全文获取类型
收费全文 | 12405篇 |
免费 | 2084篇 |
国内免费 | 2442篇 |
专业分类
化学 | 10244篇 |
晶体学 | 254篇 |
力学 | 637篇 |
综合类 | 144篇 |
数学 | 1162篇 |
物理学 | 4490篇 |
出版年
2024年 | 56篇 |
2023年 | 286篇 |
2022年 | 541篇 |
2021年 | 576篇 |
2020年 | 595篇 |
2019年 | 659篇 |
2018年 | 538篇 |
2017年 | 539篇 |
2016年 | 632篇 |
2015年 | 664篇 |
2014年 | 796篇 |
2013年 | 987篇 |
2012年 | 1069篇 |
2011年 | 1064篇 |
2010年 | 875篇 |
2009年 | 791篇 |
2008年 | 817篇 |
2007年 | 675篇 |
2006年 | 686篇 |
2005年 | 643篇 |
2004年 | 541篇 |
2003年 | 458篇 |
2002年 | 489篇 |
2001年 | 455篇 |
2000年 | 305篇 |
1999年 | 241篇 |
1998年 | 156篇 |
1997年 | 98篇 |
1996年 | 123篇 |
1995年 | 85篇 |
1994年 | 95篇 |
1993年 | 86篇 |
1992年 | 59篇 |
1991年 | 70篇 |
1990年 | 41篇 |
1989年 | 31篇 |
1988年 | 22篇 |
1987年 | 18篇 |
1986年 | 21篇 |
1985年 | 16篇 |
1984年 | 7篇 |
1983年 | 11篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1979年 | 2篇 |
1971年 | 1篇 |
1959年 | 3篇 |
1957年 | 1篇 |
1936年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
91.
92.
高强度聚焦超声(HIFU)是一种无创的热消融疗法,为保证其安全性和有效性,需要一种精度高、速度快的测温方法在其治疗过程中对温度进行监控.基于质子共振频率位移(PRFS)的磁共振温度成像(MRT)对温度具有较高的灵敏度,且与温度具有良好的线性关系,因此常被用于引导HIFU治疗.然而在实际应用中,HIFU治疗的最大隐患在于可能造成表皮灼伤,并且灼伤区域可能与焦点区域相隔较远.因此MRT的监控范围十分重要.本文基于三维回波平移成像序列,结合可控混叠的空间并行成像技术,实现了时间分辨率为3 s的快速三维温度成像.为了验证该方法的精度,本文首先设计了仿体降温实验,利用光纤温度计验证回波平移序列测温的准确度和精确度.然后在室温条件下扫描离体猪肉组织,对比加速前后的MRT的测温精确度.在HIFU加热条件下扫描离体猪肉组织,对比加速前后的MRT的测温准确度.结果显示,本文提出的方法可以在3 s内完成三维温度精准测量,对于HIFU治疗的安全监控具有重要意义. 相似文献
93.
Bei‐Bei Zhang Qian Jiang Zhi‐Xin Liao Chao Liu Shi‐Jun Liu 《Helvetica chimica acta》2013,96(7):1281-1289
Phytochemical investigation of the EtOH extract of Euphorbia sieboldiana led to the isolation of four new oleanane‐type triterpenoids, (1β,2α,3β,19β)‐1,2,3,19‐tetrahydroxyolean‐12‐en‐28‐oic acid, (1β,3β,19β)‐1,3,19‐trihydroxyolean‐12‐en‐28‐oic acid, (1β,2α,3β,16β,19β)‐1,2,3,16,19‐pentahydroxyolean‐12‐en‐28‐oic acid, and (1β,2α,3β,19β,23)‐1,2,3,19,23‐pentahydroxyolean‐12‐en‐28‐oic acid, along with 16 known compounds. Their structures were established by extensive 1D‐ and 2D‐NMR, as well as other spectral analyses. Biological evaluation of the four new triterpenoids revealed potent cytotoxic activities against HeLa and Hep‐G2 cells. 相似文献
94.
95.
In this paper, we derive the asymptotic expansions of the moments of normalized partial maxima for general error distribution. A byproduct is to deduce the convergence rates of the moments of normalized maxima to the moments of the corresponding extreme value distribution. 相似文献
96.
