (water) pycnometry, and DRIFT spectroscopy. Particles with diameters between approximately 50 and 800 nm are obtained by varying the concentrations of the reagents and reactants, the type of solvent as well as the temperature. The use of high water concentrations and post-synthetic calcination at 600 °C results in silica particles that can be considered as nonporous with respect to the size of the active molecules to be immobilized. The effect of reaction temperature on size distribution is identified. Low polydispersity is achieved by performing the reaction in a temperature range in which a change in temperature has only a weak or no effect on the final particle diameter. Upon optimization of the sol–gel process, the shape of the particles is still spherical. The agreement between experimental and geometric data is within the expected precision of the characterization techniques.     

[6,6]‐Open and [6,6]‐Closed Isomers of C70(CF2): Synthesis,Electrochemical and Quantum Chemical Investigation

Novel difluoromethylenated [70]fullerene derivatives, C₇₀(CF₂)_n (n=1–3), were obtained by the reaction of C₇₀ with sodium difluorochloroacetate. Two major products, isomeric C₇₀(CF₂) mono‐adducts with [6,6]‐open and [6,6]‐closed configurations, were isolated and their homofullerene and methanofullerene structures were reliably determined by a variety of methods that included X‐ray analysis and high‐level spectroscopic techniques. The [6,6]‐open isomer of C₇₀(CF₂) constitutes the first homofullerene example of a non‐hetero [70]fullerene derivative in which functionalisation involves the most reactive bond in the polar region of the cage. Voltammetric estimation of the electron affinity of the C₇₀(CF₂) isomers showed that it is substantially higher for the [6,6]‐open isomer (the 70‐electron π‐conjugated system is retained) than the [6,6]‐closed form, the latter being similar to the electron affinity of pristine C₇₀. In situ ESR spectroelectrochemical investigation of the C₇₀(CF₂) radical anions and DFT calculations of the hyperfine coupling constants provide evidence for the first example of an inter‐conversion between the [6,6]‐closed and [6,6]‐open forms of a cage‐modified fullerene driven by an electrochemical one‐electron transfer. Thus, [6,6]‐closed C₇₀(CF₂) constitutes an interesting example of a redox‐switchable fullerene derivative.     

Influence of the aluminum alkyl co-catalyst type in Ziegler-Natta ethene polymerization on the formation of active sites, polymerization rate, and molecular weight

The influence of the concentration of the co-catalysts triethylaluminium (TEAL), tri-iso-butylaluminium (TIBAL), tri-n-octylaluminium on the polymerization rate for standard Ziegler-Natta catalyst systems was studied. By comparing the influence of monomeric TIBAL with TEAL co-catalyst on the polymerization activity, the effect of TEAL dimerization was described. The use of the Eley-Ridealadsorption model instead of Langmuir-Hinselwood model is proposed for the absorption of monomeric aluminiumalkyl species and for the formation of active centers C*. It is further proposed that steric hindrance from different co-catalysts, which results in a higher molecular weight (MW) of polymers, is caused by active centers with reduced space for chain transfer reactions.     

Finite-temperature transitions in dipolar spin ice in a large magnetic field

We use Monte Carlo simulations to identify the mechanism that allows for phase transitions in dipolar spin ice to occur and survive for an applied magnetic field H much larger in strength than that of the spin-spin interactions. In the most generic and highest symmetry case, the spins on one out of four sublattices of the pyrochlore decouple from the total local exchange+dipolar+applied field. In the special case where H is aligned perfectly along the [110] crystallographic direction, spin chains perpendicular to H show a transition to q=X long-range order, which proceeds via a one- to three-dimensional crossover. We propose that these transitions are relevant to the origin of specific heat features observed in powder samples of the Dy2Ti2O7 spin ice material for H above 1 Tesla.