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991.
Fabrizio Innocenti Dr. Marie Eypper Edmond P. F. Lee Dr. Stefano Stranges Dr. Daniel K. W. Mok Dr. Foo‐tim Chau Prof. George C. King Prof. John M. Dyke Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(36):11452-11460
The first photoelectron band of difluorocarbene CF2, has been studied by threshold photoelectron (TPE) spectroscopy. CF2 was prepared by microwave discharge of a flowing mixture of hexafluoropropene, C3F6, and argon. A vibrationally resolved band was observed in which at least twenty‐two components were observed. In the first PE band of CF2, the adiabatic ionization energy differs significantly from the vertical ionization energy because, for the ionization CF2+ (X?2A1)+e? ← CF2 (X?1A1), there is an increase in the FCF bond angle (by ≈20°) and a decrease in the C? F bond length (by ≈0.7 Å). The adiabatic component was not observed in the experimental TPE spectrum. However, on comparing this spectrum with an ab initio/Franck–Condon simulation of this band, using results from high‐level ab initio calculations, the structure associated with the vibrational components could be assigned. This led to alignment of the experimental TPE spectrum and the computed Franck–Condon envelope, and a determination of the first adiabatic ionization energy of CF2 as (11.362±0.005) eV. From the assignment of the vibrational structure, values were obtained for the harmonic and fundamental frequencies of the symmetric stretching mode (ν1′) and symmetric bending mode (ν2′) in CF2+ (X?2A1). 相似文献
992.
Jane Brown Marie A. Colucci Simon C. Hirst Jason J. Shiers Jonathan G. Williams 《Tetrahedron letters》2008,49(33):4968-4971
Functionalised silicas 2 and 3 are effective for the cation exchange SPE purification of basic molecules containing acid-sensitive functionalities, the selective separations of mixtures of basic compounds and accelerated reaction work-ups/product isolations. 相似文献
993.
Thermophilic ethanol fermentation of wet-exploded wheat straw hydrolysate was investigated in a continuous immobilized reactor
system. The experiments were carried out in a lab-scale fluidized bed reactor (FBR) at 70°C. Undetoxified wheat straw hydrolysate
was used (3–12% dry matter), corresponding to sugar mixtures of glucose and xylose ranging from 12 to 41 g/l. The organism,
thermophilic anaerobic bacterium Thermoanaerobacter BG1L1, exhibited significant resistance to high levels of acetic acid (up to 10 g/l) and other metabolic inhibitors present
in the hydrolysate. Although the hydrolysate was not detoxified, ethanol yield in a range of 0.39–0.42 g/g was obtained. Overall,
sugar efficiency to ethanol was 68–76%. The reactor was operated continuously for approximately 143 days, and no contamination
was seen without the use of any agent for preventing bacterial infections. The tested microorganism has considerable potential
to be a novel candidate for lignocellulose bioconversion into ethanol. The work reported here also demonstrates that the use
of FBR configuration might be a viable approach for thermophilic anaerobic ethanol fermentation. 相似文献
994.
Pettersson M Unelius CR Valterová I Borg-Karlson AK 《Journal of chromatography. A》2008,1180(1-2):165-170
Volatiles released by seedlings of Norway spruce infested with the aphid Cinara pilicornis were analyzed using SPME-GC-MS. Among the stress-induced compounds released by the host plant, citronellol, cis-trans-nepetalactone and cis-trans-nepetalactol was found. These compounds originated from the aphids and they were assumed to be pheromone components for this aphid species. To determine the relative stereochemistry of the nepetalactone, a diagnostic method was developed. The method was based on multivariate analysis of tabulated relative intensities of mass fragments of the four nepetalactone diastereomers. In the practical method described, a few pairs of fragments in the mass spectra were compared and, in combination with the Kovat's index, were used to unambiguously identify the relative stereochemistry of the nepetalactone. 相似文献
995.
