Microphotoluminescence of C<Subscript>60</Subscript> Fullerites Synthesized under a Pressure of 13 GPa and Temperatures of 770–2100 K

C₆₀ fullerite samples synthesized under a pressure of P = 13 GPa and temperatures of T_s = 770 ? 2100 K were studied by scanning microphotoluminescence (MPL) at room temperature. The MPL of cleaved chip surfaces indicates the presence of emitting areas with linear dimensions from 35 to 350 μ. A band at 700 nm, which is characteristic for linear and planar C₆₀ polymers, was revealed in all 3D-polymerized fullerites too. New bands at 1100?2300 nm are observed in PL spectra of substances synthesized at 870 ≤ T_s ≤ 1270 K. Separated areas of several optically active moieties responsible for luminescence in the range 1100?2300 nm were detected by MPL cartography. The origin of this band is tentatively attributed to traps located on C₆₀-oxygen and nitrogen inclusions associated with defects of the crystal lattice.     

Ueber die Bestimmung des Formaldehyds

Ohne Zusammenfassung     

Hybrid ceramic nanosieves: stabilizing nanopores with organic links

Unprecedented hydrothermal stability in functional membranes has been obtained with hybrid organic-inorganic nanoporous materials, enabling long-term application in energy-efficient molecular separation, including dehydration up to at least 150 degrees C.     

Evaluating reproducibility and similarity of mass and intensity data in complex spectra—applications to tubulin

We present a data processing approach based on the spectral dot product for evaluating spectral similarity and reproducibility. The method introduces 95% confidence intervals on the spectral dot product to evaluate the strength of spectral correlation; it is the only calculation described to date that accounts for both the non-normal sampling distribution of the dot product and the number of peaks the spectra have in common. These measures of spectral similarity allow for the recursive generation of a consensus spectrum, which incorporates the most consistent features from statistically similar replicate spectra. Taking the spectral dot product and 95% confidence intervals between consensus spectra from different samples yields the similarity between these samples. Applying the data analysis scheme to replicates of brain tubulin CNBr peptides enables a robust comparison of tubulin isotype expression and post-translational modification patterns in rat and cow brains.     

Aminoborylene complexes of group 6 elements and iron: a synthetic, structural, and quantum chemical study

Transition-metal-borylene complexes of the type [(OC)(5)M=BR] {M=Cr, Mo, W; R=N(SiMe(3))(2), 1a-3a, Si(SiMe(3))(3), 4a} and [(OC)(4)Fe=B=N(SiMe(3))(2)] (8) were prepared by salt elimination reactions. Synthesis of the latter complex was accompanied by the formation of substantial amounts of an unusual dinuclear iron complex [Fe(2){mu-C(2)O(2)(BN(SiMe(3))(2))}(2)(CO)(6)] (9). The aminoborylene complexes of Group 6 metals were converted to trans-[(Cy(3)P)(CO)(4)M=B=N(SiMe(3))(2)] (5a-7a) by irradiation in the presence of PCy(3). Structural and spectroscopic parameters were discussed with respect to the trans-effect of the borylene ligand and the degree of M-B d(pi)-p(pi)-backbonding. Computational studies were performed on Group 6-borylene complexes. The population and topological analyses as well as the molecular orbital composition are consistent with the presence of both sigma-and pi-type interactions. There are, however, indications that the d(pi)-p(pi)-backbonding in the silylborylene complex is significantly more pronounced than in the aminoborylene complexes.     

Extractional X-ray Fluorescence Determination of Small Quantities of As,Se and Hg in Aqueous Solutions

An important problem of the monitoring of the environment is control of natural and waste waters. To elaborate the X-ray fluorescence determination of arsenic,selenium and mercury in the waters we used the extraction concentration of diethyldithiocarbamate of the elements from a strong acid solution.     

Low-temperature Crystallizational Preconcentration of Impurities in Environmental Analysis

Phenols of natural and antropogenic derivations are respected to the dangerous and wide occurring organical impurities coining in the environment with waste waters of chemical plants. Maximum permissible concentration (MPC) of phenol for unchlorinated water is 0.1 mg/l, and for chlorinated one - 0.001-0.002 mg/l. For the determination of such small contents of phenol in waters preliminary extractional or sorptional concentration is used.     

