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981.
Ratnakar Ram R. Dindoruk Birol Odikpo Greg Lewis Edward J. 《Transport in Porous Media》2019,128(1):29-43
Transport in Porous Media - We present numerical and experimental investigation on the existence of diffusion-induced compositional variations in a reservoir fluid in the absence of convective... 相似文献
982.
Maher M. Aljohani Dana Cialla-May Jürgen Popp Raja Chinnappan Khaled Al-Kattan Mohammed Zourob 《Molecules (Basel, Switzerland)》2022,27(2)
Aptamers are RNA/DNA oligonucleotide molecules that specifically bind to a targeted complementary molecule. As potential recognition elements with promising diagnostic and therapeutic applications, aptamers, such as monoclonal antibodies, could provide many treatment and diagnostic options for blood diseases. Aptamers present several superior features over antibodies, including a simple in vitro selection and production, ease of modification and conjugation, high stability, and low immunogenicity. Emerging as promising alternatives to antibodies, aptamers could overcome the present limitations of monoclonal antibody therapy to provide novel diagnostic, therapeutic, and preventive treatments for blood diseases. Researchers in several biomedical areas, such as biomarker detection, diagnosis, imaging, and targeted therapy, have widely investigated aptamers, and several aptamers have been developed over the past two decades. One of these is the pegaptanib sodium injection, an aptamer-based therapeutic that functions as an anti-angiogenic medicine, and it is the first aptamer approved by the U.S. Food and Drug Administration (FDA) for therapeutic use. Several other aptamers are now in clinical trials. In this review, we highlight the current state of aptamers in the clinical trial program and introduce some promising aptamers currently in pre-clinical development for blood diseases. 相似文献
983.
超级电容器简介 总被引:6,自引:0,他引:6
Bobby Maher 《今日电子》2006,(1):37-38
随着社会经济的发展,人们对于绿色能源和生态环境越来越关注,超级电容器作为一种新型的储能器件,因为其无可替代的优越性,越来越受到人们的重视。在一些需要高功率、高效率解决方案的设计中,工程师已开始采用超级电容器来取代传统的电池。 相似文献
984.
Jianye Zhang Heba Ali Hassan Usama Ramadan Abdelmohsen Eman Maher Zahran 《Molecules (Basel, Switzerland)》2022,27(1)
Actinobacterial natural products showed a critical basis for the discovery of new antibiotics as well as other lead secondary metabolites. Varied environmental and physiological signals touch the antibiotic machinery that faced a serious decline in the last decades. The reason was exposed by genomic sequencing data, which revealed that Actinomycetes harbor a large portion of silent biosynthetic gene clusters in their genomes that encrypt for secondary metabolites. These gene clusters are linked with a great reservoir of yet unknown molecules, and arranging them is considered a major challenge for biotechnology approaches. In the present paper, we discuss the recent strategies that have been taken to augment the yield of secondary metabolites via awakening these cryptic genes in Actinomycetes with emphasis on chemical signaling molecules used to induce the antibiotics biosynthesis. The rationale, types, applications and mechanisms are discussed in detail, to reveal the productive path for the unearthing of new metabolites, covering the literature until the end of 2020. 相似文献
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986.
Gyeong Seon Jeong Amal Cherian Kathalikkattil Robin Babu Yongchul Greg Chung Dae Won Park 《催化学报》2018,(1)
由天然的/生物单元(氨基酸)构成的金属有机框架材料(MOFs)具有自然属性和丰富的酸/碱位和官能团,因而可用于CO_2化学中.本文报道了氨基酸系含铜MOF(CuTrp,Trp=L-色氨酸)的催化效率.以甲醇为溶剂,在室温采用直接混合法合成了CuTrp催化剂,该方法具有很高的能量效率.采用X射线衍射、红外光谱、热重分析、电感耦合等离子体发射光谱法、扫描电镜和BET分析等手段对该催化剂进行了表征.采用环氧化物与CO_2环加成制备环状碳酸酯反应评价了CuTrp催化剂活性.结果表明,在无溶剂条件下,CuTrp催化剂可与四丁基溴化铵助催化剂发生协同作用.通过条件实验确定了优化的反应条件,并基于该实验结果和前期的密度泛函理论计算结果提出了反应机理.另外,CuTrp催化剂在水中也表现出令人满意的稳定性,可重复使用三次以上而活性无明显下降. 相似文献
987.
William J. Durand Gregory Blachut Michael J. Maher Stephen Sirard Summer Tein Matthew C. Carlson Yusuke Asano Sunshine X. Zhou Austin P. Lane Christopher M. Bates Christopher J. Ellison C. Grant Willson 《Journal of polymer science. Part A, Polymer chemistry》2015,53(2):344-352
This report describes the design and synthesis of a series of lamella-forming, silicon-containing block copolymers (Si-BCPs) and evaluation of these materials as potential candidates for lithographic applications. The interaction parameter χ of each Si-BCP is measured by both the mean-field theory predicted order-disorder transition and by analysis of X-ray scattering profiles. The introduction of more-polar methoxy and less-polar methylsilyl moieties increases χ to about 2–3 times that of the reference material, poly(styrene-block−4-trimethylsilylstyrene). The incremental increases appear to be essentially additive in this family of block copolymers, suggesting that improvements in χ can be predicted from appropriate monomer choice. Perpendicularly oriented thin-films of the ordered Si-BCPs generated by thermally annealing between two “neutral” polymeric surfaces and developed by etching on commercial RIE equipment show excellent image fidelity. These images demonstrate the excellent etch contrast of the Si-BCPs and document improvements in pattern fidelity that are realized with more strongly segregated BCPs. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 344–352 相似文献
988.
Hydroxide‐ion transport and stability of diblock copolymers with a polydiallyldimethyl ammonium hydroxide block
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Pepa Cotanda Nikos Petzetakis Xi Jiang Greg Stone Nitash P. Balsara 《Journal of polymer science. Part A, Polymer chemistry》2017,55(13):2243-2248
Base‐stable amphiphilic diblock copolymers with a polydiallyl dimethyl ammonium hydroxide block were synthesized and characterized to quantify hydroxide‐ion transport in the hydrated state; polystyrene was the hydrophobic block. The challenge of synthesizing a copolymer comprising blocks with very different solubility behaviors was addressed by a combination of reversible addition fragmentation chain transfer polymerization and ion metathesis. Both monomers used in the polymerization are commercially available on industrial scales. Hydroxide‐ion conductivities of 0.8 mS/cm were achieved in hot‐pressed membranes immersed in water at room temperature despite relatively low water uptake (4.2 water molecules per hydroxide ion). The stability of the polydimethyl ammonium hydroxide chains was investigated in 2 M NaOD at 60 °C. 1H NMR spectroscopy studies showed no detectable degradation after 2000 hours. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2243–2248 相似文献
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990.