In contrast to normal boronic acids, o-hydroxymethyl phenylboronic acid (benzoboroxole) has the capability of complexing glycopyranosides efficiently in neutral water. The measurement of association constants with a panel of model hexopyranosides indicates that the preferred mode of binding is through a cis-3,4-diol, such as that found in galactopyranosides, and mass spectrometric studies support a 1:1 binding stoichiometry. The complexation of glucopyranosides is weaker, and they are bound through their 4,6-diol unit. Although several factors may explain the exceptional carbohydrate-binding behavior of this class of hemiboronic acids, the relatively high Lewis acidity of benzoboroxoles is a likely contributing factor along with subtle factors such as intramolecular hydrogen bonds with other hydroxyl groups in the resulting anionic complex. These results with hexopyranosides suggest that biologically relevant cell-surface oligosaccharides could be targeted in water using oligomeric benzoboroxole receptors. 相似文献
996.
997.
Vougo-Zanda M Anokhina EV Duhovic S Liu L Wang X Oloba OA Albright TA Jacobson AJ 《Inorganic chemistry》2008,47(11):4746-4751
Three metal-oxide organic frameworks have been synthesized and characterized: vanadium 1,4-benzenedicarboxylate, V2O2F0.6(OH)1.4(BDC).0.4H 2O (1); indium 1,4-benzenedicarboxylate, In 2F2.2(OH)1.8(BDC).1.6H2O (2); and aluminum 1,4-benzenedicarboxylate Al2F3(OH)(BDC) (3). The three-dimensional structures of 1, 2, and 3 have the same framework topology as the previously reported vanadium (III) 1,4-benzenedicarboxylate, VIII2(OH)2F2(BDC). The frameworks consist of inorganic layers constructed from corner sharing ML 6 octahedra (M=V, In, Al and L=OH, F) linked by BDC ligands. The structures are related to a general class of perovskite-related layer structures with composition MM'X4. The layers show characteristic distortions that can be related to tilting of the ML 6 octahedra. In particular the structure of 1 consists of O-V distances that strongly alternate along the b axis. The electronic consequences of this distortion then create a tilting of the 1,4-benzenedicarboxylate ligand about the a axis. Crystal data: 1, orthorhombic, space group Pmna, a=7.101(2) A, b=3.8416(11) A, c=20.570(6) A; 2, orthorhombic, space group Cmcm, a=7.490(4) A, b=21.803(1) A, c=8.154(4) A; 3, monoclinic, space group P2(1)/m, a=10.7569(8) A, b=6.7615(3) A, c=7.1291(3) A, beta=76.02(1) degrees. 相似文献
998.
Statistical error distributions for enthalpies of formation as predicted by 18 different density functionals have been analyzed using a test set of 675 molecules. Systematic errors, dependent on the number of valence electrons, have been identified for some functionals. A simple empirical correction makes a significant improvement in the prediction error for these single functionals. Linear combinations of enthalpy estimates from different density functionals are identified that exploit the error correlations among the functionals and allow for further improvements in the accuracy of thermodynamic predictions. A good compromise between accuracy and computational efforts is achieved by the BLUE (best linear unbiased estimator) combination of three functionals, B3LYP, BLYP, and VSXC (polyfunctional 3 or PF3). The PF3 method has a mean absolute deviation (MAD) from experiment of 2.4 kcal/mol on the G3 set of 271 molecules. This can be compared to the MAD of 4.9 kcal/mol for B3LYP and 1.2 kcal/mol for the more costly G3 method. On the larger set of 675 molecules, the MAD for PF3 is 3.0 kcal/mol. Opportunities for further improvements in the accuracy of this method are discussed. 相似文献
999.
Background
We examined whether individual differences in hemispheric utilization can interact with the intrinsic attentional biases of the cerebral hemispheres. Evidence suggests that the hemispheres have competing biases to direct attention contralaterally, with the left hemisphere (LH) having a stronger bias than the right hemisphere. There is also evidence that individuals have characteristic biases to utilize one hemisphere more than the other for processing information, which can induce a bias to direct attention to contralateral space. We predicted that LH-biased individuals would display a strong rightward attentional bias, which would create difficulty in selectively attending to target stimuli in the left visual field (LVF) as compared to right in the performance of a bilateral flanker task. 相似文献1000.
Four aminocyclopentanols, as mimics of putative intermediates in the hydrolysis of alpha-d-galactosides, have been synthesized through a number of stereoselective transformations using the cis-fused cyclopentane-1,4-lactone (1R, 5S, 7R, 8R)-7,8-dihydroxy-2-oxabicyclo[3.3.0]oct-3-one as a chiral building block. The compounds were tested towards various glycosidases but showed no anomer selectivity in the inhibition of alpha- and beta-galactosidases. 相似文献