全文获取类型
收费全文 | 22946篇 |
免费 | 3524篇 |
国内免费 | 4685篇 |
专业分类
化学 | 17842篇 |
晶体学 | 533篇 |
力学 | 1068篇 |
综合类 | 555篇 |
数学 | 2761篇 |
物理学 | 8396篇 |
出版年
2024年 | 11篇 |
2023年 | 196篇 |
2022年 | 447篇 |
2021年 | 619篇 |
2020年 | 680篇 |
2019年 | 717篇 |
2018年 | 622篇 |
2017年 | 671篇 |
2016年 | 863篇 |
2015年 | 1018篇 |
2014年 | 1210篇 |
2013年 | 1704篇 |
2012年 | 1903篇 |
2011年 | 1986篇 |
2010年 | 1619篇 |
2009年 | 1584篇 |
2008年 | 1917篇 |
2007年 | 1778篇 |
2006年 | 1627篇 |
2005年 | 1393篇 |
2004年 | 1286篇 |
2003年 | 1040篇 |
2002年 | 1180篇 |
2001年 | 973篇 |
2000年 | 865篇 |
1999年 | 580篇 |
1998年 | 337篇 |
1997年 | 333篇 |
1996年 | 255篇 |
1995年 | 255篇 |
1994年 | 237篇 |
1993年 | 223篇 |
1992年 | 196篇 |
1991年 | 133篇 |
1990年 | 144篇 |
1989年 | 107篇 |
1988年 | 74篇 |
1987年 | 65篇 |
1986年 | 63篇 |
1985年 | 44篇 |
1984年 | 34篇 |
1983年 | 28篇 |
1982年 | 18篇 |
1981年 | 23篇 |
1980年 | 19篇 |
1979年 | 9篇 |
1978年 | 17篇 |
1976年 | 10篇 |
1974年 | 7篇 |
1973年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 390 毫秒
941.
Yuchuan Zhang Jiasheng Qian Zhuo KeXiangcheng Zhu Hong BiKangming Nie 《European Polymer Journal》2002,38(2):333-337
The intermolecular interactions between poly(vinyl chloride) (PVC) and poly(vinyl acetate) (PVAc) in tetrahydrofuran (THF), methyl ethyl ketone (MEK) and N,N′-dimethylformamide (DMF) were thoroughly investigated by the viscosity measurement. It has been found that the solvent selected has a great influence upon the polymer-polymer interactions in solution. If using PVAc and THF, or PVAc and DMF to form polymer solvent, the intrinsic viscosity of PVC in polymer solvent of (PVAc+THF) or (PVAc+DMF) is less than in corresponding pure solvent of THF or DMF. On the contrary, if using PVAc and MEK to form polymer solvent, the intrinsic viscosity of PVC in polymer solvent of (PVAc+MEK) is larger than in pure solvent of MEK. The influence of solvent upon the polymer-polymer interactions also comes from the interaction parameter term Δb, developed from modified Krigbaum and Wall theory. If PVC/PVAc blends with the weight ratio of 1/1 was dissolved in THF or DMF, Δb<0. On the contrary, if PVC/PVAc blends with the same weight ratio was dissolved in MEK, Δb>0. These experimental results show that the compatibility of PVC/PVAc blends is greatly associated with the solvent from which polymer mixtures were cast. The agreement of these results with differential scanning calorimetry measurements of PVC/PVAc blends casting from different solvents is good. 相似文献
942.
M. H. Lee C. W. Lee K. H. Hong Y. H. Choi B. H. Boo 《Journal of Radioanalytical and Nuclear Chemistry》1996,204(1):135-144
Depth distribution of239,240Pu and137Cs in the soils of South Korea have been studied. The average accumulated depositions were estimated roughly to be 54.8±32.1 Bq·m–2 for239,240Pu, 1.6±1.0 Bq· ·m–2 for238Pu and 1982.8±929.1 Bq·m–2 for137Cs. The activity ratios of239,240Pu/137Cs in soils were found to be in the narrow range of 0.0153 to 0.0364 with a mean value of 0.0230±0.006. The concentrations of239,240Pu and137Cs in soils decrease exponentially with increasing the soil depth. A significant correlation was found between the concentration of239,240Pu and that of137Cs. The activity ratios of239,240Pu/137Cs tend to increase slightly with increasing soil depth. 相似文献
943.
