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201.
The central V atom in bis[6-methyl-4-hydroxy-3-quinolinecarboxylate] mono(oxo)mono-hydroxy-vanadium(Ⅴ) (1), synthesized by the hydrothermal treatment of ethyl 6-methyl-4-hydroxy-3-quinolinecarboxylate and V2O5, has a distorted octahedral coordination geometry formed by six oxygen atoms from two oxygen atom of two hydroxy groups and two oxygen atoms of two carboxylate groups as well as one oxo group and hydroxy group. CCDC: 285592. 相似文献
202.
苯乙烯-丁二烯-苯乙烯/聚乙烯基甲基醚共混体系相容性的FT-IR及DSC研究 总被引:2,自引:0,他引:2
嵌段高聚物、均聚物共混体系相容性是近年来研究的热点。本工作以光学显微镜、DSC、FT-IR为手段,研究了三嵌段高聚物苯乙烯-丁二烯-苯乙烯(SBS);SBS-48、SBS-30,SBS-28与聚乙烯基甲基醚共混体系的相容性。DSC结果表明,随SBS中PS含量的升高,体系相容性变好,PS段分子量增大,也有助于体系相容。FT-IR结果表明PVME中COCH_3在1100cm~(-1)附近呈现的双峰的相对强度对体系的相容性十分敏感,而由于苯环C—H振动产生的698cm~(-1)峰位却不象PS/PVME体系那样随相容性的改变而有显著的改变。总而言之,嵌段高聚物SBS/均聚物PVME共混体系中,体系的相容性依赖于嵌段高聚物在体系中的组份含量及嵌段高聚物中PS的重量百分含量,PS段分子量的大小对体系相容性也有影响。 相似文献
203.
Zou Jianzhong Wu Yong Duan Chunyin Liu Yongjiang Xu Zheng 《Transition Metal Chemistry》1998,23(3):305-308
Three binuclear copper(II) complexes bridged by three different bridging ligands: μ-TPHA (terephthalato), μ-PHTA (phthalato)
and μ-TCB (tetracarboxylatobenzene) have been synthesized. The crystal structure of [{Cu(dipn)}2(μ-TPHA)](ClO4)2 where dipn = N-(3-aminopropyl)-1,3-propanediamine was solved at room temperature. The [{Cudipn}2(μ-TPHA)](ClO4)2 complex consists of a μ-terephthalato bridging binuclear copper(II) cationic unit and two non-coordinated perchlorate anions.
The TPHA ligand bridges in a bismonodentate fashion. The environment of the copper(II) ion is a distorted plane-square-planar coordination sphere. The magnetic
properties of the three complexes have been investigated in the 75–300 K range, and show that the geometry of the CuII atom is the important factor for magnetic interactions in the terephthalato bridging binuclear copper(II) complexes.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
204.
The sequence distribution and the terminal structures of poly-1,3-pentadiene chains obtained by rare earth catalyst and effect of polymerization temperature on microstructure of the polymer have been investigated by ~(13)C-NMR method. According to experimental results it was supposed that terminal active growing chain of the polymer would be four types of anti- and syn-η~3-allyl structures. When polymerization temperature was reduced, the content of cis-1,4-poly-1,3-pcntadiene increases. It can be explained by isomerization between anti- and syn-η~3-allyl. The process forming trans-1,2 unit instead of 3,4-unit were also described. 相似文献
205.
The design of new chiral ligands is the key in the development of transition metal catalyzed asymmetric synthesis. Many chiral diphosphine ligands have been prepared and applied in asymmetric catalytic reactions with excellent enantioselectivities. Among the chiral diphosphine ligands that have been reported, the atropisomeric C2-symmetric phosphines with a biaryl scaffold initiated by Noyori and co-workers with BINAP were found to have the widest application in the transition metal catalyze… 相似文献
206.
