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21.
Hiromasa Aono Dingy Wen Li Zang Damian Houde R. Blake Pepinsky David R.H. Evans 《Journal of chromatography. A》2010,1217(32):5225-5232
Protein trisulfide linkages are generated by the post-translational insertion of a sulfur atom into a disulfide bond. Molecular heterogeneity was detected in a recombinant IgG1 monoclonal antibody (mAb) and attributed to the presence of a protein trisulfide moiety. The predominant site of trisulfide modification was the bond between the heavy and light chains. The trisulfide was eliminated during purification of the IgG1 mAb via a cysteine wash step incorporated into Protein A affinity column chromatography. Analysis of the cysteine-treated mAb by electrophoresis and peptide mapping indicated that the trisulfide linkages were efficiently converted to intact disulfide bonds (13% trisulfide decreased consistently to 1% or less) without disulfide scrambling or an increase in free sulfhydryls. The on-column trisulfide conversion caused no change in protein folding detectable by hydrogen/deuterium exchange or differential scanning calorimetry. Consistent with this, binding of the mAb to its antigen in vitro was insensitive to the presence of the trisulfide modification and to its removal by the on-column cysteine treatment. Similar, high efficiency trisulfide conversion was achieved for a second IgG1 mAb using the column wash strategy (at least 7% trisulfide decreased to 1% or less). Therefore, trisulfide/disulfide heterogeneity can be eliminated from IgG1 molecules via a convenient and inexpensive procedure compatible with routine Protein A affinity capture. 相似文献
22.
Naoto Sugimoto Seiji Fukushima Yasuhiro Suzuki Yoshihisa Sakai Hiromasa Tanobe Takeshi Kurosaki Kazuto Noguchi Kimio Oguchi Hiromu Toba 《光学学报》2003,23(Z1)
A new generation of network interface card for fiber-to-the-desktop has been fabricated. The fabricated card is PC-card size and suitable for notebook PCs. It could become the key element in the coming optical Ethernet age. 相似文献
23.
Synergic Catalysis of PdCu Alloy Nanoparticles within a Macroreticular Basic Resin for Hydrogen Production from Formic Acid 下载免费PDF全文
Prof. Dr. Kohsuke Mori Dr. Hiromasa Tanaka Masahiro Dojo Prof. Dr. Kazunari Yoshizawa Prof. Dr. Hiromi Yamashita 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(34):12085-12092
Highly dispersed PdCu alloy nanoparticles have been successfully prepared within a macroreticular basic resin bearing ?N(CH3)2 functional groups. This previously unappreciated combination of alloy is first proven to be responsible for the efficient production of high‐purity H2 from formic acid (HCOOH) dehydrogenation for chemical hydrogen storage. By the addition of Cu, the electronically promoted Pd sites show significantly higher catalytic activity as well as a better tolerance towards CO poisoning as compared to their monometallic Pd counterparts. Experimental and DFT calculation studies revealed not only the synergic alloying effect but also cooperative action by the ?N(CH3)2 groups within the resin play crucial roles in achieving exceptional catalytic performances. In addition to the advantages such as, facile preparation method, free of additives, recyclable without leaching of active component, and suppression of unfavorable CO formation less than 3 ppm, the present catalytic system is cost‐effective because of the superior catalytic activity compared with that of well‐established precious PdAg or PdAu catalysts. The present catalytic system is particularly desirable for an ideal hydrogen vector in terms of potential industrial application for fuel cells. 相似文献
24.
Kazuki Abe Noriko Ogawa Hiromasa Nagase Tomohiro Endo Haruhisa Ueda 《Journal of inclusion phenomena and macrocyclic chemistry》2011,70(3-4):385-388
Although phase-solubility studies have often been used to evaluate the interaction of cyclodextrins (CDs) with various drugs, hundreds of milligrams of both CD and drug are required to prepare a phase diagram. A method that would require considerably less material for evaluating complex formation between a CD and guest compound is therefore needed. We previously reported the detection of the interactions between ??-CD and various drugs using a Biacore® system. In this study, we succeeded in immobilizing 6-monodeoxy-6-monoamino-??-CD on the gold surface of a sensor chip and in detecting the interactions between the immobilized ??-CD and various drugs. The interaction processes were kinetically analyzed using Biacore®. The surface plasmon resonance sensorgrams indicated that the association and dissociation rates of the interactions between ??-CD and drugs were faster than those between ??-CD and drugs. Although the association constants calculated from the sensorgrams were smaller than those calculated from phase-solubility studies, good correlation was shown between these data. 相似文献
25.
A novel synthetic path to sequosempervirin A was established by employing a samarium diiodide promoted intramolecular Barbier-type reaction of the lactonic iodide, in which the key structural feature, a spiro[4.5]decane ring system, could be constructed by controlling the stereochemistry of the hydroxyl group at the 8-position. The absolute configuration of natural sequosempervirin A was revised to be 4S based on this synthesis. 相似文献
26.
Yokoe H Mitsuhashi C Matsuoka Y Yoshimura T Yoshida M Shishido K 《Journal of the American Chemical Society》2011,133(23):8854-8857
Enantiocontrolled total syntheses of the breviones A, B, and C have been accomplished using a highly diastereoselective oxidative coupling of an α-pyrone with a tricyclic diene prepared from an optically pure Wieland-Miescher ketone derivative through the 7-endo-trig mode of acyl radical cyclization. 相似文献
27.
Hiromasa Kurosaki Rakesh K Sharma Masami Otsuka Masafumi Goto 《Analytical sciences》2003,19(4):647-648
The structure of 7,8-dihydroxy-4-methylcoumarin was determined by an X-ray diffraction method. The compound crystallized in the triclinic space group P1, Z = 2, with a = 7.631(2), b = 9.456(5), c = 7.075(3)A, alpha = 103.13(3), beta = 91.84(3), gamma= 68.21(3) degrees, and V= 460.9(3)A3. The X-ray crystal structure was also compared with those of 5,7-dihydroxy-4-methylcoumarin and 7-hydroxy-4-methylcoumarin. 相似文献
28.
Conjugated polymers consisting of pyrrole or an N‐substituted pyrrole bridged by methine with a mesogenic group were synthesized. Chemical structures of the products were confirmed with IR, NMR, UV–visible (UV–vis) spectroscopy, and gel permeation chromatography analysis. Liquid crystallinity was examined with differential scanning calorimetry measurements and polarizing optical microscopy observations. Liquid crystal domains of the polymer were macroscopically oriented in one direction by an external magnetic force (10 Tesla). The polymer orientation was confirmed by optical microscopy and X‐ray analysis. One of the polymers exhibited a striated fan‐shaped texture when observed with a polarizing optical microscope. This is attributed to the formation of a chiral smectic C (SmC*) phase, which is a property of ferroelectricity. Spontaneous polarization of the polymer occurred at 110 nC/cm2. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 616–629, 2005 相似文献
29.
30.
Kenkichi Murakami Hiromasa Nakanishi 《Journal of polymer science. Part A, Polymer chemistry》1976,14(1):265-270
The structural changes brought about by chemical reactions are reflected in the viscoelastic behavior of polymers. Viscoelastic behavior induced by such chemical reactions is called chemorheology. This phenomenon is not readily observed in linear polymers, because molecular flow by diffusion is generally much more rapid than relaxation or flow caused by chemical reaction. It has become possible, however, to treat chemorheology of linear polymers theoretically by taking such physical flow into consideration. The experimental results for linear polystyrene compared with the theoretical ones are described in this paper. Good agreement between theoretical results and experimental ones is obtained for monodisperse polystyrene with low concentration of accelerators. 相似文献