Zero Tension Kardar-Parisi-Zhang Equation in (d + 1)–Dimensions

The joint probability distribution function (PDF) of the height and its gradients is derived for a zero tension d + 1-dimensional Kardar-Parisi-Zhang (KPZ) equation. It is proved that the height's PDF of zero tension KPZ equation shows lack of positivity after a finite time t _c . The properties of zero tension KPZ equation and its differences with the case that it possess an infinitesimal surface tension is discussed. Also potential relation between the time scale t _c and the singularity time scale t _c.v→0 of the KPZ equation with an infinitesimal surface tension is investigated.     

Attempts at Solvolytic Generation of Phenyl Cations

New substrates and reaction conditions which may be expected to yield phenyl cation intermediates have been investigated. The approaches used were: (a) solvolysis of PhX in fluorinated alcohols, where X = ? N (O) = NOTs (tosyloxyazoxy), ? N (O) = NONf (Nf = C₄F₉SO) and ? OSO₂\documentclass{article}\pagestyle{empty}\begin{document}$ \mathop {\rm N}\limits^{\rm + } $\end{document} (CH₃)₃ōTf (Tf=CF₃SO); (b) solvolysis of ArBr, PhOTf and PhOSO₂\documentclass{article}\pagestyle{empty}\begin{document}$ \mathop {\rm N}\limits^{\rm + } $\end{document}(CH₃)₃ōTf (phenyl ‘betylate triflate’) in super-acid solvents (FSO₃H · SbF₅, SbF₅, AgSbF₆). Analysis of the product mixtures provided no evidence for the intermediacy of phenyl cations as a major pathway in any of the reactions. This result is remarkable, since the ‘betylate’, for example, is a better leaving group by a factor of at least 10⁵ than the ‘super’ leaving group triflate in the solvolysis of alkyl sulfonates. These results are a further indication of the extremely low stability of phenyl cations, as well as of the very special properties of the nitrogen leaving group in arenediazonium ions.     

Determination of lead and atmospheric particulates by flameless atomic absorption spectrometry

Flameless atomic absorption techniques were used to determine the lead and other atmospheric particulate in the city of Tehran. 640 samples were collected in 20 different stations around the city during four seasons in 1992. The radioactivity of the air samples was also measured by -ray spectrometry using high purity Ge/Li detectors, and a multichannel analyzer. The results were compared with previous measurements in the city of Tehran.     

Development of a radiotracer method for measuring CO2 uptake by cement - wood mixtures

Radiotracer method was developed for measuring¹⁴CO₂ content in cement-wood mixtures. The carbon dioxide used for the treatment was labeled with¹⁴C, a -emitting radioisotope, and samples were measured by -scintillation and liquid scintillation techniques. Test samples were prepared in the laboratory with various compositions and treated with labeled¹⁴CO₂. The tracer was released from Ba¹⁴CO₃ by lactic acid with total activity of 37 MBq. Selectivity of the technique allows to distinguish the carbon dioxide bound during the treatment and bound previously from the mbient air. Sensitivity of the method is higher than that of traditional methods and allowed determination of CO₂ content in each component of the mixture. It is 63 ng. if measured by -scintillation detector and 1.6 ng, if measured by liquid scintillation. Accuracy of the method is 0.3%.     

Synthesis and Structure Determination of Some New N‐Glycosides of 4,5‐Disubstituted‐1,2,4‐Triazole‐3‐Thiones

Some new N‐glycosides of 4‐(2‐phenylethyl)‐5‐pyridyl‐1,2,4‐triazole‐3‐thiones were synthesised by the coupling reaction of halo sugar with 4,5‐disubstituted 3H‐1,2,4‐triazole‐3‐thiones in the presence of mercuric cyanide and dry nitromethane as solvent, followed by deprotection using dry ammonia in methanol. All of the above compounds were fully characterized by means of infrared, ¹H NMR spectroscopy, mass spectroscopy and elemental analysis.     