The properties of immobilized glucose oxidase (GOD) by the complexes of diethylaminoethyl cellulose(DEAEC) with different polymers, such as polymethylacrylic acid (PMAA), polyacrylic acid (PAA), polystyrene sulfonic acid (PSSA), polyvinylaleohol (PVA), polyethylene oxide (PEO) and styrene-maleic acid copolymer (PSMA) were investigated. The activity of immobilized GOD was obviously influenced by the component of the DEAEC complexes. The relative activity of the immobilized GOD reached to maximum and over 90% of the native GOD. when the DEAEC-PMAA DEAEC-PAA complexes were used as a carrier with the molar ratio of DEAEC and polyacid of about one. Michaelis constants (Km) of the immobilized enzymes of DEAEC-GOD-PMAA and DEAEC-GOD-PAA were determined to be 1.25 and 1.00, respectively. Moreover, the immobilized GOD has a good storage stability and cyclic life. 相似文献
944.
Yujie Wang Lifang Ruan Wai-Hung Lo Hong Chua Hoi-Fu Yu 《Applied biochemistry and biotechnology》2006,132(1-3):1015-1022
Polyhydroxyalkanoates (PHAs) are polyesters of hydroxyalkanoates synthesized by numerous bacteria as intracellular carbon
and energy storage compounds and accumulated as granules in the cytoplasm of cells. In this work, we constructed two recombinant
plasmids, pBE2C1, and pBE2C1AB, containing one or two PHA synthse, genes, respectively. The two plasmids were inserted into
Bacillus subtilis DB104 to generate modified strains, B. subtilis/pBE2C1 and B. subtilis/pBE2C1AB. The two recombinants strains were subjected to fermentation and showed PHA accumulation, the first reported example
of mcl-PHA production in B. subtilis. Gas Chromatography analysis identified the compound produced by B. subtilis/pBE2C1 to be a hydroxydecanoate-co-hydroxydodecanoate (HD-co-HDD) polymer whereas that produced by B. subtilis/pBE2C1AB was a hydroxybutyrate-co-hydroxyde-canoate-co-hydroxydodecanoate (HB-HD-HDD) polymer. 相似文献
945.
James V. Beitz C.W. Williams K.-S. Hong G.K. Liu 《Journal of solid state chemistry》2005,178(2):511-520
We have assessed the feasibility of carrying out time- and wavelength-resolved laser-induced fluorescence measurements of radiation damage in glassy silica. The consequences of alpha decay of Es-253 in LaPO4 nanophases embedded in silica were probed based on excitation of 5f states of Cm3+, Bk3+, and Es3+ ions. The recorded emission spectra and luminescence decays showed that alpha decay of Es-253 ejected Bk-249 decay daughter ions into the surrounding silica and created radiation damage within the LaPO4 nanophases. This conclusion is consistent with predictions of an ion transport code commonly used to model ion implantation. Luminescence from the 6D7/2 state of Cm3+was used as an internal standard. Ion-ion energy transfer dominated the dynamics of the observed emitting 5f states and strongly influenced the intensity of observed spectra. In appropriate sample materials, laser-induced fluorescence provides a powerful method for fundamental investigation of alpha-induced radiation damage in silica. 相似文献
946.
Cancer immunotherapy with immune checkpoint inhibitors (ICIs) has revolutionized the treatment of advanced cancers. However, the tumor microenvironment (TME) functions as a formidable barrier that severely impairs the efficacy of ICIs. While the crosstalk between tumor vessels and immune cells determines the nature of anti-tumor immunity, it is skewed toward a destructive cycle in growing tumors. First, the disorganized tumor vessels hinder CD8+ T cell trafficking into the TME, disable effector functions, and even kill T cells. Moreover, VEGF, the key driver of angiogenesis, interferes with the maturation of dendritic cells, thereby suppressing T cell priming, and VEGF also induces TOX-mediated exhaustion of CD8+ T cells. Meanwhile, a variety of innate and adaptive immune cells contribute to the malformation of tumor vessels. Protumoral M2-like macrophages as well as TH2 and Treg cells secrete pro-angiogenic factors that accelerate uncontrolled angiogenesis and promote vascular immaturity. While CD8+ T and CD4+ TH1 cells suppress angiogenesis and induce vascular maturation by secreting IFN-γ, they are unable to infiltrate the TME due to malformed tumor vessels. These findings led to preclinical studies that demonstrated that simultaneous targeting of tumor vessels and immunity is a viable strategy to normalize aberrant vascular-immune crosstalk and potentiate cancer immunotherapy. Furthermore, this combination strategy has been evidently demonstrated through recent pivotal clinical trials, granted approval from FDA, and is now being used in patients with kidney, liver, lung, or uterine cancer. Overall, combining anti-angiogenic therapy and ICI is a valid therapeutic strategy that can enhance cancer immunity and will further expand the landscape of cancer treatment.Subject terms: Cancer immunotherapy, Cancer microenvironment, Tumour angiogenesis, Tumour immunology, Targeted therapies 相似文献
947.
