全文获取类型
收费全文 | 534篇 |
免费 | 13篇 |
国内免费 | 1篇 |
专业分类
化学 | 436篇 |
晶体学 | 10篇 |
力学 | 11篇 |
数学 | 9篇 |
物理学 | 82篇 |
出版年
2023年 | 2篇 |
2022年 | 4篇 |
2021年 | 9篇 |
2020年 | 15篇 |
2019年 | 11篇 |
2018年 | 9篇 |
2017年 | 9篇 |
2016年 | 16篇 |
2015年 | 5篇 |
2014年 | 14篇 |
2013年 | 40篇 |
2012年 | 40篇 |
2011年 | 49篇 |
2010年 | 13篇 |
2009年 | 12篇 |
2008年 | 16篇 |
2007年 | 26篇 |
2006年 | 25篇 |
2005年 | 22篇 |
2004年 | 17篇 |
2003年 | 18篇 |
2002年 | 16篇 |
2001年 | 8篇 |
2000年 | 11篇 |
1999年 | 7篇 |
1998年 | 4篇 |
1997年 | 3篇 |
1996年 | 3篇 |
1995年 | 6篇 |
1994年 | 3篇 |
1992年 | 5篇 |
1991年 | 6篇 |
1990年 | 5篇 |
1989年 | 8篇 |
1988年 | 3篇 |
1987年 | 6篇 |
1986年 | 7篇 |
1985年 | 6篇 |
1984年 | 12篇 |
1983年 | 4篇 |
1982年 | 4篇 |
1981年 | 5篇 |
1980年 | 5篇 |
1979年 | 9篇 |
1978年 | 6篇 |
1977年 | 5篇 |
1976年 | 5篇 |
1975年 | 4篇 |
1973年 | 2篇 |
1969年 | 2篇 |
排序方式: 共有548条查询结果,搜索用时 281 毫秒
11.
Gunter Silber Dieter Flockerzi Rajendra Singh Varma Ramamurthy Charubala Eugen Uhlmann Wolfgang Pfleiderer 《Helvetica chimica acta》1981,64(5):1704-1716
Nucleotides. XV. Synthesis and Properties of 2′O-t-Butyldimethylsilyl-5′-O-monomethoxytritylribonucleoside-3′-phosphotriesters, Starting Materials for Oligonucleotide Syntheses The syntheses of two types of fully blocked ribonucleoside 3′-phosphotriesters 6–14 have been achieved in excellent yields from 2′-O-t-butyldimethylsilyl-5′-O-monomethoxytrityl-ribonucleosides 1–5 by phosphorylation with 2-chloro- and 2,5-dichlorophenylphosphorodichloridate respectively and subsequent treatment by cyanoethanol to 6 , 8 , 10 , 12 and 14 and by p-nitrophenylethanol to 7 , 9 , 11 and 13 . These phosphotriesters are valuable starting materials for oligonucleotide syntheses due to the fact that the corresponding phosphotriesters 15–23 with free HO? C(5′) could be obtained by detritylation and the 3′-phosphodiester triethylammonium salts 24–32 by deblocking of the cyanoethyl and the 2,5-dichlorophenyl group respectively. All newly synthesized compounds have been characterized by UV.-and NMR.-spectra as well as C, H, N elementary analyses. 相似文献
12.
Treatment of 2 equiv of indole-3-aldehyde with o, m, p-xylyl, 2,5-dimethoxy-p-xylyl dibromides and 4,4′-bis(bromomethyl)-1,1′-biphenyl gave the bisalkylated products, which underwent McMurry coupling with low valent titanium to give indolophanes. Various cis-stilbenophanes with m-terphenyl building blocks were also synthesized by application of the McMurry coupling technique. 相似文献
13.
14.
Ramamurthy Charubala Eugen Uhlmann Frank Himmelsbach Wolfgang Pfleiderer 《Helvetica chimica acta》1987,70(8):2028-2038
The chemical synthesis of 3′-deoxyadenyly-(2′-5′)-3′-deoxyadenylyl-(2′-5′)-3′-deoxyadenosine ( 30 ; trimeric cordycepin) is described by three different routes using various protecting groups and applying the phosphotriester approach. The intermediates have been isolated and characterized by elemental analyses and spectroscopic means. High yields of 30 have been obtained on deprotection making this biologically very active compound available in preparative scale. 相似文献
15.
The phonon dispersion curves, phonon frequency distribution function as well as the lattice specific heat of body-centred
tetragonal indium have been deduced using a lattice dynamical model which includes central, angular and volume forces. Six
elastic constants, four zone boundary frequencies and an equilibrium condition were used in the evaluation of the force constants.
It is shown that this model is elastically consistent and satisfies the symmetry requirements of the lattice, the phonon frequencies
of indium deduced from it are in very good agreement with the experimental values of Reichardt and Smith and the theoretical
values of Garrett and Swihart, and theθ
D values compare well with the experimental values over a wide temperature range. The apparent discrepancies in the phonon
dispersion curves and theθ
D-T curves obtained from deficient models, importance of umklapp processes and the significance of angular forces in the lattice
dynamical models are discussed. 相似文献
16.
