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101.
Komatsu T Wang RM Zunszain PA Curry S Tsuchida E 《Journal of the American Chemical Society》2006,128(50):16297-16301
We present the photophysical properties of complexes of recombinant human serum albumin (rHSA) with Zn(II)-protoporphyrin IX (ZnPP) and their activities in the photosensitized reduction of water to hydrogen (H2) using methyl viologen (MV2+) as an electron relay. The ZnPP is bound in subdomain IB of wild-type rHSA [rHSA(wt] by an axial coordination of Tyr-161 and, in the rHSA(I142H/Y161L) mutant [rHSA(His], by a His-142 coordination. Both the rHSA(wt)-ZnPP and rHSA(His)-ZnPP complexes showed a long-lived photoexcited triplet state with lifetimes (tauT) of 11 and 2.5 ms, respectively. The accommodation of ZnPP into the protein matrix efficiently eliminated the collisional triplet self-quenching process. The addition of a water-soluble electron acceptor, MV2+, resulted in a significant decrease in the triplet lifetime. The transition absorption spectrum revealed the oxidative quenching of rHSA-3ZnPP* by MV2+. The quenching rate constant (kq) and backward electron transfer rate constant (kb) were determined to be 1.4 x 10(7) and 4.7 x 10(8) M(-1) s(-1) for rHSA(wt)-ZnPP. In the presence of the colloidal PVA-Pt as a catalyst and triethanolamine (TEOA) as a sacrificial electron donor, the photosensitized reduction of water to H2 takes place. The efficiency of the photoproduction of H2 was greater than that of the system using the well-known organic chromophore, tetrakis(1-methylpyridinium-4-yl)porphinatozinc(II) (ZnTMPyP4+), under the same conditions. 相似文献
102.
Seiji Yamaguchi Nao Tsuchida Kayoko Umeda Hajime Yokoyama Masahiro Miyazawa Yoshiro Hirai 《Journal of heterocyclic chemistry》2006,43(3):657-662
103.
Hiroaki Inoue Yuji Arai Tsunao Kishida Masaharu Shin-Ya Ryu Terauchi Shuji Nakagawa Masazumi Saito Shinji Tsuchida Atsuo Inoue Toshiharu Shirai Hiroyoshi Fujiwara Osam Mazda Toshikazu Kubo 《Ultrasonics》2014
The goal of this feasibility study was to examine whether sonoporation assisted transduction of siRNA could be used to ameliorate arthritis locally. If successful, such approach could provide an alternative treatment for the patients that have or gradually develop adverse response to chemical drugs. Tumor necrosis factor alpha (TNF-α) produced by synovial fibroblasts has an important role in the pathology of rheumatoid arthritis, inducing inflammation and bone destruction. In this study, we injected a mixture of microbubbles and siRNA targeting TNF-α (siTNF) into the articular joints of rats, and transduced siTNF into synovial tissue by exposure to a collimated ultrasound beam, applied through a probe 6 mm in diameter with an input frequency of 3.0 MHz, an output intensity of 2.0 W/cm2 (spatial average temporary peak; SATP), a pulse duty ratio of 50%, and a duration of 1 min. Sonoporation increased skin temperature from 26.8 °C to 27.3 °C, but there were no adverse effect such as burns. The mean level of TNF-α expression in siTNF-treated knee joints was 55% of those in controls. Delivery of siTNF into the knee joints every 3 days (i.e., 7, 10, 13, and 16 days after immunization) by in vivo sonoporation significantly reduced paw swelling on days 20–23 after immunization. Radiographic scores in the siTNF group were 56% of those in the CIA group and 61% of those in the siNeg group. Histological examination showed that the number of TNF-α positive cells was significantly lower in areas of pannus invasion into the ankle joints of siTNF- than of siNeg-treated rats. These results indicate that transduction of siTNF into articular synovium using sonoporation may be an effective local therapy for arthritis. 相似文献
104.
