On the homotopy invariance of torsion for covering spaces

We prove the homotopy invariance of torsion for covering spaces, whenever the covering transformation group is either residually finite or amenable. In the case when the covering transformation group is residually finite and when the cohomology of the covering space vanishes, the homotopy invariance was established by Lück. We also give some applications of our results.

     

Determination of ion—molecule collision frequencies by Fourier transform ion cyclotron resonance spectroscopy

It is shown that nonreactive ion—molecule collision frequencies may be determined either by analysis of the transient signal resulting from excited ion cyclotron motion or by linewidth measurement of the Fourier transform of the transient signal.     

The Reaction of Triplet 2-Methyl-1,4-Naphthoquinone (Menadione) with DNA and Polynucleotides

Abstract— The photoreaction of 2-methyl-l,4-naphthoquinone (MQ, menadione) with DNA and polynucleotides in argon-saturated aqueous solution (pH 7) was studied. Results from laser flash photolysis experiments indicate that triplet quinone reacts with DNA and polyA but not detectably with polyU by one-electron oxidation of the bases of the nucleic acid with formation of the radical anion of the quinone. Irradiation of argon-saturated solutions containing MQ and DNA or polynucleotides (polyU, polyA, polyG or polyC) with 334 nm light leads to an increase in molecular weight for single-stranded DNA, polyA and to a much less extent for polyU. This finding indicates crosslink formation with quantum yields in the range of 10⁻⁵-10⁻³     

Chromatographic classification and comparison of commercially available reversed-phase liquid chromatographic columns using principal component analysis

A total of 135 commercially available alkyl, cyano, phenyl, perfluorinated, polar embedded, enhanced polar selectivity (i.e., polar/hydrophilic endcapped), "Aqua type" and a variety of novel phases including some non-silica based stationary phases have been characterised in terms of their surface coverage, hydrophobic selectivity, shape selectivity, hydrogen bonding capacity and ion-exchange capacity at pH 2.7 and 7.6. Principal component analysis has been used to provide a simple graphical comparison of the differences/similarities between columns in the entire database and differing subsets such as "Aqua type"/enhanced polar selectivity phases. The PCA has been correlated to the phase's ability to analyse a range of hydrophilic bases.     

Spectral, electrochemical, and photophysical studies of a magnesium porphyrin-fullerene dyad

A covalently linked magnesium porphyrin-fullerene (MgPo-C60) dyad was synthesized and its spectral, electrochemical, molecular orbital, and photophysical properties were investigated and the results were compared to the earlier reported zinc porphyrin-fullerene (ZnPo-C60) dyad. The ab initio B3LYP/3-21G(*) computed geometry and electronic structure of the dyad predicted that the HOMO and LUMO are mainly localized on the MgP and C60 units, respectively. In o-dichlorobenzene containing 0.1 M (n-Bu)4NClO4, the synthesized dyad exhibited six one-electron reversible redox reactions within the potential window of the solvent. The oxidation and reduction potentials of the MgP and C60 units indicate stabilization of the charge-separated state. The emission, monitored by both steady-state and time-resolved techniques, revealed efficient quenching of the singlet excited state of the MgP and C60 units. The quenching pathway of the singlet excited MgP moiety involved energy transfer to the appended C60 moiety, generating the singlet excited C60 moiety, from which subsequent charge-separation occurred. The charge recombination rates, k(CR), evaluated from nanosecond transient absorption studies, were found to be 2-3 orders of magnitude smaller than the charge separation rate, k(CS). In o-dichlorobenzene, the lifetime of the radical ion-pair, MgPo*+-C60*-, was found to be 520 ns which is longer than that of ZnPo*+-C60*- indicating better charge stabilization in MgPo-C60. Additional prolongation of the lifetime of MgPo*+-C60*- was achieved by coordinating nitrogenous axial ligands. The solvent effect in controlling the rates of forward and reverse electron transfer is also investigated.     