T. Balakrishnan S. Hari Babu A. Perumal 《Journal of polymer science. Part A, Polymer chemistry》1990,28(6):1421-1434
The alkylation and cycloalkylation of phenylacetonitrile (PAN) with excess of 1-bromobutane and 1,4-dibromobutane respectively catalyzed by aqueous NaOH and insoluble polystyrene-bound benzyltriethylammonium chloride were studied and the rates depend upon several experimental parameters. The rate of cycloalkylation of PAN is five times faster than the alkylation and the former proceeds even in the absence of the solid catalyst. Both alkylation and cycloalkylation gave higher rates in reverse addition method than in direct addition. Deprotonation of PAN by hydroxide ion takes place without participation of the polymeric catalyst. The electrostatic force between the positive charge on the nitrogen atom of catalyst and carbanion is responsible for alkylation of active nitrile with polystyrene-bound phase-transfer catalyst. The rates of both the reactions increase with increased stirring speed, ring substitution, hydroxide ion concentration and catalyst amount and decrease with increased particle size and the degree of cross-linking of the polymer. Apparent activation energies for the reactions were calculated. The kinetic results are discussed in terms of mass transfer and a combination of intraparticle diffusion and intrinsic reactivity limitations of the rates. 相似文献
17.
Alan R. Katritzky Subbu Perumal Wojciech Kuzmierkiewicz Ping Lue John V. Greenhill 《Helvetica chimica acta》1991,74(8):1924-1930
tert- Alkyl sulfides are conveniently prepared from α-(1H-benzotriazol-1-yl)alkyl sulfides by displacement of the 1H-benzotriazol-1-yl group with Grignard reagents. The 1-[α-(alkylthio)alkyl]- and 1-[α-(arylthio)alkyl]-1H-benzotriazole intermediates are easily available by several routes: (i) displacement of the halogen from appropriate halides by sodium salts of thiols, (ii) condensation of 1H-benzotriazole and thiols with carbonyl compounds, or (iii) lithiation of N-substituted 1H-benzotriazoles and subsequent treatment with electrophiles. 相似文献
18.
Nucleotides. X. Synthesis and properties of dinucleoside monophosphates with 2′-deoxyadenosine and 1-(2′-deoxy-β-D -ribofuranosyl)-lumazines as building blocks The synthesis of various dinucleoside monophosphates 16--20 consisting of 2′-deoxyadenosine and 1-(2′-deoxy-β-D -ribofuranosyl)-lumazines via the triester approach is described. The fully protected phosphotriesters 6--10 as well as the partially deblocked intermediates 11--15 have also been isolated and characterized by physical means. Intramolecular interactions in 16--20 have been investigated by the determination of the hypochromicities and CD. spectra revealing a more or less distinct stacking effect in dependence of the 6,7-substituents in the lumazine moiety as well as the polarity of the internucleotidic linkage. Enzymatic degradations of the dinucleoside monophosphates with snake venom and spleen phosphodiesterase are depending strongly on various structural features indicating a much lower substrate specificity especially in presence of 6,7-diphenyl-lumazine as an aglycone with the latter enzyme. 相似文献
19.
P. Thirumalai Perumal 《合成通讯》2013,43(9):1353-1356
A novel oxidative cleaved product and addition product were obtained from the oxidation of alkenes with peroxydisul-phate-copper(II) systems. 相似文献
20.
A Phosphorescent Platinum(II) Bipyridyl Supramolecular Polymer Based on Quadruple Hydrogen Bonds
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Fang‐Wei Liu Dr. Li‐Ya Niu Prof. Yong Chen Prof. Vaidhyanathan Ramamurthy Prof. Li‐Zhu Wu Prof. Chen‐Ho Tung Prof. Yu‐Zhe Chen Prof. Qing‐Zheng Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(50):18132-18139
A platinum(II) bipyridyl complex bearing bis‐ureidopyrimidinone (Pt‐bisUPy) has been designed and its self‐assembling behavior has been thoroughly investigated by 1H NMR, DOSY NMR, Ubbelohde viscometry analysis, UV/Vis, and emission spectroscopies. Pt‐bisUPy underwent concentration‐dependent ring‐chain polymerization in apolar solvents. Hydrogen‐bonding interactions play an important role during the formation of the supramolecular polymers. Hydrogen‐bonded supramolecular polymers were transformed to nanoparticles in water through the miniemulsion method. These nanoparticles showed strong π–π excimeric emission. Metal‐metal‐to‐ligand charge transfer (MMLCT) from Pt–Pt interactions was not significant in the emission spectrum. The phosphorescence of the nanoparticle persisted even under aerobic conditions. The triplet state of these phosphorescent nanomaterials were long‐lived and possessed moderate emission quantum yields. Furthermore, the low toxicity of these materials promises a place for them in in vitro and in vivo bioimaging. 相似文献