Phase Transfer Catalysis Preparation of Acyl Isothiocyanates

The use of phase transfer catalysis, PTC, for nucleophillic substitution reactions is well documented.^1,2 Included among these reactions is the preparation of both alkyl³ and aryl⁴ thiocyanates. However, PTC reactions at an acyl carbon are much less common. Brándstróm⁵ has reported the preparation of acyl azides and Weber⁶ has used PTC to prepare benzoyl cyanide. Recently Illi⁷ has used PTC to acylate sterically crowded phenols.     

The Phase Transfer Catalysed Preparation of 2-Methyl-2-Trichloromethyl-3-Phenyloxirane

A phase transfer catalyst has been used to prepare the title compound and other highly chlorinated compounds from phenylpropanone and carbon tetrachloride.     

Selecting tolerances in chance-constrained programming: A multiple objective linear programming approach

An importance issue concerning the practical application of chance-constrained programming is the lack of a rational method for choosing risk levels or tolerances on the chance constraints. While there has also been much recent debate on the relationship, equivalence, usefulness, and other characteristics of chance-constrained programming relative to stochastic programming with recourse, this paper focuses on the problem of improving the selection of tolerances within the chance-constrained framework. An approach is presented, based on multiple objective linear programming, which allows the decision maker to be more involved in the tolerance selection process, but does not demand a priori decisions on appropriate tolerances. An example is presented which illustrates the approach.     

Planar Groups

In abstract algebra courses, teachers are often confronted with the task of drawing subgroup lattices. For purposes of instruction, it is usually desirable that these lattices be planar graphs (with no crossings). We present a characterization of abelian groups with this property. We also resolve the following problem in the abelian case: if the subgroup lattice is required to be drawn hierarchically (that is, in monotonic order of index within the group), when is it possible to draw the lattice without crossings?     

Charge transfer excited-state dynamics in DNA duplexes substituted with an ethynylpyrenyldeoxyuridine electron source and a fluorodeoxyuridine electron trap

Studies of six 5-(pyren-1-yl-ethynyl)-2'-deoxyuridine (U(PY))-substituted DNA duplexes in this work test and support the conclusions reported by Gaballah et al. (J. Phys. Chem. B 2005, 109, 5927-5934) based on investigations of 5-(2-pyren-1-yl-ethylenyl)-2'-deoxyuridine (U(PE))-substituted DNA hairpins. As expected because of the rigid ethynyl linker in U(PY) (compared to the flexible ethylenyl linker in U(PE)), U(PY)-substituted duplexes do not show enhanced charge transfer (CT) emission quantum yields for duplexes with 5-fluorodeoxyuridine (U(F)) electron traps near U(PY) compared to duplexes without traps. Furthermore, the average CT lifetime and emission quantum yield of U(PY)-substituted duplexes is independent of the U(F) trap location. These new results strongly suggest that the excess electron in the PY*+/dU*- CT state of U(PY) is restrained from hopping to nearby U(F) traps due to attraction to PY*+.     

Cavity resonators of metal-coated dielectric nanorods

Metallic nanoparticles bridge the length scale between atoms and crystals, exhibiting mesoscopic properties unique to their size. Thus, they have generated much interest for their potential applications as chemical or biological sensors and particularly as waveguides for light in nanoscale structures. [Y. W. C. Cao, R. C. Jin, and C. A. Mirkin, Science 297, 1536 (2002); H. J. Lezec et al., Science 297, 820 (2002); S. A. Maier, P. G. Kik, and H. A. Atwater, Appl. Phys. Lett. 81, 1714 (2002); J. M. Oliva and S. K. Gray, Chem. Phys. Lett. 379, 325 (2003)]. One important direction of research into the properties of individual metal nanoparticles involves the controlled variation of their geometry, which can yield new and tunable optical properties that simple spherical configurations do not possess. [T. S. Ahmadi, Z. L. Wang, T. C. Green, A. Henglein, and M. A. Ei-Sayed, Science 272, 1924 (1996)]. A prime example of this is the core-shell nanostructure that has a central material surrounded by differing cladding layer.     

Titration of phytic acid

Titrimetric assays for phytic acid by titration with iron(III) or thorium are described. Stannous chloride interferes in both systems, causing negative errors directly proportional to the amount of stannous chloride. The thorium:phytate ratio in the complex formed is 2:1, which is interpreted as resulting from the possession of two chelating centres by phytic acid.     

THE CHEMILUMINESCENT NO—O-ATOM REACTION

Abstract— New additional experimental data were obtained to give further information pertinent to the mechanism for the chemiluminescent NO—O-atom reaction. Results were obtained for the change of emission intensities from 10 to 300 microns pressure. Some studies were also made of the effect of various third bodies. The results support a simple two body recombination for the mechanism for the light emission: NO+O + NO₂+ hv .