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21.
Bühl M Grigoleit S Kabrede H Mauschick FT 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,12(2):477-488
59Co chemical shifts were computed at the GIAO-B3LYP level for [Co(CN)6]3-, [Co(H2O)6]3+, [Co(NH3)6]3+, and [Co(CO)4]- in water. The aqueous solutions were modeled by Car-Parrinello molecular dynamics (CPMD) simulations, or by propagation on a hybrid quantum-mechanical/molecular-mechanical Born-Oppenheimer surface (QM/MM-BOMD). Mean absolute deviations from experiment obtained with these methods are on the order of 400 and 600 ppm, respectively, over a total delta(59Co) range of about 18,000 ppm. The effect of the solvent on delta(59Co) is mostly indirect, resulting primarily from substantial metal-ligand bond contractions on going from the gas phase to the bulk. The simulated solvent effects on geometries and delta(59Co) values are well reproduced by using a polarizable continuum model (PCM), based on optimization and perturbational evaluation of quantum-mechanical zero-point corrections. 相似文献
22.
Heinrich Hillig Hendrik Küper Wolfgang Riepe Hans Peter Ritter 《Analytica chimica acta》1979,112(2):123-132
Automation of a mass spectrometer—computer system makes it possible to process up to 30 samples without attention after sample loading. An automatic sample changer introduces the samples successively into the ion source by means of a direct inlet probe. A process control unit determines the operation sequence. Computer programs are available for the hardware support, system supervision and evaluation of the spectrometer signals. The most essential precondition for automation — automatic evaporation of the sample material by electronic control of the total ion current — is confirmed to be satisfactory. The system operates routinely overnight in an industrial laboratory, so that day work can be devoted to difficult analytical problems. The cost of routine analyses is halved. 相似文献
23.
Luesch H Hoffmann D Hevel JM Becker JE Golakoti T Moore RE 《The Journal of organic chemistry》2003,68(1):83-91
The biosynthesis of the unusual amino acid 4-methylproline in the Nostoc genus of cyanobacteria was investigated on the genetic and enzymatic level. Two genes involved in the biosynthesis were cloned and the corresponding enzymes, a zinc-dependent long-chain dehydrogenase and a Delta(1)-pyrroline-5-carboxylic acid (P5C) reductase homologue, were overexpressed in Escherichia coli and biochemically characterized. Putative substrates were synthesized to test enzyme substrate specificities, and deuterium labeling studies were carried out to reveal the stereospecificities of the enzymatic reactions with respect to the substrates as well as to the coenzymes. 相似文献
24.
Floris P. J. T. Rutjes Henk Hiemstra Hendrik H. Mooiweer W. Nico Speckamp 《Tetrahedron letters》1988,29(52):6975-6978
Acid catalyzed cyclization of methoxymethyl substituted acyclic hydrazides 4 provides cyclic hydrazides 5 in moderate to good yields through the intermediacy of N,N′-di(methoxycarbonyl)hydrazinium intermediates. 相似文献
25.
Wagner J Andres H Rohrbach S Wagner D Oberer L France J 《The Journal of organic chemistry》2005,70(23):9588-9590
[Reaction: see text]. Sanglifehrin A is a novel complex natural product showing strong immunosuppressive activity and remarkably high affinity for cyclophilin A. To assess its pharmacokinetic properties in vivo, an efficient synthetic route was developed to introduce a tritium label in position C35 of sangliferin A via an oxidation/reduction strategy. The synthetic approach is particularly attractive, because the C35-oxo intermediate 7 is available in good yield on large scale and the reducing agent, lithium tri-sec-butylborotritide, is readily available. An attempt to apply a similar strategy to the alcohol in position C31 led primarily to C31-epi-hydroxy sanglifehrin A under a variety of conditions. 相似文献
26.
LiBH(4) is a powerful and selective reagent for regiospecific reduction reactions. A simple synthesis of LiB(3)H(4) at near theoretical specific radioactivity is reported. We have treated Li(3)H synthesized from tritium gas ((3)H(2), approximately 98%) with BBr(3) to produce LiB(3)H(4) (specific activity = 4120 GBq/mmol = 110 Ci/mmol. The maximum theoretical specific activity of LiB(3)H(4) is 4252 GBq/mmol = 115.04 Ci/mmol; 1 matom of (3)H = 1063 GBq = 28.76 Ci.) The tritium labeling performance of the reagent was tested by an exemplary reduction of 2-naphthaldehyde to 2-naphthalenemethanol. LiB(3)H(4) and the reduction products were characterized by a combination of (1)H, (3)H, and (11)B NMR techniques, as appropriate. 相似文献
27.
28.
By injection of the proton bound homodimer [DMF.H+.DMF] of N,N-dimethylformamide (DMF) generated in an external ion source into a mixture of DMF and a second base within the cell of a Fourier transform ion cyclotron resonance (FT-ICR) spectrometer the equilibria between [DMF.H+.DMF] and the other possible proton bound dimers [DMF.H+.base] and [base.H+.base] have been studied for 13 different bases. Strongly polar bases like aliphatic amides and dimethyl sulfoxide (DMSO) exchange both DMF in [DMF.H+.DMF] by a two step process, while the almost non-polar amines exchange only one DMF. If the base is a primary or secondary amine, the proton bound heterodimer [DMF.H+.amine] reacts further by the addition of one DMF to create a proton bound trimer [(DMF)2.H+.amine]. The affinity deltaG(DMFH+) of the bases towards protonated DMF relative to neutral DMF depends linearly on the difference deltaGB of the gas phase basicity of DMF and the other base, but different correlation lines are obtained for polar and non-polar ligands (deltaGDMFH+ = 0.44GB(base)-375 [kJ/mol] (r = 0.97) and deltaGDMFH+ = 0.46GB(base)-397 [kJ/mol] (r = 0.99), respectively). This different behavior is explained by a different character of the proton bridge in the heterodimers containing only polar ligands and those incorporating a non-polar ligand besides DMF. The former dimers contain a more or less symmetric proton bridge while the latter can be viewed as a protonated base solvated by DMF. The available data have been used to calculate the molecular pair gas phase basicity of DMF and the 13 bases used and to estimate the dissociation energies of the bonds of the proton bridge in various proton bound heterodimers. 相似文献
29.
Frunza L Kosslick H Pitsch I Frunza S Schönhals A 《The journal of physical chemistry. B》2005,109(18):9154-9159
The rotational molecular dynamics of water confined to nanoporous molecular sieves of a regular hexagonal (SBA-15) and of a foamlike pore structure was studied by dielectric spectroscopy in the frequency range from 10(-2) to 10(9) Hz and in a broad temperature interval. Two relaxation processes were observed: the process at lower frequencies is related to water molecules forming a layer, which is strongly adsorbed at the pore surface, whereas the relaxation process at higher frequencies is assigned to fluctuations of water molecules situated close to the center of the pore. The relaxation times of the low-frequency process for both materials and of the high-frequency process for the SBA-15 material have an unusual saddlelike temperature dependence, reported here for the first time. To describe this temperature dependence, a model developed for water confined to nanoporous glasses by Ryabov et al. [J. Phys. Chem. B 2001, 105, 1845] was applied, which considers two competing effects. The characteristic features of these two competing processes were compared with those reported for other porous systems. 相似文献
30.