全文获取类型
| 收费全文 | 12002篇 |
| 免费 | 1085篇 |
| 国内免费 | 951篇 |
专业分类
| 化学 | 7851篇 |
| 晶体学 | 127篇 |
| 力学 | 555篇 |
| 综合类 | 121篇 |
| 数学 | 1135篇 |
| 物理学 | 4249篇 |
出版年
| 2025年 | 19篇 |
| 2024年 | 165篇 |
| 2023年 | 288篇 |
| 2022年 | 440篇 |
| 2021年 | 534篇 |
| 2020年 | 587篇 |
| 2019年 | 673篇 |
| 2018年 | 466篇 |
| 2017年 | 412篇 |
| 2016年 | 604篇 |
| 2015年 | 590篇 |
| 2014年 | 680篇 |
| 2013年 | 822篇 |
| 2012年 | 996篇 |
| 2011年 | 951篇 |
| 2010年 | 688篇 |
| 2009年 | 597篇 |
| 2008年 | 665篇 |
| 2007年 | 610篇 |
| 2006年 | 508篇 |
| 2005年 | 394篇 |
| 2004年 | 286篇 |
| 2003年 | 259篇 |
| 2002年 | 286篇 |
| 2001年 | 265篇 |
| 2000年 | 172篇 |
| 1999年 | 209篇 |
| 1998年 | 153篇 |
| 1997年 | 104篇 |
| 1996年 | 94篇 |
| 1995年 | 73篇 |
| 1994年 | 75篇 |
| 1993年 | 67篇 |
| 1992年 | 57篇 |
| 1991年 | 56篇 |
| 1990年 | 53篇 |
| 1989年 | 43篇 |
| 1988年 | 29篇 |
| 1987年 | 19篇 |
| 1986年 | 16篇 |
| 1985年 | 8篇 |
| 1984年 | 5篇 |
| 1983年 | 8篇 |
| 1982年 | 3篇 |
| 1981年 | 2篇 |
| 1980年 | 2篇 |
| 1979年 | 2篇 |
| 1959年 | 2篇 |
| 1936年 | 1篇 |
排序方式： 共有10000条查询结果，搜索用时 15 毫秒
71.
The crystal structure of the title compound 2-[(P, P-Diphenoxy)phosphono(p-methyl)benzyl]-1, 2-benzisoselenazol-3(2H)-one, C27H22NO4PSe, was determined by single crystal X-ray diffraction. It crystallizes in the triclinic system, space group P(No. 2) with Mr=534.41, a=9.761(2), b=10.304(2), c=13.396(3), α=110.97(3), β=107.70(3). γ=90.02(3)°, V=1190(1) 3, Z=2, Dx=1.492 g/cm3, λ=0.71073, μ=1.6596 mm-1 and F(000)=544. The structure was solved by direct methods. The final R factor is 0.068 and Rw is 0.074 for 2500 unique observed reflections [I≥3σ(I)]. The results presented herein indicate that the selenium-containing bicyclic moiety is a coplanar structure and that two adjacent molecules are symmetrically linked to each other forming a dimer through the Se(1c)...O=P(1) bonding interaction with an intermolecular Se(1c)...O distance of 2.797 . 相似文献
72.
Jia Guogang 《Journal of Radioanalytical and Nuclear Chemistry》1994,185(2):255-264
A rapid and accurate method for the determination of90Sr in environmental soil has been developed; the procedure includes soil leaching by hydrochloric acid, oxalate precipitation, decontamination from210Bi, separation by HDEHP extraction chromatography column, yttrium oxalate precipitation and -counting. The interference of210Bi was found and studies have been made for the decontamination of90Y from210Bi by Bi2S3 precipitation giving a decontamination factor of 1.05·103. The analytical results obtained by the improved rapid method for 12 soil samples were comparable to that obtained by a previous method within a relative error of 20%. Studies of vertical distribution of90Sr in an environmental soil profile have shown that 90% of the90Sr deposits in the 30 cm surface soil of the earth with a highest concentration of 3.40 Bq/kg. When 50 g soil was analyzed, the yield of yttrium was 73±17% with a detection limit of 0.26 Bq/kg. 相似文献
73.