QuEChERS前处理结合HPLC-Q-TOF/MS非靶向快速筛查凉茶中的非法添加物 总被引:1,自引:0,他引:1
建立了QuEChERS法净化,结合高效液相色谱-四极杆-飞行时间质谱法(HPLC-Q-TOF/MS)非靶向快速筛查凉茶中未知非法添加物的方法。凉茶中的非法添加物经0.5%乙酸-乙腈提取,氨丙基粉净化,C_(18)色谱柱(100 mm×2.1 mm,1.7μm)分离,HPLC-Q-TOF/MS测定。利用8种质控化合物建立的筛查方法检出限为2.0~10μg/kg,定量下限为5.0~25μg/kg。3个不同加标水平的平均回收率为75.8%~95.6%,RSD(n=6)为2.1%~6.5%。在该定量方法基础上利用目标化合物特征离子的精确质量数、同位素匹配、二级碎片信息进行数据库匹配,无标准品情况下非靶向筛查非法添加物。结果表明,该方法无需标准品即可快速筛查凉茶中的非法添加西药,能应用于凉茶样品的实际筛查。应用该方法对50份散装凉茶样品进行测定,其中10份凉茶样品检出对乙酰氨基酚,含量为4.14~2 188 mg/kg。该方法快速、准确、分析通量高,可为凉茶中非法添加物的快速筛查和质量控制提供重要依据。 相似文献
207.
Tetragonal tungsten bronze K0.71Nd0.028WO3 was synthesized by rare earth co-permeation method using Keggin type POMs of α-K10[SiCu3(OH2)W9O37]·6H2O (abbreviated as SiW9Cu3) as precursor. XRD, XPS, XRF, TG-DTA were used to characterize the resulting material. The XPS results indicate that Nd has permeated and diffused into the body of the sample and exists in tungsten bronze in the form of K0.71Nd0.028WO3. The results of TG-DTA show that K0.71Nd0.028WO3 begins to decompose at 320 ℃. The consequence of DC four-probe shows that the conductivity of the sample permeated by rare earth is 103 times higher than that of the sample only permeated by methanol at room temperature. The conductivity of the sample only permeated by methanol is only 10-3 S·cm-1 but the conductivity of the sample permeated by rare earth is 1.65 S·cm-1. 相似文献
208.
Poly(L -lactide-co-β-malic acid) was obtained after the hydrogenolysis of the copolymer of L -lactide (L-LA) and β-benzyl malate (MA). 1H-NMR demonstrated that the composition of the copolymer was identical to the feeding dose. Thermal property study revealed the morphology of the copolymer could be changed from semi-crystalline to amorphous with increasing hydrophilic β-malic acid content. The copolymers with 8 and 13 mol% β-malic acid content possessed enough mechanical property for fabricating cell scaffold. Degradation result demonstrated that most of the hydrophilic β-malic acid units broke down from the copolymer within 1 week and the ester bond between L -lactide and β-malic acid hydrolyzed prior to the inner ester bond of poly(L -lactide) (PLLA). Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
209.
Zn-Al-Ce三元类水滑石的制备及性质研究 总被引:8,自引:1,他引:8
采用共沉淀法,水热合成层状化合物一硝酸根柱撑锌铝铈三元类水滑石,分别测定了各种单一金属盐溶液及M^2 /M^3 摩尔比为2,Ce^3 /Al^3 摩尔比为0.25的混合金属盐的NaOH滴定曲线,并利用XRD对不同条件下合成产物进行物相分析。实验结果表明:在M^2 /M^2 =2,Ce^3 /Al^3 =0.07~0.50,pH=5.8~6.5条件下进行多种离子共沉淀,并经120℃、6h水热处理后,均能合成结构单一的ZnAlCe—HTLLcs,利用TG—DTlA、FT—IR、ICP对合成物进行了表征,筛选出适宜的合成条件,并对HTLcs层状结构的热行为进行初步研究,结果表明ZnAlCe—HTLcs热稳定性较差,层间结合水、层板羟基及层间客体物种(NO3^-)失去温度在240℃左右,易于转化为复合氧化物,将此复合氧化物应用于NO的催化?肖除反应,680℃下NO的转化率高达近100%。 相似文献
210.
研究新型无毒无机颜料,逐步取代如铅铬黄、镉黄等无机颜料,日益引人注意。我们以价廉易得的自云石凹凸棒、蒙脱石、凹凸棒石粘土矿为原料,制得黄色硅酸盐类无毒新型颜料。研究了该类颜料的骨架结构与成分,及其发色机理。工艺过程如下: 相似文献