Applications of Inorganic Polymeric Materials, III: Polyphosphazenes

Polyphosphazenes form one of the most important and interesting classes of inorganic polymers having a backbone of alternating phosphorus and nitrogen atoms with phosphorus atom bearing two organic side groups. The most important feature of these polymers is the synthesis route which allows the side groups to be changed over a wide range to obtain a broad variety of products with different properties from elastomers to glasses, water soluble to hydrophobic polymers, bioinert to bioactive materials, and electrical insulators to conductors. In this paper, some novel applications of these polymers in biomedical materials and advanced devices are reviewed.     

SILICA PHOSPHORIC ACID/NaNO2 AS A NOVEL HETEROGENEOUS SYSTEM FOR THE COUPLING OF THIOLS TO THEIR CORRESPONDING DISULFIDES

Silica phosphoric acid was prepared via reaction of silica chloride (I) and phosphoric acid. Thiols can be readily converted to their corresponding thionitrites with a combination of silica phosphoric acid (II), wet SiO ₂ , and sodium nitrite in dichloromethane at room temperature. Disulfides result from the homolytic cleavage of the sulfur–nitrogen bond of the unstable thionitrite and subsequent coupling of the resultant thiyl radicals.     

A simple accurate model for prediction of deflagration temperature of energetic compounds

A novel general method is introduced to predict deflagration temperature of organic energetic compounds containing at least –NNO₂, –ONO₂, or –CNO₂ groups. Deflagration temperature is an important safety parameter in working with dangerous energetic compounds and their environmental problems. It is shown that the contribution of some molecular structure parameters can be used to interpret thermal decomposition of an energetic compound. For 86 energetic materials (corresponding to 102 measured values) with different molecular structures, the new correlation has the root mean square (rms) and the average deviations of 23.8 and 19.0 K, respectively. The new method is also tested for some energetic compounds with complex molecular structures, e.g., two new organic energetic molecules N,N′-bis(1,2,4-triazol-3yl)-4,4′-diamino-2,2′,3,3′,5,5′,6,6′-octanitroazobenzene (BTDAONAB) and 2,4,6-trinitrophloroglucinol.     

Diastereoselective synthesis of pyrrolo[1, 2-c]imidazoles using chiral thiohydantoins,malononitrile, and aldehydes and evaluation of their antioxidant and antibacterial activities

Diastereoselective synthesis of pyrrolo[1,2-c]imidazoles is reported from three-component reaction of chiral thiohydantoins, aldehydes, and malononitrile in the presence of NEt₃. The antioxidant properties of the obtained products were evaluated by 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging assay. Among the products, compound 4l possessing NH₂ and NH groups and bromine atom at 4-position of the aromatic ring displayed the highest antioxidant activity (90%). Also, their antibacterial activities were explored against gram-positive and gram-negative bacteria using disc diffusion method. Among the synthesized compounds, 4a with chlorine atom at para position of the aromatic ring, and methyl group (the smallest alkyl group) at 7-position, displayed the best antibacterial activity against the tested gram-positive bacteria.     

Exo/endo stereocontrolled synthesis of spiroindoloindolizidines by using classical and microwave conditions via the 1,3-dipolar cycloaddition reaction

Using both classical reflux and microwave-mediated conditions, a series of new spiroindoloindolizidines was synthesized by multicomponent 1,3-dipolar cycloaddition of azomethine ylides in unprecedented exo/endo stereocontrolled. Both conditions easily afforded two identical and separable exo/endo diastereomeric ratios of cycloadducts. However, the ratio of two diastereomeric products obtained from conventional conditions was reversed in all examined cases when the reactions were explored under microwave-mediated conditions. As expected, utilizing the microwave-assisted conditions produced higher yields and reaction rates compared to classical conditions. The structure and exact stereochemistry of synthesized cycloadducts were determined by applying various 2D-NMR spectroscopic techniques and single-crystal X-ray diffraction. Finally, the mechanism of the reaction has been briefly investigated by using density functional theory (DFT) calculations.