全文获取类型
收费全文 | 1474篇 |
免费 | 161篇 |
国内免费 | 134篇 |
专业分类
化学 | 958篇 |
晶体学 | 3篇 |
力学 | 30篇 |
综合类 | 15篇 |
数学 | 230篇 |
物理学 | 533篇 |
出版年
2024年 | 2篇 |
2023年 | 13篇 |
2022年 | 30篇 |
2021年 | 40篇 |
2020年 | 55篇 |
2019年 | 39篇 |
2018年 | 32篇 |
2017年 | 44篇 |
2016年 | 67篇 |
2015年 | 60篇 |
2014年 | 74篇 |
2013年 | 118篇 |
2012年 | 89篇 |
2011年 | 83篇 |
2010年 | 92篇 |
2009年 | 98篇 |
2008年 | 110篇 |
2007年 | 94篇 |
2006年 | 100篇 |
2005年 | 89篇 |
2004年 | 79篇 |
2003年 | 68篇 |
2002年 | 50篇 |
2001年 | 58篇 |
2000年 | 36篇 |
1999年 | 29篇 |
1998年 | 21篇 |
1997年 | 20篇 |
1996年 | 12篇 |
1995年 | 14篇 |
1994年 | 10篇 |
1993年 | 10篇 |
1992年 | 8篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 5篇 |
1988年 | 2篇 |
1987年 | 3篇 |
1986年 | 1篇 |
1985年 | 3篇 |
1980年 | 1篇 |
1975年 | 1篇 |
1973年 | 1篇 |
1972年 | 1篇 |
1969年 | 1篇 |
排序方式: 共有1769条查询结果,搜索用时 15 毫秒
51.
Chen He Ban‐Kun Jin Wei‐Dong He Xue‐Song Ge Jing Tao Jing Yang Sheng‐Qi Chen 《Journal of polymer science. Part A, Polymer chemistry》2013,51(10):2142-2149
Long‐subchain hyperbranched polystyrene (lsc‐hp PSt) with uniform subchain length was obtained through copper‐catalyzed azide‐alkyne cycloaddition click chemistry from seesaw macromonomer of PSt having one alkynyl group anchored at the chain centre and two azido group attached to both chain ends [alkynyl‐(PSt‐N3)2]. After precipitation fraction, different portions of lsc‐hp PSt having narrow overall molecular weight distribution were obtained for further grafting with alkynyl‐capped poly(N‐isopropylacrylamide) (alkynyl‐PNIPAM), which was obtained via single‐electron transfer living radical polymerization of NIPAM with propargyl 2‐bromoisobutyrate as the initiator and grafted onto the peripheral azido groups of lsc‐hp PSt via click chemistry. Thus, amphiphilic lsc‐hp PSt grafted with PNIPAM chains (lsc‐hp PSt‐g‐PNIPAM) was obtained and would have star‐like conformation in tetrahydrofuran (THF). By replacing THF with water, lsc‐hp PSt‐g‐PNIPAM was dissolved at molecular level in aqueous solution due to the hydrophilicity of PNIPAM and exhibited thermal induced shrinkage of PNIPAM arms. The water‐insoluble lsc‐hp PSt would collapse densely and could be served as a reservoir to absorb hydrophobic chemicals in aqueous solution. The influence of overall molecular weight of lsc‐hp PSt on the absorption of pyrene was studied. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
52.
53.
We provide a new class of interior solution of a(2+1)-dimensional anisotropic star in Finch and Skea spacetime corresponding to the BTZ black hole. We develop the model by considering the MIT bag model EOS and a particular ansatz for the metric function grrproposed by Finch and Skea [M.R. Finch and J.E.F. Skea, Class. Quantum.Grav. 6(1989) 467]. Our model is free from central singularity and satisfies all the physical requirements for the acceptability of the model. 相似文献
54.
Seung Hyun Sung William B. Farnham Heidi E. Burch Yefim Brun Kai Qi Thomas H. Epps 《Journal of Polymer Science.Polymer Physics》2019,57(24):1663-1672
We demonstrate the directional alignment of perpendicular‐lamellae domains in fluorinated three‐armed star block polymer (BP) thin films using solvent vapor annealing with shear stress. The control of orientation and alignment was accomplished without any substrate surface modification. Additionally, three‐armed star poly(methyl methacrylate‐block‐styrene) [PMMA‐PS] and poly(octafluoropentyl methacrylate‐block‐styrene) were compared to their linear analogues to examine the impact of fluorine content and star architecture on self‐assembled BP feature sizes and interdomain density profiles. X‐ray reflectometry results indicated that the star BP molecular architecture increased the effective polymer segregation strength and could possibly facilitate reduced polymer domain spacings, which are useful in next‐generation nanolithographic applications. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 1663–1672 相似文献
55.
A star edge coloring of a graph is a proper edge coloring such that every connected 2-colored subgraph is a path with at most 3 edges. Deng et al. and Bezegová et al. independently show that the star chromatic index of a tree with maximum degree is at most , which is tight. In this paper, we study the list star edge coloring of -degenerate graphs. Let be the list star chromatic index of : the minimum such that for every -list assignment for the edges, has a star edge coloring from . By introducing a stronger coloring, we show with a very concise proof that the upper bound on the star chromatic index of trees also holds for list star chromatic index of trees, i.e. for any tree with maximum degree . And then by applying some orientation technique we present two upper bounds for list star chromatic index of -degenerate graphs. 相似文献
56.