Qian Wei Rong Zhang Qin Wang Xin Jia Yan Quan Wei Yu Fu Xia Yan 《Natural product research》2020,34(9):1320-1325
AbstractAs part of our continuing efforts to explore bioactive compounds from natural resources, a new iridoid glycoside, adoxosidic acid-6′-oleuroperic ester (1), together with one known phenylethanoid glycoside (2) and two known flavonoid glycosides (3–4) were isolated from the fruit of Forsythia suspensa. The structure of the new compound (1) was elucidated through 1D and 2D NMR spectroscopic data and HR-ESIMS. Interestingly, compound 1 was a monoterpene ester of one iridoid glycoside. Compounds 2–4 were identified as calceolarioside A (2), kaempferol-3-O-rutinoside (3), kampferol-3-O-robinobioside (4) on the basis of NMR spectroscopic data analyses and comparison with the data reported in the literature. The antiviral activity aganisist influenza A (H5N1) virus of compound 1 was studied as well. 相似文献
74.
Siquan Zhang Guang Cheng Liping Guo Ning Wang Prof. Bien Tan Prof. Shangbin Jin 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(15):6063-6070
Methods to synthesize crystalline covalent triazine frameworks (CTFs) are limited and little attention has been paid to development of hydrophilic CTFs and photocatalytic overall water splitting. A route to synthesize crystalline and hydrophilic CTF-HUST-A1 with a benzylamine-functionalized monomer is presented. The base reagent used plays an important role in the enhancement of crystallinity and hydrophilicity. CTF-HUST-A1 exhibits good crystallinity, excellent hydrophilicity, and excellent photocatalytic activity in sacrificial photocatalytic hydrogen evolution (hydrogen evolution rate up to 9200 μmol g−1 h−1). Photocatalytic overall water splitting is achieved by depositing dual co-catalysts in CTF-HUST-A1, with H2 evolution and O2 evolution rates of 25.4 μmol g−1 h−1 and 12.9 μmol g−1 h−1 in pure water without using sacrificial agent. 相似文献
75.
Dr. Shuo Tao Dr. Xiaolei Li Dr. Xiaoge Wang Dr. Ying Wei Yunling Jia Dr. Jing Ju Dr. Yuanhui Cheng Prof. Huaisheng Wang Prof. Shuwen Gong Dr. Xingjun Yao Haixu Gao Cunyin Zhang Qiqi Zang Prof. Zhijian Tian 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(9):3483-3487
The synthesis of hierarchical nanosized zeolite materials without growth modifiers and mesoporogens remains a substantial challenge. Herein, we report a general synthetic approach to produce hierarchical nanosized single-crystal aluminophosphate molecular sieves by preparing highly homogeneous and concentrated precursors and heating at elevated temperatures. Accordingly, aluminophosphate zeotypes of LTA (8-rings), AEL (10-rings), AFI (12-rings), and -CLO (20-rings) topologies, ranging from small to extra-large pores, were synthesized. These materials show exceptional properties, including small crystallites (30–150 nm), good monodispersity, abundant mesopores, and excellent thermal stability. A time-dependent study revealed a non-classical crystallization pathway by particle attachment. This work opens a new avenue for the development of hierarchical nanosized zeolite materials and understanding their crystallization mechanism. 相似文献
76.