Molecular triads composed of ferrocene,C60, and nitroaromatic entities: electrochemical,computational, and photochemical investigations

Synthesis and physicochemical characterization of a series of molecular triads composed of ferrocene, C(60), and nitroaromatic entities are reported. Electrochemical studies revealed multiple redox processes involving all three redox active ferrocene, C(60), and nitrobenzene entities. Up to eight redox couples within the accessible potential window of o-dichlorobenzene containing 0.1 M (TBA)ClO(4) are observed. A comparison between the measured redox potentials with those of the starting compounds revealed absence of any significant electronic interactions between the different redox entities. The geometric and electronic structure of the triads are elucidated by using ab initio B3LYP/3-21G methods. In the energy-optimized structures, as predicted by electrochemical studies, the first HOMO orbitals are found to be located on the ferrocene entity, while the first LUMO orbitals are mainly on the C(60) entity. The coefficients of the subsequent LUMO orbitals track the observed site of electrochemical reductions of the triads. The photochemical events of the triads are probed by both steady-state and time-resolved techniques. The steady-state emission intensities of the triads and the starting dyad, 2-(ferrocenyl)fulleropyrrolidine, are found to be completely quenched compared to fulleropyrrolidine bearing no redox active substituents. The subpicosecond and nanosecond transient absorption spectral studies revealed efficient charge separation (and rapid charge recombination) in the triads, and this has been attributed to the close spacing of the redox entities of the triad to one another.     

Pretreatment of softwood by acid-catalyzed steam explosion followed by alkali extraction

A process for converting lignocellulosic biomass to ethanol hydrolyzes the hemicellulosic fraction to soluble sugars (i.e., pretreatment), followed by acid- or enzyme-catalyzed hydrolysis of the cellulosic fraction. Enzymatic hydrolysis may be improved by using an alkali to extract a fraction of the lignin from the pretreated material. The removal of the lignin may increase the accessibility of the cellulose to enzymatic attack, and thus improve overall economics of the process, if the alkali-treated material can still be effectively converted to ethanol. Pretreated Douglas fir produced by a sulfuric-acid-catalyzed steam explosion was treated with NaOH, NH₄OH, and lime to extract some of the lignin. The treated material, along with an untreated control sample, was tested by an enzymatic-digestion procedure, and converted to ethanol by simultaneous saccharification and fermentation using a glucose-fermenting yeast. NaOH was most effective at removing lignin (removed 29%), followed by NH4OH and lime. However, the susceptibility of the treated material to enzymatic digestion was lower than the control and decreased with increasing lignin removal. Ethanol production was similar for the control and NaOH-treated material, and lower for NH₄OH- and lime-treated material.     

Energy transfer followed by electron transfer in a supramolecular triad composed of boron dipyrrin, zinc porphyrin, and fullerene: a model for the photosynthetic antenna-reaction center complex

The first example of a working model of the photosynthetic antenna-reaction center complex, constructed via self-assembled supramolecular methodology, is reported. For this, a supramolecular triad is assembled by axially coordinating imidazole-appended fulleropyrrolidine to the zinc center of a covalently linked zinc porphyrin-boron dipyrrin dyad. Selective excitation of the boron dipyrrin moiety in the boron dipyrrin-zinc porphyrin dyad resulted in efficient energy transfer (k(ENT)(singlet) = 9.2 x 10(9) s(-)(1); Phi(ENT)(singlet) = 0.83) creating singlet excited zinc porphyrin. Upon forming the supramolecular triad, the excited zinc porphyrin resulted in efficient electron transfer to the coordinated fullerenes, resulting in a charge-separated state (k(cs)(singlet) = 4.7 x 10(9) s(-)(1); Phi(CS)(singlet) = 0.9). The observed energy transfer followed by electron transfer in the present supramolecular triad mimics the events of natural photosynthesis. Here, the boron dipyrrin acts as antenna chlorophyll that absorbs light energy and transports spatially to the photosynthetic reaction center, while the electron transfer from the excited zinc porphyrin to fullerene mimics the primary events of the reaction center where conversion of the electronic excitation energy to chemical energy in the form of charge separation takes place. The important feature of the present model system is its relative "simplicity" because of the utilized supramolecular approach to mimic rather complex "combined antenna-reaction center" events of photosynthesis.     

Photoelectric detection and estimation of carbon monoxide with granules coated with palladous silicomolybdate

A colorimetric method for continuous detection and spot-test estimation of carbon monoxide in air is described. Measurements are made of the decrease in photoelectric current when the incident light changes after contact with translucent granules of silica gel coated with palladous silicomolybdate, which changes its color from yellow to green and blue in the presence of carbon monoxide. The scale of a microammeter in a specially designed instrument, incorporating a photoelectric cell and mechanical devices for exposing the granules simultaneously to gas and light, is calibrated in terms of the volume percentage of carbon monoxide. Concentrations, from one down to about 0.001 % can be estimated with an accuracy of about 10%. A measurement may be made in one minute.