全文获取类型
收费全文 | 24873篇 |
免费 | 4264篇 |
国内免费 | 4142篇 |
专业分类
化学 | 18696篇 |
晶体学 | 285篇 |
力学 | 1455篇 |
综合类 | 297篇 |
数学 | 3213篇 |
物理学 | 9333篇 |
出版年
2024年 | 41篇 |
2023年 | 518篇 |
2022年 | 846篇 |
2021年 | 956篇 |
2020年 | 1085篇 |
2019年 | 1145篇 |
2018年 | 875篇 |
2017年 | 889篇 |
2016年 | 1256篇 |
2015年 | 1306篇 |
2014年 | 1492篇 |
2013年 | 1931篇 |
2012年 | 2105篇 |
2011年 | 2254篇 |
2010年 | 1633篇 |
2009年 | 1618篇 |
2008年 | 1721篇 |
2007年 | 1447篇 |
2006年 | 1349篇 |
2005年 | 1160篇 |
2004年 | 965篇 |
2003年 | 789篇 |
2002年 | 909篇 |
2001年 | 694篇 |
2000年 | 592篇 |
1999年 | 557篇 |
1998年 | 434篇 |
1997年 | 354篇 |
1996年 | 359篇 |
1995年 | 290篇 |
1994年 | 280篇 |
1993年 | 252篇 |
1992年 | 174篇 |
1991年 | 190篇 |
1990年 | 172篇 |
1989年 | 121篇 |
1988年 | 111篇 |
1987年 | 69篇 |
1986年 | 71篇 |
1985年 | 82篇 |
1984年 | 41篇 |
1983年 | 36篇 |
1982年 | 31篇 |
1981年 | 18篇 |
1980年 | 7篇 |
1979年 | 9篇 |
1978年 | 6篇 |
1977年 | 5篇 |
1957年 | 4篇 |
1936年 | 5篇 |
排序方式: 共有10000条查询结果,搜索用时 93 毫秒
991.
Xiao Jun-An Cheng Xiu-Liang Peng Hai Li Jin-Lian Xie Zhen-Zhen Chen Wen-Qiang Liu Zhi-Ping Xiao Qi Su Wei Yang Hua 《中国科学:化学(英文版)》2020,63(6):785-791
A diastereoselectivity-controllable formal [3+2]-cycloaddition of arylvinyl oxirane 2,2-diesters with cyclic N-sulfonyl imines is developed, affording the corresponding tricyclic oxazolidine derivatives in moderate to excellent yields with excellent diastereoselectivities in the presence of palladium(0) or scandium(III) triflate. This protocol allows selective synthesis of diastereomers of tricyclic oxazolidine derivatives under switchable and mild conditions. Further transformations of the obtained products were conducted by removing ester groups and arylvinyl moieties. 相似文献
992.
Two LnIII ions are sandwiched by dinuclear CoII building blocks derived from a tris‐triazamacrocyclic ligand bearing pendant carboxylic acid functionality, 1,3,5‐tris((4,7‐bis(2‐carboxyethyl)‐1,4,7‐triazacyclonon‐1‐yl)methyl)‐benzene (H6L), giving rising to two nanoscale heterometallic metal–organic cages formulated as [Co4Ln2(LH2.5)2(H2O)4]·(ClO4)6·NO3·nH2O [Ln = Dy, n = 12 ( 1 ); Ln = Yb, n = 9 ( 2 )], whose internal cavity accommodates a guest NO3? anion. Their hexanuclear cage‐like architectures are maintained both in solution and solid states as confirmed by mass spectrum as well as X‐ray diffraction experiments. These two cages display ligand‐based fluorescence emissions and therefore both were chosen to be operated as fluorescent chemosensors for the detection of nitroaromatic compounds. Attractively, these metal–organic cages allow highly selective and sensitive detection of picric acid (PA) over other nitroaromatics in solution and suspension, and the fluorescence resonance energy transfer (FRET) between the cage probes and PA is mainly responsible for the remarkable detection efficiency. 相似文献
993.
994.
Xuan Hao Dr. Hongsen Zhang Dr. Qi Liu Dr. Jingyuan Liu Dr. Rongrong Chen Dr. Jing Yu Prof. Milin Zhang Peili Liu Prof. Jun Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(2):590-597
Enrichment of UVI is an urgent project for nuclear energy development. Herein, magnetic graphitic carbon nitride nanosheets were successfully prepared by in situ anchoring of pyrrhotite (Fe7S8) on the graphitic carbon nitride nanosheet (CNNS), which were used for capturing UVI. The structural characterizations of Fe7S8/CNNS-1 indicated that the CNNS could prevent the aggregation of Fe7S8 and the saturation magnetization was 4.69 emu g−1, which meant that it was easy to separate the adsorbent from the solution. Adsorption experiments were performed to investigate the sorption properties. The results disclosed that the sorption data conformed to the Langmuir isotherm model with the maximum adsorption capacity of 572.78 mg g−1 at 298 K. The results of X-ray photoelectron spectroscopy (XPS) demonstrated that the main adsorption mechanism are as follows: UVI is adsorbed on the surface of Fe7S8/CNNS-1 through surface complexation initially, then it was reduced to insoluble UIV. Thereby, this work provided an efficient and easy to handle sorbent material for extraction of UVI. 相似文献
995.
