Arylation with aryllead triacetates produced in situ by mercury-lead exchange

Reaction of a diarylmercury with lead tetraacetate to give an aryllead triacetate has been found to be a rapid reaction. The in situ generation of aryllead triacetates is thus an attractive alternative to the use of the purified reagents in the various electrophilic arylation reactions of these compounds.     

Equilibria in complexes of N-heterocyclic molecules,part XII. The reaction of hydroxide and alkoxide Ions with platinum(II) complexes of 5-nitro-1,10-phenanthroline and 2,2′-bipyridyl

Summary Bis-(5-nitro-1,10-phenanthroline)platinum(II) dichloride and diperchlorate have been prepared. The reaction between the parent cation and hydroxide ion has been studied using 1 FI n.m.r. spectroscopy and found to involve attack at the ligand. The bis-(2,2-bipyridyl)platinum(II) ion has been shown to be highly reactive towards methoxide ion. The dissociation of a 2,2-bipyridyl ligand is preceded by attack at the ligand.Part XI: R. D. Gillard, t.. A. P. Kane-Maguire and P. A. Williams,Transition Met. Chem., 2, 47 (1977).On leave from the University of Baghdad, Iraq.     

Interfacial electrical properties of DNA-modified diamond thin films: intrinsic response and hybridization-induced field effects

We have investigated the frequency-dependent interfacial electrical properties of nanocrystalline diamond films that were covalently linked to DNA oligonucleotides and how these properties are changed upon exposure to complementary and noncomplementary DNA oligonucleotides. Frequency-dependent electrical measurements at the open-circuit potential show significant changes in impedance at frequencies of >10(4) Hz when DNA-modified diamond films are exposed to complementary DNA, with only minimal changes when exposed to noncomplementary DNA molecules. Measurements as a function of potential show that at 10(5) Hz, the impedance is dominated by the space-charge region of the diamond film. DNA molecules hybridizing at the interface induce a field effect in the diamond space-charge layer, altering the impedance of the diamond film. By identifying a range of impedances where the impedance is dominated by the diamond space-charge layer, we show that it possible to directly observe DNA hybridization, in real time and without additional labels, via simple measurement of the interfacial impedance.     

Homoatomic P --> P coordination: a versatile synthetic approach to polyphosphorus dications

Polyphosphorus dications have been synthesised and comprehensively characterised as diphosphine (dppe, dmpe and dpph) linked Ar2P+ Lewis acids (Ar = C6H5); this application of unique homoatomic coordination chemistry provides important building blocks for extended systems.     

Stéréochimie des réactions de substitution des alcoxygermanes par les organolithiens et par les réactifs de Grignard

The reactions of organolithium reagents and Grignard reagents with optically active alkoxygermanes R₃GeOR′ have been studied [R₃GeOR′ = ()-i-PrPhNpGeOCH₃, ()-i-PrPhNPGeOMen and ()-MePhNpGeOMen]. Saturated reagents (e.g. butyllithium) give retention of configuration at germanium whilst unsaturated reagents (e.g. allyl- or benzyllithium) lead to inversion.     

Some symmetry-induced isotope effects in the kinetics of recombination reactions

Symmetry-induced isotope effects in recombination and collision-induced dissociation reactions are discussed. Progress on understanding the anomalous isotope effects in ozone is reviewed. Then, calculations are performed for the simpler reaction xNe+yNe+H<-->xNeyNe+H, where x and y label either identical or different isotopes. The atomic masses in the model are chosen so that symmetry is the only difference between the systems. Starting from a single potential energy surface, the properties of the bound, quasibound, and continuum states of the neon dimer are calculated. Then, the vibration rotation infinite order sudden approximation is used to calculate cross sections for all possible inelastic and dissociative processes. A rate constant matrix that exactly satisfies detailed balance is constructed. It allows recombination to occur both via direct three-body collisions and via tunneling into the quasibound states of the energy transfer mechanism. The eigenvalue rate coefficients are determined. Significant isotope effects are clearly found, and their behavior depends on the pressure, temperature, and mechanism of the reaction. Both spin statistics and symmetry breaking produce isotope effects. Under most conditions the breaking of symmetry enhances the rates, but a wide spectrum of effects is observed; they range from isotope effects with a normal mass dependence to huge, mass-independent isotope effects to cancellation and even to reversal of the isotope effects. This is the first calculation of symmetry-induced isotope effects in recombination rates from first principles. The relevance of the present effects to ozone recombination is discussed.     

