全文获取类型
收费全文 | 176178篇 |
免费 | 14174篇 |
国内免费 | 23682篇 |
专业分类
化学 | 144553篇 |
晶体学 | 2990篇 |
力学 | 3431篇 |
综合类 | 1820篇 |
数学 | 24355篇 |
物理学 | 36885篇 |
出版年
2024年 | 232篇 |
2023年 | 2086篇 |
2022年 | 2709篇 |
2021年 | 4960篇 |
2020年 | 5487篇 |
2019年 | 5140篇 |
2018年 | 4413篇 |
2017年 | 5302篇 |
2016年 | 6062篇 |
2015年 | 5592篇 |
2014年 | 7485篇 |
2013年 | 13975篇 |
2012年 | 10889篇 |
2011年 | 10379篇 |
2010年 | 8971篇 |
2009年 | 11312篇 |
2008年 | 11684篇 |
2007年 | 11913篇 |
2006年 | 10534篇 |
2005年 | 8754篇 |
2004年 | 8250篇 |
2003年 | 7017篇 |
2002年 | 8684篇 |
2001年 | 5093篇 |
2000年 | 4550篇 |
1999年 | 4082篇 |
1998年 | 3617篇 |
1997年 | 2880篇 |
1996年 | 2637篇 |
1995年 | 2522篇 |
1994年 | 2270篇 |
1993年 | 1896篇 |
1992年 | 1814篇 |
1991年 | 1201篇 |
1990年 | 970篇 |
1989年 | 914篇 |
1988年 | 786篇 |
1987年 | 586篇 |
1986年 | 550篇 |
1985年 | 644篇 |
1984年 | 543篇 |
1983年 | 298篇 |
1982年 | 533篇 |
1981年 | 688篇 |
1980年 | 616篇 |
1979年 | 635篇 |
1978年 | 527篇 |
1977年 | 393篇 |
1976年 | 336篇 |
1973年 | 212篇 |
排序方式: 共有10000条查询结果,搜索用时 343 毫秒
911.
Kenji Hara Keiji Iwahashi Satoru Takakusagi Kohei Uosaki Masaya Sawamura 《Surface science》2007,601(22):5127-5132
Functionalization of self-assembled monolayer (SAM) of alkanethiolate with metal containing unit is one of the versatile methods to obtain functional surfaces such as heterogeneous catalysts. However, organic molecules that strongly bind to transition metals at SAM terminal are limited. Recently N-heterocyclic carbenes (NHCs) such as cyclic diaminocarbenes have emerged as strongly σ-donating ligands forming a robust bond with broad spectrum of transition metals. In the present study, for the purpose of establishment of a new robust basement for heterogeneous metal catalysts, a SAM of the alkanethiolate terminated with NHC-rhodium(I) complex moiety was prepared by utilizing a newly designed disulfide molecule bearing NHC-metal complex terminals. X-ray photoelectron spectroscopy (XPS) analysis and angle resolved XPS measurement revealed successful formation of the Rh-complex-terminated SAM on a gold substrate. Infrared reflection absorption spectroscopy (IRRAS) analysis suggested that the linker methylene chains connecting the rhodium complex moiety and the gold surface are in a loosely packed structure. This unique chemical species, NHC, would be a promising candidate as a basement for the construction of functional surface. 相似文献
912.
T. Schäfer 《The European Physical Journal A - Hadrons and Nuclei》2007,31(4):403-408
We review many-body calculations of the equation of state of dilute neutron matter in the context of effective-field theories
of the nucleon-nucleon interaction. 相似文献
913.
D. Boilley A. Marchix B. Jurado K. -H. Schmidt 《The European Physical Journal A - Hadrons and Nuclei》2007,33(1):47-52
We propose a new formula for the saddle-to-scission time that is more general that the one based on Kramers' approach. Its
validity and applicability is then studied in detail. Such a formula is useful for the evaluation of the fission time of very
heavy nuclei. 相似文献
914.
Andrea Vietri 《Graphs and Combinatorics》2007,23(1):111-121
We analyse 3-subset difference families of Z2d+1⊕Z2d+1 arising as reductions (mod 2d+1) of particular families of 3-subsets of Z⊕Z. The latter structures, namely perfect d-families, can be viewed as 2-dimensional analogues of difference triangle sets having the least scope. Indeed, every perfect d-family is a set of base blocks which, under the natural action of the translation group Z⊕Z, cover all edges {(x,y),(x′,y′)} such that |x−x′|, |y−y′|≤d. In particular, such a family realises a translation invariant (G,K3)-design, where V(G)=Z⊕Z and the edges satisfy the above constraint. For that reason, we regard perfect families as part of the hereby defined translation designs, which comprise and slightly generalise many structures already existing in the literature. The geometric context allows
some suggestive additional definitions. The main result of the paper is the construction of two infinite classes of d-families. Furthermore, we provide two sporadic examples and show that a d-family may exist only if d≡0,3,8,11 (mod 12). 相似文献
915.
