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排序方式: 共有163条查询结果,搜索用时 281 毫秒
71.
采用新型二元致孔剂Pluronic F127/十二胺,通过两步溶胶-凝胶法合成了辛基杂化整体柱,并用于稠环物质、苯系物以及水体中8种生物毒素的毛细管液相色谱分离分析.在整体柱的形貌方面,F127的加入使材料由聚集球状结构转变成双连续孔结构,并实现了对材料通孔、骨架以及骨架上介孔的尺寸调节,得到了更适于小分子分离的结构.此外,通过减少十二胺用量使凝胶化时间延长,显著降低了灌柱的难度以及灌柱时可能引起的材料不均匀和重复性差的问题.优化后的辛基杂化整体柱保持了良好的机械稳定性和高渗透性,塔板数为49000/m,与传统的制备方法相比柱效明显提高.在对稠环物质、苯系物等典型小分子的测试中均得到了良好的分离效果.新型二元致孔剂的辛基杂化整体柱制备更容易,形貌控制简单,稳定性好,实用性显著增强. 相似文献
72.
Two novel polynuclear complexes{NaFe4(μ4-O)(L)4(μ2-Cl)[Fe(CN)5NO](H2O)(DMF)2}(1) and{NaFe4(μ4-O)(L)4(μ2-OEt)[Fe(CN)5NO](H2O)(DMF)2}(2) have been prepared using the tetradentate N-(2-hydroxyethyl)-3-methoxysalicylaldimine Schiff-base ligand (H2L) with the help of[Fe(CN)5NO]2-linkers,where the ligand was in situ synthesized through the condensation of o-vanillin and e... 相似文献
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Growth of aligned single-walled carbon nanotubes under ac electric fields through floating catalyst chemical vapour deposition 下载免费PDF全文
Through floating catalyst chemical vapour deposition(CVD) method,well-aligned isolated single-walled carbon nanotubes (SWCNTs) and their bundles were deposited on the metal electrodes patterned on the SiO2/Si surface under ac electric fields at relatively low temperature(280℃). It was indicated that SWCNTs were effectively aligned under ac electric fields after they had just grown in the furnace.The time for a SWCNT to be aligned in the electric field and the effect of gas flow were estimated. Polarized Raman scattering was performed to characterize the aligned structure of SWCNTs. This method would be very useful for the controlled fabrication and preparation of SWCNTs in practical applications. 相似文献
75.
我们合成、表征了苯并 1 8 冠 6(B1 8 C 6)与K2 [Pd (SCN) 4 ],K2 [Pt(SCN) 4 ]生成的一维链状配合物 [K(B1 8 C 6) ]2 [Pd(SCN) 4 ]( 1 ) ,[K(B1 8 C 6) ]2 [Pt(SCN) 4 ]( 2 )和[K(B1 8 C 6) ]2 [Pt(SCN) 4 ]·C2 H4Cl2 ( 3 ) .其中 3为三斜晶系 ,空间群P1 [化学学报 2 0 0 2 ,60 ( 8) ,1 465 ].厦门大学胡盛志教授认为该化合物的空间群应为P 1 .经将原始数据重新还原、修正 ,3的空间群的确为P 1 ,现予以更正 .配合物 3部分结构数据由表 1给出 ,其非氢原子坐标和热参数列于表 2 ,部分键长和键角列于表 3 .晶体结构和堆积图… 相似文献
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Luminescent properties of Tm3+-doped GdYTaO4 are studied for exploring their potential applications in temperature and pressure sensing.Two main emission peaks from 3H4→3H6 transition of Tm3+are investigated.Intensity ratio between the two peaks evolves exponentially with temperature and has a highest sensitivity of 0.014 K?1 at 32 K.The energy difference between the two peaks increases linearly with pressure increasing at a rate of 0.38 meV/GPa.Intensity ratio between the two peaks and their emission lifetimes are also analyzed for discussing the pressure-induced variation of the sample structure.Moreover,Raman spectra recorded under high pressures indicate an isostructural phase transition of GdYTaO4 occurring at 4.46 GPa. 相似文献
78.
Wei-Min Jiang 《中国物理 B》2022,31(6):66801-066801
High mobility quasi two-dimensional electron gas (2DEG) found at the CaZrO3/SrTiO3 nonpolar heterointerface is attractive and provides a platform for the development of functional devices and nanoelectronics. Here we report that the carrier density and mobility at low temperature can be tuned by gate voltage at the CaZrO3/SrTiO3 interface. Furthermore, the magnitude of Rashba spin-orbit interaction can be modulated and increases with the gate voltage. Remarkably, the diffusion constant and the spin-orbit relaxation time can be strongly tuned by gate voltage. The diffusion constant increases by a factor of ~ 19.98 and the relaxation time is reduced by a factor of over three orders of magnitude while the gate voltage is swept from -50 V to 100 V. These findings not only lay a foundation for further understanding the underlying mechanism of Rashba spin-orbit coupling, but also have great significance in developing various oxide functional devices. 相似文献
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银离子高效液相色谱-质谱法分析血清中甘油三酯类化合物的组成 总被引:1,自引:0,他引:1
针对甘油三酯(TAG)类化合物的复杂性,建立了分析小鼠血清中TAG类化合物的方法。采用经典的氯仿-甲醇溶剂体系对血中的TAG类化合物进行提取。脂质提取物经Varian ChromSpher 5 Lipids柱分离,在0.75 mL/min的流速下以乙腈-正己烷(1:99, v/v)为流动相进行等度洗脱,采用大气压化学电离源正离子模式电离,质谱增强型全扫描、增强型子离子扫描和中性丢失扫描模式检测。根据银离子色谱对双键的保留规律以及质谱所给出的碎片离子信息,对血清中TAG类化合物进行了结构鉴定。结果表明采用该方法可以从小鼠血清中鉴定到66个TAG类化合物以及5个胆固醇酯。该方法简单,重现性好,可通用于其他样品中TAG类化合物的检测。 相似文献
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