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91.
92.
The generation mechanism of the screech tone in the helical oscillation mode is mainly investigated using a series of instantaneous schlieren photographs. From the photographs, five evanescent sound sources are observed as prominent points along the jet axis. The sound source for the dominant helical oscillation mode is found to be the second prominent point which moves along a circular orbit in a plane perpendicular to the jet axis and just downstream of the rear edge of the third shock cell. It is shown that the speed of a moving sound source is supersonic and that the Mach cone generated by the moving sound source forms the helical-shaped wave front of the screech tone for the helical oscillation mode of the jet. This idea of the moving sound source is well supported by a measured directionality of the screech tone. Sound sources of the other oscillation modes appearing in the other pressure ratio ranges are also described. 相似文献
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94.
T. Yamaya K. Umeda T. Suehiro K. Takimoto R. Wada E. Takada M. Fukada J. Schimizu Y. Okuma 《Physics letters. [Part B]》1980,90(3):219-223
The (d, 6Li) reaction was studied at Ed = 54.25 MeV on the target nuclei 12C, 16O, 24Mg, 40Ca and 58Ni. The data were analyzed with finite-range DWBA calculations. The absolute values of the α-cluster spectroscopic factors and the target mass dependence of the relative Sα were in agreement with those in the (p, pα) reaction at Ep = 100 and 157 MeV. The theoretical calculations of the relative Sα were in better agreement with the experimental data at higher energy than at the lower energies. 相似文献
95.
Umeda Y Furihata K Sakuda S Nagasawa H Ishigami K Watanabe H Izumikawa M Takagi M Doi T Nakao Y Shin-ya K 《Organic letters》2007,9(21):4239-4242
In the course of our screening program for regulators of a molecular chaperone GRP78 expression, we isolated a novel inhibitor of GRP78 expression, designated as prunustatin A, from Streptomyces violaceoniger 4521-SVS3. The planar structure of prunustatin A was determined to be an oxidized type of the neoantimycin family. Its absolute stereochemistry was established to be 2R, 4S, 6S, 7R, 9S, and 29S by analyzing chemically degraded components obtained from the derivative of prunustatin A. 相似文献
96.
Satoshi Aihara Norihiko Kamata Masato Umeda Shin-Ichi Kanezaki Koji Nagumo Daiyo Terunuma Koji Yamadam 《Optical Review》1999,6(5):393-395
We observed an electroluminescence (EL) of poly bis(p-propoxyphenyl)silane (PBPPS) from a double-layer device with an electron transport layer of 8-hydroxyquinoline aluminum (Alq3) for the first time. The EL spectrum at 77 K consisted of a PBPPS emission at 3.0 eV, which coincided with the photoluminescence spectrum, and a broad emission band between 1.8 and 2.7 eV. 相似文献
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99.
Performance benchmark tests of the multireference perturbation theory (MRPT2) calculation in the GAMESS suite of programs have been performed on a 128-node PC cluster system. The benchmark results point to two kinds of problems with GAMESS: network delay and slow access to disk files. To overcome these bottlenecks, we employ (semi-)direct atomic orbital integral calculations and a new algorithm for the "global sum" operation. These modifications produce remarkable performance improvements, especially in the 128-node PC cluster system, which was almost twice as fast in our version as in the original version. The modification of "global sum" also improved the performance of other types of molecular orbital calculations in GAMESS, such as density functional theory. 相似文献
100.
A new series of radioiodinated analogues of 1-[2-(3,4-dimethoxyphenyl)ethyl]-4-(3-phenylpropyl)piperazine (SA4503) was synthesized and evaluated as a potential brain sigma-1 receptor imaging ligands by single photon emission computed tomography (SPECT). Iodinated analogues of SA4503 (4a-c) were prepared from piperazine in a high yield. The in vitro competition binding studies using [3H] DTG (sigma-1, 2), [3H] (+)-pentazocine (sigma-1), and [3H] DTG in the presence of carbetapentane (sigma-2) as sigma receptor selective radioligands were revealed that iodinated analogues 4a-c possess high affinities to sigma receptors (IC50: 4a=7.1, 4b=31.0, and 4c=77.3 nM). In particular, the affinity of 4a, bearing iodine at ortho position on the phenyl ring, was 4.4 times greater than SA4503, and 3 times greater than that of haloperidol. The meta-iodo analogue 4b was the same to SA4503, the lead compound. The radioiodinated derivatives, [125I] 4a, 4b were synthesized no-carrier-added from the corresponding tributyltin precursors by the iododestannylation reaction with high yields. The binding of [125I] 4a, 4b have been characterized in the rat brain membranes. These compounds were indicated single population binding to sigma receptor with high affinity (4a: Kd=1.86+/-0.34 nM, Bmax=205+/-28.9 fmol/mg protein, 4b: Kd=3.30+/-0.51 nM, Bmax=231.5+/-13.8 fmol/mg protein). In vitro blocking studies were confirmed that the high specificity of 4a, 4b. These results suggest that radioiodinated 4a and 4b are promising sigma receptors imaging ligand for pursuing further in vivo studies. 相似文献