2,947 research outputs found
Arene oxidation with malonoyl peroxides
Malonoyl peroxide 7, prepared in a single step from the commercially available diacid, is an effective reagent for the
oxidation of aromatics. Reaction of an arene with peroxide 7 at room temperature leads to the corresponding protected phenol
which can be unmasked by aminolysis. An ionic mechanism consistent with the experimental findings and supported by isotopic
labeling, Hammett analysis, EPR investigations and reactivity profile studies is proposed
Investigating Ca II emission in the RS CVn binary ER Vulpeculae using the Broadening Function Formalism
The synchronously rotating G stars in the detached, short-period (0.7 d),
partially eclipsing binary, ER Vul, are the most chromospherically active
solar-type stars known. We have monitored activity in the Ca II H & K reversals
for almost an entire orbit. Rucinski's Broadening Function Formalism allows the
photospheric contribution to be objectively subtracted from the highly blended
spectra. The power of the BF technique is also demonstrated by the good
agreement of radial velocities with those measured by others from less crowded
spectral regions. In addition to strong Ca II emission from the primary and
secondary, there appears to be a high-velocity stream flowing onto the
secondary where it stimulates a large active region on the surface 30 - 40
degrees in advance of the sub-binary longitude. A model light curve with a spot
centered on the same longitude also gives the best fit to the observed light
curve. A flare with approximately 13% more power than at other phases was
detected in one spectrum. We suggest ER Vul may offer a magnified view of the
more subtle chromospheric effects synchronized to planetary revolution seen in
certain `51 Peg'-type systems.Comment: Accepted to AJ; 17 pages and 16 figure
Methanol-to-Olefins Catalysis with Hydrothermally Treated Zeolite SSZ-39
Zeolite SSZ-39 is evaluated for catalyzing the methanol-to-olefins (MTO) reaction. By steaming NH_4–SSZ-39, Al can be removed from framework positions, resulting in an increase in framework-Si/AlT and thus a lowered active acid site density. The Si/Al_T ratios can be controlled by the steaming temperatures. SSZ-39 steamed at 750 °C, with preserved pore volume and morphology, is an excellent MTO catalyst, as high, stable olefin selectivities, long time-on-stream activity, and low alkane production are observed. Moreover, interesting propylene/ethylene/butylene ratios of 2.8/1/1.1 are obtained, likely related to the shape of the AEI cage. By Cu^(2+)-exchanging SSZ-39, evidence is provided to show that Al_T sites in close proximity (high AlT density) produce the unwanted effects (higher alkane-make and carbonaceous deposits) in nonsteamed materials during MTO
First-principles study on the intermediate compounds of LiBH
We report the results of the first-principles calculation on the intermediate
compounds of LiBH. The stability of LiBH and LiBH has been examined with the ultrasoft pseudopotential method based on
the density functional theory. Theoretical prediction has suggested that
monoclinic LiBH is the most stable among the candidate
materials. We propose the following hydriding/dehydriding process of LiBH
via this intermediate compound : LiBHLiBH LiH HLiH B H. The hydrogen content and enthalpy of the first
reaction are estimated to be 10 mass% and 56 kJ/mol H, respectively, and
those of the second reaction are 4 mass% and 125 kJ/mol H. They are in good
agreement with experimental results of the thermal desorption spectra of
LiBH. Our calculation has predicted that the bending modes for the
-phonon frequencies of monoclinic LiBH are lower than
that of LiBH, while stretching modes are higher. These results are very
useful for the experimental search and identification of possible intermediate
compounds.Comment: 7 pages, 5 figures, submitted to PR
Organic fuel cell methods and apparatus
A liquid organic, fuel cell is provided which employs a solid electrolyte membrane. An organic fuel, such as a methanol/water mixture, is circulated past an anode of a cell while oxygen or air is circulated past a cathode of the cell. The cell solid electrolyte membrane is preferably fabricated from Nafion.TM.. Additionally, a method for improving the performance of carbon electrode structures for use in organic fuel cells is provided wherein a high surface-area carbon particle/Teflon.TM.-binder structure is immersed within a Nafion.TM./methanol bath to impregnate the electrode with Nafion.TM.. A method for fabricating an anode for use in a organic fuel cell is described wherein metal alloys are deposited onto the electrode in an electro-deposition solution containing perfluorooctanesulfonic acid. A fuel additive containing perfluorooctanesulfonic acid for use with fuel cells employing a sulfuric acid electrolyte is also disclosed. New organic fuels, namely, trimethoxymethane, dimethoxymethane, and trioxane are also described for use with either conventional or improved fuel cells
Organic fuel cell methods and apparatus
