全文获取类型
收费全文 | 701篇 |
免费 | 24篇 |
国内免费 | 1篇 |
专业分类
化学 | 589篇 |
晶体学 | 14篇 |
力学 | 5篇 |
数学 | 55篇 |
物理学 | 63篇 |
出版年
2024年 | 2篇 |
2023年 | 5篇 |
2022年 | 23篇 |
2021年 | 19篇 |
2020年 | 12篇 |
2019年 | 8篇 |
2018年 | 12篇 |
2017年 | 12篇 |
2016年 | 15篇 |
2015年 | 25篇 |
2014年 | 17篇 |
2013年 | 28篇 |
2012年 | 54篇 |
2011年 | 81篇 |
2010年 | 26篇 |
2009年 | 26篇 |
2008年 | 44篇 |
2007年 | 51篇 |
2006年 | 47篇 |
2005年 | 42篇 |
2004年 | 41篇 |
2003年 | 26篇 |
2002年 | 27篇 |
2001年 | 4篇 |
2000年 | 4篇 |
1999年 | 5篇 |
1998年 | 1篇 |
1997年 | 4篇 |
1996年 | 6篇 |
1995年 | 11篇 |
1994年 | 8篇 |
1993年 | 4篇 |
1992年 | 4篇 |
1991年 | 3篇 |
1988年 | 4篇 |
1986年 | 1篇 |
1985年 | 6篇 |
1984年 | 1篇 |
1982年 | 4篇 |
1981年 | 2篇 |
1980年 | 5篇 |
1979年 | 2篇 |
1977年 | 1篇 |
1976年 | 1篇 |
1934年 | 1篇 |
1905年 | 1篇 |
排序方式: 共有726条查询结果,搜索用时 15 毫秒
1.
2.
3.
Muhammad Faisal Nobuaki Sato Armando T. Quitain Hiroyuki Daimon Koichi Fujie 《国际化学动力学杂志》2007,39(3):175-180
The kinetics and pathway of hydrothermal decomposition of aspartic acid were studied using a continuous‐flow tubular reactor. The reaction was carried out in the temperature range of 200–260°C and at a pressure of 20 MPa. Deamination was the primary reaction, indicated by the presence of significant amount of ammonia, fumaric acid, or maleic acid in the products. Other reaction products were pyruvic acid, malic acid, and traces of succinic and lactic acid. Traces of alanine were also detected, showing the possibility of decomposing high‐molecular weight amino acids to obtain simple amino acids such as glycine or alanine. Results on the effect of reaction parameters demonstrated that decomposition of aspartic acid is highly temperature dependent under hydrothermal conditions. For a slight temperature difference of 60°C (from 200 to 260°C), the first‐order reaction rate constants of 0.003 significantly increased to 0.231 s?1. The activation energy was 144 kJ/mol, as calculated by the Arrhenius equation. No significant effect was exhibited by other reaction parameters such as pH and pressure. The results are useful in controlling the hydrolysis of proteinaceous materials toward high yield of aspartic acid under hydrothermal conditions. © 2007 Wiley Periodicals, Inc. 39: 175–180, 2007 相似文献
4.
Dimitri Markushevich Vladimir B. Matveev Armando Treibich 《Letters in Mathematical Physics》2006,76(2-3):109-109
5.
Dore Augusto Clemente Armando Marzotto Giovanni Valle 《Journal of chemical crystallography》1988,18(2):147-156
The crystal and molecular structure of thiamine monochloride (C12H17N4OSCl) was determined by X-ray diffraction and refined to a finalR value of 0.042. The compound crystallizes in the monoclinic system, space groupP21/a, with cell constantsa=18.929(4),b=11.663(2),c=6.376(2) Å and=96.72(8)°. The thiamine molecule is anhydrous and unprotonated, and the torsion angles at the methylene carbon show that it possesses anF conformation. The dihedral angle value of 84.16(6)° between thiazolium and pyrimidine rings is in the normal range found for the thiamine withF conformation, protonated or not, hydrated or not. Thiamine therefore has the same conformation notwithstanding protonation or hydration, with the rings similarly oriented in all the crystal structures containing thiamine. 相似文献
6.
Armando J. L. Pombeiro Raymond L. Richards 《Monatshefte für Chemie / Chemical Monthly》1992,123(8-9):749-756
Summary Reactions oftrans-[M(N2)2(dppe)2] (A;M=Mo, W;dppe=Ph
2PCH2CH2PPh
2) with ethyldiazoacetate, N2CHCOOEt, yield the bisdiazoalkane speciestrans-[M(N2CHCOOEt)2(dppe)2], upon simple replacement of the dinitrogen ligand by ethyldiazoacetate. However, diazomethane, N2CH2, reacts withA with loss of N2 to give products which we tentatively formulate as containing methylene ligands,trans-[M(CH2)2(dppe)2].
