首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   19788篇
  免费   1306篇
  国内免费   2478篇
化学   14016篇
晶体学   308篇
力学   294篇
综合类   127篇
数学   3271篇
物理学   3102篇
无线电   2454篇
  2024年   26篇
  2023年   220篇
  2022年   462篇
  2021年   591篇
  2020年   679篇
  2019年   496篇
  2018年   399篇
  2017年   507篇
  2016年   527篇
  2015年   448篇
  2014年   578篇
  2013年   1181篇
  2012年   837篇
  2011年   1127篇
  2010年   895篇
  2009年   1260篇
  2008年   1190篇
  2007年   1189篇
  2006年   1113篇
  2005年   1054篇
  2004年   1130篇
  2003年   908篇
  2002年   823篇
  2001年   654篇
  2000年   646篇
  1999年   501篇
  1998年   405篇
  1997年   427篇
  1996年   419篇
  1995年   399篇
  1994年   409篇
  1993年   326篇
  1992年   290篇
  1991年   195篇
  1990年   147篇
  1989年   147篇
  1988年   110篇
  1987年   99篇
  1986年   94篇
  1985年   69篇
  1984年   65篇
  1982年   55篇
  1981年   64篇
  1980年   60篇
  1979年   84篇
  1978年   68篇
  1977年   58篇
  1976年   46篇
  1974年   22篇
  1973年   23篇
排序方式: 共有10000条查询结果,搜索用时 406 毫秒
101.
The dynamic external hashing proposed in this paper allocates records according to the spiral storage technique. Separators derived from the signature technique are used for distinguishing primary from overflow records and for subdividing overflow chains into segments allocated into the primary file. Single access retrieval is obtained by means of a main memory index with an entry per bucket and containing separators and pointers. While this method uses a larger index than other recent proposals, it is much more convenient regarding load factor and insertion cost. Furthermore, file expansion is directed by various control parameters, thus allowing the user to choose the most suitable policy for his application.  相似文献   
102.
Summary An analysis of five different datasets of inhibitors of serotonin uptake has yielded quantitative structure/ activity relationships (QSARs) which delineate the role of steric and hydrophobic properties essential for inhibition by phenylethylamine-type analogues.  相似文献   
103.
1IntroductionStabilityintermsoftwomeasures,thisconceptenableustounifyava-rietyofstabilityconceptsandtoofferageneralandunifiedframeworkforinvestigationofstabilitytheory.AndtheoriginalLiapunovtheoremshavebeenextended,generalizedandweakenedinvariousaspects[3…  相似文献   
104.
以MCl2和配体L(L=1,10-菲罗啉-5,6-二酮)为原料,合成了标题配合物MLCl2,M=NiⅡ,CuⅡ,ZnⅡ,并经元素分析、热谱、IR和摩尔电导表征.三者均为四配位的电中性配合物,热稳定性高于500K,易溶于DMF、DMSO和吡啶,可溶于乙腈和水.它们在DMF中于350nm和315nm附近显示出强的M-L荷移跃迁  相似文献   
105.
In this paper, we present three constructions for anti‐mitre Steiner triple systems and a construction for 5‐sparse ones. The first construction for anti‐mitre STSs settles two of the four unsettled admissible residue classes modulo 18 and the second construction covers such a class modulo 36. The third construction generates many infinite classes of anti‐mitre STSs in the remaining possible orders. As a consequence of these three constructions we can construct anti‐mitre systems for at least 13/14 of the admissible orders. For 5‐sparse STS(υ), we give a construction for υ ≡ 1, 19 (mod 54) and υ ≠ 109. © 2005 Wiley Periodicals, Inc. J Combin Designs 14: 237–250, 2006  相似文献   
106.
A decomposition heuristics for the container ship stowage problem   总被引:3,自引:0,他引:3  
In this paper we face the problem of stowing a containership, referred to as the Master Bay Plan Problem (MBPP); this problem is difficult to solve due to its combinatorial nature and the constraints related to both the ship and the containers. We present a decomposition approach that allows us to assign a priori the bays of a containership to the set of containers to be loaded according to their final destination, such that different portions of the ship are independently considered for the stowage. Then, we find the optimal solution of each subset of bays by using a 0/1 Linear Programming model. Finally, we check the global ship stability of the overall stowage plan and look for its feasibility by using an exchange algorithm which is based on local search techniques. The validation of the proposed approach is performed with some real life test cases. This work has been developed within the research area: “The harbour as a logistic node” of the Italian Centre of Excellence on Integrated Logistics (CIELI) of the University of Genoa, Italy  相似文献   
107.
