Effect of the pH of the medium on the electronic absorption spectra and structure of 3-methyl-1-phenyl-4-phenylazo-5-pyrazolone

On the basis of the electronic absorption spectra it was found that 3-methyl-1-phenyl-4-phenylazo-5-pyrazolone exists in acidic solutions in mono- and diprotonated forms. It was established by means of calculations by the Pariser—Parr—Pople (PPP) method that in the neutral and protonated forms the quinone hydrazone tautomer of the phenylazopyrazolone is more stable than the azo tautomer, and it was determined that the protonation center is the N₍₂₎ atom of the pyrazolone ring. The diprotonated form is most likely the quinone hydrazone tautomer protonated at the heteroring N₍₂₎ atom and the -nitrogen atom of the azo group. In an alkaline medium the phenylazopyrazolone exists in the form of an anion with predominance of the azo form. The effect of substituents ion the diazo component of the phenylazopyrazolone on the long-wave bands of the electronic absorption spectra in various media was explained on the basis of calculation of the distribution of the -electron density during electron transitions.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1331–1336, October, 1991.     

Stereochemie von Metallocenen, 40. Mitt.

Starting from optically active methylferrocene-- and--carboxylic acids (1 a and1 b) of known absolute configuration and enantiomeric purity about 15 chiral ferrocenes (of each isomeric series— and ) were obtained by suitable ligand transformations. Thereby (almost) all possible chiral combinations of the ligands CH₃, COOH (COO^–), COOCH₃, CN and NH₂ (NH₃ ⁺) were accessible which are necessary for a potential test of approximations of chirality functions for compounds with basic symmetry C_5v. The chiroptical properties of these disubstituted ferrocenes are recorded.Preliminary tests using a shortened Ansatz revealed large discrepancies between calculated () and found [M]_D-values. Possible reasons for this failure are discussed.

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61. Mitt. über Ferrocenderivate

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39. Mitt.:A. Meyer, H. Neudeck undK. Schlögl, Chem. Ber.110, 1403 (1977).

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60. Mitt.:V. Rapi, K. Schlögl undB. Steinitz, J. Organometal. Chem.94, 87 (1975).     

A Safe Way of Performing Some Dangerous Experiments. II. Construction of a Safety Dropper

Due to the high safety risks, chemistry instructors avoid demonstrating many remarkable experiments based on the addition of a liquid to a solid. Well-known examples of such demonstrations are various pyrotechnic mixtures of potassium chlorate and sugar (sucrose), which are usually activated with a drop of concentrated sulfuric acid. Other attractive demonstrations are the addition of water to freshly prepared magnesium phosphide and addition of water to burning magnesium. In all of these demonstrations the reaction that takes place immediately is very vigorous and can be hazardous for the instructor. Because chemistry teachers and instructors usually try to avoid performing experiments that include a hazard, a number of highly attractive experiments may remain unknown to the public. Using a simple homemade device called a safety dropper, one can perform all of these experiments with complete safety, both for the audience and the demonstrator. Details for performing some of these experiments as well as for the construction of the safety dropper are given in this paper. Video clips of demonstrations are included as an aid for inexperienced instructors.     

Radiation-induced polymerization of cyclohexene sulfide in the solid state

Radiation-induced solid-state polymerization of cyclohexene sulfide has been investigated. Differential thermal analysis shows that this compound has a phase transition point at ?74°C and behaves as a plastic crystal in the temperature range from ?74 to ?20°C (melting point). By rapid cooling, this plastic crystal was easily supercooled, and below ?166°C a glassy crystal, i.e., a supercooled nonequilibrium state of plastic crystal, was obtained. In-source polymerization proceeded in the plastic crystalline state. Postpolymerization of glassy crystalline monomer irradiated at ?196°C occurred above ?166°C (glass transition point) during subsequent heating.     

First-order transitions in spherical models: Finite-size scaling

Finite-size behavior near the first-order phase boundary of ferromagnetic spherical models is investigated for block- and cylinder-shaped systems ind dimensions. The bulk thermodynamic singularities are rounded and, asymptotically for large size, obey appropriate scaling laws. Both short-range interactions and long-range couplings, decaying like 1/r^d+ with >0, are analyzed: the short-range results agree precisely with a recently developed scaling theory forO(n) symmetric systems in the limitn. More generally, the scaling functions are universal, depending only on . Explicit aspects of the shape and interactions enter only in the spin wave or Goldstone mode contributions which appear, technically, as corrections to scaling. An appendix analyzes the truncation error in the approximation, by many-fold sums, of multivariate integrals with integrands diverging like [_ja_{j j} ² ]^- as 0.     

Mechanism of the cyclization of dimethyl diethynyl silane with selenium tetrabromide: Computational and structural studies, and monitoring

The structure of 2,4-dibromo-2-dibromomethyl-3,3-dimethyl-1-selena-3-silacyclopentene-4, formed by regioselective electrophilic addition of SeBr₄ to dimethyl diethynyl silane, has been determined using X-ray analysis technique. Quantum chemistry methods were used to study elementary stages of the reaction. It was found that the first stage consisted of SeBr₄ conversion into bimolecular complex Br₂?SeBr₂, initiated by dimethyl diethynyl silane. Possible formation of five-membered and six-membered heterocycles involves different cyclization mechanisms. The formation of only five-membered heterocycle is explained by kinetically preferable ring closure through four-center transition state. The conclusions obtained by calculations were confirmed by monitoring of the reaction using ¹H NMR method.     

Synthesis and anion binding properties of 2,5-diamidothiophene polypyrrole Schiff base macrocycles

[reaction: see text] Two easy-to-synthesize polypyrrolic 2,5-diamidothiophene Schiff base macrocycles are reported, along with their anion binding properties as determined via UV-vis spectroscopic titrations carried out in dichloroethane. There is a striking difference between the interactions with anions of the two macrocycles, a finding ascribed to differences in their rigidity. For example, the more flexible dipyrromethane-derived macrocycle displays a 1.2:1 hydrogen sulfate versus nitrate selectivity, while its more rigid bipyrrole-derived congener shows a 7.4:1 selectivity in favor to hydrogen sulfate.