Electron-impact fragmentation of penta-fluorophenyldimethylsilyl ethers of some sterols of biological importance

The mass spectral properties under medium and high resolution of a new protecting group for sterols is described and its ability to direct fragmentation is compared with established derivatives. The mass spectra obtained are characterised by strong molecular ions which fragment to produce a more even ion distribution than the familiar TMS ethers. This results in enhanced abundance of hydrocarbon fragments, with molecular structural details given greater prominence than is found with other derivatives.     

Anhand der Methode der Konfigurationenwechselwirkung berechnete Dipolmomente einiger nichtalternierender Kohlenwasserstoffe in angeregtem Singulett- und Triplettzustand

Ohne ZusammenfassungDie Verfasser erachten es für ihre angenehme Pflicht, an dieser Stelle Frl. N. Grozdanova für ihre Hilfe bei der Zusammenstellung des Programms für die Elektronenrechenmaschine den verbindlichsten Dank auszusprechen.     

Activation analysis of alkaline rocks. A comparison between destructive and non-destructive methods

The United States Geological Survey reference sample AGV-1 andesite, and three alkaline rocks from the apatite mine of Jacupiranga, Brasil, were analyzed by thermal neutron activation analysis using destructive and non-destructive methods, and high resolution Ge(Li) gamma-ray detectors. One of the rocks, a carbonatite, was also analyzed by instrumental activation analysis with epithermal neutrons. A greater number of elements can be determined using the radiochemical separation, but the precision and accuracy attained by INAA and RNAA were of the same order for most of the elements analyzed. Epithermal activation was more advantageous for tantalum, terbium and holmium. Comparison of the analytical results for USGS reference sample (AGV-1) with the data published by others gave good agreement. Statistical tests used for comparison of the results of destructive and non-destructive methods, as well as other results are presented.     

A combinatorial algorithm for calculating ligand binding

We consider the problem of predicting the mode of binding of a small molecule to a receptor site on a protein. One plausible approach, given a rigid molecule and its geometry, is to search directly for the orientation in space that maximizes the degree of contact. The computation time required for such a naive procedure is proportional to n³m³, where n is the number of points in the site where binding can occur, and m is the number of atoms in the ligand. We give an alternative, combinatorial approach, in which only “contact–no-contact” criteria are considered. We relate this problem to the well-known combinatorial problem of finding cliques in a graph and show that we can use a solution to the clique problem not only to solve our original problem, but also the problem of avoiding energetically unfavorable matches. Our experience with this method indicates that the computation time required is proportional to nm^2.8, with a lower constant of proportionality than that of the naive procedure.     

The investigation of natural compounds by HPLC. III. A study of sesquiterpene lactones of the guaiane type by microcolumn HPLC

Two comparable methods of microcolumn high-performance liquid chromatography (HPLC) have been developed for the sesquiterpene lactones leucomicin, matricarin, austricin, and anhydroaustricin and for the drug isolated from the epigeal part ofArtemisia leucodes.     

Atomic Absorption Assay of Noble Metals in Ores with the Use of Sample Decomposition by Ultrasound

An atomic absorption assay of gold, silver, and palladium in various types of ores is performed with the use of ultrasound at the fire assay stage. It is shown that ultrasound can reduce the temperature and duration of fusion and increase the recovery of noble metals into the lead button.     

Efficacy testing of disinfectants

The U.S. Environmental Protection Agency's (EPA) Office of Pesticide Programs (OPP) has the responsibility for regulating antimicrobial products, including sporicides, used to treat and decontaminate inanimate surfaces. In response to the anthrax (Bacillus anthracis) attacks of 2001 and the associated need for verifying the performance of chemicals for building decontamination, the EPA initiated research in late 2003 to evaluate and improve efficacy test methods for sporicides. The OPP Microbiology Laboratory located at the Environmental Science Center, Ft. Meade, MD is the lead laboratory. Through funding provided by EPA's Office of Research and Development (Safe Buildings Program), a collaborative research plan has been established to address several key issues. Research is currently being conducted on 2 fronts: (1) the evaluation of quantitative methodology for assessing the efficacy of sporicides, and (2) the development and comparative testing of selected modifications to improve the AOAC Sporicidal Activity Test (AOAC Method 966.04). Future studies will include the evaluation of candidate surrogates of B. anthracis using a quantitative method, and a multilaboratory validation study of a quantitative method-surrogate combination. The General Referee is serving as the Principal Investigator for all research described in this report, and has the overall responsibility for the technical conduct of the projects. In cases where the General Referee has oversight of projects that involve official collaborative studies and validation support from AOAC INTERNATIONAL, AOAC officials and the Committee Chair will determine the appropriate mechanism for formal study review. The 2003 General Referee report provides the background on the development and direction of the research projects. The preliminary data, general conclusions, next steps, and recommendations are provided in this report.     

Recherches sur la formation et la transformation des esters LXXVII [1]. Etude à l'aide de H2[18O] de la scission de quelques monoesters phosphoreux et de l'acide propargyl-benzènephosphonique

(1) Monopotassium phosphite KH₂PO₃ heated at 300°C with CO[¹⁸O] exchanges one atom of oxygen after 3 hours, one to two atoms after 6 hours, and its three O atoms after 12 hours; the probable mecanism of this exchange is discussed. When the same treatment is carried out in the presence of o-phenylene diamine hydrochloride, the exchange is total (three O) after 3 hours at 300°C. Treated by this last procedure, benzenephosphonic acid C₆H₅PO(OH)₂ undergoes equally a total exchange of its O atoms in 3 hours.