全文获取类型
收费全文 | 3347篇 |
免费 | 441篇 |
国内免费 | 101篇 |
专业分类
化学 | 3466篇 |
晶体学 | 81篇 |
力学 | 7篇 |
综合类 | 5篇 |
数学 | 78篇 |
物理学 | 162篇 |
无线电 | 90篇 |
出版年
2024年 | 9篇 |
2023年 | 58篇 |
2022年 | 54篇 |
2021年 | 90篇 |
2020年 | 149篇 |
2019年 | 100篇 |
2018年 | 94篇 |
2017年 | 66篇 |
2016年 | 185篇 |
2015年 | 157篇 |
2014年 | 203篇 |
2013年 | 244篇 |
2012年 | 218篇 |
2011年 | 175篇 |
2010年 | 152篇 |
2009年 | 196篇 |
2008年 | 235篇 |
2007年 | 256篇 |
2006年 | 205篇 |
2005年 | 222篇 |
2004年 | 202篇 |
2003年 | 112篇 |
2002年 | 52篇 |
2001年 | 53篇 |
2000年 | 54篇 |
1999年 | 62篇 |
1998年 | 53篇 |
1997年 | 49篇 |
1996年 | 45篇 |
1995年 | 39篇 |
1994年 | 19篇 |
1993年 | 15篇 |
1992年 | 9篇 |
1991年 | 3篇 |
1990年 | 6篇 |
1989年 | 5篇 |
1988年 | 7篇 |
1987年 | 5篇 |
1986年 | 2篇 |
1985年 | 5篇 |
1984年 | 6篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1980年 | 3篇 |
1979年 | 3篇 |
1978年 | 1篇 |
1977年 | 3篇 |
1976年 | 1篇 |
1974年 | 1篇 |
1971年 | 1篇 |
排序方式: 共有3889条查询结果,搜索用时 9 毫秒
1.
Michael C. W. Chan Dr. 《化学:亚洲杂志》2008,3(1):18-27
The notion of weak attractive ligand–polymer interactions is introduced, and its potential application, importance, and conceptual links with “cooperative” ligand–substrate interactions are discussed. Synthetic models of weak attractive ligand–polymer interactions are described, in which intramolecular weak C? H???F? C interactions (the existence of which remains contentious) have been detected by NMR spectroscopy and neutron and X‐ray diffraction experiments. These C? H???F? C interactions carry important implications for the design of catalysts for olefin polymerization, because they provide support for the practical feasibility of ortho‐F???Hβ ligand–polymer contacts proposed for living Group 4 fluorinated phenoxyimine catalysts. The notion of weak attractive noncovalent interactions between an “active” ligand and the growing polymer chain is a novel concept in polyolefin catalysis. 相似文献
2.
The self‐complementary tetrameric propargyl triols 8, 14, 18 , and 21 were synthesized to investigate the duplex formation of self‐complementary, ethynylene‐linked UUAA, AAUU, UAUA, and AUAU analogues with integrated bases and backbone (ONIBs). The linear synthesis is based on repetitive Sonogashira couplings and C‐desilylations (34–72% yield), starting from the monomeric propargyl alcohols 9 and 15 and the iodinated nucleosides 3, 7, 11 , and 13 . Strongly persistent intramolecular H‐bonds from the propargylic OH groups to N(3) of the adenosine units prevent the gg‐type orientation of the ethynyl groups at C(5′). As such, an orientation is required for the formation of cyclic duplexes, this H‐bond prevents the formation of duplexes connected by all four base pairs. However, the central units of the UAUA and AAUU analogues 18 and 14 associate in CDCl3/(D6)DMSO 10 : 1 to form a cyclic duplex characterized by reverse Hoogsteen base pairing. The UUAA tetramer 8 forms a cyclic UU homoduplex, while the AUAU tetramer 21 forms only linear associates. Duplex formation of the O‐silylated UUAA and AAUU tetramers is no longer prevented. The self‐complementary UUAA tetramer 22 forms Watson–Crick‐ and Hoogsteen‐type base‐paired cyclic duplexes more readily than the sequence‐isomeric AAUU tetramer 23 , further illustrating the sequence selectivity of duplex formation. 相似文献
3.
Organophosphorus compounds have been applied in two ways in chemical synthesis. They can either be used as a reagent in a step of the synthesis (for example, in the Wittig reaction) or they can be incorporated directly into the target molecule. This second application, in particular, has expanded greatly in the last few years with the preparation of low-coordination phosphorus compounds. These include the phosphaalkynes, which are of great interest to organic and inorganic chemists. Phosphaalkynes have been employed in the synthesis of heterocyclic compounds, phosphaarenes and their valence isomers, and polycyclic compounds. Further applications have been the use of phosphaalkynes as new ligand systems in complex chemistry and their cyclooligomerization with organometallic reagents. While the chemical properties of phosphaalkynes have little in common with those of nitriles, they are in many ways very similar to those of the isoelectronic acetylenes. 相似文献
4.