The surface tension of aqueous solutions of a sodium chloride (NaCl)-decyl methyl sulfoxide (DeMS) mixture was measured as a function of the total molality of the mixture and the mole fraction of DeMS in the mixture at 298.15 K under atmospheric pressure. The total surface density of the mixture and the mole fraction of DeMS in the adsorbed film and micelle were numerically evaluated by applying the thermodynamic treatment of surfactant mixture to the NaCl-DeMS mixture. Miscibility of NaCl and DeMS in the adsorbed film and micelle was clarified by use of the phase diagram of adsorption and micelle formation. Positive adsorption of NaCl was observed in the presence of DeMS and attributed to attractive interaction between the polar head group of DeMS molecule and Na+ or Cl- ions in the adsorbed film and micelle. The results were compared with those of NaCl-octyl methyl sulfoxide and NaCl-decyldimethylphosphine oxide mixtures to elucidate the structure effect of nonionic surfactant on the miscibility. 相似文献
105.
Tomoyuki Kobayashi Junji Yamamoto Takao Hirajima Hidemi Ishibashi Naoto Hirano Yong Lai Vladimir S. Prikhod'ko Shoji Arai 《Journal of Raman spectroscopy : JRS》2012,43(8):1126-1133
To assess the ability of densimetry for CO2 fluid in CO2 inclusions, we compare two methods, microthermometry and Raman microspectroscopic densimetry for CO2. The comparative experiment was performed for nine CO2 inclusions in three mantle xenoliths. The results are as follows: (1) microthermometry precisely determines CO2 density with the range of 0.65 to 1.18 g/cm3 compared with Raman microspectroscopic densimetry; (2) CO2 density obtained by Raman microspectroscopic densimetry is fairly consistent with that by microthermometry; (3) it is hard to determine CO2 density in CO2 inclusion with diameter of less than around 3 µm using microthermometry; and (4) microthermometry can be applied only to the CO2 inclusion whose CO2 density ranges from around 0.65 to 1.18 g/cm3, whereas the Raman microspectroscopic densimetry is applicable to CO2 density ranging from 0.1 to 1.24 g/cm3. The above features carry the potential for estimation of depth origin of mantle‐derived rocks. The depth where the rocks were trapped by host magma can be estimated using both geothermometric data and CO2 fluid density in CO2 inclusions in the rocks. Typical precisions of density of CO2 in CO2 inclusions obtained by the Raman microspectroscopic densimetry (~0.01 g/cm3) and by the microthermometry (< 0.001 g/cm3) correspond to uncertainties in the depth origin of 2.4 km and < 1.7 km, respectively, at 1000 ± 50 °C. In case of the mantle under 750–1250 °C and 1 GPa, the CO2 fluid has a density ranging from 1.06 g/cm3 to 1.21 g/cm3, which are well measured by the Raman microspectroscopic densimetry. Combination of both densimetries for CO2 in mantle minerals elucidates the deep structure of the Earth. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
106.
Hidemi Ishibashi Masashi Arakawa Junji Yamamoto Hiroyuki Kagi 《Journal of Raman spectroscopy : JRS》2012,43(2):331-337
The relationship between Mg# [ = 100 Mg/(Mg + Fe) in mol] and the Raman shift was analyzed precisely for olivine [(Mg, Fe)2SiO4] samples with Mg# between 100 and 62.8. Two prominent peaks at 826–820 cm−1 (peak 1) and 858–849 cm−1 (peak 2) and three subordinate peaks at 883–881 cm−1 (peak 3), 920–914 cm−1 (peak 4), and 967–951 cm−1 (peak 5) were observed to shift monotonously to lower wavenumbers with decreasing Mg#. The ΔMg#( = Mg#ref − Mg#) versus Δν(= νref − ν) can be linearly regressed for each peak as ΔMg# = A Δν, where ν is a peak wavenumber of olivine with Mg# ranging from 100 to 62.8, and νref is that of olivine with a reference value of Mg#, namely, Mg#ref. We set Mg#ref as 100 (i.e.pure forsterite Mg2SiO4) whereas A is a regression parameter (5.789, 4.294, 12.34, 6.348, and 2.09, respectively,for peaks 1, 2, 3, 4, and 5). This equation enables us to avoid small inter‐laboratory differences of wavenumber calibration. The equation for peak 2 yields estimations of Mg# in geologically satisfactory precision, ± 1 Mg# (1σ) in the Mg# range of 100–62.8. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
107.
