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1.
KL Britton HF Rogers Y Asano T Dairi Y Kato TJ Stillman DW Rice 《Acta crystallographica. Section D, Biological crystallography》1998,53(4):124-126
The novel NAD+-linked opine dehydrogenase from a soil isolate Arthrobacter sp. strain 1C belongs to an enzyme superfamily whose members exhibit quite diverse substrate specificites. Crystals of this opine dehydrogenase, obtained in the presence or absence of co-factor and substrates, have been shown to diffract to beyond 1.8 ? resolution. X-ray precession photographs have established that the crystals belong to space group P21212, with cell parameters a = 104.9, b = 80.0, c = 45.5 ? and a single subunit in the asymmetric unit. The elucidation of the three-dimensional structure of this enzyme will provide a structural framework for this novel class of dehydrogenases to enable a comparison to be made with other enzyme families and also as the basis for mutagenesis experiments directed towards the production of natural and synthetic opine-type compounds containing two chiral centres. 相似文献
2.
R. F. Storey J. S. Wiggins A. D. Puckett 《Journal of polymer science. Part A, Polymer chemistry》1994,32(12):2345-2363
Bioabsorbable poly(ester-urethane) networks were synthesized from ethyl 2,6-diisocyanatohexanoate (L -lysine diisocyanate) (LDI) and a series of polyester triols. LDI was synthesized by refluxing L-lysine monohydrochloride with ethanol to form the ester, which was subsequently refluxed with 1,1,1,3,3,3-hexamethyldisilazane to yield a silazane-protected intermediate. This product was then phosgenated using triphosgene. Polyester triols were synthesized from D,L-lactide, ?-caprolactone, or comonomer mixtures thereof, using glycerol as initiator and stannous octoate as catalyst. Polyurethane networks were cured using [NCO]/[OH] = 1.05 and stannous octoate (0.05 wt %) for 24 h at room temperature and pressure and 24 h at 50°C and 0.1 mm Hg. LDI-based polyurethane networks were totally amorphous and possessed very low sol contents. Networks based on poly (D,L-lactide) triols were rigid (Tg ∽ 60°C) with ultimate tensile strengths of ~ 40–70 MPa, tensile moduli of ~ 1.2–2.0 GPa, and ultimate elongations of ~ 4–10%. Networks based on ?-caprolactone triols were low-modulus elastomers with tensile strengths and moduli of ~ 1–4 MPa and ~ 3–6 GPa, respectively, and ultimate elongations of ~ 50–300%. Networks based on copolymers displayed physical properties consistent with monomer composition and were tougher than the networks based on the homopolymers. Tensile strengths for the copolymers were ~ 3–25 MPa with ultimate elongations up to 600%. Hydrolytic degradation under simulated physiological conditions showed that D ,L -lactide homopolymer networks were the most resistant to degradation, undergoing virtually no change in mass or physical properties for 60 days. ?-Caprolactone-based networks were resistant to degradation for 40 days, and high-lactide copolymer-based networks suffered substantial losses in physical properties after only 3 days. © 1994 John Wiley & Sons, Inc. 相似文献
3.
Although 7-methoxy- and 6,7-dimethoxy-2-methyl-4-vinyl-isocarbostyrils could not be isolated and characterised, they have been generated in situ and shown to undergo cyclo-addition reactions with typical dienophiles. The enol acetate of 2-methyl-4-acetylisocarbostyril has also been trapped as its adduct with maleic anhydride and with p-benzoquinone. 相似文献
4.
Gyarfas BJ Wiggins B Zosel M Hipps KW 《Langmuir : the ACS journal of surfaces and colloids》2005,21(3):919-923
Scanning tunneling microscopy (STM) is utilized to study the solution-solid interface formed between Au(111) and solutions of coronene in hexanoic, heptanoic, and octanoic acids. In all three cases adsorbed coronene is observed and lays flat on the metal surface. Heptanoic and hexanoic acid solutions produce a hexagonal symmetry monolayer. For the heptanoic and hexanoic cases, dipole-image dipole interactions and H bonding stabilize a surface structure in which 12 acid molecules surround each coronene and produce a coronene spacing of 1.45 nm. In the case of octanoic acid as solvent, the incorporation of the solvent into the monolayer is not as strongly favored. The coronene spacing can range from close-packed (1.2 nm) with no solvent presumed present in the monolayer, to 1.50 nm with up to 12 solvent molecules surrounding each coronene. The close-packed regions have hexagonal symmetry, as do those with the largest (1.5 nm) spacing. Heptanoic acid solutions give the clearest STM images and are associated with the most stable two-component monolayer. The present paper demonstrates that non-covalent interactions at the solution-metal interface can lead to complex multicomponent monolayer structures. 相似文献
5.
6.
