1-Cyanoimidazole as a Mild and Efficient Electrophilic Cyanating Agent

A mild and high-yielding cyanating reaction of amine, sulfur, and carbanion nucleophiles is reported here using 1-cyanoimidazole as an electrophilic cyanating agent.     

Dry etch damage and its effect on electronic and optical nanostructures

The creation of nano-structures in 3–5 semiconductors is currently of great interest. If the conventional route of pattern definition in a resist followed by pattern transfer is used, this implies in most cases electron beam lithography and some form of dry etching. Using electron beam lithography, patterns of 10nm width on 40nm centre to centre spacing can be transfered to metal lines on thin substrates; even on normal wafers, linewidths of 25nm on 60nm spacing are achievable with state of the art machines.If the creation of a raised structure is necessary because of the physics of the situation, it is important to consider the damage which may be introduced by dry etching. The methods by which dry etch damage can be revealed are discussed, and the ways in which it can be reduced mentioned. Progress towards understanding the microscopic nature of the damage will be reviewed. Examples are drawn from etching of GaAs/GaAlAs in Silicon tetrachloride and methane/hydrogen.     

Pronounced negative thermal expansion from a simple structure: cubic ScF(3)

Scandium trifluoride maintains a cubic ReO(3) type structure down to at least 10 K, although the pressure at which its cubic to rhombohedral phase transition occurs drops from >0.5 GPa at ～300 K to 0.1-0.2 GPa at 50 K. At low temperatures it shows strong negative thermal expansion (NTE) (60-110 K, α(l) ≈ -14 ppm K(-1)). On heating, its coefficient of thermal expansion (CTE) smoothly increases, leading to a room temperature CTE that is similar to that of ZrW(2)O(8) and positive thermal expansion above ～1100 K. While the cubic ReO(3) structure type is often used as a simple illustration of how negative thermal expansion can arise from the thermally induced rocking of rigid structural units, ScF(3) is the first material with this structure to provide a clear experimental illustration of this mechanism for NTE.     

Direct kinetics study of the product‐forming channels of the reaction of isoprene‐derived hydroxyperoxy radicals with NO

A direct kinetics study of the product‐forming channels of the reaction of isoprene‐derived hydroxyalkylperoxy radicals with NO has been performed at 100 Torr pressure and 298 K using the turbulent flow technique with high‐pressure chemical ionization mass spectrometry for the detection of reactants and products. For comparative purposes, a similar study was also performed for the reaction of 1‐ and 2‐butene‐derived hydroxyalkylperoxy radicals with NO. The measured hydroxyalkylnitrate product channel branching ratios were determined to be 0.061, 0.068, and 0.070 for the 1‐butene, 2‐butene, and isoprene systems, respectively. The results are compared to previous measurements of the hydroxyalkylnitrate‐branching ratios for these systems, and the atmospheric significance of the results is discussed. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 353–361, 2007     

Diffuse reflectance laser flash photolysis of adsorbed molecules

Recent progress which allows laser flash photolysis investigation of opaque materials by using diffuse reflectance from analysing sources for the detection of laser induced transient species is described. Experimental details of nanosecond and picosecond diffuse reflectance laser photolysis systems are presented and methods of analysis of data are discussed. The potential of the technique for studying elementary reactions at interfaces is demonstrated with particular reference to bimolecular reactions of (a) the triplet state of acridine adsorbed on various porous silica surfaces and (b) ion-electron recombination following multi-photon ionisation of diphenyl polyenes adsorbed on γ-alumina. The mechanisms of formation and decay of these transient adsorbed species are discussed.     

Wetting, mixing, and phase transitions in Langmuir-Gibbs films

Millimolar bulk concentrations of the surfactant cetyltrimethylammonium bromide (CTAB) induce spreading of alkanes, H(CH(2))(n)H (denoted C(n)) 12< or =n< or =21, on the water surface, which is not otherwise wet by these alkanes. The novel Langmuir-Gibbs film (LGF) formed is a liquidlike monolayer comprising both alkanes and CTAB tails. Upon cooling, an ordering transition occurs, yielding a hexagonally packed, quasi-2D crystal. For 11< or =n< or =17 this surface-frozen LGF is a crystalline monolayer. For 18< or =n< or =21 the LGF is a bilayer with a crystalline, pure-alkane, upper monolayer, and a liquidlike lower monolayer. The phase diagram and film structure were determined by x-ray, ellipsometry, and surface tension measurements. A thermodynamic theory accounts quantitatively for the observations.     

Fusing multiple Bayesian knowledge sources

We address the problem of information fusion in uncertain environments. Imagine there are multiple experts building probabilistic models of the same situation and we wish to aggregate the information they provide. There are several problems we may run into by naively merging the information from each. For example, the experts may disagree on the probability of a certain event or they may disagree on the direction of causality between two events (e.g., one thinks A causes B while another thinks B causes A). They may even disagree on the entire structure of dependencies among a set of variables in a probabilistic network. In our proposed solution to this problem, we represent the probabilistic models as Bayesian Knowledge Bases (BKBs) and propose an algorithm called Bayesian knowledge fusion that allows the fusion of multiple BKBs into a single BKB that retains the information from all input sources. This allows for easy aggregation and de-aggregation of information from multiple expert sources and facilitates multi-expert decision making by providing a framework in which all opinions can be preserved and reasoned over.