A linear optical unambiguous discrimination of hyperentangled Bell states is proposed for two‐photon systems entangled in both the polarization and momentum degrees of freedom (DOFs) assisted by time bin. This unambiguous discrimination scheme can completely identify 16 orthogonal hyperentangled Bell states using only linear optical elements, where the function of the auxiliary entangled Bell state is replaced by time bin. Moreover, the possibility of extending this scheme for distinguishing hyperentangled Bell states in n DOFs is discussed, and it shows that hyperentangled Bell states in n ( ) DOFs can be distinguished with k ( ) auxiliary entangled states of additional DOFs by introducing a time delay, which decreases the auxiliary entanglement resource required for unambiguous discrimination of hyperentangled Bell state. Therefore, this scheme provides a new way for distinguishing hyperentangled states with current technology, which will extend the application of discrimination of hyperentangled states via linear optics to other quantum information protocols besides hyperdense coding schemes in the future. 相似文献
996.
Yuan Li Li Kai Song Xin Sun Huaying Ning Ping Sun Xin 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2019,93(12):2373-2382
Russian Journal of Physical Chemistry A - The mechanism of PH3 oxidation is investigated at B3LYP/6-311+g (d, p) level using density functional theory calculation with n = 0–6 water molecules... 相似文献
997.
The intramolecular hydroacylation of 1,2-disubstituted alkenes was considered to be a challenging task due to the side reactions resulted from the lack of additional substituent at 1-position and the low activity caused by the steric hindrance of substituent at 2-position, and an asymmetric version has not been considered possible due to problems associated with the racemization of the products. We have partially solved these problems. Catalyzed by an activated diphosphine-Rh complex and reacted in a selected dihalogenated solvent, the intramolecular hydroacylation of o-(2-arylvinyl)benzaldehydes provided the corresponding 2-aryl-1-indanones in high yields, and its asymmetric variant using o-(2-alkylvinyl)benzaldehydes afforded chiral 2-alkyl-1-indanones in high yields and with moderate enantioselectivities. 相似文献
998.
Lin-Lin Zhang Bing-Chao Da Shao-Hua Xiang Shuai Zhu Zi-Yun Yuan Zhen Guo Bin Tan 《Tetrahedron》2019,75(12):1689-1696
Quinones, precursors of aromatic structures, were firstly employed as the electrophiles for the organocatalytic Michael addition/cyclization cascade reaction with versatile 3-isothiocyanato oxindoles. Chiral bifunctional organocatalyst was appropriate for this enantioselective transformation to afford a variety of novel spirooxindoles, possessing a spirocyclic stereocenter adjacent to the aromatic ring, via asymmetric double arylation. These synthesized spirooxindoles are very difficult to access by the reported methods and were obtained in excellent chemical yields with excellent enantioselectivities. 相似文献
999.
Ganoderma mushrooms are widely used as effective medicines for treating and preventing chronic diseases. In this study, five new meroterpenoids, dayaolingzhiols A (1) and B (2) featuring a 6/6/6 ring system, dayaolingzhiols C?E (3–5) harboring a γ-lactone motif, along with eight known ones (6–13), were purified from G. lucidum. To clarify their chemical structures, spectroscopic and ECD and OR computational methods were used. In addition, the inhibition of all the new meroterpenoids against AChE was evaluated, disclosing that (+)-4 and (±)-5 possess potent AChE inhibitory activities with respective IC50 values of 8.52?±?1.90?μM and 7.37?±?0.52?μM. 相似文献
1000.
空间填充设计在计算机试验中应用十分广泛,当拟合回归模型时,正交的空间填充设计保证了因子效应估计的独立性.基于广义正交设计,文章给出了构造二阶正交拉丁超立方体设计和列正交设计的方法,新构造的设计不仅满足任意两列之间相互正交,还能保证每一列与任一列元素平方组成的列以及任两列元素相乘组成的列都正交.当某些正交的空间填充设计不存在时,具有较小相关系数的近似正交设计可作为替代设计使用.设计构造的灵活性为计算机试验在实践中的广泛应用提供了必要的支持. 相似文献