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排序方式: 共有68条查询结果,搜索用时 156 毫秒
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McDonough JE Weir JJ Carlson MJ Hoff CD Kryatova OP Rybak-Akimova EV Clough CR Cummins CC 《Inorganic chemistry》2005,44(9):3127-3136
The kinetics of the oxidative addition of PhSeSePh and PhTeTePh to the stable 17-electron complex *Cr(CO)3C5Me5 have been studied utilizing stopped-flow techniques. The rates of reaction are first-order in each reactant, and the enthalpy of activation decreases in going from Se (deltaH(double dagger) = 7.0 +/- 0.5 kcal/mol, deltaS(double dagger) = -22 +/- 3 eu) to Te (deltaH(double dagger) = 4.0 +/- 0.5 kcal/mol, deltaS(double dagger) = -26 +/- 3 eu). The kinetics of the oxidative addition of PhSeH and *Cr(CO)3C5Me5 show a change in mechanism in going from low (overall third-order) to high (overall second-order) temperatures. The enthalpies of the oxidative addition of PhE-EPh to *Cr(CO)3C5Me5 in toluene solution have been measured and found to be -29.6, -30.8, and -28.9 kcal/mol for S, Se, and Te, respectively. These data are combined with enthalpies of activation from kinetic studies to yield estimates for the solution-phase PhE-EPh bond strengths of 46, 41, and 33 kcal/mol for E = S, Se, and Te, respectively. The corresponding Cr-EPh bond strengths are 38, 36, and 31 kcal/mol. Two methods have been used to determine the enthalpy of hydrogenation of PhSeSePh in toluene on the basis of reactions of HSPh and HSePh with either *Cr(CO)3C5Me5 or 2-pyridine thione. These data lead to a thermochemical estimate of 72 kcal/mol for the PhSe-H bond strength in toluene solution, which is in good agreement with kinetic studies of H atom transfer from HSePh at higher temperatures. The reaction of H-Cr(CO)3C5Me5 with PhSe-SePh is accelerated by the addition of a Cr radical and occurs via a rapid radical chain reaction. In contrast, the reaction of PhTe-TePh and H-Cr(CO)3C5Me5 does not occur at any appreciable rate at room temperature, even in the presence of added Cr radicals. This is in keeping with a low PhTe-H bond strength blocking the chain and implies that H-TePh < or = 63 kcal/mol. Structural data are reported for PhSe-Cr(CO)3C5Me5 and PhS-Cr(CO)3C5Me5. The two isostructural complexes do not show signs of an increase in steric strain in terms of metal-ligand bonds or angles as the Cr-EPh bond is shortened in going from Se to S. Bond strength estimates of the PhE-H and PhE-EPh derived from density functional theory calculations are in reasonable agreement with experimental data for E = Se but not for E = Te. The nature of the singly occupied molecular orbital of the *EPh radicals is calculated to show increasing localization on the chalcogenide atom in going from S to Se to Te. 相似文献
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Bolton RD Bowman JD Cooper MD Frank JS Hallin AL Heusi PA Hoffman CM Hogan GE Mariam FG Matis HS Mischke RE Nagle DE Piilonen LE Sandberg VD Sanders GH Sennhauser U Werbeck R Williams RA Wilson SL Hofstadter R Hughes EB Ritter MW Grosnick D Wright SC Highland VL McDonough J 《Physical review letters》1986,56(23):2461-2464
35.
Cation–π Interactions Contribute to Substrate Recognition in γ‐Butyrobetaine Hydroxylase Catalysis 下载免费PDF全文
Jos J. A. G. Kamps Amjad Khan Dr. Hwanho Choi Robert K. Lesniak Dr. Jürgen Brem Dr. Anna M. Rydzik Dr. Michael A. McDonough Prof. Christopher J. Schofield Prof. Timothy D. W. Claridge Dr. Jasmin Mecinović 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(4):1270-1276
γ‐Butyrobetaine hydroxylase (BBOX) is a non‐heme FeII‐ and 2‐oxoglutarate‐dependent oxygenase that catalyzes the stereoselective hydroxylation of an unactivated C?H bond of γ‐butyrobetaine (γBB) in the final step of carnitine biosynthesis. BBOX contains an aromatic cage for the recognition of the positively charged trimethylammonium group of the γBB substrate. Enzyme binding and kinetic analyses on substrate analogues with P and As substituting for N in the trimethylammonium group show that the analogues are good BBOX substrates, which follow the efficiency trend N+>P+>As+. The results reveal that an uncharged carbon analogue of γBB is not a BBOX substrate, thus highlighting the importance of the energetically favorable cation–π interactions in productive substrate recognition. 相似文献
36.
We find explicit PD-sets for partial permutation decoding of the generalized Reed-Muller codes from the affine geometry designs of points and lines in dimension 3 over the prime field of order p, using the information sets found in [8].
This work was supported by the DoD Multidisciplinary University Research Initiative (MURI) program administered by the Office
of Naval Research under Grant N00014-00-1-0565. 相似文献
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John A. Howarter Ming Liu Walter G. McDonough Christopher Soles Gale A. Holmes 《Journal of Polymer Science.Polymer Physics》2017,55(23):1711-1717
It is understood that the ballistic resistance of aromatic polyamide fibers is related to the fiber's ultimate tensile strength, strain‐to‐failure, and Young's modulus. Ideal high‐performance ballistic materials maximize these properties while minimizing material density. Equally important is long‐term mechanical and chemical stability: the fibers should not exhibit performance loss over their lifetime. However, less is known quantitatively about their modes of degradation, and experimental methods to quantify the aging and degradation in these fibers are critical. Multiple variations of next generation high‐performance fibers have been investigated under chemical and mechanical accelerated aging conditions. Performance losses have been empirically correlated to chemical degradation of the polymer chain and nanostructural changes in the fiber morphology through X‐ray photoelectron spectroscopy (XPS). Here, we introduce positron annihilation lifetime spectroscopy measurements as a sensitive method to quantify the early onset of damage in the flexed fibers as quantified through changes in the nanoscale void structure in the material. Published 2017.? J. Polym. Sci., Part B: Polym. Phys. 2017 , 55 , 1711–1717 相似文献
40.
Dominguez-Medina S McDonough S Swanglap P Landes CF Link S 《Langmuir : the ACS journal of surfaces and colloids》2012,28(24):9131-9139
We present in situ observations of adsorption of bovine serum albumin (BSA) on citrate-stabilized gold nanospheres. We implemented scattering correlation spectroscopy as a tool to quantify changes in the nanoparticle brownian motion resulting from BSA adsorption onto the nanoparticle surface. Protein binding was observed as an increase in the nanoparticle hydrodynamic radius. Our results indicate the formation of a protein monolayer at similar albumin concentrations as those found in human blood. Additionally, by monitoring the frequency and intensity of individual scattering events caused by single gold nanoparticles passing the observation volume, we found that BSA did not induce colloidal aggregation, a relevant result from the toxicological viewpoint. Moreover, to elucidate the thermodynamics of the gold nanoparticle-BSA association, we measured an adsorption isotherm which was best described by an anticooperative binding model. The number of binding sites based on this model was consistent with a BSA monolayer in its native state. In contrast, experiments using poly(ethylene glycol)-capped gold nanoparticles revealed no evidence for adsorption of BSA. 相似文献