948.
Photophysical properties of porphyrin tapes 总被引:1,自引:0,他引:1
Cho HS Jeong DH Cho S Kim D Matsuzaki Y Tanaka K Tsuda A Osuka A 《Journal of the American Chemical Society》2002,124(49):14642-14654
The novel fused Zn(II)porphyrin arrays (Tn, porphyrin tapes) in which the porphyrin macrocycles are triply linked at meso-meso, beta-beta, beta-beta positions have been investigated by steady-state and time-resolved spectroscopic measurements along with theoretical MO calculations. The absorption spectra of the porphyrin tapes show a systematic downshift to the IR region as the number of porphyrin pigments increases in the arrays. The fused porphyrin arrays exhibit a rapid formation of the lowest excited states (for T2, approximately 500 fs) via fast internal conversion processes upon photoexcitation at 400 nm (Soret bands), which is much faster than the internal conversion process of approximately 1.2 ps observed for a monomeric Zn(II)porphyrin. The relaxation dynamics of the lowest excited states of the porphyrin tapes were accelerated from approximately 4.5 ps for the T2 dimer to approximately 0.3 ps for the T6 hexamer as the number of porphyrin units increases, being explained well by the energy gap law. The overall photophysical properties of the porphyrin tapes were observed to be in a sharp contrast to those of the orthogonal porphyrin arrays. The PPP-SCI calculated charge-transfer probability indicates that the lowest excited state of the porphyrin tapes (Tn) resembles a Wannier-type exciton closely, whereas the lowest excited state of the directly linked porphyrin arrays can be considered as a Frenkel-type exciton. Conclusively, these unique photophysical properties of the porphyrin tapes have aroused much interest in the fundamental photophysics of large flat organic molecules as well as in the possible applications as electric wires, IR sensors, and nonlinear optical materials. 相似文献
949.
S.H. LiuX.F. Qian J. YinL. Hong X.L. WangZ.K. Zhu 《Journal of solid state chemistry》2002,168(1):259-262
Ag2S nanoparticles in hyperbranched polyurethane matrix were prepared through the in situ reaction with thioacetamide as the sulfur source at room temperature. Transmission electron microscopic analysis revealed a uniform spherical shape for Ag2S nanoparticles, with an average size of about 4-10 nm and a narrow size distribution. X-ray powder diffraction and UV-vis spectroscopy were also used to characterize the obtained nanoparticles 相似文献
950.
Guangdong Zhou Zhanlin Xu Xiaohong Guo Hong Zhuang Yanan Li Xueju Lü Tiexin Cheng Wenxing Li Kaiji Zhen 《Reaction Kinetics and Catalysis Letters》2005,85(1):57-64
Summary The oxidation of hexanol in the presence of the Keggin-type heteropoly compounds (HPCs) H3PMonW12-nO40 (denoted as PMonW12-n, n=0,1) and Na5PW11ZO39 (denoted as PW11Z, Z = Mn, Fe, Co, Ni, Cu and Zn) was carried out to produce hexanal and hexanoic acid. The reaction was conducted in tert-butanol (t-BuOH), using cetylpyridinium bromide (CPB) salts of HPA and 15% aqueous H2O2 as oxidant under mild condition. The PMoW11 catalyst showed higher hexanol conversion of 25%, the lowest selectivity to hexanal of 64.4% and an efficient utilization of H2O2 of 34%. Over the transition metal substituted PW11Z catalysts decomposition of H2O2 was rapid. For these PW11Z catalysts, the efficient utilization of H2O2 decreased to 9% or even lower. By means of IR, UV-visible and GC-MS techniques the catalysts were characterized. 相似文献