全文获取类型
收费全文 | 21104篇 |
免费 | 3447篇 |
国内免费 | 2367篇 |
专业分类
化学 | 15079篇 |
晶体学 | 263篇 |
力学 | 1269篇 |
综合类 | 193篇 |
数学 | 2093篇 |
物理学 | 8021篇 |
出版年
2024年 | 76篇 |
2023年 | 480篇 |
2022年 | 690篇 |
2021年 | 778篇 |
2020年 | 848篇 |
2019年 | 816篇 |
2018年 | 683篇 |
2017年 | 634篇 |
2016年 | 992篇 |
2015年 | 998篇 |
2014年 | 1133篇 |
2013年 | 1470篇 |
2012年 | 1905篇 |
2011年 | 1914篇 |
2010年 | 1271篇 |
2009年 | 1121篇 |
2008年 | 1317篇 |
2007年 | 1293篇 |
2006年 | 1153篇 |
2005年 | 1025篇 |
2004年 | 731篇 |
2003年 | 635篇 |
2002年 | 580篇 |
2001年 | 444篇 |
2000年 | 416篇 |
1999年 | 480篇 |
1998年 | 364篇 |
1997年 | 380篇 |
1996年 | 317篇 |
1995年 | 304篇 |
1994年 | 304篇 |
1993年 | 252篇 |
1992年 | 197篇 |
1991年 | 199篇 |
1990年 | 184篇 |
1989年 | 120篇 |
1988年 | 86篇 |
1987年 | 90篇 |
1986年 | 61篇 |
1985年 | 44篇 |
1984年 | 44篇 |
1983年 | 25篇 |
1982年 | 25篇 |
1981年 | 18篇 |
1980年 | 14篇 |
1975年 | 2篇 |
1957年 | 4篇 |
1936年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Dr. Lipeng Zhai Dr. Siwen Cui Boli Tong Prof. Weihua Chen Dr. Zijie Wu Prof. Constantinos Soutis Prof. Donglin Jiang Prof. Guangshan Zhu Prof. Liwei Mi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(26):5784-5788
Covalent organic frameworks (COFs) enable precise integration of various organic building blocks into porous skeletons through topology predesign. Here, we report the first example of COFs by integrating electron withdrawing bromine group onto the skeletons for triboelectric nanogenerators (TENG). The resulting framework exhibits high surface area and good crystallinity. Thus, the bromine functionalized COF has more regular aligned π columns and arrays over the skeleton than bare COFs, which in turn significantly enhances charge transport ability. As a result, bromine functionalized COFs showed higher electrical output performance at 5 Hz with a peak value of short circuit current density of 43.6 μA and output voltage of 416 V, which is 2 and 1.3 times higher than those of bare COFs (21.6 μA and 318 V), respectively. These results demonstrated that this strategy for engineering electron withdrawing groups on the skeleton could open a new aspect of COFs for developing TENG devices. 相似文献
992.
993.
Long‐Zhang Dong Lei Zhang Jiang Liu Qing Huang Meng Lu Wen‐Xin Ji Ya‐Qian Lan 《Angewandte Chemie (International ed. in English)》2020,59(7):2659-2663
A series of stable heterometallic Fe2M cluster‐based MOFs ( NNU‐31‐M , M=Co, Ni, Zn) photocatalysts are presented. They can achieve the overall conversion of CO2 and H2O into HCOOH and O2 without the assistance of additional sacrificial agent and photosensitizer. The heterometallic cluster units and photosensitive ligands excited by visible light generate separated electrons and holes. Then, low‐valent metal M accepts electrons to reduce CO2, and high‐valent Fe uses holes to oxidize H2O. This is the first MOF photocatalyst system to finish artificial photosynthetic full reaction. It is noted that NNU‐31‐Zn exhibits the highest HCOOH yield of 26.3 μmol g?1 h?1 (selectivity of ca. 100 %). Furthermore, the DFT calculations based on crystal structures demonstrate the photocatalytic reaction mechanism. This work proposes a new strategy for how to design crystalline photocatalyst to realize artificial photosynthetic overall reaction. 相似文献
994.
Kun Lu Ju Huang Li Ren Chao Li Yejun Guan Bingwen Hu Hao Xu Jingang Jiang Yanhang Ma Peng Wu 《Angewandte Chemie (International ed. in English)》2020,59(15):6258-6262
Precisely controlled crystal growth endows zeolites with special textural and catalytic properties. A nanosheet mordenite zeolite with a thickness of ca. 11 nm, named as MOR‐NS, has been prepared using a well‐designed gemini‐type amphiphilic surfactant as bifunctional structure‐directing agent (SDA). Its benzyl diquarternary ammonium cations structurally directed the formation of MOR topology, whereas the long and hydrophobic hexadecyl tailing group prevented the extensive crystal growth along b axis. This kind of orientated crystallization took place through the inorganic–organic interaction between silica species and SDA molecules present in the whole process. The thin MOR nanosheets, with highly exposed (010) planes and 8‐membered ring (MR) windows, exhibited a much improved ethylene selectivity (42.1 %) for methanol‐to‐olefin (MTO) reactions when compared with conventional bulk MOR crystals (3.3 %). 相似文献
995.
