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851.
Synthesis of Novel α‐(Acyloxy)‐α‐(quinolin‐4‐yl)acetamides by a Three‐Component Reaction between an Isocyanide,Quinoline‐4‐carbaldehyde,and Arenecarboxylic Acids 下载免费PDF全文
Jafar Taran Ali Ramazani Sang Woo Joo Katarzyna Ślepokura Tadeusz Lis 《Helvetica chimica acta》2014,97(8):1088-1096
Novel α‐(acyloxy)‐α‐(quinolin‐4‐yl)acetamides were synthesized by the Passerini three‐component reaction between an isocyanide, quinoline‐4‐carbaldehyde, and arenecarboxylic acids in H2O. The reactions were carried out in one pot at room temperature with quantitative yields. 相似文献
852.
The efficacy of photodynamic therapy (PDT) depends upon the amount of photosensitizer accumulated in the malignant tissues. Radachlorin is a popular photosensitizer used in photodynamic therapy to treat various types of cancer. In this study, we have studied the main organelles responsible for the accumulation of radachlorin in human anaplastic thyroid cancer in vitro and in vivo. The optimal time window for uptake and clearance of radachlorin also was studied. Confocal microscopic images confirmed that the radachlorin is mainly acquired by mitochondria and partially by lysosome and endoplasmic reticulum. Studies also showed that the maximum amount of radachlorin was accumulated within 3–6 h after the treatment. Radachlorin also showed a higher affinity toward malignant tumors compared to the other organs in mice xenograft model. Uptake of radachlorin reached an optimum amount within 6 h and most of the radachlorins were also cleared from the body in next 48 h. Therefore, detailed information regarding exact accumulation sites and a time window in which maximum amount of drug is accumulated and cleared were obtained by this study. Hence, not only the efficacy of the treatment can be increased but the phototoxicity after the treatment also can be controlled. 相似文献
853.
Ki Mun Jung Lyn C Thomas Mee Chi So 《The Journal of the Operational Research Society》2015,66(10):1656-1668
Data-based scorecards, such as those used in credit scoring, age with time and need to be rebuilt or readjusted. Unlike the huge literature on modelling the replacement and maintenance of equipment there have been hardly any models that deal with this problem for scorecards. This paper identifies an effective way of describing the predictive ability of the scorecard and from this describes a simple model for how its predictive ability will develop. Using a dynamic programming approach one is then able to find when it is optimal to rebuild and when to readjust a scorecard. Failing to readjust or rebuild a scorecard when they aged was one of the defects in credit scoring identified in the investigations into the sub-prime mortgage crisis. 相似文献
854.
Yong Kyun Sim Suhyun Jung Jung Yun LimJuhyun Kim Seong-Ho KimBong Keun Song Bum Tae KimHyuk Lee Seongsoon Park 《Tetrahedron letters》2011,52(9):1041-1043
A facile process was developed to manufacture biocatalyst-conjugated magnetic nanobeads, which afford no loss of the intrinsic activity and enantioselectivity of biocatalysts. Up to 90% of their activities remained after six-time recycling in aqueous media. 相似文献
855.
Hyun Min ParkByul Nim Oh Jin Hoon KimWu Qiong In Hong HwangKwang-Deog Jung Cheal Kim Jinheung Kim 《Tetrahedron letters》2011,52(43):5581-5584
In this study, an assay to quantify the presence of aluminum ions with a receptor containing naphthol and quinoline moieties was developed using a turn-on fluorescence enhancement approach. Upon treatment with aluminum ions, the fluorescence of the receptor was enhanced at 510 nm due to the formation of a complex between the ligand and aluminum ions at room temperature. As the concentration of Al3+ was increased, the fluorescence gradually increased. Other metal ions, such as K+, Ag+, Ca2+, Mg2+, Zn2+, Mn2+, Co2+, Ni2+, Cu2+, Cd2+, Cr3+, Fe3+, In3+, had no significant effect on the fluorescence. 相似文献
856.
Reaction of [AuCl(SMe2)] with NaL·H2O (L = ethyl(pyridine-4-yl methyl)dithiocarbamate (epdtc) or methyl(2-(pyridin-2-yl)ethyl)dithiocarbamate (mpdtc)) affords
a series of neutral dinuclear gold(I) complexes bridged by each dithiocarbamate ligand, [Au(L)]2. The successive reaction of [Au(L)]2 with organic acids such as isophthalic acid (m-pa) and maleic acid (ma) produces 1:1 adducts, [Au(L)]2·(organic acid). The crystal structure of [Au(L)]2·(m-pa) is a 1D polymer formed via hydrogen bonds between the free pyridyl and the carboxylic acid moiety. For the dinuclear
moiety, strong intradinuclear aurophilic interactions (Au(I)–Au(I) = 2.7783(8) Å and 2.7525(7) Å) exist, but interdinuclear
interactions are weak (3.2551(8)–3.2733(8) Å). The dinuclear gold(I) complexes, [Au(epdtc)]2 and [Au(mpdtc)]2, show a bright luminescence at 562.5 and 552.0 nm in solid state, respectively, but their organic acid adducts, [Au(L)]2·(organic acid), have no luminescent properties. This dramatic difference in properties between the gold(I) complexes and
their adducts may be ascribed to the weakness of the internuclear Au(I)–Au(I) interaction including crystal packing. 相似文献
857.
