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排序方式: 共有336条查询结果,搜索用时 15 毫秒
1.
Mishra SR Bachmann KT Bernstein RH Blair RE Foudas C Lefmann WC Leung WC Oltman E Quintas PZ Sciulli FJ Shaevitz MH Smith WH Merritt FS Oreglia MJ Schellman H Schumm BA Borcherding F Fisk HE Lamm MJ Marsh W Merritt KW Yovanovitch DD Bodek A Budd HS Sakumoto WK 《Physical review letters》1989,63(2):132-135
2.
Single Crystal Investigations on Fluoroperovskites MPdF3 (M = Rb, K) and PdF2 Single crystal investigations on PdF2 (violet) confirm the tetragonale rutile structure [1, 2] with a = 495.44(3) pm, c = 338.48(3) pm, Z = 2, space group P42/mnm-D (No. 136) (xF = 0.3058(8)). RbPdF3 and KPdF3 have been obtained. RbPdF3 and KPdF3 both ruby-red single crystals crystallize cubic (perovskite-structure), space group Pm3m-O (No. 221) with a = 429.41(8) pm (RbPdF3) respectively a = 424.30(4) pm (KPdF3). 相似文献
3.
4.
Arroyo CG King BJ Bachmann KT Bazarko AO Bolton T Foudas C Lefmann WC Leung WC Mishra SR Oltman E Quintas PZ Rabinowitz SA Sciulli FJ Seligman WG Shaevitz MH Merritt FS Oreglia MJ Schumm BA Bernstein RH Borcherding F Fisk HE Lamm MJ Marsh W Merritt KW Schellman HM Yovanovitch DD Bodek A Budd HS de Barbaro P Sakumoto WK Kinnel T Sandler PH Smith WH 《Physical review letters》1994,72(22):3452-3455
5.
Zhou J Kelly WL Bachmann BO Gunsior M Townsend CA Solomon EI 《Journal of the American Chemical Society》2001,123(30):7388-7398
Using a single ferrous active site, clavaminate synthase 2 (CS2) activates O(2) and catalyzes the hydroxylation of deoxyguanidinoproclavaminic acid (DGPC), the oxidative ring closure of proclavaminic acid (PC), and the desaturation of dihydroclavaminic acid (and a substrate analogue, deoxyproclavaminic acid (DPC)), each coupled to the oxidative decarboxylation of cosubstrate, alpha-ketoglutarate (alpha-KG). CS2 can also catalyze an uncoupled decarboxylation of alpha-KG both in the absence and in the presence of substrate, which results in enzyme deactivation. Resting CS2/Fe(II) has a six-coordinate Fe(II) site, and alpha-KG binds to the iron in a bidentate mode. The active site becomes five-coordinate only when both substrate and alpha-KG are bound, the latter still in a bidentate mode. Absorption, CD, MCD, and VTVH MCD studies of the interaction of CS2 with DGPC, PC, and DPC provide significant molecular level insight into the structure/function correlations of this multifunctional enzyme. There are varying amounts of six-coordinate ferrous species in the substrate complexes, which correlate to the uncoupled reaction. Five-coordinate ferrous species with similar geometric and electronic structures are present for all three substrate/alpha-KG complexes. Coordinative unsaturation of the Fe(II) in the presence of both cosubstrate and substrate appears to be critical for the coupling of the oxidative decarboxylation of alpha-KG to the different substrate oxidation reactions. In addition to the substrate orientation relative to the open coordination position on the iron site, it is hypothesized that the enzyme can affect the nature of the reactivity by further regulating the binding energy of the water to the ferrous species in the enzyme/succinate/product complex. 相似文献
6.
We have exactly enumerated all sequences and conformations of hydrophobic-polar (HP) proteins with chains of up to 19 monomers on the simple cubic lattice. For two variants of the HP model, where only two types of monomers are distinguished, we determined and statistically analyzed designing sequences, i.e., sequences that have a nondegenerate ground state. Furthermore we were interested in characteristic thermodynamic properties of HP proteins with designing sequences. In order to be able to perform these exact studies, we applied an efficient enumeration method based on contact sets. 相似文献
7.
Bertelsen S Halland N Bachmann S Marigo M Braunton A Jørgensen KA 《Chemical communications (Cambridge, England)》2005,(38):4821-4823
The first organocatalytic enantioselective alpha-bromination of aldehydes and ketones is presented; a C2-symmetric diphenylpyrrolidine catalyst afforded the alpha-brominated aldehydes in good yields and up to 96% ee, while ketones were alpha-brominated by a C2-symmetric imidazolidine in up to 94% ee; furthermore, the organocatalytic enantioselective alpha-iodination of aldehydes is also demonstrated to proceed with up to 89% ee. 相似文献
8.
Abstract Fourier transform infrared (FTIR) spectroscopy is an effective and nondestructive method for monitoring cellular alterations. Combining the advantages of FTIR spectroscopy with the challenge of cellular characterization, the main objective of this review is to collect information related to the spectroscopic identification of blood cells, focusing on specific biochemical features of leukemia cells detected through FTIR spectral analysis. Some interesting results obtained by different authors regarding human promyelocytic leukemia, white blood cells, chronic lymphocytic leukemia, and human peripheral blood mononuclear cells are presented. In addition, the characterization of two types of cells, namely, leukemia T and a healthy human blood cells, is reported and the identification of biochemical markers provides important information that, associated with clinical examination, can assist in the diagnosis of diseases. 相似文献
9.
Association and Dissociation of Grignard Reagents RMgCl and Their Turbo Variant RMgCl⋅LiCl
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Christoph Schnegelsberg Sebastian Bachmann Marlene Kolter Thomas Auth Dr. Michael John Prof. Dr. Dietmar Stalke Prof. Dr. Konrad Koszinowski 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(23):7752-7762
Grignard reagents RMgCl and their so‐called turbo variant, the highly reactive RMgCl?LiCl, are of exceptional synthetic utility. Nevertheless, it is still not fully understood which species these compounds form in solution and, in particular, in which way LiCl exerts its reactivity‐enhancing effect. A combination of electrospray‐ionization mass spectrometry, electrical conductivity measurements, NMR spectroscopy (including diffusion‐ordered spectroscopy), and quantum chemical calculations is used to analyze solutions of RMgCl (R=Me, Et, Bu, Hex, Oct, Dec, iPr, tBu, Ph) in tetrahydrofuran and other ethereal solvents in the absence and presence of stoichiometric amounts of LiCl. In tetrahydrofuran, RMgCl forms mononuclear species, which are converted into trinuclear anions as a result of the concentration increase experienced during the electrospray process. These trinuclear anions are theoretically predicted to adopt open cubic geometries, which remarkably resemble structural motifs previously found in the solid state. The molecular constituents of RMgCl and RMgCl?LiCl are interrelated via Schlenk equilibria and fast intermolecular exchange processes. A small portion of the Grignard reagent also forms anionic ate complexes in solution. The abundance of these more electron‐rich and hence supposedly more nucleophilic ate complexes strongly increases upon the addition of LiCl, thus rationalizing its beneficial effect on the reactivity of Grignard reagents. 相似文献
10.
We study weakly disordered quantum wires whose width is large compared to the Fermi wavelength. It is conjectured that such wires display universal metallic behavior as long as their length is shorter than the localization length (which increases with the width). The random matrix theory that accounts for this behavior—the DMPK theory—rests on assumptions that are in general not satisfied by realistic microscopic models. Starting from the Anderson model on a strip, we show that a twofold scaling limit nevertheless allows to recover rigorously the fundaments of DMPK theory, thus opening a way to settle some conjectures on universal metallic behavior. 相似文献