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91.
P.A. Butler I.Y. Lee J.O. Newton Y. El-Masri M.M. Aleonard P. Colombani R.M. Diamond F.S. Stephens R.W. Lougheed E.K. Hulet 《Physics letters. [Part B]》1977,68(2):122-124
Excitation functions and angular distributions have been measured for the fission of 232Th, 238U, 244Pu and 248Cm induced by 86Kr and 136Xe ions at energies in the vicinity of the Coulomb barrier. No large differences as a function of either target or projectile were found. These results suggest that the main process occuring is not Coulomb fission. 相似文献
92.
93.
Roger Stephens 《Spectrochimica Acta Part B: Atomic Spectroscopy》1985,40(9):1259-1266
The technique has the advantage of allowing isotopic differences to be detected using a standard atmospheric atomiser and a conventional hollow cathode source. The measurements are sufficiently robust to tolerate a limited variability of sample composition, background absorption from matrix species, and some instrumental parameters such as source intensity. Different isotopes show different responses with varying magnetic field strength across the atomiser. This allows a distinction to be made between the isotopes even though only a single source of natural isotopic composition is used. Results illustrating this behaviour are given for Pb206, Pb207, Pb208. 相似文献
94.
Green JS Ovchinnikov VM Evans RG Akli KU Azechi H Beg FN Bellei C Freeman RR Habara H Heathcote R Key MH King JA Lancaster KL Lopes NC Ma T MacKinnon AJ Markey K McPhee A Najmudin Z Nilson P Onofrei R Stephens R Takeda K Tanaka KA Theobald W Tanimoto T Waugh J Van Woerkom L Woolsey NC Zepf M Davies JR Norreys PA 《Physical review letters》2008,100(1):015003
Metal foil targets were irradiated with 1 mum wavelength (lambda) laser pulses of 5 ps duration and focused intensities (I) of up to 4x10;{19} W cm;{-2}, giving values of both Ilambda;{2} and pulse duration comparable to those required for fast ignition inertial fusion. The divergence of the electrons accelerated into the target was determined from spatially resolved measurements of x-ray K_{alpha} emission and from transverse probing of the plasma formed on the back of the foils. Comparison of the divergence with other published data shows that it increases with Ilambda;{2} and is independent of pulse duration. Two-dimensional particle-in-cell simulations reproduce these results, indicating that it is a fundamental property of the laser-plasma interaction. 相似文献
95.
Jason S. Howell Benjamin O. Stephens David S. Boucher 《Journal of Polymer Science.Polymer Physics》2015,53(16):1089-1097
Solubility parameters are certain measurable quantities that are observed to influence the ability of a solvent to fully dissolve a polymer. Current theory partitions the intermolecular forces between dispersion, polar, and hydrogen bonding interactions, thereby generating a three‐dimensional solubility parameter space. The Hansen solubility parameters of a polymer are taken to be the center of a sphere obtained from the best fit of the coordinates of good solvents in the parameter space. Investigations of several polymers (lignin, polyethersulfone, and bitumen) show that the convex hull of all known good solvents in the three‐dimensional parameter space also gives a meaningful interpretation of the solubility region. Several methods for computing the convex solubility parameters of a polymer from the convex solubility region are described. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1089–1097 相似文献
96.
A comparison of the abilities of time-dependent density-functional theory (TDDFT) and coupled cluster (CC) theory to reproduce experimental sodium D-line specific rotations for 13 conformationally rigid organic molecules is reported. The test set includes alkanes, alkenes, and ketones with known absolute configurations. TDDFT calculations make use of gauge-including atomic orbitals and give origin-independent specific rotations. CC rotations are computed using both the origin-independent dipole-velocity and origin-dependent dipole-length representations. The mean absolute deviations of calculated and experimental rotations are of comparable magnitudes for all three methods. The origin-independent DFT and CC methods give the same sign of [alpha]D for every molecule except norbornanone. For every large-rotation ketone and alkene for which DFT and CC yield the incorrect sign as compared to liquid-phase experimental data, the corresponding optical rotatory dispersion (ORD) curve is bisignate, suggesting that the two models cannot reliably reproduce the relative excitation energies and antagonistic rotational strengths of multiple competing electronic states that contribute to the total long-wavelength rotation. Several potential sources of error in the theoretical treatments are considered, including basis set incompleteness, vibrational and temperature effects, electron correlation, and solvent effects. 相似文献
97.