A liquid organic, fuel cell is provided which employs a solid electrolyte membrane. An organic fuel, such as a methanol/water mixture, is circulated past an anode of a cell while oxygen or air is circulated past a cathode of the cell. The cell solid electrolyte membrane is preferably fabricated from Nafion.TM.. Additionally, a method for improving the performance of carbon electrode structures for use in organic fuel cells is provided wherein a high surface-area carbon particle/Teflon.TM.-binder structure is immersed within a Nafion.TM./methanol bath to impregnate the electrode with Nafion.TM.. A method for fabricating an anode for use in a organic fuel cell is described wherein metal alloys are deposited onto the electrode in an electro-deposition solution containing perfluorooctanesulfonic acid. A fuel additive containing perfluorooctanesulfonic acid for use with fuel cells employing a sulfuric acid electrolyte is also disclosed. New organic fuels, namely, trimethoxymethane, dimethoxymethane, and trioxane are also described for use with either conventional or improved fuel cells
Aqueous liquid feed organic fuel cell using solid polymer electrolyte membrane
A liquid organic fuel cell is provided which employs a solid electrolyte membrane. An organic fuel, such as a methanol/water mixture, is circulated past an anode of a cell while oxygen or air is circulated past a cathode of the cell. The cell solid electrolyte membrane is preferably fabricated from Nafion.TM.. Additionally, a method for improving the performance of carbon electrode structures for use in organic fuel cells is provided wherein a high surface-area carbon particle/Teflon.TM.-binder structure is immersed within a Nafion.TM./methanol bath to impregnate the electrode with Nafion.TM.. A method for fabricating an anode for use in a organic fuel cell is described wherein metal alloys are deposited onto the electrode in an electro-deposition solution containing perfluorooctanesulfonic acid. A fuel additive containing perfluorooctanesulfonic acid for use with fuel cells employing a sulfuric acid electrolyte is also disclosed. New organic fuels, namely, trimethoxymethane, dimethoxymethane, and trioxane are also described for use with either conventional or improved fuel cells
Organic fuel cell methods and apparatus
A liquid organic fuel cell is provided which employs a solid electrolyte membrane. An organic fuel, such as a methanol/water mixture, is circulated past an anode of a cell while oxygen or air is circulated past a cathode of the cell. The cell solid electrolyte membrane is preferably fabricated from Nafion.TM.. Additionally, a method for improving the performance of carbon electrode structures for use in organic fuel cells is provided wherein a high surface-area carbon particle/Teflon.TM.-binder structure is immersed within a Nafion.TM./methanol bath to impregnate the electrode with Nafion.TM.. A method for fabricating an anode for use in a organic fuel cell is described wherein metal alloys are deposited onto the electrode in an electro-deposition solution containing perfluorooctanesulfonic acid. A fuel additive containing perfluorooctanesulfonic acid for use with fuel cells employing a sulfuric acid electrolyte is also disclosed. New organic fuels, namely, trimethoxymethane, dimethoxymethane, and trioxane are also described for use with either conventional or improved fuel cells
Photo-fragmentation spectroscopy of benzylium and 1-phenylethyl cations
The electronic spectra of cold benzylium (C6H5-CH2+) and 1-phenylethyl
(C6H5-CH-CH3+)cations have been recorded via photofragment spectroscopy.
Benzylium and 1-phenylethyl cations produced from electrosprayed benzylamine
and phenylethylamine solutions, respectively, were stored in a cryogenically
cooled quadrupole ion trap and photodissociated by an OPO laser, scanned in
parts of the UV and visible regions (600-225 nm). The electronic states and
active vibrational modes of the benzylium and 1-phenylethyl cations as well as
those of their tropylium or methyl tropylium isomers have been calculated with
ab initio methods for comparison with the spectra observed. Sharp vibrational
progressions are observed in the visible region while the absorption features
are much broader in the UV. The visible spectrum of the benzylium cation is
similar to that obtained in an argon tagging experiment [V. Dryza, N. Chalyavi,
J.A. Sanelli, and E.J. Bieske, J. Chem. Phys. 137, 204304 (2012)], with an
additional splitting assigned to Fermi resonances. The visible spectrum of the
1-phenylethyl cation also shows vibrational progressions. For both cations, the
second electronic transition is observed in the UV, around 33 000 cm-1 (4.1
eV), and shows a broadened vibrational progression. In both cases the S2
optimized geometry is non planar. The third electronic transition observed
around 40 000 cm-1 (5.0 eV) is even broader with no apparent vibrational
structures, which is indicative of either a fast non-radiative process or a
very large change in geometry between the excited and the ground states. The
oscillator strengths calculated for tropylium and methyl tropylium are weak.
Therefore, these isomeric structures are most likely not responsible for these
absorption features. Finally, the fragmentation pattern changes in the second
and third electronic states: C2H2 loss becomes predominant at higher excitation
energies, for both cations
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