全文获取类型
收费全文 | 109714篇 |
免费 | 17691篇 |
国内免费 | 12579篇 |
专业分类
化学 | 76374篇 |
晶体学 | 1228篇 |
力学 | 6257篇 |
综合类 | 748篇 |
数学 | 13397篇 |
物理学 | 41980篇 |
出版年
2024年 | 370篇 |
2023年 | 2209篇 |
2022年 | 3913篇 |
2021年 | 4133篇 |
2020年 | 4462篇 |
2019年 | 4237篇 |
2018年 | 3967篇 |
2017年 | 3571篇 |
2016年 | 5329篇 |
2015年 | 5262篇 |
2014年 | 6364篇 |
2013年 | 8279篇 |
2012年 | 9796篇 |
2011年 | 9978篇 |
2010年 | 7008篇 |
2009年 | 6713篇 |
2008年 | 7029篇 |
2007年 | 6279篇 |
2006年 | 5835篇 |
2005年 | 4890篇 |
2004年 | 3848篇 |
2003年 | 3096篇 |
2002年 | 2817篇 |
2001年 | 2362篇 |
2000年 | 2041篇 |
1999年 | 2154篇 |
1998年 | 1823篇 |
1997年 | 1634篇 |
1996年 | 1630篇 |
1995年 | 1429篇 |
1994年 | 1298篇 |
1993年 | 1038篇 |
1992年 | 932篇 |
1991年 | 815篇 |
1990年 | 691篇 |
1989年 | 528篇 |
1988年 | 395篇 |
1987年 | 355篇 |
1986年 | 346篇 |
1985年 | 272篇 |
1984年 | 189篇 |
1983年 | 156篇 |
1982年 | 130篇 |
1981年 | 84篇 |
1980年 | 63篇 |
1979年 | 26篇 |
1978年 | 24篇 |
1976年 | 22篇 |
1975年 | 22篇 |
1957年 | 28篇 |
排序方式: 共有10000条查询结果,搜索用时 4 毫秒
981.
伏安型植物组织生物微电极的研究:混合不同植物组织碳糊微电极的研究 总被引:3,自引:0,他引:3
由于香蕉组织中含有的氧化酶能够生物催化氧化多巴胺,去甲肾上腺素,L-多巴等,大大地提高了植物组织电极的灵敏度;又由于茄子组织中所含有的氧化酶在催化氧化儿茶酚的同时,能有效地抑制抗坏血酸在电极上的反应,将上述两种植物组织混合制成电极,使其更适于神经递质的测定,线性范围:2.4×10^-6--9.8×10^-4mol/L;检出下限3.2×10^-7mol/L。 相似文献
982.
Polycondensation of a cresol mixture (C(m)) with formaldehyde (F) in basic aqueous solutions leads to formation of highly cross-linked C(m)F aquagels that can be supercritically dried with carbon dioxide to form organic C(m)F aerogels. Aerogels synthesized with different catalyst contents and reactant concentrations are characterized by low-temperature nitrogen adsorption. The present experimental results suggest that the C(m)F aerogels are typical mesoporous materials and have almost no micropores in bulk. The microstructure of the organic C(m)F aerogels can be controlled and tailored effectively by varying synthesis conditions during the initial sol-gel process. C(m)F organic aerogels with specific surface area as high as 627 m(2)/g and corresponding pore volume 2.06 ml/g have been obtained with a dominant pore size of 30 nm. C(m)F organic aerogels with peaky pore size distributions concentrated at 11 nm have also been prepared. 相似文献
983.
A highly effective Cu-Ru catalyzed addition of terminal alkynes to imines via C-H activation has been achieved in water or under solvent-free conditions. 相似文献
984.
Isolation of lipase producer and its performance in enantioselective hydrolysis of glycidyl butyrate
A racemic glycidyl butyrate resolving strain, preliminarily identified as a Rhizopus sp., had been isolated from soil. Its extracellular lipase was found to enantioselectively hydrolyze the (S)-enantiomer of
the chiral ester, with optimal activities at pH 5.3 and 42°C. Higher en antioselectivity of theenzyme was observed at lower
temperatures, while the best anantioselectivity was obtained at pH 5.5–6.0, with an, E value (enantiomeric ratio) of 57. 相似文献
985.