Harry Wiggins Ansie Harding 《International Journal of Mathematical Education in Science & Technology》2017,48(8):S16-S29
ABSTRACTThis paper presents an enrichment case study to showcase a possible avenue for attending to the needs of academically strong mathematics students. We report on a group of university students who were presented with the opportunity of exploring a specific first year mathematics topic deeper, using an inquiry-based learning approach as part of an enrichment programme. Following the intervention, students completed a questionnaire and a few were interviewed to establish their experiences of the enrichment programme. We discuss the successes and pitfalls of the intervention and report on the impact it had on the participants. 相似文献
7.
In Vivo Endoscopic Tissue Identification by Rapid Evaporative Ionization Mass Spectrometry (REIMS) 下载免费PDF全文
Dr. Julia Balog Dr. Sacheen Kumar James Alexander Ottmar Golf Dr. Juzheng Huang Tom Wiggins Nima Abbassi‐Ghadi Dr. Attila Enyedi Dr. Sandor Kacska James Kinross Prof. George B. Hanna Prof. Jeremy K. Nicholson Prof. Zoltan Takats 《Angewandte Chemie (International ed. in English)》2015,54(38):11059-11062
Gastrointestinal cancers are a leading cause of mortality, accounting for 23 % of cancer‐related deaths worldwide. In order to improve outcomes from these cancers, novel tissue characterization methods are needed to facilitate accurate diagnosis. Rapid evaporative ionization mass spectrometry (REIMS) is a technique developed for the in vivo classification of human tissue through mass spectrometric analysis of aerosols released during electrosurgical dissection. This ionization technique was further developed by utilizing surface induced dissociation and was integrated with an endoscopic polypectomy snare to allow in vivo analysis of the gastrointestinal tract. We tested the classification performance of this novel endoscopic REIMS method in vivo. It was shown to be capable of differentiating between healthy layers of the intestinal wall, cancer, and adenomatous polyps based on the REIMS fingerprint of each tissue type in vivo. 相似文献
8.
S. Wiggins 《Zeitschrift für Angewandte Mathematik und Physik (ZAMP)》1999,46(1):585-616
In this paper we develop analytical techniques for proving the existence of chaotic dynamics in systems where the dynamics is generated by infinite sequences of maps. These are generalizations of the Conley-Moser conditions that are used to show that a (single) map has an invariant Cantor set on which it is topologically conjugate to a subshift on the space of symbol sequences. The motivation for developing these methods is to apply them to the study of chaotic advection in fluid flows arising from velocity fields with aperiodic time dependence, and we show how dynamics generated by infinite sequences of maps arises naturally in that setting. Our methods do not require the existence of a homoclinic orbit in order to conclude the existence of chaotic dynamics. This is important for the class of fluid mechanical examples considered since one cannot readily identify a homoclinic orbit from the structure of the equations.¶We study three specific fluid mechanical examples: the Aref blinking vortex flow, Samelson's tidal advection model, and Min's rollup-merge map that models kinematics in the mixing layer. Each of these flows is modelled as a type of "blinking flow", which mathematically has the form of a linked twist map, or an infinite sequence of linked twist maps. We show that the nature of these blinking flows is such that it is possible to have a variety of "patches" of chaos in the flow corresponding to different length and time scales. 相似文献
9.
In this paper we derive two rigorous properties of residence-time distributions for flows in pipes and mixers motivated by computational results of Khakhar et al. [Chem. Eng. Sci. 42, 2909 (1987)], using some concepts from ergodic theory. First, a curious similarity between the isoresidence-time plots and Poincare maps of the flow observed in Khakhar et al. is resolved. It is shown that in long pipes and mixers, Poincare maps can serve as a useful guide in the analysis of isoresidence-time plots, but the two are not equivalent. In particular, for long devices isoresidence-time sets are composed of orbits of the Poincare map, but each isoresidence-time set can be comprised of many orbits. Second, we explain the origin of multimodal residence-time distributions for nondiffusive motion of particles in pipes and mixers. It is shown that chaotic regions in the Poincare map contribute peaks to the appropriately defined and rescaled axial distribution functions. (c) 1999 American Institute of Physics. 相似文献
10.
Zheng Chen Daniel R. Dreyer Zong‐quan Wu Kelly M. Wiggins Zhenhua Jiang Christopher W. Bielawski 《Journal of polymer science. Part A, Polymer chemistry》2011,49(6):1421-1426
The synthesis and characterization of a novel family of main‐chain carbazole‐containing polymers using copper‐catalyzed azide‐alkyne cycloaddition chemistry is reported. The reactions were performed under mild conditions using readily available copper catalysts and ligands, which afforded polymeric products with Mws up to 18 kDa. Using a range of techniques, the polymers were found to exhibit a glass transition temperature (Tg) of 85 °C, high thermal stability (Td = 274 °C), and high photoluminescent quantum efficiency (?f = 0.29; λem = 448 nm), which underscore their potential for use in organic light‐emitting diodes or other emissive devices, particularly where efficient blue emission is of value. The approach described offers practical advantages over other synthetic methods used to prepare main‐chain carbazole‐containing polymers, especially with regard to the lack of need for rigorously inert conditions and the absence of byproducts generated during the polymerization reaction. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献