全文获取类型
收费全文 | 2343篇 |
免费 | 69篇 |
国内免费 | 8篇 |
专业分类
化学 | 1739篇 |
晶体学 | 28篇 |
力学 | 22篇 |
数学 | 168篇 |
物理学 | 463篇 |
出版年
2022年 | 15篇 |
2021年 | 19篇 |
2020年 | 30篇 |
2019年 | 25篇 |
2018年 | 21篇 |
2017年 | 17篇 |
2016年 | 46篇 |
2015年 | 53篇 |
2014年 | 43篇 |
2013年 | 94篇 |
2012年 | 106篇 |
2011年 | 126篇 |
2010年 | 87篇 |
2009年 | 66篇 |
2008年 | 122篇 |
2007年 | 154篇 |
2006年 | 132篇 |
2005年 | 116篇 |
2004年 | 127篇 |
2003年 | 121篇 |
2002年 | 99篇 |
2001年 | 63篇 |
2000年 | 50篇 |
1999年 | 19篇 |
1998年 | 37篇 |
1997年 | 21篇 |
1996年 | 35篇 |
1995年 | 29篇 |
1994年 | 30篇 |
1993年 | 20篇 |
1992年 | 21篇 |
1991年 | 31篇 |
1990年 | 30篇 |
1989年 | 26篇 |
1988年 | 21篇 |
1987年 | 17篇 |
1986年 | 30篇 |
1985年 | 31篇 |
1984年 | 32篇 |
1983年 | 21篇 |
1982年 | 24篇 |
1981年 | 23篇 |
1980年 | 24篇 |
1979年 | 15篇 |
1978年 | 18篇 |
1977年 | 25篇 |
1976年 | 12篇 |
1975年 | 14篇 |
1974年 | 13篇 |
1973年 | 16篇 |
排序方式: 共有2420条查询结果,搜索用时 250 毫秒
121.
122.
Jianhuai Ye Dr. Sayaka Hatano Prof. Dr. Manabu Abe Prof. Dr. Ryohei Kishi Yusuke Murata Prof. Dr. Masayoshi Nakano Prof. Dr. Waldemar Adam 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(7):2299-2306
In the photochemical denitrogenation of 1,4‐diaryl‐2,3‐diazabicyclo[2.2.1]heptane ( AZ6 ) bearing sterically hindered substituents, a curious new absorption band at about 450 nm was observed under low‐temperature matrix conditions, together with the previously well‐characterized planar singlet diradical pl‐1 DR6 with λmax=≈580 nm. The 450 nm species was electron paramagnetic resonance (EPR)‐silent. Instead of generating the planar diradical pl‐1 DR6 and the precursor azoalkane AZ6 upon warming, the ring‐closed bicyclo[2.1.0]pentane derivative SB6 , that is, the AZ6 denitrogenation product was identified. Based on product analysis, low‐temperature spectroscopic observations, high‐level quantum‐mechanical computations, viscosity effect, and laser‐flash photolysis, the puckered singlet diradicaloid puc‐1 DR6 was assigned to the new 450 nm absorption. The latter was detected experimentally at the same time as the planar singlet diradical pl‐1 DR6 . Sterically demanding substituents as well as viscosity impediments were essential for the detection of the experimentally hitherto unknown puckered singlet cyclopentane‐1,3‐diyl diradicaloid puc‐1 DR6 , that is, the third isomer in homolysis. The present findings should stimulate future work on the mechanistically fascinating stereoselectivity documented in the formation of bicyclo[2.1.0]pentanes during the 2,3‐diazabicyclo[2.2.1]heptane denitrogenation. 相似文献
123.
124.
A new method has been developed for the generation and subsequent reaction of ynolates in a micro flow reactor system. This new procedure allowed for ynolates to be prepared at 0 °C or ambient temperature within 1 min via a reductive lithiation reaction, whereas the corresponding batch processes generally require low temperature control and extended reaction times of up to 1 h. The resulting ynolates were applied to the olefination of carbonyl compounds, with the reactions reaching completion in a much shorter reaction time in the continuous flow reactor than the batch reactor. These results highlight the practical utility of the ynolate reaction, and represent the first reported example of the use of lithium naphthalenide in a flow microreactor, which would contribute to progress of the flash chemistry. 相似文献
125.