Reaction de Cycloaddition dipolaire-1,3-des thiazolones et des selenazolones mesoioniques avec l'acetylene dicarboxylate de methyle—II: Influence de la nature des substituants sur la reactivite observee et sur la nature des produits obtenus

Mesoionic thiazolones and selenazolones react with dimethyl acetylene dicarboxylate to give thiophenes or pyridones. We show that the reactivity of the mesoionic thiazolones towards dimethyl acetylene dicarboxylate may be explained by second order perturbation theory, limited to frontier orbitals. The influence of the temperature and of the nature of the substituants on the evolution of the primary cycloadduct can be explained by a competition between a retro Diels-Alder reaction giving a thiophene and a desulfurisation or a deselenurisation giving a pyridone.     

A concise asymmetric synthesis of the ADE fragment of nakadomarin A

The ADE fragment of nakadomarin A has been synthesized in nine linear steps from commercial material. The key transformation is an asymmetric azomethine ylide [1,3]-dipolar cycloaddition to establish the AD-spirocyclic system containing three of the four stereocenters of the natural product. [reaction: see text]     

ENHANCEMENT OF THE SENSITIVITY OF RADIATIVE and NON-RADIATIVE DETECTION TECHNIQUES IN THE STUDY OF PHOTOSENSITIZATION BY WATER SOLUBLE SENSITIZERS USING A REVERSE MICELLE SYSTEMS*,†

The study of photosensitization processes in aqueous solution is complicated by the unsuit-ability of water as solvent for the commonly used techniques for monitoring radiative and non-radiative relaxation processes. The infrared luminescence method is hampered by the relatively weak intensity of emission and short lifetime of singlet molecular oxygen, O₂(¹Δ_g), in water. Photoacoustic and photothermal detection of the dominant non-radiative relaxation process for O₂(¹Δ_g) is also inhibited by the unfavorable physico-chemical properties of water which reduce the sensitivities of these techniques for the study of sensitizers in aqueous with respect to non-aqueous media. Such problems have been alleviated by incorporating the sensitizer in the aqueous core of aerosol OT reverse micelles. It is demonstrated that the sensitivity of both radiative and non-radiative detection depends not on the local environment of the sensitizer but on the overall composition of the medium, which, in the case of reverse micelle solutions, is predominantly hydrocarbon. This produces a 4.5 and 6-fold enhancement of the sensitivity of luminescence and optoacoustic detection, respectively, in comparison to purely aqueous solution. The utility of the method is demonstrated for Rose Bengal, where quantum yields of intersystem crossing (φ_isc) of 0.78 (LIOAC) and singlet oxygen generation (φ_δ) of 0.81 (LIOAC) and 0.80 (TRLD) were measured. Phenazine was also studied for comparative purposes and to corroborate values obtained for Rose Bengal.     

An efficient preparation of isosteric phosphonate analogues of sphingolipids by opening of oxirane and cyclic sulfamidate intermediates with alpha-lithiated alkylphosphonic esters

D-erythro-(2S,3R,4E)-Sphingosine-1-phosphonate (1), the isosteric phosphonate analogue of naturally occurring sphingosine 1-phosphate (1a), and D-ribo-phytosphingosine 1-phosphonate (2), the isosteric phosphonate analogue of D-ribo-phytosphingosine-1-phosphate (2a), were synthesized starting with methyl 2,3-O-isopropylidene-d-glycerate (4) and D-ribo-phytosphingosine (3), respectively. Oxirane 12 was formed in eight steps from 4, and cyclic sulfamidate 22 was formed in five steps from 3. The phosphonate group was introduced via regioselective ring-opening reactions of oxirane 12 and cyclic sulfamidate 22 with lithium dialkyl methylphosphonate, affording 13 and 23, respectively. The synthesis of 1 was completed by S(N)2 displacement of chloromesylate intermediate 14b with azide ion, followed by conversion of the resulting azido group to a NHBoc group and deprotection. The synthesis of 2 was completed by cleavage of the acetal, N-benzyl, and alkyl phosphonate ester groups.