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951.
《应用有机金属化学》2017,31(7)
The reactions of R3SnCl (R = Me, Bu or Ph) with sodium 4‐phenylbutyrate, Na(OPhb), in EtOH yielded three polymeric triorganotin carboxylates, namely [R3Sn(OPhb)]n (R = Me ( 1 ), Bu ( 2 ) or Ph ( 3 )). All complexes were spectroscopically characterized using Fourier transform infrared, 119Sn Mössbauer, 1H NMR, 13C{1H} NMR and 119Sn{1H} NMR spectral techniques. In addition, the crystal structures of 1 and 3 were determined using single‐crystal X‐ray diffraction. Their polymeric structures are sustained by bridging carboxylates which connect two five‐coordinate Sn(IV) centres. Each metallic cation displays a distorted trigonal bipyramidal coordination geometry (Addison's parameters ranging from 0.84 in 1 to 0.77–0.91 in 3 ), with the oxygen atoms occupying the apical positions and the organic groups at the equatorial corners. The one‐dimensional zigzag chains of 1 propagate along the b ‐axis, whereas 3 displays wave‐like double polymeric chains along the b ‐axis. For both 1 and 3 , parallel one‐dimensional polymeric chains are interconnected by C─H⋅⋅⋅π interactions. The antifungal activity of 1 – 3 was screened against Candida albicans (ATCC 18804), C. tropicalis (ATCC 750), C. glabrata (ATCC 90030), C. parapsilosis (ATCC 22019), C. lusitaniae (CBS 6936) and C. dubliniensis (clinical isolate 28). The antifungal activity of 3 was noteworthy since it was not only more active than 1 and 2 , but also more active than the control drugs (nystatin and fluconazole nitrate) in some cases. 相似文献
952.
Transition metal complexes of Mn(II) and Ni(II) have been synthesized with novel bioactive Schiff's base ligand. Schiff's base ligand i.e. benzoylacetone‐bis(2‐amino‐4‐methylbenzothioazole) has been synthesized via condensation reaction between 2‐amino‐4‐methylbenzothioazole and benzoylacetone in 2:1 ratio, respectively. Synthesized ligand has been characterized using elemental analysis, infra‐red, 1H–NMR and mass spectroscopy techniques. Characterization of complexes was based on magnetic moment, molar conductance, elemental analysis, electronic spectra, infra‐red and EPR spectroscopic techniques. Molar conductance data suggest that metal complexes are non‐electrolytic in nature. Therefore, these complexes are formulated as [M(L)X2], where M = Mn(II), Ni(II), L = Schiff's base ligand, X = Cl?, CH3COO?, NO3?. Data of characterization study suggest octahedral geometry for Mn(II) and Ni(II) complexes. Geometry of metal complexes was also optimized with the help of computational study i.e. molecular modelling. Computational study also suggests octahedral geometry for complexes. Free ligand as well as its all metal complexes have been screened against the growth of pathogenic bacteria (E.coli, S.aureus) and fungi (C.albicans, C.krusei, C.parapsilosis, C.tropicalis) to assess their inhibition potential. The inhibition data revealed that metal complexes exhibit higher inhibition potential against the growth of bacteria and fungi microorganisms than free ligand. 相似文献
953.
The structure of liquid indium in a wide temperature range has been investigated by means of X-ray diffraction and reverse Monte Carlo methods. Analysis of temperature dependence of the interatomic distances and coordination numbers allowed us to determine the existence of structural transformation in a liquid state. Moreover, it was found that at a temperature of 640 K thermal expansion coefficients, estimated from temperature dependence of interatomic distances, change its sign from negative to positive confirming the transformations in structure of liquid indium which are observed by temperature variations. 相似文献
954.
955.
《Journal of computational chemistry》2018,39(19):1354-1358
Alchemical free energy (AFE) calculations based on molecular dynamics (MD) simulations are key tools in both improving our understanding of a wide variety of biological processes and accelerating the design and optimization of therapeutics for numerous diseases. Computing power and theory have, however, long been insufficient to enable AFE calculations to be routinely applied in early stage drug discovery. One of the major difficulties in performing AFE calculations is the length of time required for calculations to converge to an ensemble average. CPU implementations of MD‐based free energy algorithms can effectively only reach tens of nanoseconds per day for systems on the order of 50,000 atoms, even running on massively parallel supercomputers. Therefore, converged free energy calculations on large numbers of potential lead compounds are often untenable, preventing researchers from gaining crucial insight into molecular recognition, potential druggability and other crucial areas of interest. Graphics Processing Units (GPUs) can help address this. We present here a seamless GPU implementation, within the PMEMD module of the AMBER molecular dynamics package, of thermodynamic integration (TI) capable of reaching speeds of >140 ns/day for a 44,907‐atom system, with accuracy equivalent to the existing CPU implementation in AMBER. The implementation described here is currently part of the AMBER 18 beta code and will be an integral part of the upcoming version 18 release of AMBER. © 2018 Wiley Periodicals, Inc. 相似文献
956.