Tae Kyu Kim Euh Duck Jeong Chae Young Oh Min Seob Shin Jong-Pil Kim Ok-Sang Jung Hongsuk Suh Fazlur Rahman Nawaz Khan Myung Ho Hyun Jong Sung Jin 《Chemical Papers》2011,65(6):863-872
A series of neutral gelators and cationic amphiphiles derived from 1,2 diphenylethylenediamine (I) and 1,2-cyclohexanediamine (II) was synthesised. Helical silica nanotubes were prepared utilising these organic gelators through sol-gel polycondensation
of tetraethoxy silane, (TEOS-silica source). Right- and left-handed helical nanotubes respectively were obtained from a 1:
1 mass mixture of optically active, (1S,2S)-III-(1S,2S)-V neutral gelator and (1S,2S)-IV-(1S,2S)-VI cationic amphiphile and a 1: 1 mass mixture of optically active, (1R,2R)-III-(1R,2R)-V neutral gelator and (1R,2R)-IV-(1R,2R)-VI cationic amphiphile, indicating that the handedness of the helical nanotubes varied with the change in the neutral gelator
precursors used. The nanotubes were characterised by SEM images. 相似文献
858.
The amorphous and crystalline phase behavior, spherulite morphology, and interactions between amorphous poly(vinyl acetate)
(PVAc) and poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid) (PHBV) were examined using differential scanning calorimetry,
polarized-light optical and scanning electron, atomic-force microscopy (DSC, POM, SEM, AFM), and small-angle X-ray scattering
(SAXS). The PHBV/PVAc blend was found to be miscible with an almost linear T
g-composition relationship, indicating perfect homogeneity. Interaction parameter by melting point depression is a negative
value of χ = −0.32, suggesting quite favorable interaction strength. With the intimate interaction between the amorphous PVAc and crystalline
PHBV polymers, effects of PVAc on the spherulitic morphology of PHBV are quite significant. Owing to the higher T
g of PVAc (than that of PHBV), the spherulite growth rate of PHBV was depressed by increasing PVAc content in blends. Neat
PHBV exhibits ring-banded spherulites when crystallized at Tc = 60 ~ 110° C {T_{\rm{c}}} = {6}0\sim {11}0^\circ {\hbox{C}} ; however, with increasing PVAc content in the blends, the temperature range at which the PHBV/PVAc blends exhibit ring-banded
spherulites remains similar but the regularity increases, and the inter-ring spacing significantly decreases. In addition,
the spherulite size and ring-band patterns therein are strongly dependent on T
max (190 vs. 220 °C, respectively, for erasing prior nuclei), from which the blends were quenched to a T
c (60–110 °C) for crystallization. For PHBV/PVAc blends crystallized at the same T
c from different T
max, higher T
max tends to erase nuclei, leading to larger spherulites. However, such larger spherulites owing to higher T
max are not necessarily packed with thicker lamellae. 相似文献
859.
Functionalized magnetic nanoparticles, composed of both inorganic and organic components, have recently been examined as promising platforms for detection and separation applications. This unique class of nanomaterials can retain not only beneficial features of both the inorganic and organic components, but can also provide the ability to systematically tune the properties of the hybrid materials through the combination of appropriate functional components. This tutorial review focuses on the recent development of functionalized magnetic nanoparticles for use in biological and environmental applications, in which these chromogenic and fluorogenic chemosensors can selectively detect and separate specific toxic metal ions. 相似文献
860.
Chi Won Kim Jungmin Ahn Sung Min Kim Tae Hwan Noh Ok-Sang Jung 《Transition Metal Chemistry》2011,36(5):545-551
Type studies on competitive polyatomic anion versus acetonitrile coordination in the self-assembly of a series of [Ag2(X)
m
(bip)(NCCH3)
n
](X)2−m
(X− = NO3
−, CF3SO3
−, ClO4
−, BF4
−, and PF6
−; m = 0, 2; n = 0, 2, 4; bip = 1,4-bis(2-isonicotinoyloxyethyl)piperazine) were carried out. Each bip spacer acts as an N4 tetradentate ligand and is linked to four silver(I) centers through two pyridine and two piperazine moieties, producing a
double strand consisting of two 20-membered ring units. The coordinating environment around the silver(I) center is subtly
determined by the competition of the polyatomic anions with acetonitrile, that is, by the Ag···NCCH3 versus Ag···X interactions. The coordinating ability of acetonitrile is inversely proportional to the order of the coordination
ability of the Hoffmeister series of polyatomic anions, NO3
− ≫ CF3SO3
− > ClO4
− > BF4
− ≫ PF6
−. 相似文献