A. V. Afonin 《Russian Chemical Bulletin》1996,45(5):1142-1144
The analysis of the effect of the solvents on the proton chemical shifts in1H NMR spectra of 2-vinyloxypyridine indicates that the C—H...N interaction of weak intramolecular hydrogen bond type hinders the formation of intermolecular hydrogen C—H...X and C-H... bonds. The protonating solvents reduce the intramolecular C—H...N interaction due to association with the N atom of the pyridine cycle.Translated fromIzvestiya Akademii Nauk. Seriya Khimieheskaya, No. S, pp. 1202–1204, May, 1996. 相似文献
5.
Safoklov B. B. Atovmyan E. G. Nikonova L. A. Tkachev V. V. Aldoshin S. M. 《Russian Chemical Bulletin》2002,51(12):2224-2229
Pyrrole-2-carbaldehyde isonicotinoylhydrazone (1) and its hydrate [1·H2O] (2) were studied by single-crystal X-ray diffraction analysis. The introduction of the pyrrole substituent into N"-substituted isonicotinic hydrazide (INH) causes the intramolecular redistribution of the electron density compared to those in INHs studied earlier, which increases the basicity of the hydrazone nitrogen atom (N") involved in intermolecular hydrogen bonding. This effect has not been observed in the structures of N"-substituted INHs and benzhydrazides studied previously. Intermolecular hydrogen bonds play a decisive role in the formation of the crystal structures of 1 and 2. 相似文献
6.
We discuss the impact of density functional electronic structure calculations for understanding the organometallic chemistry of transition metal (TM) surface complexes and clusters. Examples will cover three types of systems, mainly of interest in the context of heterogeneous catalysis: (i) supported carbonyl complexes of rhenium on MgO and of rhodium in zeolites, (ii) TM clusters with CO ligands and adsorbates, and (iii) metal clusters exhibiting chemical bonds with atomic carbon. The first group of case studies promotes the concept that surface groups of oxide supports are bonded to TM complexes in the same way as common (poly-dentate) ligands are bonded in coordination compounds. The second group of examples demonstrates various “ligand effects” of TM clusters. Finally, we illustrate how carbido centers stabilize TM clusters and modify the propensity for adsorption at the surface of such clusters. 相似文献
7.
The MNDO method has been modified for the calculation of the properties of complexes with hydrogen bonds S-H-X, X = N, O, F, S. The results obtained are in good agreement with the experimental data. 相似文献
8.
In this study, we investigated how the presence of multiple intermolecular interaction sites influences the heteromeric supramolecular assembly of N-[(3-pyridinylamino) thioxomethyl] carbamates with fluoroiodobenzenes. Three targets—R-N-[(3-pyridinylamino) thioxomethyl] carbamate (R = methyl, ethyl, and isobutyl)—were selected and crystallized, resulting in three parent structures, five co-crystals, and one co-crystal solvate. Three hydrogen-bonded parent crystal structures were stabilized by N-H···N hydrogen bonding and assembled into layers that stacked on top of one another. Molecular electrostatic potential surfaces were employed to rank binding sites (Npyr > C=S > C=O) in order to predict the dominant interactions. The N-H⋯H hydrogen bond was replaced by I⋯Npyr in 3/6 cases, I⋯C=S in 4/6 cases, and I⋯O=C in 1 case. Interestingly, the I⋯C=S halogen bond coexisted twice with I⋯Npyr and I⋯O=C. Overall, the MEPs were fairly reliable for predicting co-crystallization outcomes; however, it is crucial to also consider factors such as molecular flexibility. Finally, halogen-bond donors are capable of competing for acceptor sites, even in the presence of strong hydrogen-bond donors. 相似文献
9.
Abstract. A novel germanate compound, |[Ni(dien)2]3(H2O)3|[Ge7O13F5]2(designated JU‐85, dien = diethylenetriamine), was solvothermally synthesized. The structure of JU‐85 was determined by single‐crystal X‐ray diffraction and further characterized by powder X‐ray diffraction, inductively coupled plasma, infrared spectroscopy, elemental analysis, and thermogravimetric analysis. JU‐85 has dissymmetric chains constructed from diagonally linked Ge7 building units and various Ni(dien)22+ complexes formed in situ during the synthesis. Compared with its structural analogue, FJ‐6, JU‐85 contains less complex cations and different host‐guest assembly. Besides the diagonal linkage in JU‐85, other dissymmetric linkages of Ge7 building units were enumerated, which could be used as the stereogenic centers for the design of novel chiral germanate compounds. 相似文献
10.