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991.
本文将气液色谱法用于测定环丁砜含盐溶液中以烃、芳烃、氯代烃、醇和酮为溶质的盐效应常数,结果表明,大多数溶质的盐效应关系可用Setschenow方程描述;负离子的性质对盐效应的影响比正离子更重要;负离子的电子向氯代烃中氯原子3d空轨道的迁移作用对其k_s的影响很大。 相似文献
992.
人造芥子油中异硫氰酸烯丙酯与硫氰酸烯丙酯的气相色谱分析 总被引:4,自引:0,他引:4
采用2m×3mm玻璃柱,涂布0.5%EGA的80~100目GaschromQ为固定相,以异辛醇为内标物,分析芥子油中异硫氰酸烯丙酯与硫氰酸烯丙酯异构体。该方法既可用于人造芥子油的含量分析,也可用于市售芥子油的质量鉴定。 相似文献
993.
本文对CT联合血清同型半胱氨酸(HCY)、β2-微球蛋白(β2-M)在下肢动脉狭窄闭塞性疾病中的诊断价值进行分析。选取上海市金山区中西医结合医院收治的120例疑似下肢动脉狭窄闭塞性疾病患者进行研究,选取同期健康体检者120例作为对照组,对患者进行CT检查、血清HCY和β2-M水平检查,并比较了CT诊断下肢动脉狭窄闭塞情况、两组患者血清HCY和β2-M水平,以明确CT、HCY、β2-M诊断价值及误诊率、漏诊率。结果显示,120例疑似患者中,CT检测出646节段病变血管,其中轻度狭窄155节段,中度狭窄257节段,重度狭窄143节段,血管完全闭塞91节段;研究组患者血清HCY、β2-M水平明显高于对照组,两组比较差异有统计学意义(P<0.05);HCY的AUC为0.863,截断值>21.75(μmol/L),诊断敏感性为79.00%,特异性为80.00%,β2-M的AUC为0.837,截断值>2.98(μmol/mL),诊断敏感性为75.25%,特异性为65.21%;CT诊断阳性率为67.50%,HCY诊断阳性率为69.17%,β2-M诊断阳性率为67.50%,三者联合诊断阳性率为82.50%,联合诊断阳性率高于CT、HCY、β2-M单独诊断阳性率(P<0.05);CT、HCY、β2-M单一检测对下肢动脉狭窄闭塞性疾病均有较高灵敏度、特异性及准确度,但三者联合诊断灵敏度、特异性及准确度最高,误诊率、漏诊率最低。本文证实了采用CT联合血清HCY、β2-M诊断下肢动脉狭窄闭塞性疾病诊断灵敏度、特异性及准确度高,误诊率、漏诊率低。 相似文献
994.
Zhang Yongqiang Wang Baiquan Xu Shansheng Zhou Xiuzhong Sun Jie 《Transition Metal Chemistry》1999,24(6):722-725
Reactions of diiron complexes (E)[5-t-BuC5H3)Fe(CO)]2(-CO)2 [E = Me2Si (1), Me2SiSiMe2 (2), and Me2SiOSiMe2 (3)] with iodine in CHCl3 yielded diiodide complexes (E)[5-t-BuC5H3)Fe(CO)2I]2 [E=Me2Si (5), Me2SiSiMe2 (6), and Me2SiOSiMe2 (7)]. Like (1–3), complexes (5–7) also exists as mixtures of cis and trans isomers even though the Fe–Fe bond in (1–3) has been cleaved. When the pure isomers (1–3) reacted with iodine respectively in CHCl3, the cis isomers (1c–3c) yielded only the cis products (5c–7c), whereas the trans isomers (1t–3t) yielded only the trans isomers (5t–7t). This indicates that iodination of bridged diiron complexes is stereospecific. Similar treatment of trans-(Me2Si)[{5-t-(heptyl)C5H3}Fe(CO)]2(-CO)2 (4t) with iodine gave only the trans product (Me2Si)[{5-t-(heptyl)C5H3}Fe(CO)2I]2 (8t). The molecular structure of (5t) was determined by X-ray diffraction. 相似文献
995.
996.