Raman spectra, atomic force microscope (AFM) images, hardness (H) and Young's modulus (E) measurements were carried out in order to characterize carbon thin films obtained from a C60 ion beam on silicon substrates at different deposition energies (from 100 up to 500 eV). The mechanical properties were studied via the nanoindentation technique. It has been observed by Raman spectroscopy and AFM that the microstructure presents significant changes for films deposited at energies close to 300 eV. However, these remarkable changes have not been noticeable on the mechanical properties: apparently H and E increase with higher deposition energy up to ∼11 and ∼116 GPa, respectively. These values are underestimated if the influence of the film roughness is not taken into account.  相似文献   
108.
This paper aims at reporting on the synthesis of a heterograft copolymer by combining the “grafting onto” process based on atom transfer radical addition (ATRA) and the “grafting from” process by atom transfer radical polymerization (ATRP). The statistical copolymerization of ε‐caprolactone (εCL) and α‐chloro‐ε‐caprolactone (αClεCL) was initiated by 2,2‐dibutyl‐2‐stanna‐1,3‐dioxepane (DSDOP), followed by ATRA of parts of the chlorinated units of poly(αClεCL‐co‐εCL) on the terminal double bond of α‐MeO,ω‐CH2?CH? CH2? CO2‐poly(ethylene oxide) (PEO). The amphiphilic poly(εCL‐g‐EO) graft copolymer collected at this stage forms micelles as supported by dynamic light scattering (DLS) and transmission electron microscopy (TEM). The unreacted pendant chloro groups of poly(εCL‐g‐EO) were used to initiate the ATRP of styrene with formation of copolymer with two populations of randomly distributed grafts, that is PEO and polystyrene. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6015–6024, 2006  相似文献   
109.
Novel catalytic systems, prepared in situ by the oxidative addition of 8‐hydroxyquinoline ligands to bis(1,5‐cyclooctadiene)nickel(0) and activated by methylaluminoxane, were studied in ethylene polymerization. When 8‐hydroxyquinoline was employed, only oligomeric products were obtained. On the contrary, 5,7‐dinitro‐8‐hydroxyquinoline gave linear polyethylene (PE), but with a modest activity. For the catalyst based on 5‐nitro‐8‐hydroxyquinoline, the productivity was largely dependent on the content of free trimethylaluminum (TMA) present in the commercial aluminoxane. The progressive optimization of the TMA/oligomeric methylaluminoxane ratio increased the productivity, which reached 700 kg of PE/(mol of Ni × h), by an order of magnitude. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 200–206, 2006  相似文献   
110.
Well‐defined polystyrene‐ (PSt) or poly(ε‐caprolactone) (PCL)‐based polymers containing mid‐ or end‐chain 2,5 or 3,5‐ dibromobenzene moieties were prepared by controlled polymerization methods, such as atom transfer radical polymerization (ATRP) or ring opening polymerization (ROP). 1,4‐Dibromo‐2‐(bromomethyl)benzene, 1,3‐dibromo‐5‐(bromomethyl)benzene, and 1,4‐dibromo‐2,5‐di(bromomethyl)benzene were used as initiators in ATRP of styrene (St) in conjunction with CuBr/2,2′‐bipyridine as catalyst. 2,5‐Dibromo‐1,4‐(dihydroxymethyl)benzene initiated the ROP of ε‐caprolactone (CL) in the presence of stannous octoate (Sn(Oct)2) catalyst. The reaction of these polymers with amino‐ or aldehyde‐functionalized monoboronic acids, in Suzuki‐type couplings, afforded the corresponding telechelics. Further functionalization with oxidable groups such as 2‐pyrrolyl or 1‐naphthyl was attained by condensation reactions of the amino or aldehyde groups with low molecular weight aldehydes or amines, respectively, with the formation of azomethine linkages. Preliminary attempts for the synthesis of fully conjugated poly(Schiff base) with polymeric segments as substituents, by oxidative polymerization of the macromonomers, are presented. All the starting, intermediate, or final polymers were structurally analyzed by spectral methods (1H NMR, 13C NMR, and IR). © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 727–743, 2006  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号