全文获取类型
收费全文 | 5915篇 |
免费 | 210篇 |
国内免费 | 28篇 |
专业分类
化学 | 3955篇 |
晶体学 | 71篇 |
力学 | 161篇 |
数学 | 438篇 |
物理学 | 1528篇 |
出版年
2024年 | 5篇 |
2023年 | 35篇 |
2022年 | 122篇 |
2021年 | 155篇 |
2020年 | 104篇 |
2019年 | 106篇 |
2018年 | 86篇 |
2017年 | 93篇 |
2016年 | 149篇 |
2015年 | 170篇 |
2014年 | 219篇 |
2013年 | 378篇 |
2012年 | 422篇 |
2011年 | 456篇 |
2010年 | 293篇 |
2009年 | 244篇 |
2008年 | 426篇 |
2007年 | 364篇 |
2006年 | 374篇 |
2005年 | 307篇 |
2004年 | 288篇 |
2003年 | 237篇 |
2002年 | 234篇 |
2001年 | 169篇 |
2000年 | 112篇 |
1999年 | 98篇 |
1998年 | 54篇 |
1997年 | 29篇 |
1996年 | 45篇 |
1995年 | 58篇 |
1994年 | 36篇 |
1993年 | 40篇 |
1992年 | 30篇 |
1991年 | 16篇 |
1990年 | 31篇 |
1989年 | 29篇 |
1988年 | 14篇 |
1987年 | 15篇 |
1985年 | 22篇 |
1984年 | 10篇 |
1983年 | 11篇 |
1982年 | 14篇 |
1981年 | 13篇 |
1980年 | 10篇 |
1979年 | 3篇 |
1978年 | 4篇 |
1977年 | 5篇 |
1975年 | 3篇 |
1974年 | 3篇 |
1969年 | 3篇 |
排序方式: 共有6153条查询结果,搜索用时 15 毫秒
991.
Won-Moon Choi Il-Doo Chung Neung-Ju Lee Young-Woo Lee Chang-Sik Ha Won-Jei Cho 《Journal of polymer science. Part A, Polymer chemistry》1998,36(13):2177-2184
The new monomer, α-methoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil (METFU), was synthesized by the reaction of 5-fluorouracil (5-FU) and exo-3,6-epoxy-1,2,3,6-tetrahydrophthalic anhydride (ETA) in order to prepare polymers containing 5-FU moiety. Poly(α-methoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil) [poly(METFU)], poly(α-methoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouraci-co-acrylic acid) [poly(METFU-co-AA)], and poly(α-methoxy-exo-3,6-epoxy-1,2,3,6-tetrahydrophthaloyl-5-fluorouracil-co-vinyl acetate) [poly(METFU-co- VAc)] were synthesized by photopolymerizations using 2,2-dimethoxy-2-phenylacetophenone (DMP) as an initiator. The synthesized METFU and the polymers were identified by FTIR and 1H-NMR spectroscopies. The contents of METFU in poly(METFU-co-AA) and poly(METFU-co-VAc) determined by elemental analysis were 52 and 60 mol %, respectively. The average molecular weights and polydispersity indices determined with GPC were as follows: M n = 9,400, M w = 11,400 M w/M n = 1.21 for poly(METFU), M n = 14,400, M w = 26,800, M w/M n = 1.86 for poly(METFU-co-AA), and M n = 23,100, M w = 33,000, M w/M n = 1.43 for poly(METFU-co-VAc). The in vitro cytotoxicities of samples were evaluated with mouse mammary carcinoma (FM3A), mouse leukemia (P388), and human histiocytic lymphoma (U937) as cancer cell lines, and mouse liver cells (AC2F) as a normal cell line. The in vivo antitumor activities of synthesized polymers against mice bearing the sarcoma 180 tumor cell line were greater than those of 5-FU at concentrations of 0.8 and 80 mg/kg. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2177–2184, 1998 相似文献
992.