Soloveichik G Her JH Stephens PW Gao Y Rijssenbeek J Andrus M Zhao JC 《Inorganic chemistry》2008,47(10):4290-4298
The ammonia complex of magnesium borohydride Mg(BH4)2.2NH3 (I), which contains 16.0 wt % hydrogen, is a potentially promising material for hydrogen storage. This complex was synthesized by thermal decomposition of a hexaaammine complex Mg(BH4)2.6NH3 (II), which crystallizes in the cubic space group Fm3 m with unit cell parameter a=10.82(1) A and is isostructural to Mg(NH3) 6Cl2. We solved the structure of I that crystallizes in the orthorhombic space group Pcab with unit cell parameters a=17.4872(4) A, b=9.4132(2) A, c=8.7304(2) A, and Z=8. This structure is built from individual pseudotetrahedral molecules Mg(BH4)2.2NH3 containing one bidentate BH4 group and one tridentate BH4 group that pack into a layered crystal structure mediated by N-H...H-B dihydrogen bonds. Complex I decomposes endothermically starting at 150 degrees C, with a maximum hydrogen release rate at 205 degrees C, which makes it competitive with ammonia borane BH 3NH3 as a hydrogen storage material. 相似文献
98.
Reliability of high-throughput genotyping of whole genome amplified DNA in SNP genotyping studies 总被引:1,自引:0,他引:1
Berthier-Schaad Y Kao WH Coresh J Zhang L Ingersoll RG Stephens R Smith MW 《Electrophoresis》2007,28(16):2812-2817
Whole genome amplification (wga) of DNA is being widely implemented in many laboratories to extend the life of samples only available in limited quantities for genetic analysis. We determined the reliability of wgaDNA genotypes in three sets of replicates from the same individuals: (i) 23 pairs of genomic DNA (gDNA), (ii) 43 pairs gDNA versus wgaDNA, and (iii) 29 pairs of independently amplified wgaDNA. Amplification was performed using multiple displacement amplification (MDA). Genotyping was successful for both DNA types for 1268 out of 1534 SNPs from 164 cardiovascular candidate genes assayed in a single Illumina panel. Amplified DNA failed for 77 SNPs (6%) that were genotyped successfully with genomic material. Percent of successful SNP calls, and concordance between pairs and kappa statistics (kappa) were determined. A total of 54 110 genotypes from gDNA-wgaDNA pairs were available for concordance analysis. Mean kappa for gDNA-wgaDNA pairs was 0.99. Concordance between gDNA-wgaDNA pairs was higher than amongst wgaDNA pairs (mean kappa for the 29 independently amplified pairs of wgaDNA was 0.95; interquartile range: 0.93-1.00). A statistical analysis of those SNPs which failed to genotype from amplified DNA only revealed that those loci were more likely to be closer to the telomeres and in locally GC-rich sequences. In summary, the MDA method produces wgaDNA samples that can be genotyped using high-throughput technology with a very high reproducibility to the original DNA but with slightly lower call rates. DNA amplification methodologies provide a useful solution for current and future large-scale genetic analyses especially with limited quantities of samples and DNA. 相似文献
99.
Stephens PJ Pan JJ Devlin FJ Krohn K Kurtán T 《The Journal of organic chemistry》2007,72(9):3521-3536
The absolute configurations (ACs) of the iridoid natural products, plumericin (1) and isoplumericin (2), have been re-investigated using vibrational circular dichroism (VCD) spectroscopy, electronic circular dichroism (ECD) spectroscopy, and optical rotatory dispersion (ORD). Comparison of DFT calculations of the VCD spectra of 1 and 2 to the experimental VCD spectra of the natural products, (+)-1 and (+)-2, leads unambiguously to the AC (1R,5S,8S,9S,10S)-(+) for both 1 and 2. In contrast, comparison of time-dependent DFT (TDDFT) calculations of the ECD spectra of 1 and 2 to the experimental spectra of (+)-1 and (+)-2 does not permit definitive assignment of their ACs. On the other hand, TDDFT calculations of the ORD of (1R,5S,8S,9S,10S)-1 and -2 over the range of 365-589 nm are in excellent agreement with the experimental data of (+)-1 and (+)-2, confirming the ACs derived from the VCD spectra. Thus, the ACs initially proposed by Albers-Sch?nberg and Schmid are shown to be correct, and the opposite ACs recently derived from the ECD spectra of 1 and 2 by Els?sser et al. are shown to be incorrect. As a result, the ACs of other iridoid natural products obtained by chemical correlation with 1 and 2 are not in need of revision. 相似文献
100.
Aldous DW Stephens NF Lightfoot P 《Dalton transactions (Cambridge, England : 2003)》2007,(22):2271-2282
Nine new vanadium oxyfluorides, containing ten different oligomeric vanadium (oxy)fluoride anions have been prepared by solvothermal synthesis in water-ethylene glycol and using organic cations as co-crystallising agents. Crystal structures are reported for each. Amongst the ten structure types, five represent previously unobserved moieties, including one monomeric unit (cis-[VOF4(H2O)]2-), two dimers ([V2O2F6(H2O)2]2- and [V2O2F8]4-) and two tetramers (both isomers of composition [V4O4F14]6-). Structural relationships between the various units are discussed, together with some rationalisation of their occurrence as a function of synthetic variables. 相似文献