Bin‐Wen Liu Xiao‐Ming Jiang Bing‐Xuan Li Hui‐Yi Zeng Guo‐Cong Guo 《Angewandte Chemie (International ed. in English)》2020,59(12):4856-4859
A large nonlinear optical (NLO) coefficient and a wide band gap are two crucial but contradictory parameters that are difficult to achieve simultaneously in a single infrared (IR) NLO compound. A salt‐inclusion chalcogenide (SIC), Li[LiCs2Cl][Ga3S6] ( 1 ), was prepared that presents a nanosized tunnel framework constructed from monotype chalcogenide tetrahedra. Highly oriented covalent GaS4 tetrahedra in the host lead to a moderate second harmonic generation response (0.7 AgGaS2), and ionic guests effectively broaden the band gap to the widest value (4.18 eV) among all IR NLO chalcogenides, thereby achieving a remarkable balance between NLO efficiency and band gap. 相似文献
996.
Jiang Tian Liu Hannes Hase Sarah Taylor Ingo Salzmann Pat Forgione 《Angewandte Chemie (International ed. in English)》2020,59(18):7146-7153
A library of symmetrical linear oligothiophene was prepared employing decarboxylative cross‐coupling reaction as the key transformation. Thiophene potassium carboxylate salts were used as cross‐coupling partners without the need of co‐catalyst, base, or additives. This method demonstrates complete chemoselectivity and is a comprehensive greener approach compared to the existing methods. The modularity of this approach is demonstrated with the preparation of discreet oligothiophenes with up to 10 thiophene repeat units. Symmetrical oligothiophenes are prototypical organic semiconductors where their molecular electrical doping as a function of the chain length can be assessed spectroscopically. An oligothiophene critical length for integer charge transfer was observed to be 10 thiophene units, highlighting the potential use of discrete oligothiophenes as doped conduction or injection layers in organic electronics applications. 相似文献
997.
Wenbin Wang Yutang Wang Ruoou Yang Qunlei Wen Youwen Liu Zheng Jiang Huiqiao Li Tianyou Zhai 《Angewandte Chemie (International ed. in English)》2020,59(39):16974-16981
Electrochemical synthesis based on electrons as reagents provides a broad prospect for commodity chemical manufacturing. A direct one‐step route for the electrooxidation of amino C?N bonds to nitrile C≡N bonds offers an alternative pathway for nitrile production. However, this route has not been fully explored with respect to either the chemical bond reforming process or the performance optimization. Proposed here is a model of vacancy‐rich Ni(OH)2 atomic layers for studying the performance relationship with respect to structure. Theoretical calculations show the vacancy‐induced local electropositive sites chemisorb the N atom with a lone pair of electrons and then attack the corresponding N(sp3)?H, thus accelerating amino C?N bond activation for dehydrogenation directly into the C≡N bond. Vacancy‐rich nanosheets exhibit up to 96.5 % propionitrile selectivity at a moderate potential of 1.38 V. These findings can lead to a new pathway for facilitating catalytic reactions in the chemicals industry. 相似文献
998.
Jiang Wang Pan‐Lin Shao Xin Lin Baode Ma Jialin Wen Xumu Zhang 《Angewandte Chemie (International ed. in English)》2020,59(41):18166-18171
An unprecedented Ir/f‐amphox‐catalyzed asymmetric hydrogenation of racemic 2,3‐syn‐dihydroxy‐1,4‐diones is presented involving dynamic kinetic resolution, which produces (1R,2R,3R,4R)‐tetraols. This protocol constitutes an efficient and straightforward approach to accessing sugar alcohols bearing four contiguous stereocenters. The strategy exhibits various advantages over existing methods, including excellent yields (up to 98 %), exceptional stereoselectivities (up to 99:1 dr, 99.9 % ee), operational simplicity and substrate generality. Moreover, the nature of the reaction was revealed as a stepwise transformation by in situ Fourier‐transform infrared spectroscopy and isolation of intermediates. 相似文献
999.
Chang Su Jin‐Song Gong Jin‐Peng Ye Ji‐Meng He Rui‐Yi Li Min Jiang Yan Geng Yan Zhang Jing‐Hua Chen Zheng‐Hong Xu Jin‐Song Shi 《Macromolecular bioscience》2020,20(9)
Keratin is widely recognized as a high‐quality renewable protein resource for biomedical applications. Despite their extensive existence, keratin resources such as feathers, wool, and hair exhibit high stability and mechanical properties because of their high disulfide bond content. Consequently, keratin extraction is challenging and its application is greatly hindered. In this work, a biological extraction strategy is proposed for the preparation of bioactive keratin and the fabrication of self‐assembled keratin hydrogels (KHs). Based on moderate and controlled hydrolysis by keratinase, keratin with a high molecular weight of approximately 45 and 28 kDa that retain its intrinsic bioactivities is obtained. The keratin products show excellent ability to promote cell growth and migration and are conferred with significant antioxidant ability because of their intrinsically high cysteine content. In addition, without the presence of any cross‐linking agent, the extracted keratin can self‐assemble into injectable hydrogels. The KHs exhibit a porous network structure and 3D culture ability, showing potential in promoting wound healing. This enzyme‐driven keratin extraction strategy opens up a new approach for the preparation of keratin that can self‐assemble into injectable hydrogels for biomedical engineering. 相似文献
1000.
Wang C. Cheng S. Y. Zhao W. W. Yang X. N. Zhou K. Z. Tian J. J. Jiang D. F. Ma P. H. 《Crystallography Reports》2020,65(7):1156-1160
Crystallography Reports - This paper reports on the supramolecular self-assembly of cyclopentano cucurbit[5]uril (CyP5Q[5]), L-phenylalanine (L-Phe), and cadmium ions. The crystal structure is... 相似文献