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131.
132.
系数倍率和卡尔曼滤波紫外分光光度法同时测定发洗剂中的苯酚、间苯二酚和水杨酸 总被引:1,自引:0,他引:1
用系数倍率和卡尔曼滤波紫外分光光度法同时测定发洗剂中苯酚、间苯二酚、水杨酸的含量,苯酚、间苯二酚、水杨酸的线性回归方程分别为:A=0.00546 0.01762X,r=0.9999;A=0.00245 0.01606X,r=0.9999;A=-0.00748 0.02491X.r=0.9999。回收率分别为97.8%~102.3%、99.9%~102.3%、99.3%~103.2%。 相似文献
133.
二烷基磷(膦)酸钠盐萃取体系的相行为 总被引:4,自引:0,他引:4
用二烷基磷(膦)酸钠盐NaA作为阴离子表面活性剂,测定了NaA-醇-油-水体系W/O型微乳液中水的增溶量,用类三元相 图单相微乳区,测定了NaDTMPP-HDTMPP-煤油-水(含Na2SO4)体系相的变化,并讨论了溶剂、醇、温度、含盐量等对相行为的影响。 相似文献
134.
The combination of photoredox catalysis and enamine catalysis has enabled the development of an enantioselective aerobic oxidative cross-dehydrogenative coupling between glycine derivatives and simple ketones or aldehydes, which provides an efficient approach for the rapid synthesis of enantiopure unnatural α-alkyl α-amino acid derivatives in good yield with excellent diastereo- (up to >99 : 1) and enantioselectivities (up to 97% ee). This process includes the direct photoinduced oxidation of glycine derivatives to an imine intermediate, followed by the asymmetric Mannich-type reaction with an enamine intermediate generated in situ from a ketone or aldehyde and a chiral secondary amine organocatalyst. This mild method allows the direct formation of a C–C bond with simultaneous installation of two new stereocenters without wasteful removal of functional groups.A visible-light-induced enantioselective aerobic oxidative cross-dehydrogenative coupling between glycine derivatives and simple ketones or aldehydes is achieved. 相似文献
135.
Click and Release: A Chemical Strategy toward Developing Gasotransmitter Prodrugs by Using an Intramolecular Diels–Alder Reaction 下载免费PDF全文
Dr. Xingyue Ji Dr. Cheng Zhou Dr. Kaili Ji Robert E. Aghoghovbia Zhixiang Pan Vayou Chittavong Prof. Dr. Bowen Ke Prof. Dr. Binghe Wang 《Angewandte Chemie (International ed. in English)》2016,55(51):15846-15851
Prodrug strategies have been proven to be a very effective way of addressing delivery problems. Much of the chemistry in prodrug development relies on the ability to mask an appropriate functional group, which can be removed under appropriate conditions. However, developing organic prodrugs of gasotransmitters represent unique challenges. This is especially true with carbon monoxide, which does not have an easy “handle” for bioreversible derivatization. By taking advantage of an intramolecular Diels–Alder reaction, we have developed a prodrug strategy for preparations of organic CO prodrugs that are stable during synthesis and storage, and yet readily release CO with tunable release rates under near physiological conditions. The effectiveness of the CO prodrug system in delivering a sufficient quantity of CO for possible therapeutic applications has been studied using a cell culture anti‐inflammatory assay and a colitis animal model. These studies fully demonstrate the proof of concept, and lay a strong foundation for further medicinal chemistry work in developing organic CO prodrugs. 相似文献
136.
等离子体质谱法测定大米、茶叶中痕量稀土元素 总被引:2,自引:0,他引:2
采用ICP—MS等离子体质谱法和使用HNO3+H2O2混酸体系高压密闭微波前处理样品联合技术,同时测定了大米、茶叶样品中15种稀土元素(La、Ce、Pr、Nd、Sm、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb、Lu、Y)含量。对消化条件、测定方法和等离子体质谱测定条件进行了优化选择,并进行了国家标准物质的对照分析质量验证。结果表明,检测方法的准确度达90%-110%,相对标准偏差(RSD)〈8%,仪器检出限为50—70ng/kg。该法快速灵敏,准确可靠,能够满足检测要求。 相似文献
137.
In this letter, we report a multifunctional high-performance Nd:glass laser system. Laser pulses from an all-fiber front end are first amplified by a regenerative amplifier to 10 mJ level, and then further amplified in a four-pass amplifier. The laser system can provide 10.3-J, 3-ns laser pulses at 1053-nm wavelength. The shot-to-shot energy stability is better than 1.5% (RMS). The output laser beam is near diffraction limit. Binary amplitude masks are used to maintain a flat top near-field profile with a 71% fill factor. After the frequency conversion process, 7 and 5.5 J pulses at 526.5 and 351 nm are obtained, respectively. 相似文献
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140.
A series of iridium complexes ( 1 – 5 ), which consist of two 2‐(2,4‐difluorophenyl)pyridine (dfppy)‐based primary ligands and one pyridinylphosphinate ancillary ligand, have been investigated theoretically for screening highly efficient deep‐blue light‐emitting materials. Compared with the reported dfppy‐based emitter 1 , the designed iridium complexes 3 – 5 with the introduction of a stronger electron‐withdrawing (–CN, –CF3 , or o‐carborane) group and a bulky electron‐donating (tert‐butyl) group in dfppy ligands can be achieved to display the emission peaks at 443, 442, and 447 nm, respectively. The electronic structures, absorption and emission properties, radiative and nonradiative processes of their excited states, and charge injection and transport properties of the iridium complexes are analyzed in detail. The calculated results show that designed iridium complexes have comparable radiative and nonradiative rate constants with 1 , and are expected to have similar quantum efficiency with 1 . Meanwhile, these designed complexes keep the advantages of the charge transport properties of 1 , indicating that they are potential iridium complexes for efficient deep‐blue phosphorescence. This work provides more in‐depth understanding the structure–property relationship of dfppy‐based iridium complexes, and shed lights on molecular design for deep‐blue phosphorescent metal complexes. 相似文献