全文获取类型
收费全文 | 15339篇 |
免费 | 2809篇 |
国内免费 | 1822篇 |
专业分类
化学 | 10971篇 |
晶体学 | 154篇 |
力学 | 1132篇 |
综合类 | 64篇 |
数学 | 1654篇 |
物理学 | 5995篇 |
出版年
2024年 | 15篇 |
2023年 | 339篇 |
2022年 | 345篇 |
2021年 | 484篇 |
2020年 | 630篇 |
2019年 | 585篇 |
2018年 | 530篇 |
2017年 | 483篇 |
2016年 | 836篇 |
2015年 | 728篇 |
2014年 | 919篇 |
2013年 | 1129篇 |
2012年 | 1459篇 |
2011年 | 1444篇 |
2010年 | 982篇 |
2009年 | 920篇 |
2008年 | 1070篇 |
2007年 | 944篇 |
2006年 | 855篇 |
2005年 | 761篇 |
2004年 | 530篇 |
2003年 | 430篇 |
2002年 | 397篇 |
2001年 | 334篇 |
2000年 | 288篇 |
1999年 | 306篇 |
1998年 | 262篇 |
1997年 | 232篇 |
1996年 | 266篇 |
1995年 | 266篇 |
1994年 | 186篇 |
1993年 | 147篇 |
1992年 | 151篇 |
1991年 | 145篇 |
1990年 | 125篇 |
1989年 | 101篇 |
1988年 | 85篇 |
1987年 | 67篇 |
1986年 | 50篇 |
1985年 | 41篇 |
1984年 | 30篇 |
1983年 | 25篇 |
1982年 | 14篇 |
1981年 | 16篇 |
1980年 | 9篇 |
1978年 | 2篇 |
1972年 | 1篇 |
1957年 | 6篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
51.
Qin Yin Shou-Guo Wang Xiao-Wei Liang De-Wei Gao Jun Zheng Shu-Li You 《Chemical science》2015,6(7):4179-4183
An organocatalytic asymmetric chlorinative dearomatization of naphthols was realized for the first time, providing chiral naphthalenones with a Cl-containing all-substituted stereocenter in excellent yields and enantioselectivity (up to 97% yield and 96% ee). The reaction features mild reaction conditions, good tolerance of diverse functional groups and simple reaction operation. 相似文献
52.
Polypyrrole Shell@3D‐Ni Metal Core Structured Electrodes for High‐Performance Supercapacitors 下载免费PDF全文
Gao‐Feng Chen Yu‐Zhi Su Pan‐Yong Kuang Zhao‐Qing Liu Dao‐Yi Chen Xu Wu Nan Li Prof. Shi‐Zhang Qiao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(12):4614-4621
Three‐dimensional (3D) nanometal films serving as current collectors have attracted much interest recently owing to their promising application in high‐performance supercapacitors. In the process of the electrochemical reaction, the 3D structure can provide a short diffusion path for fast ion transport, and the highly conductive nanometal may serve as a backbone for facile electron transfer. In this work, a novel polypyrrole (PPy) shell@3D‐Ni‐core composite is developed to enhance the electrochemical performance of conventional PPy. With the introduction of a Ni metal core, the as‐prepared material exhibits a high specific capacitance (726 F g?1 at a charge/discharge rate of 1 A g?1), good rate capability (a decay of 33 % in Csp with charge/discharge rates increasing from 1 to 20 A g?1), and high cycle stability (only a small decrease of 4.2 % in Csp after 1000 cycles at a scan rate of 100 mV s?1). Furthermore, an aqueous symmetric supercapacitor device is fabricated by using the as‐prepared composite as electrodes; the device demonstrates a high energy density (≈21.2 Wh kg?1) and superior long‐term cycle ability (only 4.4 % and 18.6 % loss in Csp after 2000 and 5000 cycles, respectively). 相似文献
53.
54.
Yaogang Hu Peng Teng Wenyang Gao Xiaobing Zuo Lukasz Wojtas Randy W. Larsen Shengqian Ma Jianfeng Cai 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(6):2501-2507
Foldamers offer an attractive opportunity for the design of novel molecules that mimic the structures and functions of proteins and enzymes including biocatalysis and biomolecular recognition. Herein we report a new class of nonnatural helical sulfono‐γ‐AApeptide foldamers of varying lengths. The crystal structure of the sulfono‐γ‐AApeptide monomer S6 illustrates the intrinsic folding propensity of sulfono‐γ‐AApeptides, which likely originates from the bulkiness of tertiary sulfonamide moiety. The two‐dimensional solution NMR spectroscopy data for the longest sequence S1 demonstrates a 10/16 right‐handed helical structure. Optical analysis using circular dichroism further supports well‐ defined helical conformation of sulfono‐γ‐AApeptides in solution containing as few as five building blocks. Future development of sulfono‐γ‐AApeptides may lead to new foldamers with discrete functions, enabling expanded application in chemical biology and biomedical sciences. 相似文献
55.
A coarse-grained molecular dynamics simulation model was developed in this study to investigate the friction process occurring between Fe and polytetrafluoroethylene(PTFE).We investigated the effect of an external load on the friction coefficient of Fe–PTFE using the molecular dynamics simulations and experimental methods.The simulation results show that the friction coefficient decreases with the external load increasing,which is in a good agreement with the experimental results.The high external load could result in a larger contact area between the Fe and PTFE layers,severer springback as a consequence of the deformed PTFE molecules,and faster motion of the PTFE molecules,thereby affecting the friction force and normal force during friction and consequently varying the friction coefficient. 相似文献
56.
57.
58.
59.
60.
The Effect of Metal‐Ligand Affinity on Fe3O4_Supported Co–Rh Catalysts for Dicyclopentadiene Hydroformylation 下载免费PDF全文
Yubo Ma Shaojun Qing Nana Li Letao Zhang Shouzhu Li Zhixian Gao Hongyi Li Wumanjiang Eli Tianfu Wang 《国际化学动力学杂志》2015,47(10):621-628
The catalytic performances of Co‐Rh/Fe3O4 catalysts modified with phosphine ligands (PPh3) and its analogues on dicyclopentadiene hydroformylation were evaluated. Among these catalysts, Co‐Rh/Fe3O4 modified with tris(p‐trifluoromethylphenyl)phosphine was determined to be effective for monoformyltricyclodecanes production, whereas Co‐Rh/Fe3O4 modified with PPh3 or tri‐p‐tolylphosphine was effective for the diformyltricyclodecanes production. To investigate the ligand effects, the complex catalyst system (Co‐Rh/Fe3O4 and phosphine ligand) was subjected to pretreatment with syngas and then characterized by thermogravimetry and differential thermal analysis (TG‐DTA). It was determined that the threshold decomposition temperature reflected the corresponding Rh‐phosphine interaction strength, affecting the catalytic selectivity toward different products. A weak Rh‐phosphine interaction was desirable to produce monoformyltricyclodecanes with fast reaction kinetics, whereas a strong Rh‐phosphine complex was required for the synthesis of diformyltricyclodecanes. In addition to the selectivity rule shown in the PPh3 series, experiments with other ligands also demonstrated similar selectivity trends. 相似文献