Akira Mori Hitoshi Takeshita Ryoji Mori Shinji Takematsu Manabu Takemoto Seiji Ujiie 《Liquid crystals》2013,40(2):171-178
Two kinds of monocyclic troponoid mesogens, 2,5-dialkanoyloxytropones (4) and 5-alkanoyloxy2-alkoxytropones (5), were prepared. The former showed monotropic smectic A phases and the virtual isotropic liquid-smectic A transitions of the latter were determined by extrapolation of results in a binary phase diagram. Comparing the mesogenic properties between the tropones 4 and the 2-alkanoyloxy-5-alkoxytropones (1), the alkanoyloxy group at C-5 enhances both the melting points and the transition temperatures of the smectic A phases. From the comparison between 5 and 1, the alkanoyloxy group at C-2 lowers the melting points. 相似文献
126.
The preparation, characterization and ammonia and water adsorption properties of edge-rich carbon nanofibers (CNFs) were studied, including platelet CNFs (PCNFs) and cup-stacked CNFs (CSCNFs). Since PCNFs and CSCNFs have many chemically active exposed edges, functionalization by oxidizing the edges was carried out by ozone stream and by nitric acid. Transmission electron microscopy, N2 adsorption isotherms and temperature-programmed desorption analysis showed that the nitric acid treatment partly destroyed the graphite structure of the PCNFs and created acid functional groups and micropores, whereas the ozone treatment created functional groups without damaging the structure. Ammonia adsorption isotherms clarified that NH3 adsorption on PCNFs and CSCNFs occurred mainly on oxygen-containing groups, whereas the adsorption on activated carbon fibers (ACFs) occurred on both oxygen-containing groups and the carbon surface without the functional groups, and the CSCNFs showed larger amounts of adsorbed ammonia compared to the PCNFs. Especially at a relatively low pressure range (<0.2 atm), the PCNFs/CSCNFs/ACFs showed the same ammonia adsorption mechanism; that is, the one-to-one interaction between oxygen atoms in the functional groups and hydrogen atoms in ammonia molecules. In addition, the adsorption on the ACFs appeared to occur mainly by interaction with the carbon surface at relatively high pressure (0.3–1.0 atm). Our experimental results and previous findings suggest that NH3 adsorption on PCNFs is due mainly to NH…O hydrogen bonding between oxygen-containing groups and ammonia rather than to chemical bonding. 相似文献
127.
Hisanao Yamamoto Akira Fujita Miyuki Harada Mitsukazu Ochi 《Molecular Crystals and Liquid Crystals》2014,588(1):41-50
A liquid crystalline epoxy resin (LCE) having α-methylstilbene as a mesogenic unit and an ethylene-oxy unit as a spacer (DGE(C2-MS-C2)) was synthesized and characterized. DGE (C2-MS-C2) has a lower melting point (MP) compared to the diglycidylether of 4,4′-dihydroxy-α-methylstilbene (DGEDHMS). The curing of DGE (C2-MS-C2) with diaminodiphenylethane (DDEt) in a mesophase generated a liquid crystalline (LC) network, which have a more highly layered structure than DGEDHMS. The LC network showed extensively large fracture energy on a tensile test. Introducing spacers outside the mesogen unit promotes the mesogen unit to form a highly ordered structure, which enhances the versatility of LC epoxy resins. 相似文献
128.
129.
Prof. Dr. Manabu Yamada Fumiya Uemura Dr. Uma Maheswara Rao Kunda Prof. Dr. Takenori Tanno Prof. Dr. Hiroshi Katagiri Prof. Dr. Fumio Hamada 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(38):8393-8399
Alkanes composed of C−C and C−H show a low electric polarization, and therefore, there is only very weak interaction between alkanes and adsorbents. Thus, it is difficult to separate a specific alkane from a mixture of alkanes by adsorption. Here, two activated “channel-like” crystals generated from brominated thiacalix[4]arene propyl ethers, which adopt 1,3-alternate and partial cone conformations, recognize specific alkane vapors depending on alkane-shape and -size, sorting in three-type alkane guests such as linear, branched, and cyclic alkanes. Two activated crystals, which are prepared by removal of solvent upon heating under reduced pressure, incorporate branched and/or cyclic alkane vapors by a unique “gate-opening” mechanism via a crystal transformation in the process. Linear alkane vapors do not trigger gate opening and are not taken up by the activated crystals. The shape and size molecular-recognition properties of the activated crystals promises considerable usefulness for the separation of linear, branched, and cyclic alkanes. 相似文献
130.