Jing?Zhou Yuqi?Liu Liming?Tang Xinchen?Teng Ning?Tang Zhongxian?HuangEmail author 《中国科学B辑(英文版)》2003,46(1):64-74
Two mutants of the zinc finger protein, ZNF191 (243–368) I323W and R327W, are successfully obtained by site-directed mutagenesis.
The fluorescence spectrum is used to study the interaction between these two mutants and the oligonucleotides. The influence
of the mutation on the interaction has been studied using ethidium bromide (EB) as the fluorescence probe. The binding constants
of the I323W-DNA and R327W-DNA have been calculated and the possible binding models have been discussed. 相似文献
997.
Wang GC Zhou YH Morikawa Y Nakamura J Cai ZS Zhao XZ 《The journal of physical chemistry. B》2005,109(25):12431-12442
The decomposition of methanol on the Ni(111) surface has been studied with the pseudopotential method of density functional theory-generalized gradient approximation (DFT-GGA) and with the repeated slab models. The adsorption energies of possible species and the activation energy barriers of the possible elementary reactions involved are obtained in the present work. The major reaction path on Ni surfaces involves the O-H bond breaking in CH(3)OH and the further decomposition of the resulting methoxy species to CO and H via stepwise hydrogen abstractions from CH(3)O. The abstraction of hydrogen from methoxy itself is the rate-limiting step. We also confirm that the C-O and C-H bond-breaking paths, which lead to the formation of surface methyl and hydroxyl and hydroxymethyl and atom hydrogen, respectively, have higher energy barriers. Therefore, the final products are the adsorbed CO and H atom. 相似文献
998.
利用分子束技术改变甲烷的平动能E_k来研究E_k及其法向分量E_n对甲烷在Ni表面及La薄膜上激活解离吸附的影响。对CH_4/Ni及CH_4/La系统, 当甲烷的平动能E_k分别低于58.5 kJ·mol~(-1)及52.3 kJ·mol~(-1)时, 没观察到甲烷的解离吸附。当甲烷的平动能超过此阈值时, 即对CH_4/Ni系统, 当Ek=58.5增至63.8 kJ·mol~(-1)时, 初始沾着几率s_0由0至0.54线性增加; 对CH_4/La系统, 当E_k=52.3增至63.8 kJ·mol~(-1)时, S_0由0至0.49线性增加。这些结果表明, 两个系统的化学吸附是不经过前趋态的直接化学吸附。最后求出CH_4/Ni, CH_4/La系统的表观活化能分别为46.8 kJ·mol~(-1)和38.1 kJ·mol~(-1)。 相似文献
999.
Lifang Yang Haifeng He Hongqing Cao Xinhua Wan Qi-feng Zhou Department of Polymer Science & Engineering College of Chemistry & Molecular Engineering Peking University Beijing China 《高分子科学》2002,(5):401-407
Four new rod-coil diblock molecules, which had well-defined para-phenylene oligomers (PPP, from biphenyl toquinquephenyl) as rigid segments and poly(ethylene oxide) (PEO, M_w ca. 750) as flexible segments, were synhesized. Thechemical structure and the number of repeating unit in PEO coil and PPP rod were characterized by ~1H-NMR and MALDI-TOF mass spectromeny. The diblock oligomers showed good solubility in common organic solvents and aggregated in wateras characterized by a blue shift in UV-vis absorption spectra, a red shift in emission spectra, quenching of the fluorescenceand formation of the microfibrilla and fractal-like structures. The formation of different supramolecular structures meant thatthis effort might lead to commercial important highly organized functional materials. 相似文献
1000.
Titanate nanoribbons were prepared via a hydrothermal treatment of rutile-type TiO2 powders in a 10 M NaOH solution at 200 °C for 48 h. The as-prepared titanate nanoribbons were then hydrothermally post-treated at 150 °C for 12-36 h. The titanate nanoribbons before and after hydrothermal post-treatment were characterized with FESEM, XRD, TEM, UV-VIS and nitrogen adsorption-desorption isotherms. The results showed that the hydrothermal post-treatment not only promoted the phase transformation from titanate to anatase TiO2, but also was beneficial to the removal of Na+ ions remained in the titanate nanoribbons. After hydrothermal post-treatment, the TiO2 samples retained the one-dimensional structure feature of the titanate nanoribbons and showed an obvious increase in the specific surface area and the pore volume. 相似文献