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排序方式: 共有269条查询结果,搜索用时 140 毫秒
81.
82.
Akhtaruzzaman M Tomura M Zaman MB Nishida J Yamashita Y 《The Journal of organic chemistry》2002,67(22):7813-7818
Three novel 4,7-bis(n-pyridylethynyl)-2,1,3-benzothiadiazoles (n = 2, 3, and 4) were synthesized by using the Sonogashira cross-coupling reaction of 4,7-dibromo-2,1,3-benzothiadiazole with the corresponding ethynylpyridines in the presence of a Pd(II) catalyst. The viologen analogues were also prepared by methylation of pyridyl nitrogen atoms. X-ray structure analysis of these compounds revealed the linear molecular structures with unusual columnar crystal structures. Insertion of a benzothiadiazole moiety into the acetylene-pyridine skeleton brings about a large increase in electron affinity and the bispyridyl compounds obtained here show high fluorescence quantum yields. 相似文献
83.
M. K. Suleymanov R. G. Nazmitdinov E. I. Shahaliev O. B. Abdinov A. Ajaz A. Zaman K. H. Khan Z. Wazir 《Bulletin of the Russian Academy of Sciences: Physics》2012,76(10):1089-1092
A new statistical method is proposed for the analysis of experimental data obtained in nucleus-nucleus collisions at high energies which borrows from ideas developed using the Random Matrix Theory. The method allows us to detect regions with correlation effects in the momentum distributions of secondary particles. 相似文献
84.
85.
Haladhara Naik Guinyun Kim Kwangsoo Kim Muhammad Zaman Sung-Chul Yang Muhammad Sahid Manwoo Lee Sung-Gyun Shin Ashok Goswami Moo-Hyun Cho 《Journal of Radioanalytical and Nuclear Chemistry》2014,300(3):1121-1130
The independent isomeric yield ratios of 95m,gNb from the natMo(γ, pxn) reactions with bremsstrahlung end-point energies of 45, 50, 55, 60, and 70 MeV were determined by an activation and an off-line γ-ray spectrometric technique at the Pohang accelerator laboratory (PAL), Korea. The isomeric yield ratios of 95m,gNb from the natZr(p, xn) reactions were also determined in eight different proton energies within 19.4–44.7 MeV by a stacked-foil activation and an off-line γ-ray spectrometric technique using the MC-50 cyclotron of Korea Institute of Radiological and Medical Sciences (KIRAMS), Korea. The measured isomeric yield ratios of 95m,gNb from the present work and the literature data in the natMo(γ, pxn) and natZr(p, xn) reactions were compared with the similar literature data in the natMo(p, αxn) reactions. It was found that the isomeric yield ratio of 95m,gNb increases with projectile energy, which indicate the effect of excitation energy. However, at the same excitation energy, the isomeric yield ratios of 95m,gNb in the natZr(p, xn) and natMo(p, αxn) reactions are higher than those in the natMo(γ, pxn) reaction, which indicates the role of input angular momentum. The isomeric yield ratios of 95m,gNb in the natMo(γ, pxn), natZr(p, xn), and natMo(p, αxn) reactions were also calculated using computer code TALYS 1.4. The calculated isomeric yield ratios of 95m,gNb from three reactions increase with excitation energy. However, in all the three reactions, the calculated values are significantly higher than the experimental data. 相似文献
86.
Summary A point source at an interface between a homogeneous layer of finite depth and an inhomogeneous half-space is considered.
The transmitted wave and the dispersion relation for the Love waves is calculated analytically.
The authors of this paper have agreed to not receive the proofs for correction. 相似文献
87.
Two new pyranoisoflavones, auriculasin and isoauriculasin were isolated from M. auriculata and assigned structures 1 and 3 respectively. The structure assigned earlier to isoauriculatin has been revised to 4. 相似文献
88.
Summary To develop a preconcentration technique for trace elements in aqueous solution, the adsorption behaviour of some metal ions and their oxinates on a weak carboxylic acid resin (Zeokarb-226) in the H+ form was investigated. Results indicate that under the conditions of the experiment, the resin behaves like a chelating ion-exchanger and that by selecting appropriate conditions, a group of ions such as U(VI), Th(IV), Pb(II), Hg(II), Fe(III) may be separated from many other ions.
Adsorptionsverhalten einiger Metallionen und ihrer Oxinate an Zeokarb-226
Zusammenfassung Das Adsorptionsverhalten einiger Metallionen und ihrer Oxinate an dem schwachen Carbonsäureharz Zeokarb-226 (H+-Form) wurde untersucht, um ein Anreicherungsverfahren für Spurenelemente in wäßriger Lösung zu entwickeln. Die Ergebnisse zeigen, daß sich das Harz unter den gegebenen Bedingungen als Chelataustauscher verhält und geeignet ist für die selektive Anreicherung von z.B. U(VI), Th(IV), Pb(II), Hg(II) und Fe(III).相似文献
89.
Dr. Shenghua Chen Dr. Chengliang Ye Dr. Ziwei Wang Dr. Peng Li Dr. Wenjun Jiang Dr. Zechao Zhuang Dr. Jiexin Zhu Dr. Xiaobo Zheng Dr. Shahid Zaman Dr. Honghui Ou Lei Lv Dr. Lin Tan Dr. Yaqiong Su Dr. Jiang Ouyang Prof. Dingsheng Wang 《Angewandte Chemie (International ed. in English)》2023,62(50):e202315621
Electrochemical CO2 reduction reaction (CO2RR) over Cu catalysts exhibits enormous potential for efficiently converting CO2 to ethylene (C2H4). However, achieving high C2H4 selectivity remains a considerable challenge due to the propensity of Cu catalysts to undergo structural reconstruction during CO2RR. Herein, we report an in situ molecule modification strategy that involves tannic acid (TA) molecules adaptive regulating the reconstruction of a Cu-based material to a pathway that facilitates CO2 reduction to C2H4 products. An excellent Faraday efficiency (FE) of 63.6 % on C2H4 with a current density of 497.2 mA cm−2 in flow cell was achieved, about 6.5 times higher than the pristine Cu catalyst which mainly produce CH4. The in situ X-ray absorption spectroscopy and Raman studies reveal that the hydroxyl group in TA stabilizes Cuδ+ during the CO2RR. Furthermore, theoretical calculations demonstrate that the Cuδ+/Cu0 interfaces lower the activation energy barrier for *CO dimerization, and hydroxyl species stabilize the *COH intermediate via hydrogen bonding, thereby promoting C2H4 production. Such molecule engineering modulated electronic structure provides a promising strategy to achieve highly selective CO2 reduction to value-added chemicals. 相似文献
90.