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41.
Vu H.H. Nguyen Son H. Doan Tram T. Van Phuc H. Pham Tran T.N. Nguyen Ngoc N. Nguyen Thach N. Tu Nam T.S. Phan 《应用有机金属化学》2019,33(4)
Iron‐based metal–organic framework VNU‐20 was utilized as a heterogeneous catalyst for cascade reactions between ketoximes and dibenzyl ether to produce 2,4,6‐triphenylpyridines. Additionally, benzyl alcohol and (dimethoxymethyl)benzene could be used as an alternative starting materials for the transformation. The oxidant exhibited a remarkable impact on the reactions, and di‐tert‐butylperoxide was the most appropriate candidate. The VNU‐20 displayed higher efficiency than many homogeneous and heterogeneous catalysts. The catalyst was reusable for the cascade reactions without a noticeable deterioration in catalytic activity. This transformation is new, and would offer alternative routes to triphenylpyridines utilizing ketoximes as building blocks. 相似文献
42.
E. Goya-Jorge T.Q. Doan M.L. Scippo M. Muller R.M. Giner S.J. Barigye 《SAR and QSAR in environmental research》2020,31(3):209-226
ABSTRACTThe aryl hydrocarbon receptor (AhR) plays an important role in several biological processes such as reproduction, immunity and homoeostasis. However, little is known on the chemical-structural and physicochemical features that influence the activity of AhR antagonistic modulators. In the present report, in vitro AhR antagonistic activity evaluations, based on a chemical-activated luciferase gene expression (AhR-CALUX) bioassay, and an extensive literature review were performed with the aim of constructing a structurally diverse database of contaminants and potentially toxic chemicals. Subsequently, QSAR models based on Linear Discriminant Analysis and Logistic Regression, as well as two toxicophoric hypotheses were proposed to model the AhR antagonistic activity of the built dataset. The QSAR models were rigorously validated yielding satisfactory performance for all classification parameters. Likewise, the toxicophoric hypotheses were validated using a diverse set of 350 decoys, demonstrating adequate robustness and predictive power. Chemical interpretations of both the QSAR and toxicophoric models suggested that hydrophobic constraints, the presence of aromatic rings and electron-acceptor moieties are critical for the AhR antagonism. Therefore, it is hoped that the deductions obtained in the present study will contribute to elucidate further on the structural and physicochemical factors influencing the AhR antagonistic activity of chemical compounds. 相似文献
43.
Study of a circuit-breaker arc with self-generated flow. I. Energytransfer in the high-current phase
Gleizes A. Rahal A.M. DeLacroix H. Van Doan P. 《IEEE transactions on plasma science. IEEE Nuclear and Plasma Sciences Society》1988,16(6):606-614
This study deals with the first phase of operation, corresponding to the energy transfer between arc and gas and to the pressure rise. The experimental study is devoted to measurements of current, arc voltage, and pressure variations in N2 and SF6. For currents of the order of 10 kA the mean measured electric field was about 32 V/cm in SF6 and 36 V/cm in N2. Through a bibliographical study and a modeling approach of the interruption arc, an analysis of the role of the different mechanisms of energy transfer between the arc and SF6 was conducted. With a 10 kA pulse, about 80% of the transfer is found to be due to convection and the rest to radiation from the arc. This transfer results in an overpressure of nearly 1 bar in SF6 and 2 bar in N2. It appears that the operation of this type of circuit breaker is limited to high currents: for currents below 7 kA the overpressure is lower than 0.5 bar, which does not provide efficient blowing at current zero 相似文献
44.
Wang San-Lang Yu Hao-Ting Tsai Min-Hsiung Doan Chien Thang Nguyen Van Bon Do Van Chung Nguyen Anh Dzung 《Research on Chemical Intermediates》2018,44(8):4903-4911
Research on Chemical Intermediates - The purpose of this study was to reclaim squid pens for the production of chitosanases and biosorbents of food colorants and industrial dyes via Bacillus cereus... 相似文献
45.
Nguyen Tan Thanh Nguyen Ngoc Tuan Ping-Chung Kuo Doan Manh Dung Doan Lan Phuong Dinh Thi Truong Giang 《Natural product research》2018,32(20):2392-2397
A new tirucallane-type triterpenoid igniarine (1), and four known compounds meshimakobnol A (2), meshimakobnol B (3), ergosterol (4) and ergosterol peroxide (5), were purified from the methanol extracts of the fruiting bodies of Phellinus igniarius (DC. ex Fr.) Quél. The structure of 1 was elucidated using a combination of 1D and 2D NMR techniques and HR-ESI-MS analyses. In addition, the isolated compounds were examined for their cytotoxicity against several tumour cell lines and part of the tested compounds demonstrated weak cytotoxicity. 相似文献
46.
Tinh Cao Thanh Chuong Thai Doan 《Journal of Optimization Theory and Applications》2022,194(2):570-596
Journal of Optimization Theory and Applications - In this paper, we first present strong conic linear programming duals for convex quadratic semi-infinite problems with linear constraints and... 相似文献
47.