Gong WT Li XC Ning GL Zhu L Wang L Lin Y 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):835-839
Two novel phenylated pyrylium compounds, silver (I)-bridged 2,3,4,5-tetraphenylpyrylium perchlorate (P1) and its silver (I)-free pyrylium ligand (P2) were prepared from 1,2,3,4-tetraphenylcyclopentadiene to examine their spectroscopic behaviors. The UV/vis absorption and fluorescent emission spectra of P1 and P2, measured in three solvents (acetonitrile, dichloromethane and toluene), reveal that the photophysical behaviors are closely related to silver (I) fragment, and strongly dependent on solvent polarity. In polar acetonitrile, P1 displays longer absorption wavelength and much lower fluorescent emission intensity than P2, although they exhibit much similarity in shape. In contrast, in nonpolar toluene, while P2 shows an apparent absorption band at 338 nm, P1 displays a tail-like line without absorption band observed. All the spectra obtained indicate a better coplanarity and a stronger intra-molecular charge transfer in P1 due to the effect of silver (I) fragment. Additionally, the 1H NMR spectra of P1 and P2, which were recorded under the same conditions, indicate that the silver (I) fragment reinforces pyrylium ring's capacity to localize the formal positive charge within the heterocyclic ring. 相似文献
986.
A simple approach to a diverse set of chiral trisoxazolines is described. Deprotonation of bisoxazolines 2, followed by treatment of 2-chloromethyloxazolines 3, affords chiral trisoxazolines, including chiral homo- and hetero-trisoxazolines in good to high yields. These trisoxazolines are successfully applied in the asymmetric reaction of indole with benzylidene malonate, and ee's up to 93% were obtained. 相似文献
987.
Arrayed structures are desirable for many applications, but the fabrication of many material arrays remains a significant challenge. As a prominent II-VI semiconductor, large-scale arrayed ZnS structure has not been easily fabricated. Here, we introduce a simple structure conversion route for the synthesis of novel arrayed structures, and large-scale tube-like ZnS structure arrays and cable-like ZnS-ZnO composite arrays were successfully prepared through sulfuration conversion from arrayed rod-like ZnO structure based on a hydrothermal method at low temperature. XRD, EDS, SEM, TEM and PL are used to confirm the formation of the novel arrayed structure and trace the conversion process. The results show that the conversion ratio can be conveniently tailored by the reaction time, and the PL properties of the obtained materials can be adjusted through the conversion ratio. Especially, the cable-like structure holds the PL properties of both ZnO and ZnS structures. This simple solution method can be further extended to the preparation of other semiconductor sulfide and selenide, and can amplify the application field of large-scale arrays of semiconductors. 相似文献
988.
The selectivity of a column system, S, defined by equation 28, includes a variation coefficient (β) of plate number with capacity ratio which has a large influence on the peak capacity, as shown in Fig. 18. Some typical chromatograms are given. In order to predict S for a column system from Kovat's Index, equations 40 and 41 are given to calculate the constant of the carbon number rule for squalane at different temperatures or for different stationary phases. The specific retention value of heptane on squalane at different temperatures can be calculated from equation 42. The nonpolarity index, defined by equation 43, was used to calculate the retention value of heptane on various stationary phases. In liquid chromatography, the order of elution may be reversed by changing the composition of the eluent on the same chemically bonded silica (manufactured in China). The linear relations between the log retention values of different kinds of solutes or of a single solute on the silicas of different surface areas when using the same eluent are given. 相似文献
989.
Supported iron tetrasulfophthalocyanine can efficiently catalyze the degradation of organic pollutants by H2O2 under visible light irradiation in an aqueous solution, and the catalyst can be easily recycled without apparent loss of activity. 相似文献
990.
Aihua Zhang Kun Liu Lan Li Siyu Ma Zonghe Li 《International journal of quantum chemistry》2005,104(3):373-378
The ring‐closing reaction of 5′‐adenosine monophosphate (5′‐AMP) to generate cyclic 3′, 5′‐adenosine monophosphate (cAMP) and H2O was theoretically investigated at the B3LYP/6‐31G**level. It was found that the ring‐closing reaction of 5′‐AMP may proceed in a synchronous way or in a stepwise way. For the latter, the reaction is a multichannel elimination reaction including inner H transfer. The potential energy surface of Path 3 is lowest in all the ring‐closing reaction paths. In addition, H shuttling reaction with the participation of a water molecule to act as a shuttle were also studied at the same level. The calculations indicate that the participation of a water molecule facilitates hydrogen transfer reaction. Our present calculations rationalized all the possible reaction channels. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2005 相似文献