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991.
This empirical analysis of CD data for 7-membered lactams includes examples of all twelve possible structural types in which the lactam is fused to a cyclohexane ring as part of a polycyclic compound. The CD behaviour of several classes of lactams shows ‘dOgura's sign rule’ to be an over-simplification. The signs and values of Δ? for lactams in which the second ring is fused at the 3,4- or 6,7-positions of the lactam ring show considerable deviations from the “normal’ values for 4,5- or 5,6-fused lactams.No simple pattern of group contributions emerged from this analysis, but a correlation of CD behaviour with the torsion angle in the C-CO-NH-C structural component is suggested, on the basis of a study of Dreiding models, and is supported by the result of an X-ray crystallographic analysis of one of the lactams.This study of CD data is extended to a smaller group of lactones with a seven-membered ring, most of which show Cotton effects opposite in sign and of smaller magnitude than those of the corresponding lactams. 相似文献
992.
Maria A. Curtin Irwin A. Taub Kenneth Kustin Narith Sao Jeremy R. Duvall Katharine I. Davies Christopher J. Doona Edward W. Ross 《Research on Chemical Intermediates》2004,30(6):647-661
The slow reaction between peroxodisulfate and formate is significantly accelerated by ascorbate at room temperature. The products of this induced oxidation, CO2 and oxalate (C2O2–
4), were analyzed by several methods and the kinetics of this reaction were measured. The overall mechanism involves free radical species. Ascorbate reacts with peroxodisulfate to initiate production of the sulfate radical ion (SO–
4), which reacts with formate to produce carbon dioxide radical ion (CO–
2) and sulfate. The carbon dioxide radical reacts with peroxodisulfate to form CO2 or self-combines to form oxalate. Competition occurring between these two processes determines the overall fate of the carbon dioxide radical species. As pH decreases, protonation of the carbon dioxide radical ion tends to favor production of CO2. 相似文献
993.
A novel supramolecular strategy to prepare bidentate ligands via the assembly of functionalised monomeric ligands on a dimeric zinc(II) porphyrin template is presented; the assembled bidentate ligands show chelating behaviour and their rhodium complexes display enhanced selectivity in the hydroformylation compared to the non-template analogue. 相似文献
994.
Shoeib T Cunje A Hopkinson AC Siu KW 《Journal of the American Society for Mass Spectrometry》2002,13(4):408-416
Collision-induced dissociation experiments on the Ag+-phenylalanine complex using several collision energies were shown to yield ten different fragment ions. Unambiguous assignment of these fragment ions were made by careful analysis of deuterium labeling experiments. The losses of H2O, CO, CO2, and AgH were commonly observed; also encountered were the losses of H2, Ag, and H. Deuterium labeling experiments and density functional calculations have been employed to probe fragmentation mechanisms that account for all experimental results. 相似文献
995.
The synthesis and transition temperatures of some trans-4-alkylcyclohexylethyl-substituted 2,3-difluorobiphenyls 总被引:1,自引:0,他引:1
Terphenyls with two lateral ortho-fluoro-substituents have proved to be excellent host materials for ferroelectric (SC*) mixtures. The compounds reported here are biphenyls with the same arrangement of lateral substituents but with a trans-4-alkylcyclohexylethyl moiety as one of the terminal substituents. Such three ring systems retain the ability to generate the SC mesophase and have low melting points. Low temperature lithiation procedures were used to prepare phenylboronic acids, which were then used in palladium catalysed cross-coupling procedures to prepare the desired compounds. The effect of molecular structure on the mesophase types and thermal stabilities is discussed and comparisons are made with analogous terphenyls and biphenyls with open chain terminal substituents. 相似文献
996.
B.W. Clare P.J. Jennings J.C.L. Cornish G. Talukder C.P. Lund G.T. Hefter 《Journal of computational chemistry》1993,14(12):1423-1428
A set of simple models of hydrogenated amorphous silicon (a-Si:H) consisting of hypothetical silane molecules with diamond or similar lattices was studied by the semiempirical AM1 method. Densities of states and infrared spectra were calculated for the silane molecules and similar molecules with dangling bonds disorder, and with boron or phosphorus substitution to simulate doping. Some examples are presented, and a comparison is made with experimental properties of a-Si:H. It is proposed to use these models in a study of the Staebler–Wronski photodegradation of a-Si:H and other aspects of amorphous silicon technology. © John Wiley & Sons, Inc. 相似文献
997.
The effect of low-energy ion bombardment on CD4/O2 and CF3X (X=F, Cl, Br) plasma etching has been assessed by applying controlled rf bias voltages on polystyrene (PS) and polymethylmethacrylate (PMMA) samples. In both cases ion bombardment has been found to have a chemical effect. In the case of CF4/O2 discharges, ion bombardment has been found to change the relative etching efficiency of different mixtures. In the case of CF3X plasmas, ion bombardment has been found to alter PMMA and PS etch rates in a different way. In particular, the ratios between CF4 and CF3X (X=Cl, Br) etch rates of PS have been found to decrease with increasing bias voltage. This effect has been tentatively attributed to an ion bombardment-induced enhancement of the reaction between the aromatic ring and halogen molecules formed in CF3Cl and CF3Br discharges. 相似文献
998.
Abstract— The weak and reversible binding of the antifungal drug, griseofulvin (GF), to calf thymus DNA has been demonstrated by difference spectroscopy and the quenching of the fluorescence of GF by DNA observed. The value of K n was determined to be 800 M -1 by fluorescence quenching titration. Adenosine and guanosine also exhibit difference spectra with GF and quench GF fluorescence indicating that they may be the site of both binding and energy transfer. The in vitro photosensitization of DNA by griseofulvin is shown to occur. It is proposed that the clinically observed in vivo photosensitizing action of griseofulvin may result from binding followed by excitation energy transfer and that this may also be important in the antifungal activity of the drug. 相似文献
999.
A method for isoelectric focusing of apolipoprotein E in an immobilized pH gradient with added carrier ampholytes has been developed. This method is an improvement over conventional isoelectric focusing of apolipoprotein E with respect to resolution, reproducibility, and simplicity. Since monosialo isoforms are resolved from the normally cofocusing asialo isoforms, unique patterns are obtained for all 6 common apolipoprotein E phenotypes. The method can also be applied to the screening of apolipoprotein A and C isoforms. Delipidated very low density lipoproteins (VLDL) have been used as the source of apolipoprotein E and C. Apolipoprotein A isoforms were focused directly from detergent-treated serum. Immunodetection of apolipoprotein E using capillary transfer was found to be compatible with the described method. 相似文献
1000.
Phosphonomethylation of 2-aminoethanethiol and thiazolidine gives the unexpected dimethylene diphosphonic acid 6. 相似文献