Yoshiki Shibuya Ryoichi Tatara Yivan Jiang Yang Shao‐Horn Jeremiah A. Johnson 《Journal of polymer science. Part A, Polymer chemistry》2019,57(3):448-455
The properties of polymeric materials are dictated not only by their composition but also by their molecular architecture. Here, by employing brush‐first ring‐opening metathesis polymerization (ROMP), norbornene‐terminated poly(ethylene oxide) (PEO) macromonomers ( MM‐n , linear architecture), bottlebrush polymers ( Brush‐n , comb architecture), and brush‐arm star polymers ( BASP‐n , star architecture), where n indicates the average degree of polymerization (DP) of PEO, are synthesized. The impact of architecture on the thermal properties and Li+ conductivities for this series of PEO architectures is investigated. Notably, in polymers bearing PEO with the highest degree of polymerization, irrespective of differences in architecture and molecular weight (~100‐fold differences), electrolytes with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as an Li+ source exhibit normalized ionic conductivities (σn) within only 4.9 times difference (σn = 29.8 × 10?5 S cm?1 for MM‐45 and σn = 6.07 × 10?5 S cm?1 for BASP‐45 ) at a concentration of Li+ r = [Li+]/[EO] = 1/12 at 50 °C. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 448–455 相似文献
57.
Ikhlas Gadwal Prakash P. Wadgaonkar Amol B. Ichake Shivshankar R. Mane 《Journal of polymer science. Part A, Polymer chemistry》2019,57(2):146-156
A new approach was developed for synthesis of certain A3B3‐type of double hydrophilic or amphiphilic miktoarm star polymers using a combination of “grafting onto” and “grafting from” methods. To achieve the synthesis of desired miktoarm star polymers, acetyl protected poly(ethylene glycol) (PEG) thiols (Mn = 550 and 2000 g mol?1) were utilized to generate A3‐type of homoarm star polymers through an in situ protective group removal and a subsequent thiol–epoxy “click” reaction with a tris‐epoxide core viz. 1,1,1‐tris(4‐hydroxyphenyl)ethane triglycidyl ether. The secondary hydroxyl groups generated adjacent to the core upon the thiol–epoxy reaction were esterified with α‐bromoisobutyryl bromide to install atom transfer radical polymerization (ATRP) initiating sites. ATRP of N‐isopropylacrylamide (NIPAM) using the three‐arm star PEG polymer fitted with ATRP initiating sites adjacent to the core afforded A3B3‐type of double hydrophilic (PEG)3[poly(N‐isopropylacrylamide)] (PNIPAM)3 miktoarm star polymers. Furthermore, the generated hydroxyl groups were directly used as initiator for ring‐opening polymerization of ε‐caprolactone to prepare A3B3‐type of amphiphilic (PEG)3[poly(ε‐caprolactone)]3 miktoarm star polymers. The double hydrophilic (PEG)3(PNIPAM)3 miktoarm star polymers showed lower critical solution temperature around 34 °C. The preliminary transmission electron microscopy analysis indicated formation of self‐assembly of (PEG)3(PNIPAM)3 miktoarm star polymer in aqueous solution. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 146–156 相似文献
58.
Dr. Zafar Mahmood Noreen Rehmat Prof. Shaomin Ji Prof. Jianzhang Zhao Shanshan Sun Dr. Mariangela Di Donato Prof. Mingde Li Maria Teddei Prof. Yanping Huo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(65):14912-14918
Zinc(II) bis(dipyrrin) complexes, which feature intense visible absorption and efficient symmetry breaking charge transfer (SBCT) are outstanding candidates for photovoltaics but their short lived triplet states limit applications in several areas. Herein we demonstrate that triplet excited state dynamics of bis(dipyrrin) complexes can be efficiently tuned by attaching electron donating aryl moieties at the 5,5′-position of the complexes. For the first time, a long lived triplet excited state (τT=296 μs) along with efficient ISC ability (ΦΔ=71 %) was observed for zinc(II) bis(dipyrrin) complexes, formed via SBCT. The results revealed that molecular geometry and energy gap between the charge transfer (CT) state and triplet energy levels strongly control the triplet excited state properties of the complexes. An efficient triplet–triplet annihilation upconversion system was devised for the first time using a SBCT architecture as triplet photosensitizer, reaching a high upconversion quantum yield of 6.2 %. Our findings provide a blueprint for the development of triplet photosensitizers based on earth abundant metal complexes with long lived triplet state for revolutionary photochemical applications. 相似文献
59.
60.
2,3-Disubstituted Fluorene Scaffold for Efficient Green Phosphorescent Organic Light-Emitting Diodes
Jia-Jia Wei Yong-Jian Yang Dr. Xiang-Yang Liu Dr. Runlai Li Prof. Dr. Shu-an Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(39):e202200756
Fluorene is a classic three-membered polycyclic aromatic hydrocarbon, and it has been widely used in optoelectronic devices. Here we explore a simple and efficient strategy for the derivatization at the 2- and 3- positions in fluorene unit. By introducing different types of substituents, we design two pairs of 2,3-disubstituted fluorene isomers and use them as host materials for phosphorescent organic light-emitting diodes (PHOLEDs). The green PHOLEDs hosted by these fluorene derivatives realize high external quantum efficiencies (EQE) over 20 % with low efficiency roll-off. Particularly, the devices hosted by 2TRz3TPA and 2TPA3TRz achieve nearly 24 % EQE and 104 lm W−1 power efficiency. These results clearly demonstrate that the 2,3-disubstituted fluorene platforms are potentially useful for constructing host materials. 相似文献