Analysis of a Population Genetics Model with Mutation, Selection, and Pleiotropy

We investigate a population genetics model introduced by Waxman and Peck⁽¹⁾ incorporating mutation, selection, and pleiotropy (one gene affecting several unrelated traits). The population is infinite, and continuous variation of genotype is allowed. Nonetheless, Waxman and Peck showed that if each gene affects three or more traits, then the steady-state solution of the model can have a nonzero fraction of the population with identical alleles. We use a recursion technique to calculate the distribution of alleles at finite times as well as in the infinite-time limit. We map Waxman and Peck's model into the mean-field theory for Bose condensation, and a variant of the model onto a bound-state problem in quantum theory. These mappings aid in delineating the region of parameter space in which the unique genotype occurs. We also discuss our attempts to correlate the statistics of DNA-sequence variation with the degree of pleiotropy of various genes.     

Detection of volatile metabolites of <Emphasis Type="Italic">Escherichia coli</Emphasis> by multi capillary column coupled ion mobility spectrometry

Detection and immediate quantification of microbial metabolic activities is of high interest in fields as diverse as biotechnology and infection biology. Interestingly, the most direct signals of microbial metabolism, the evolution of volatile metabolites, is largely ignored in the literature, and rather, metabolite concentrations in the microbial surrounding or even disruptive methods for intracellular metabolite measurements (i.e., metabolome analysis) are favored. Here, the development of a multi capillary column coupled ion mobility spectrometer (MCC-IMS) was described for the detection of volatile organic compounds from microbes and the MCC-IMS was used for characterization of metabolic activity of growing Escherichia coli. The MCC-IMS chromatogram of the microbial culture off-gas of the acetone-producing E. coli strain BL21 pLB4 revealed four analytes that positively correlated with growth, which were identified as ethanol, propanone (acetone), heptan-2-one, and nonan-2-one. The occurrence of these analytes was cross-validated by solid-phase micro-extraction coupled with gas chromatography mass spectrometry analysis. With this information in hand, the dynamic relationship between the E. coli biomass concentration and the metabolite concentrations in the headspace was measured. The results suggest that the metabolic pathways of heptan-2-one and nonan-2-one synthesis are regulated independent of each other. It is shown that the MCC-IMS in-line off-gas analysis is a simple method for real-time detection of microbial metabolic activity and discussed its potential for application in metabolic engineering, bioprocess control, and health care.     

Chemistry of 2,2,6,6,-tetramethyl-3,5-heptanedione (Hthd) modification of zirconium and hafnium propoxide precursors

The modification of different zirconium propoxide and hafnium propoxide precursors with 2,2,6,6,-tetramethyl-3,5-heptanedione (Hthd) was investigated by characterization of the isolated modified species. The complexes [Zr(OnPr)3(thd)](2), [Zr(OnPr)(OiPr)2(thd)]2, Zr(OiPr)(thd)3, [Hf(OnPr)3(thd)]2, and Hf(OiPr)(thd)3 were isolated and characterized. The structure of the n-propoxide analogue of Zr(OiPr)(thd)3 could not be refined, but its existence was clearly demonstrated by XRD and 1H NMR. The modification of the propoxide precursors involves mono- and trisubstituted intermediate compounds and does not involve a disubstituted compound; thus, the commercial product that is claimed to be "Zr(OiPr)2(thd)2" and is most commonly used for the MOCVD preparation of ZrO2 does not exist. No evidence was found for the presence of such a compound in either zirconium- or hafnium-based systems. Formation of the dimeric hydroxo-di-thd-substituted complex, [Hf(OH)(OiPr)(thd)2]2, which could be isolated only for hafnium-based systems, occurs on microhydrolysis. All heteroleptic intermediates are eventually transformed to the thermodynamically stable Zr(thd)4 or Hf(thd)4) The compounds obtained from isopropoxide precursors showed a higher stability than those with n-propoxide ligands or a combination of both types. In addition, it is important to note that residual alcohol facilitates the transformation and strongly enhances its rate. The unusually low solubility and volatility of MIV(thd)4 has been shown to be due to close packing and strong van der Waals interactions in the crystal structures of these compounds.