Wei Wang Xue-Mei ZhaoJing-Li Wang Xin GengJun-Fang Gong Xin-Qi Hao Mao-Ping Song 《Tetrahedron letters》2014
Primary aromatic amides can be synthesized from aldehydes and hydroxylamine hydrochloride in the presence of Cs2CO3. Various aromatic aldehydes (include some heteroaromatic aldehydes) are able to generate the corresponding aromatic amides in moderate to excellent yields. 相似文献
97.
Jia‐Xuan Yan Hu Li Xiang‐Wei Liu Jiang‐Ling Shi Xin Wang Zhang‐Jie Shi 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(19):5045-5049
3,4‐Dihydroquinolinones were synthesized by the palladium‐catalyzed, oxidative‐addition‐initiated activation and arylation of inert C(sp3) H bonds. Pd(OAc)2 and P(o‐tol)3 were used as the catalyst and ligand, respectively, to improve the efficiency of the reaction. A further advantage of this reaction is that it could be performed in air. A relatively rare seven‐membered palladacycle was proposed as a key intermediate of the catalytic cycle. 相似文献
98.
The creation of hierarchical nanostructures in polymeric materials has been intensively studied due to the great potential to tailor their physicochemical properties. Although much success has been achieved over the past decades in block copolymers, hierarchical structure engineering in polymer blends remains a great challenge. Here, the formation of hierarchical lamellae‐in‐lamella nanostructures from polymer blends via controlled nonequilibrium freezing is reported. Polymer blends are first dissolved in molten hexamethylbenzene (HMB) to form a homogeneous melt. When cooled to below its melting temperature, the HMB is crystallized and depleted, and the polymers are directionally solidified. This process is rapid enough that phase separation of the polymer blends is kinetically trapped at the nanoscale level. Then, the polymer blend epitaxially crystallizes onto the HMB inside the nanophase, resulting in the hierarchical lamellae‐in‐lamella structure. This structure is stable under ambient conditions and tunable depending on the annealing temperature and blending ratio.
99.
In order to reduce greenhouse gas emissions, developing flame retardants from bio-based resources has aroused extensive interest in recent years. In this work, we utilized furfural(biomass) and 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide(DOPO) to synthesize a biobased co-curing agent(FGD) to combine with 4,4'-diaminodiphenyl methane(DDM) for obtaining a low-phosphorus loading flame-retardant epoxy thermosets. The introduction of FGD decreased the activation energy of the curing progress, enhanced the mechanical properties of the epoxy thermosets, and did not affect the glass transition temperature of the epoxy thermosets. EP-5.0 had a lower thermal degradation rate and a doubled char yield compared with EP-0. The phosphorus content of EP-5.0 was only 0.45 wt%, while EP-5.0 reached the UL-94 V-0 rating with a high LOI value of 32%. Compared with EP-0, the PHRR of EP-2.5 and EP-5.0 decreased by 22.3% and 31.3%, respectively. The SEM results showed that the addition of FGD made the char residues more uniform and denser, which could effectively prevent combustible volatiles from escaping from the degradation area to the flame area and isolate the heat transfer so that the epoxy thermosets had an excellent flame-retardant performance. 相似文献
100.
Joseph Israel Gurti Prof. Xun-Lei Ding Ya-Ya Wang Yan Chen Dr. Wei Li Dr. Xin Wang 《Chemphyschem》2022,23(14):e202200124
The reaction of N2 with trinuclear niobium and tungsten sulfide clusters Nb3Sn and W3Sn (n=0–3) was systematically studied by density functional theory calculations with TPSS functional and Def2-TZVP basis sets. Dissociations of N−N bonds on these clusters are all thermodynamically allowed but with different reactivity in kinetics. The reactivity of Nb3Sn is generally higher than that of W3Sn. In the favorite reaction pathways, the adsorbed N2 changes the adsorption sites from one metal atom to the bridge site of two metal atoms, then on the hollow site of three metal atoms, and at that place, the N−N bond dissociates. As the number of ligand S atoms increases, the reactivity of Nb3Sn decreases because of the hindering effect of S atoms, while W3S and W3S2 have the highest reactivity among four W3Sn clusters. The Mayer bond order, bond length, vibrational frequency, and electronic charges of the adsorbed N2 are analyzed along the reaction pathways to show the activation process of the N−N bond in reactions. The charge transfer from the clusters to the N2 antibonding orbitals plays an essential role in N−N bond activation, which is more significant in Nb3Sn than in W3Sn, leading to the higher reactivity of Nb3Sn. The reaction mechanisms found in this work may provide important theoretical guidance for the further rational design of related catalytic systems for nitrogen reduction reactions (NRR). 相似文献