Daisuke Suzuki Tomoyo Yamagata Koji Horigome Kiyoshi Shibata Akira Tsuchida Tsuneo Okubo 《Colloid and polymer science》2012,290(2):107-117
Influence of the gel size on the morphology, phase diagram, and reflection spectroscopy of the colloidal crystals of thermo-sensitive
gel spheres, poly (N-isopropylacrylamide) (pNIPAm), was discussed by adding the data of two gel samples of pNIPAm(400–5) and pNIPAm(600–5) of
412 nm (at 25 °C) and 220 nm (at 45 °C) and of 517 nm (at 20 °C) and 294 nm (at 45 °C), respectively. Colloidal single crystals
formed, but not so large compared with the giant crystals of small pNIPAm gels reported previously. The suspensions even with
ion-exchange resins were turbid and hard to observe the single crystals clearly with the naked eyes as gel size increased.
The critical concentration of melting decreased sharply as the suspensions were deionized with coexistence of the mixtures
of cation- and anion-exchange resins. The critical concentration increased as the gel size increased and/or dispersion temperature
increased. Density of the gel spheres increased as their size increased. These results demonstrated that the colloidal crystallization
takes place by the extended electrical double layers formed around the gel spheres in addition of the excluded volume effect of the gels. Contribution of the electrical double layers on the crystallization increased sharply as temperature increased
and gel concentration decreased, respectively. The contribution also increased slightly as sphere size increased, when comparison
was made at the same gel concentration in wt.%. The present work clarified that the colloidal interfaces, which are inevitable
for the formation of the electrical double layers, are formed between the water phase and gel spheres, though the gel spheres
contain a lot of water molecules at the inner sphere region. 相似文献
108.
Noguchi M Nakamura M Ohno A Tanaka T Kobayashi A Ishihara M Fujita M Tsuchida A Mizuno M Shoda S 《Chemical communications (Cambridge, England)》2012,48(45):5560-5562
An efficient chemo-enzymatic process for construction of the α-linked disaccharide unit (GlcNAcα1-4Gal) found in gastric mucin has been developed. The process consists of a one-step preparation of a novel triazine type glycosyl donor in water and the subsequent transglycosylation to a galactose derivative catalysed by α-N-acetylglucosaminidase. 相似文献
109.
Hidemi Nagao Yasuhito Ohta Takashi Yoshimoto Hiroaki Saito Jun Maki Hiroyuki Kawabe Koji Ohta Kiyoshi Nishikawa 《International journal of quantum chemistry》2001,84(6):686-693
We calculate the optical properties such as the polarization, the (hyper)polarizabilities, the critical vector potential, etc., in terms of the non‐Hermitian Anderson model of a 6‐site ring model. The dependence of the optical properties on the delocalization transition is investigated. It is found that all the total optical properties nonlinearly increase with the increase of the delocalization. © 2001 John Wiley & Sons, Inc. Int J Quantum Chem, 2001 相似文献
110.
A. Tsuchida K. Taguchi E. Takyo H. Yoshimi S. Kiriyama T. Okubo M. Ishikawa 《Colloid and polymer science》2000,278(9):872-877
Rate coefficients (k) in the colloidal crystallization of monodispersed silica spheres in the presence of sodium chloride are studied in microgravity
achieved by parabolic flights of an aircraft. Time-resolved reflection spectroscopy is made with a continuous circulating-type
stopped-flow cell system. The k values decrease as the salt concentration increases both at 0 and 1 G and those in microgravity are smaller than those in
normal gravity by 16% (maximum), especially in water and in the presence of a small amount of the salt lower than 2 × 10−6 mol/l. The rates in flight at 1 G are larger by 15% (maximum) compared with those at 1 G on the ground. The k values obtained at 0 G, 1 G in flight and 1 G on the ground agree excellently with each other for the suspensions with 3 × 10−6 and 4 × 10−6 mol/l sodium chloride. Disappearance of the downward diffusion of spheres and no convection of the suspensions are important
for retardation in microgravity.
Received: 20 January 2000 Accepted: 9 March 2000 相似文献