Yuting Wang Dr. Wei Zhou Ranran Jia Prof. Yifu Yu Prof. Bin Zhang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(13):5388-5392
Unveiling the active phase of catalytic materials under reaction conditions is important for the construction of efficient electrocatalysts for selective nitrate reduction to ammonia. The origin of the prominent activity enhancement for CuO (Faradaic efficiency: 95.8 %, Selectivity: 81.2 %) toward selective nitrate electroreduction to ammonia was probed. 15N isotope labeling experiments showed that ammonia originated from nitrate reduction. 1H NMR spectroscopy and colorimetric methods were performed to quantify ammonia. In situ Raman and ex situ experiments revealed that CuO was electrochemically converted into Cu/Cu2O, which serves as an active phase. The combined results of online differential electrochemical mass spectrometry (DEMS) and DFT calculations demonstrated that the electron transfer from Cu2O to Cu at the interface could facilitate the formation of *NOH intermediate and suppress the hydrogen evolution reaction, leading to high selectivity and Faradaic efficiency. 相似文献
77.
Yiliang Wang Liu-Pan Yang Xiang Zhao Lei Cui Jian Li Xueshun Jia Jianhui Fang Chunju Li 《Molecules (Basel, Switzerland)》2020,25(24)
Conformational exchanges of synthetic macrocyclic acceptors are rather fast, which is rarely studied in the absence of guests. Here, we report multiple stimuli-responsive conformational exchanges between two preexisting conformations of 2,2′,4,4′-tetramethoxyl biphen[3]arene (MeBP3) macrocycle. Structures of these two conformations are both observed in solid state, and characterized by 1H NMR, 13C NMR and 2D NMR in solution. In particular, conformational exchanges can respond to solvents, temperatures, guest binding and acid/base addition. The current system may have a role to play in the construction of molecular switches and other stimuli-responsive systems. 相似文献
78.
Gaseous reactant involved heterogeneous catalysis is critical to the development of clean energy, environmental management, health monitoring, and chemical synthesis. However, in traditional heterogeneous catalysis with liquid–solid diphase reaction interfaces, the low solubility and slow transport of gaseous reactants strongly restrict the reaction efficiency. In this minireview, we summarize recent advances in tackling these drawbacks by designing catalytic systems with an air–liquid–solid triphase joint interface. At the triphase interface, abundant gaseous reactants can directly transport from the air phase to the reaction centre to overcome the limitations of low solubility and slow transport of the dissolved gas in liquid–solid diphase reaction systems. By constructing a triphase interface, the efficiency and/or selectivity of photocatalytic reactions, enzymatic reactions, and (photo)electrochemical reactions with consumption of gaseous reactants oxygen, carbon dioxide, and nitrogen are significantly improved.Gaseous reactant involved liquid–solid diphase interface reactions can be significantly enhanced using rationally designed and constructed air–liquid–solid triphase systems. 相似文献
79.
Huan Li Lei Guo Xiaoliang Feng Liping Huo Shengqing Zhu Lingling Chu 《Chemical science》2020,11(19):4904
A selective, sequential C–O decarboxylative vinylation/C–H arylation of cyclic alcohol derivatives enabled by visible-light photoredox/nickel dual catalysis is described. This protocol utilizes a multicomponent radical cascade process, i.e. decarboxylative vinylation/1,5-HAT/aryl cross-coupling, to achieve efficient, site-selective dual-functionalization of saturated cyclic hydrocarbons in one single operation. This synergistic protocol provides straightforward access to sp3-enriched scaffolds and an alternative retrosynthetic disconnection to diversely functionalized saturated ring systems from the simple starting materials.A selective, sequential C–O decarboxylative vinylation/C–H arylation of cyclic alcohol derivatives enabled by visible-light photoredox/nickel dual catalysis has been described. 相似文献
80.
Mian Chang Jiayou Yu Shaojun Wang Liping Yang Yi Yang Shihao Cai Shouheng Shi Yan Wang P. W. Zhu 《中国科学B辑(英文版)》1997,40(5):529-534
A synthetical equation is proposed to characterize the essential features of the inverse “S” type curve on the basis of summing-up
simulation approach of “S” type curve. The two physical variables in the model obtained are discussed and the detailed method
used to determine the parameters is given. The model is then presented to describe the crystallization of poly(caryleher ether
ketone) (PEEK) and thermal decomposition of poly(amide-imide) (PAI) respectively. It is found that some thermal characteristic
parameters can be well estimated from the model simu-lated in computer. 相似文献