连续变化法测定络合物组成和稳定常数是大学化学中的经典学生实验。但针对1:2和1:3的络合反应,实验教科书的设计中可能出现数据点过少也就是溶液配制过少的问题。如果按照要求配制溶液,由于没有完全反应的混合溶液,而其他混合溶液给出的数据又都呈良好的线性,就缺少了用来估算曲线的数据点,结果是,将没有足够的数据对稳定常数进行估算。对这种可能出现的数据点过少的实验设计的原因、结果和解决方法进行了探讨。 相似文献
957.
Anastasios K. Papageorgiou Evangelos M. Papoutsis-Kiachagias Kyriakos C. Giannakoglou 《国际流体数值方法杂志》2022,94(1):59-75
This article contributes to the development of methods for shape optimization under uncertainties, associated with the flow conditions, based on intrusive Polynomial Chaos Expansion (iPCE) and continuous adjoint. The iPCE to the Navier–Stokes equations for laminar flows of incompressible fluids is developed to compute statistical moments of the Quantity of Interest which are, then, compared with those obtained through the Monte Carlo method. The optimization is carried out using a continuous adjoint-enabled, gradient-based loop. Two different formulations for the continuous adjoint to the iPCE PDEs are derived, programmed, and verified. Intrusive PCE methods for the computation of the statistical moments require mathematical development, derivation of a new system of governing equations and their numerical solution. The development is presented for a chaos order of two and two uncertain variables and can be used as a guide to those willing to extend this development to a different set of uncertain variables or chaos order. The developed method and software, programmed in OpenFOAM, is applied to two optimization problems pertaining to the flow around isolated airfoils with uncertain farfield conditions. 相似文献
958.
Kamlesh Madhusudan Makwana Dr. Radhakrishnan Mahalakshmi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(12):4147-4156
A popular strategy in the de novo design of stable β‐sheet structures for various biomedical applications is the incorporation of aromatic pairs at the non‐hydrogen‐bonding (NHB) position. However, it is important to explicitly understand how aryl pair packing at the NHB region is coordinated with backbone structural rearrangements, and to delineate the benefits and drawbacks associated with stereopositional choice of dissimilar aromatic pairs. Here, we probe the consequences of flipped Trp/Tyr pairs by using engineered permutants at the NHB position of dodecapeptide β‐hairpins, proximal and distal to the turn. Extensive conformational analysis of these peptides using NMR and CD spectroscopy reveal that a classic Edge‐to‐Face and Face‐to‐Edge geometry at the proximal and distal aromatic pairs, respectively, in YW‐WY, is the most stabilizing. Such a preferred packing geometry in YW‐WY results in a highly twisted β‐sheet backbone, with Trp always providing a ‘Face’ orientation to its dissimilar aromatic partner Tyr. Flipping the proximal and/or distal aromatic pair distorts the ideal T‐shaped geometry, and results in alternate aryl arrangements that can adversely affect strand twist and β‐sheet stability. Our study reveals the existence of a strong stereopositional influence on the packing of dissimilar aromatic pairs. Our findings highlight the importance of modeling physical interaction forces while designing protein and peptide structures for functional applications. 相似文献
959.
依据相关光谱式红外气体传感器检测原理,以系统中红外光与气体反应的气室为研究对象,利用光学设计专用软件Tracepro对理想红外朗伯光源在不同反射镜类型下光源的最佳位置进行了仿真分析;通过建立光路传输系统的数学模型,对气室不同结构尺寸下的光功率输出、以及气室内壁反射率对传感系统性能的影响进行了仿真与优化.在理论模型的基础上,根据仿真结果,确定了最佳气室模型的参数组合.实验结果表明,通过对气室中红外光源的位置、反射镜类型、气室长度等部分进行适当的优化修改后,可使探测器接收信号幅度得到明显提高,将有利于后级电路的信号放大、数模转换等处理过程,从而提高气体浓度检测的灵敏度和精度. 相似文献
960.
刘明 《数学的实践与认识》2014,(20)
综合评价指数是一种广义上的统计指数,在讨论了综合评价指数与一般统计指数不同的基础上,引述了综合评价指数一般编制步骤并详细分析研究了综合评价指数编制过程中的权重确定,提出了基于等权设计思想的加权修正综合评价指数编制方法,最后以甘肃省装备制造产业为例进行了展示. 相似文献