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91.
吡啶酮偶氮分散染料光谱性能 总被引:1,自引:0,他引:1
吡啶酮分散染料应用性能优异 ,其色谱主要为黄色及橙色 ,尤以黄色为主 [1~ 3]。Cheng和 Peng等 [2 ,3] 对以氨基噻二唑类和苯系芳胺为重氮组分的吡啶酮类染料的可见光谱及互变异构进行了研究 ,Ertan等 [4 ] 研究了以氨基噻唑和氨基苯并噻唑为重氮组分的吡啶酮偶氮染料的可见光谱 ,结果表明上述染料色谱主要仍为黄色。为得到具有更深色谱的吡啶酮类染料 ,我们用不同的重氮组分合成了一系列吡啶酮分散染料 ,研究了其在不同溶剂及不同 p H值下的光谱 ,发现该类染料亦可达到红、甚至蓝色谱 ,其中染料 1 a、1 b及 2 b3个染料结构未见报道。O2 … 相似文献
92.
《Analytical letters》2012,45(4):823-833
Abstract A simple, sensitive, and specific spectrophotometric method for the measurement of nitrite in water has been developed and optimum reaction conditions along with other analytical parameters have been evaluated. The azo dye, 4‐(1‐methyl‐1‐mesitylcylobutane‐3‐yl)‐2‐(p‐N,N‐dimethylazobenzene)‐1,3‐thiazole was synthesized with the reaction of 4‐(1‐methyl‐1‐mesitylcylobutane‐3‐yl)‐2‐aminothiazole and N,N‐dimethyl aniline in acidic medium. Obtained azo dye has been characterized by infrared (IR), 1H nuclear magnetic resonance (NMR), and microanalysis methods. The dye shows an absorption maximum at 482 nm. The method is optimized for acid concentration, pH, amount of reagents required, time, and interfering species. All the determinations were carried out at this wavelength throughout the work. At an analytical wavelength of 482 nm, Beer's law is obeyed over the concentration range 0.05 to 2.00 µg nitrite per mL analyte. The molar absorptivity, Sandell's sensitivity, and relative standard deviation are 2.03×104 L mol?1 cm?1±251.3 (95%), 2.28×10?3 µg cm?2, and 2.74% (n=10), respectively. The detection limit of the method is 0.012 µg ml?1 of nitrite ion. The method was succesfully applied to the determination of nitrite in tap water and lake water. 相似文献
93.
《Analytical letters》2012,45(10):1887-1900
Abstract Preliminary investigations by a batch method are described for aiming at the flow determination of free chlorine in water with novel chemiluminescence (CL) detection. The CL originates from the reaction of xanthene dyes with free chlorine, Cl2, HOCl, and OCl?. Through the measurements of CL decay curves, fundamental CL characteristics were explored from the analytical point of view. Among xanthene dyes tested, eosin Y. eosin B. pyronin B. and rhodamine 6G were found to be promising CL reagents with such sensitivity and selectivity that free chlorine can be readily determined in tap water. In particular. these CL systems have the special advantage of being insensitive to oxo acids of chlorine and chloramine. Recommended flow systems are proposed. 相似文献
94.
《Analytical letters》2012,45(10):2153-2167
Abstract Three single‐chain fragment variable (scFv) fusion structures were constructed for use in rapid and sensitive detection of nucleocapsid protein (NP) of Hantaan virus. The detection of NPs on glass chips was signalized by enzyme labeling or fluorescence dye Cy3, or Cy5 cluster nanoparticles. The sensitivity of the methods with different signal systems was evaluated and compared. The detection limits of scFv‐alkaline phosphatase fusion, fluorescence labeling (scFv‐Cy3), and nanoparticles labeling (scFv‐SBP‐streptavidin‐nanoparticle) were 0.1 µg/mL, 1 ng/mL, and 0.1 ng/mL NP, respectively, which were all lower than that in a conventional enzyme‐linked immunosorbent assay (ELISA) (1 µg/mL). Twenty Hantaan virus isolates were detected using the proposed methods. 相似文献
95.
96.
在阴离子型和非离子型表面活性剂组成的反胶束体系中研究了直径为11~14nm的AgCl微粒子与菁染料之间的作用,讨论了AgCl纳米粒子对菁染料的吸附及荧光猝灭现象. 相似文献
97.