(+/-)-7beta,8alpha-Dihydroxy-9beta,10beta-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (DE-1) undergoes reaction with anhydrous HCl in dioxane to yield predominantly ( approximately 94%) a single chlorohydrin. This chlorohydrin was assigned structure 9, in which the chloro goup at C-10 is located cis to the C-9 hydroxyl group, on the basis of its (1)H NMR spectrum. This result is in contrast to the reaction of a diastereomeric benzo[a]pyrene 7,8-diol 9,10-epoxide (DE-2) with HCl, which yields only trans-chlorohydrin 8. The hydrolysis of cis-chlorohydrin 9 in 10:90 dioxane-water solutions yields the same ratio of tetrols ( approximately 89% cis/11% trans) as that formed by acid-catalyzed hydrolysis of DE-1. This result again contrasts with the hydrolysis of trans-chlorohydrin 8, which undergoes hydrolysis to give tetrols in a ratio different from that from acid-catalyzed hydrolysis of DE-2. A marked common ion rate depression in the hydrolysis of cis-chlorohydrin 9 is observed, which shows that hydrolysis proceeds via an intermediate carbocation that has a sufficient lifetime to be trapped by external chloride ion. The observation that DE-1 reacts with HCl to give mainly the cis-chlorohydrin is rationalized by quantum chemical calculations that suggest that the cis-chlorohydrin is more stable than the epimeric trans-chlorohydrin. 相似文献
48.
Smoukov SK Quaroni L Wang X Doan PE Hoffman BM Que L 《Journal of the American Chemical Society》2002,124(11):2595-2603
Despite the current availability of several crystal structures of purple acid phosphatases, to date there is no direct evidence for solvent-derived ligands occupying terminal positions in the active enzyme. This is of central importance, because catalysis has been shown to proceed through the direct attack on a metal-bound phosphate ester by a metal-activated solvent-derived moiety, which has been proposed to be either (i) a hydroxide ligand terminally bound to the ferric center or (ii) a bridging hydroxide. In this work we use (2)H Q-band (35 GHz) pulsed electron-nuclear double resonance (ENDOR) spectroscopy to identify solvent molecules coordinated to the active mixed-valence (Fe(3+)Fe(2+)) form of the dimetal center of uteroferrin (Uf), as well as to its complexes with the anions MoO(4), AsO(4), and PO(4). The solvent-derived coordination of the dinuclear center of Uf as deduced from ENDOR data includes a bridging hydroxide and a terminal water/hydroxide bound to Fe(2+) but no terminal water/hydroxide bound to Fe(3+). The terminal water is lost upon anion binding while the hydroxyl bridge remains. These results are not compatible with a hydrolysis mechanism involving a terminal Fe(3+)-bound nucleophile, but they are consistent with a mechanism that relies on the bridging hydroxide as the nucleophile. 相似文献
49.
Synthesis of linear and star‐like poly(ε‐caprolactone)‐b‐poly{γ‐2‐[2‐(2‐methoxy‐ethoxy)ethoxy]ethoxy‐ε‐caprolactone} amphiphilic block copolymers using zinc undecylenate
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Katherine E. Washington Ruvanthi N. Kularatne Jia Du Matthew J. Gillings Jack C. Webb Nicolette C. Doan Michael C. Biewer Mihaela C. Stefan 《Journal of polymer science. Part A, Polymer chemistry》2016,54(22):3601-3608
Linear and star‐like amphiphilic diblock copolymers were synthesized by the ring‐opening polymerization of ε‐caprolactone and γ‐2‐[2‐(2‐methoxyethoxy)ethoxy]ethoxy‐ε‐caprolactone monomers using zinc undecylenate as a catalyst. These polymers have potential applications as micellar drug delivery vehicles, therefore the properties of the linear and 4‐arm star‐like structures were examined in terms of their molecular weight, viscosity, thermodynamic stability, size, morphology, and drug loading capacity. Both the star‐like and linear block copolymers showed good thermodynamic stability and degradability. However, the star‐like polymers were shown to have increased stability at lower concentrations with a critical micelle concentration (CMC) of 5.62 × 10?4 g L?1, which is less than half the concentration of linear polymer needed to form micelles. The star‐like polymeric micelles showed smaller sizes when compared with their linear counterparts and a higher drug loading capacity of doxorubicin, making them better suited for drug delivery purposes. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3601–3608 相似文献
50.
Khang H. Trinh Phuong H. Tran Thanh T. Nguyen Son H. Doan Minh-Vien Le Tung T. Nguyen Nam T.S. Phan 《应用有机金属化学》2020,34(4):e5515
A strontium-doped lanthanum cobaltite perovskite, La0.6Sr0.4CoO3, was prepared and utilized as a recyclable heterogeneous catalyst for the direct oxidative C(sp3)─H/C(sp2)─H coupling reaction between cyclic ethers and alkenes or coumarins to achieve corresponding α-functionalized ethers. The α-functionalization of cyclic thioethers or amides with alkenes or coumarins was also achieved via this protocol. The La0.6Sr0.4CoO3 catalyst exhibited better performance than a variety of homogeneous and heterogeneous catalysts. Utilizing a recyclable catalyst would offer a greener option for the direct oxidative C(sp3)─H/C(sp2)─H coupling reaction. To our best knowledge, the C(sp3)─H/C(sp2)─H coupling between olefins and ethers to generate α-functionalized ethers using a heterogeneous catalyst has not been previously reported, and the α-functionalization of cyclic thioethers or amides with alkenes or coumarins is new. 相似文献