全文获取类型
收费全文 | 25793篇 |
免费 | 4747篇 |
国内免费 | 4149篇 |
专业分类
化学 | 19920篇 |
晶体学 | 565篇 |
力学 | 1368篇 |
综合类 | 329篇 |
数学 | 2855篇 |
物理学 | 9652篇 |
出版年
2024年 | 24篇 |
2023年 | 406篇 |
2022年 | 529篇 |
2021年 | 757篇 |
2020年 | 984篇 |
2019年 | 1107篇 |
2018年 | 856篇 |
2017年 | 867篇 |
2016年 | 1218篇 |
2015年 | 1312篇 |
2014年 | 1472篇 |
2013年 | 1977篇 |
2012年 | 2425篇 |
2011年 | 2449篇 |
2010年 | 1913篇 |
2009年 | 1856篇 |
2008年 | 2034篇 |
2007年 | 1712篇 |
2006年 | 1732篇 |
2005年 | 1525篇 |
2004年 | 1262篇 |
2003年 | 982篇 |
2002年 | 1080篇 |
2001年 | 827篇 |
2000年 | 645篇 |
1999年 | 526篇 |
1998年 | 333篇 |
1997年 | 260篇 |
1996年 | 221篇 |
1995年 | 188篇 |
1994年 | 211篇 |
1993年 | 154篇 |
1992年 | 101篇 |
1991年 | 131篇 |
1990年 | 88篇 |
1989年 | 69篇 |
1988年 | 72篇 |
1987年 | 33篇 |
1986年 | 42篇 |
1985年 | 53篇 |
1984年 | 28篇 |
1983年 | 26篇 |
1982年 | 21篇 |
1981年 | 22篇 |
1980年 | 15篇 |
1979年 | 18篇 |
1978年 | 15篇 |
1977年 | 13篇 |
1976年 | 9篇 |
1975年 | 11篇 |
排序方式: 共有10000条查询结果,搜索用时 390 毫秒
991.
We introduce a graphical representation of DNA primary sequences by taking four special vectors in a 3-D space to represent the four nucleic acid bases in DNA sequences, so that a DNA primary sequence is denoted in a 3-D space by a successive vector sequence which is a directed walk on the space. It is demonstrated that this representation has no overlap and intersection and allows numerical characterization. 相似文献
992.
合成甲醇的催化剂Rh-ZnO/MWNTs的研究 总被引:2,自引:0,他引:2
研究新型的由多壁碳纳米管(MWNTs)负载的, ZnO助催的铑基甲醇合成催化剂. 当铑含量达到4%(w)时,催化剂具有较高的比表面积(99.6 m2•g-1), 催化剂的反应活化能为68.8 kJ•mol-1.在563 K, 1 MPa下,催化剂的最高催化活性和甲醇选择性分别为411.4 mg/gcat.•h和96.7%. TEM、TPR和TPD等表征结果显示,碳纳米管能增加Rh在催化剂表面的分散度,提高催化剂的还原温度并能增加氢物种的吸附量,这些结果将有助于更好地了解催化剂中各组分间的协同作用和催化活性中心本质. 相似文献
993.
A quantitative analysis method for penicillins including ampicillin (AmP), benzyl penicillin (BP), oxacillin (OA) and amoxycillin (AmO) is proposed that makes use of the totally internally reflected resonance light scattering (TIR-RLS) signal from the penicillin at the H2O/CCl4 interface in the presence of cetyltrimethylammonium bromide (CTMAB), and enables the pharmacokinetics of penicillin taken orally and excreted through urine to be monitored. Penicillin is coadsorbed with CTMAB at the H2O/CCl4 interface in neutral solution, resulting in the formation of ion associates that display greatly enhanced TIR-RLS signals (maximum at 368–372 nm). This enhanced TIR-RLS intensity was found to be proportional to the penicillin concentration over the range 0.2×10–6 to 2.2×10–6 mol L–1, with limits of determination (3) of 5.0×10–8 to 7.0×10–8 mol L–1. Pharmacokinetics studies performed using the present method show that the excretion of orally-taken ampicillin through urine has a half-time of 1.05 h and an excremental quantum over 8 h of 49.3%, respectively. 相似文献
994.
Nakanishi M Eguchi A Akuta T Nagoshi E Fujita S Okabe J Senda T Hasegawa M 《Current protein & peptide science》2003,4(2):141-150
Improving the performance of non-viral gene-delivery vehicles that consist of synthetic compounds and nucleic acids is a key to successful gene therapy. Supplementing synthetic vehicles with various biological functions by using natural or artificial peptides is a promising approach with which to achieve this goal. One of the obstacles hindering this effort is that some of the potentially useful peptides, especially those with many basic amino acid residues, interfere with the formation of the complex owing to strong electrostatic interactions with the nucleic acid. In this review, we describe our recent work in examining the potential of these peptides in gene delivery, using a recombinant lambda phage particle as the model for the gene-delivery complex. Lambda phage encapsulates large duplex DNA in a rigid polyplex-like shell with a diameter of 55 nm, and can display various peptides on this capsid, independently of particle formation. By examining the expression of marker genes encapsulated in the phage capsid, we have demonstrated that the protein transduction domain of HIV Tat protein and the nuclear localization signal derived from SV40 T antigen can remarkably facilitate the delivery of these marker genes across the two major barriers, the cell membrane and the nuclear membrane, respectively. Our results indicate that these basic peptides can constitute effective components of synthetic gene-transfer complexes, as long as sufficient copies are displayed on the outer surface of the complex. 相似文献
995.