建立了微波消解-石墨炉原子吸收光谱法测定植物染发剂中重金属铅、镉和铜的方法.采用L9(34)正交设计讨论了固液比、消解剂体积比、消解时间和消解压力对样品消解效果的影响,最佳的消解条件:固液比(g/mL)为1∶12,HNO3/H2O2(V/V)为4∶1,消解时间为5min,消解压力1.5MPa.在最佳微波消解条件下,进行了精密度实验、回收率实验,相对标准偏差为1.05%~3.35%,回收率为96.67%~105.43%.微波消解法处理植物染发剂样品,试剂用量少、消解完全、快速、简便,而且测定结果的精密度、准确度较好. 相似文献
98.
Jian‐Ging Chen Ken‐Yen Liu Chia‐Yuan Chen Chia‐Yu Lin Kuan‐Chieh Huang Yi‐Hsuan Lai Chun‐Guey Wu King‐Fu Lin Kuo‐Chuan Ho 《Journal of polymer science. Part A, Polymer chemistry》2010,48(22):4950-4957
This study reports the characteristics of gel‐type dye‐sensitized solar cells (DSSCs), fabricated with gel‐type electrolyte containing poly‐1,1′‐(methylenedi‐4,1‐phenylene)bismaleimide (PBMI), or poly‐1,1′‐(3,3′‐dimethyl‐1,1′‐biphenyl‐4,4′‐diyl)bismaleimide (PDBBMI), or poly‐N,N′‐(4‐methyl‐1,3‐phenylene)bismaleimide (PMPBMI), prepared by in situ polymerization of the corresponding monomer without an initiator at 30 °C. Incorporating 0.3 wt % content of exfoliated alkyl‐modified nanomica (EAMNM) into PBMI‐gelled electrolyte leads to higher short‐circuit current density (Jsc = 17.14 mA cm?2) and efficiency (η = 7.02%) than that of neat PBMI‐gel electrolyte (Jsc = 15.32 mA cm?2, η = 6.41%). Incorporating 0.3 wt % EAMNM into PBMI‐gelled electrolyte results in remarkably stable device performance under continuous light soaking under one sun (100 mW cm?2) at 55 °C. The efficiency of DSSCs based on PBMI/0.3 wt % EAMNM‐gelled electrolyte drops by only 1.7% (η = 6.93%) after 500 h of continuous light soaking. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
99.
Ken‐Yen Liu Chiao‐Ling Hsu Shun‐Hsing Chang Jian‐Ging Chen Kuo‐Chuan Ho King‐Fu Lin 《Journal of polymer science. Part A, Polymer chemistry》2010,48(2):366-372
A new crosslinkable light sensitizer, Ru(2,2′‐bipyridine‐4,4′‐bicarboxylic acid)(4,4′‐bis(11‐dodecenyl)‐2,2′‐bipyridine)(NCS)2, denoted as Ru‐C for titanium oxide nanocrystalline‐based solar cells was synthesized with its crosslinking properties invesitigated by Fourier‐transform infrared and UV‐vis absorption spectroscopies. After crosslinking by itself or copolymerizing with methyacrylic acid, their sensitized solar cells with poly(methylacrylate)‐gelled electrolyte system not only attained more than 5% of power conversion efficiency at AM 1.5 illumination (100 mW/cm2), but also gave rise to long storage life. To the best our knowledge, this is the first crosslinkable dye ever applied to the DSSC in the literature. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 366–372, 2010 相似文献
100.
The fluorescence properties of novel 6-butyl-2,3-dicyano-7-methyl-6H-1,4-diazepine styryl dyes having mono-, di-, tri-, and tetra(ethyleneglycol) units were examined. The mono(ethylenglycol) derivative was solid at room temperature, whereas the di-, tri-, and tetra(ethylenglycol) derivatives were oily. The monoethyleneglycol derivative showed weak aggregation-induced emission enhancement with fluorescence maximum at 649 nm, which comes from J-aggregates. The fluorescence of oily di-, tri-, and tetra(ethyleneglycol) derivatives in neat form was very weak. No aggregation-induced emission enhancement was observed for the oily derivatives. 相似文献