Herstellung von Bisdiazoalkan- und ähnlichen Komplexen aus den Reaktionen von Diazoverbindungen mit Distickstoffkomplexen des Typstrans-[M(N2)2(Ph 2PCH2CH2PPh 2)2] mitM=Mo oder W
Zusammenfassung Die Reaktion vontrans-[M(N2)2(dppe)2] (A:dppe=Ph 2PCH2CH2PPh 2 undM=Mo oder W) mit Ethyldiazoacetat, N2CHCOOEt, ergab nach einfachem Austausch des Distickstoffliganden mit Ethyldiazoacetat die Bisdiazoalkanetrans-[M(N2CHCOOEt)2(dppe)2]. Diazomethan (N2CH2) hingegen reagierte mitA unter Verlust von N2 zu Produkten, die tentativ alstrans-[M(CH2)2(dppe)2] mit Methylenliganden formuliert wurden.相似文献
7.
Armando J.L. Pombeiro Christopher J. Pickett Raymond L. Richards 《Journal of organometallic chemistry》1982,224(3):285-294
The isocyanide complexes trans-[ReCl(CNR)(dppe)2] (R Me, But, C6H4CH3-4, C6H4CH3-2, C6H4Cl-4, C6H4OCH3-4 and C6H3Cl2-2,6; dppe Ph2PCH2CH2PPh2) have been prepared by isocyanide displacement of dinitrogen from the parent complex trans-[ReCl(N2)(ddpe)2]. Their redox properties have been studied by cyclic voltammetry and are interpreted on the basis of the electronic properties and the geometry of the ligating isocyanides which are believed to be bent in these complexes, appearing to exhibit ligand parameter (PL) values ca. +0.3 V higher than those which would be expected for linear geometry. A very high polarisability (B ? 3.4) is observed for the {ReCl(dppe)2} site. 相似文献
8.
DellaGreca M Iesce MR Previtera L Temussi F Zarrelli A Mattia CA Puliti R 《The Journal of organic chemistry》2002,67(25):9011-9015
Androst-4-ene-3,17-dione (1) and 17alpha-methyltestosterone (2) are dimerized in the solid-state by UV radiation. These substances were selected by a search in the CSD among the steroid enones presenting in the crystalline state an intermolecular short contact between a hydrogen alpha to a carbonyl group and the oxygen of an enone system. Dimerization occurs by transfer of the hydrogen to the oxygen and connection between the two involved carbons. Androst-4-ene-3,17-dione (1) affords dimer 3 and trimer 4, both formed by connection of the C-16 of a molecule with the C-3 of a near one. Irradiation of 17alpha-methyltestosterone (2) gives the isomeric trienones 5 and 6. These compounds are reasonably formed by dehydration of unisolated intermediate products 7 and/or 8 obtained by coupling of two molecules through a linkage between the C-2 and the C-3' carbons. The formation mechanisms of the photoproducts are satisfactory explained on the basis of the molecular arrangement of the monomers in the crystal state. Modeling of the dimeric molecules was done using molecular mechanics calculations. A single-crystal X-ray of the dimer of androst-4-ene-3,17-dione confirms the structural interpretation of spectral data. The conformer found in the solid-state agrees well with the results of molecular mechanics calculations. 相似文献
9.
Armando Treibich 《Acta Appl Math》1994,36(1-2):27-48
We construct all tangential covers as zeroes of a particular set of polynomials. The resulting pointed curves give rise, through the Krichever dictionary, to elliptic KP solitons. We then give a criterion to detect the so-called hyperelliptic-tangential covers, which give rise to elliptic KdV solitons. Finally we construct new examples of the latter covers and write down the corresponding (doubly periodic finite-gap) source potentials.Dedicated to the memory of J.-L. Verdier 相似文献
10.
Sílvia S. P. R. Almeida Joo J. R. Fraústo Da Silva Armando J. L. Pombeiro 《Journal of organometallic chemistry》1993,450(1-2)
Treatment of a THF solution of trans-[ReCl(N2)(dppe)2] (dppe = Ph2PCH2CH2PPh2) with a 1-alkyne HCCR (R =tBu, CO2Me, CO2Et, or C6H4Me-4), in the presence of Tl[BF4]/[NH4][BF4], under sunlight, affords the corresponding carbyne-fluoro complexes trans-[ReF(CCH2R)(dppe)2][BF4] in an unprecedented single-pot synthesis. Further reaction with [BU4N]OH leads to the vinylidenefluoro compounds trans-[ReF(=C=CHR)(dppe)2] (R = CO2Me, CO2Et, or C6H4Me-4). 相似文献