根据p53基因的序列设计并合成了能特异性检测p53 mRNA的分子信标(MB), 发展了一种快速定量测定细胞内总RNA提取物中p53 mRNA的方法. 采用鼻咽癌(CNE2)细胞系和经RNA干扰技术降低p53基因表达的CNE2-p53RNAi细胞系, 抽提总RNA并用MB检测, 验证了MB的检测对象是p53 mRNA. 将该方法应用于多种肿瘤细胞内p53基因表达水平的分析, 表达变化趋势与经典的mRNA分析方法RT-PCR检测结果相符. 在此基础上, 用MB对5-氟尿嘧啶(5-Fu)处理的肺腺癌细胞(A549)进行了p53 mRNA的体外定量检测, 结果表明采用MB能够快速地获知该药物对细胞内p53 mRNA表达影响的信息. 相似文献
996.
We report a convenient method for quantitative non-covalent functionalization of single-walled carbon nanotubes (SWNT) with phthalocyanine (Pc) compounds, in which a surface coverage of 49% was achieved. The effect of several process parameters on the functionalization process was elucidated. Firstly, as-produced SWNT gave the largest extent of functionalization compared with purified SWNT and as-produced multi-walled carbon nanotubes (MWNT). Secondly, the extent of functionalization was sensitive to the specific molecular structures of the Pc compounds. Finally, in terms of solvent selection, dimethylformamide (DMF) was found to give the largest extent of functionalization, which is then followed by chloroform (CHCl3) and 1,2-dichlorobenzene (ODCB). The method reported in this paper provides new insights on the interactions between Pc molecules and carbon nanotubes and paves the way for rational control of the degree of functionalization, which is an important step from the perspective of carbon nanotube applications.
Electronic supplementary material Supplementary material for this article is avilable at and is accessible for authorised users. 相似文献
997.
Korupoju SR Mangayarkarasi N Zacharias PS Mizuthani J Nishihara H 《Inorganic chemistry》2002,41(16):4099-4101
New homo trinuclear Zn(II) complexes [Zn(3)L(1)(micro-OAc)](ClO(4))(2).3CHCl(3).H(2)O, 1, and [Zn(3)L(1)(micro-OAc)].ClO(4).PF(6).5CH(3)OH.H(2)O, 2, and hetero trinuclear complex [Zn(2)CuL(1)(micro-OAc)](ClO(4))(2).3CHCl(3).H(2)O,3, of optically active hexaaza triphenolic macrocycle H(3)L(1) were synthesized and crystallographically characterized. The cation [Zn(3)L(1)(micro-OAc)](+) structure of 1 and 2 closely resembles the trinuclear Zn(II) active site of P1 nuclease. The distorted tetrahedral geometry of Zn3 was successfully reproduced at Cu1 in complex 3. The complexes 2 and 3 cleave CT DNA at 37 and 50 degrees C. 相似文献
998.
Jeremy R. Lizotte Brian M. Erwin Ralph H. Colby Timothy E. Long 《Journal of polymer science. Part A, Polymer chemistry》2002,40(4):583-590
The feasibility of utilizing stable free‐radical polymerization (SFRP) in the synthesis of well‐defined poly(2‐vinylnaphthalene) homopolymers has been investigated. Efforts to control molecular weight by manipulating initiator concentration while maintaining a 2,2,6,6‐tetramethylpiperidinyl‐1‐oxy (TEMPO):benzoyl peroxide (BPO) molar ratio of 1.2:1 proved unsuccessful. In addition, systematic variations of the TEMPO: BPO molar ratio did not result in narrow molecular weight distributions. In situ Fourier transform infrared spectroscopy (FTIR) indicated that the rate of monomer disappearance under SFRP and thermal conditions were identical. This observation indicated a lack of control in the presence of the stable free radical, TEMPO. The similarities in chemical structure between styrene and 2‐vinylnaphthalene suggested thermally initiated polymerization occurred via the Mayo mechanism. A kinetic analysis of the thermal polymerization of styrene and 2‐vinylnaphthalene suggested that the additional fused ring in 2‐vinylnaphthalene increased the propensity for thermal polymerization. The observed rate constant for thermal polymerization of 2‐vinylnaphthalene was determined using in situ FTIR spectroscopy and was one order of magnitude greater than styrene, assuming pseudo‐first‐order kinetics. Also, an Arrhenius analysis indicated that the activation energy for the thermal polymerization of 2‐vinylnaphthalene was 30 kJ/mol less than styrene. © 2002 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 583–590, 2002; DOI 10.1002/pola.10131 相似文献
999.
沙林酸印迹聚邻苯二胺纳米膜制备及结构表征 总被引:9,自引:0,他引:9
采用电化学聚合法合成了对有机磷毒剂沙林具有特异识别的聚邻苯二胺(PPD)分子印迹纳米膜(iPPD).利用石英晶体微天平(QCM)证实了印迹效应的存在,并用循环伏安法(CV)、AFM、XPS进行了系统的结构表征.结果表明,分子印迹膜的膜厚约20 nm,膜的表面呈“石林”状,疏松多孔,具有良好的吸附性能.分子印迹主要影响聚合物的三维排列,而聚合物的化学组成没有发生改变.该种分子印迹纳米膜在选择性检测军用毒剂沙林中具有良好的应用前景. 相似文献
1000.