Won Jung Yoon Jae Hoon Ryu Cheolhoon Cheong Kyu Yong Choi 《Macromolecular theory and simulations》1998,7(3):327-332
Molecular weight averages have long been used as a measure of polymer molecular weight properties in industrial polymer manufacturing processes. With a kinetic model, it is possible to directly calculate the polymer chain length distribution by integrating an infinite number of the polymer population balance equations. However, when the polymer chain length is very large, such a direct integration of polymer population balance equations can be computationally demanding. In this paper, the method of finite molecular weight moments is applied to the calculation of polymer chain length distribution in a batch free radical thermal polymerization of styrene. The weight fraction of a finite chain length interval is directly calculated in conjunction with a kinetic model. The method of calculation is illustrated through model simulations. 相似文献
993.
Miscibility behavior and rheological properties with mechanical spectroscopy study of both poly(3-hydroxybutyrate) (PHB)/poly(ethylene oxide) (PEO) and biodegradable synthetic aliphatic polyester (BDP)/linear low density polyethylene (LLDPE) were investigated. Blends of BDP with LLDPE were immiscible, showing two separate Tg values in all compositions; whereas blends of PHB with PEO were miscible, showing a single Tg in the whole range of compositions. However, the shear viscosities of both synthetic and biosynthetic blend systems decrease with increasing shear rate. When a modified Cole-Cole plot of the blend system is further considered, the logG′-logG” plot shows little sensitivity to a variation in both LLDPE composition for synthetic BDP and PEO composition for biosynthetic PHB. Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (P(3HB-co-3HV)) random copolymers were also investigated. 相似文献
994.
995.
996.
Peddaboodi Gopikrishna Huijeong Choi Do Hui Kim Jun Ho Hwang Youngwan Lee Hyeonwoo Jung Gyeonghwa Yu Telugu Bhim Raju Eunji Lee Youngu Lee Shinuk Cho BongSoo Kim 《Chemical science》2021,12(42):14083
The concurrent enhancement of short-circuit current (JSC) and open-circuit voltage (VOC) is a key problem in the preparation of efficient organic solar cells (OSCs). In this paper, we report efficient and stable OSCs based on an asymmetric non-fullerene acceptor (NFA) IPC-BEH-IC2F. The NFA consists of a weak electron-donor core dithienothiophen[3,2-b]-pyrrolobenzothiadiazole (BEH) and two kinds of strong electron-acceptor (A) units [9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile (IPC) with a tricyclic fused system and 2-(5,6-difluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile (IC2F)]. For comparison, the symmetric NFAs IPC-BEH-IPC and IC2F-BEH-IC2F were characterised. The kind of flanking A unit significantly affects the light absorption features and electronic structures of the NFAs. The asymmetric IPC-BEH-IC2F has the highest extinction coefficient among the three NFAs owing to its strong dipole moment and highly crystalline feature. Its highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels lie between those of the IPC-BEH-IPC and IC2F-BEH-IC2F molecules. The IPC group also promotes molecular packing through the tricyclic π-conjugated system and achieves increased crystallinity compared to that of the IC2F group. Inverted-type photovoltaic devices based on p-type polymer:NFA blends with PBDB-T and PM6 polymers as p-type polymers were fabricated. Among all these devices, the PBDB-T:IPC-BEH-IC2F blend device displayed the best photovoltaic properties because the IPC unit provides balanced electronic and morphological characteristics. More importantly, the PBDB-T:IPC-BEH-IC2F-based device exhibited the best long-term stability owing to the strongly interacting IPC moiety and the densely packed PBDB-T:IPC-BEH-IC2F film. These results demonstrate that asymmetric structural modifications of NFAs are an effective way for simultaneously improving the photovoltaic performance and stability of OSCs.A 9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile (IPC) moiety in asymmetric non-fullerene acceptors promotes the formation of a densely packed crystalline structure, enabling efficient and long-term stable organic solar cells. 相似文献
997.
998.
999.
1000.