We introduce new classes of 2-weight cyclic codes which are direct sums of 1-weight irreducible cyclic codes
相似文献
916.
Yozo Miura Hiroyuki Dote Hiroyuki Kubonishi Kenichi Fukuda Tomoko Saka 《Journal of polymer science. Part A, Polymer chemistry》2007,45(6):1159-1169
A dendritic macroinitiator having 16 TEMPO‐based alkoxyamines, Star‐16 , was prepared by the reaction of a dendritic macroinitiator having eight TEMPO‐based alkoxyamines, [G‐3]‐OH , with 4,4′‐bis(chlorocarbonyl)biphenyl. The nitroxide‐mediated radical polymerization (NMRP) of styrene (St) from Star‐16 gave 16‐arm star polymers with PDI of 1.19–1.47, and NMPR of 4‐vinylpyridine from the 16‐arm star polymer gave 16‐arm star diblock copolymers with PDI of 1.30–1.43. The ring‐opening polymerization of ε‐caprolactone from [G‐3]‐OH and the subsequent NMRP of St gave AB8 9‐miktoarm star copolymers with PDI of 1.30–1.38. The benzyl ether linkages of the 16‐arm star polymers and the AB8 9‐miktoarm star copolymers were cleaved by treating with Me3SiI, and the resultant poly(St) arms were investigated by size exclusion chromatography (SEC). The SEC results showed PDIs of 1.23–1.28 and 1.18–1.22 for the star polymers and miktoarm stars copolymers, respectively, showing that they have well‐controlled poly(St) arms. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 1159–1169, 2007. 相似文献
917.
Reaction of arenesulfonylimines of methyl trifluoropyruvate with 1,3-C,N-and-N,N-binucleophiles led to a variety of N-sulfonylated fluorine-containing heterocycles, including the fused ones.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2171–2175, November, 2007. 相似文献
918.
N-Acylalkylation of neutral and anionic N-nucleophiles with α-halocarbonyl compounds was investigated by quantum chemical methods
in terms of the density functional theory and by experimental methods for 2,3-dihydroimidazo[2,1-b]quinazolin-1(10)H-5-one, its N-anion, and simpler model structures. High reactivity of these reagents is determined primarily by stabilization
of transition states (TS) by bridge bonds involving halogen or nitrogen atoms rather than by conjugation, as has been commonly
accepted. Bridged TS are formed by both the substitution mechanism S
N
2 and the addition-elimination mechanism. α-Haloalkyl-substituted zwitterions, which are potential intermediates of stepwise
N-acylalkylation of neutral N-nucleophiles, do not exist in the isolated state, but they are rather efficiently stabilized
upon solvation. These zwitterions, as well as analogous O-anions generated from anionic N-nucleophiles, can serve as intermediates
of N-acylalkylation, as was demonstrated by localization of the corresponding TS.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1150–1164, June, 2007. 相似文献
919.
Ignacio Villanueva 《Mathematische Nachrichten》2003,250(1):98-103
We clarify and prove in a simpler way a result of Taskinen about symmetric operators on C(Kn), K an uncountable metrizable compact space. To do this we prove that, for any compact space K and any n ∈ ?, the symmetric injective n–tensor product of C(K), , is complemented in C(BC(K)*), a result of independent interest. The techniques we develop allow us to extend the result in several directions. We also show that the hypothesis of metrizability and uncountability cannot be removed. 相似文献
920.
A photoemission study of molybdenum hexacarbonyl adsorption and decomposition on TiO2(1 1 0) surface
The adsorption and decomposition of molybdenum hexacarbonyl on (1 1 0) TiO2 surfaces were studied using both core levels and valence band photoemission spectroscopies. It was found that after an adsorption at 140 K, when going back to room temperature, only a small part of molybdenum compounds, previously present at low temperature, remained on the TiO2 surface. This indicates that the desorption temperature on such a surface is lower than the decomposition one. The use of photon irradiation to decompose the hexacarbonyl molecule was also studied. It was shown that during such a decomposition molecular fragments were chemisorbed on the surface allowing a higher amount of metal to remain on the surface. It was also shown that it was possible to get rid of adsorbed subcarbonyl groups and to organize the metal atoms by thermal treatments at temperatures as low as 400 K, i.e. much lower than the one needed to obtain the same structures using physical vapour deposition (PVD). Moreover, due to lower used temperatures, this chemical way of deposition allows a better control of the interface than during PVD growth. 相似文献