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971.
Yohei Ishikawa Tomokatsu Hayakawa Koji Inoue Masayuki Nogami 《Journal of Sol-Gel Science and Technology》2013,65(3):324-328
Transparent, luminescent films of Pr3+-doped (Ca0.6Sr0.4)TiO3 (CSTO) have been prepared for cathodo-excitation of pure red luminescence by a sol–gel method from a stabilized sol with Ca2+, Sr2+, Pr3+ ions and titanium-isopropoxide in acetic acid. The structure and surface morphology of the obtained films are characterized by X-ray diffraction and Atomic Force Microscopy, respectively. The photoluminescence and cathodoluminescence (CL) properties of the films are evaluated. The films exhibit a strong single line of 1D2 → 3H4 red photoluminescence of Pr3+ ions doped, which increases almost linearly with the number of the dip-coated layers. It is also found that strong single red photoemission is observed and the CL intensity increases with increasing acceleration voltage. The results demonstrate that it is potential for application in field-emission display devices. 相似文献
972.
Anoklase J.‐L. Ayitou Dr. Gaku Fukuhara Elango Kumarasamy Prof. Dr. Yoshihisa Inoue Prof. Dr. J. Sivaguru 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(13):4327-4334
Enantiospecific axial‐to‐point chiral transfer in light‐induced transformations was efficient under elevated pressure at high temperatures. Model photoreactions with atropisomeric compounds showed higher enantioselectivity in the photoproducts under elevated pressure. The ee values in the photoproducts were rationalized based on the increased stability of optically pure atropisomeric compounds at elevated pressure, even at high temperatures. 相似文献
973.
Automatic analyzer for highly polar carboxylic acids based on fluorescence derivatization–liquid chromatography
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Kenichiro Todoroki Tatsuki Nakano Yasuhiro Ishii Kanoko Goto Ryoko Tomita Toshihiro Fujioka Jun Zhe Min Koichi Inoue Toshimasa Toyo'oka 《Biomedical chromatography : BMC》2015,29(3):445-451
A sensitive, versatile, and reproducible automatic analyzer for highly polar carboxylic acids based on a fluorescence derivatization–liquid chromatography (LC) method was developed. In this method, carboxylic acids were automatically and fluorescently derivatized with 4‐(N,N‐dimethylaminosulfonyl)‐7‐piperazino‐2,1,3‐benzoxadiazole (DBD‐PZ) in the presence of 4‐(4,6‐dimethoxy‐1,3,5‐triazin‐2‐yl)‐4‐methylmorpholinium chloride by adopting a pretreatment program installed in an LC autosampler. All of the DBD‐PZ‐carboxylic acid derivatives were separated on the ODS column within 30 min by gradient elution. The peak of DBD‐PZ did not interfere with the separation and the quantification of all the acids with the exception of lactic acid. From the LC‐MS/MS analysis, we confirmed that lactic acid was converted to an oxytriazinyl derivative, which was further modified with a dimethoxy triazine group of 4‐(4,6‐dimethoxy‐1,3,5‐triazin‐2‐yl)‐4‐methylmorpholinium chloride (DMT‐MM). We detected this oxytriazinyl derivative to quantify lactic acid. The detection limits (signal‐to‐noise ratio = 3) for the examined acids ranged from 0.19 to 1.1 µm , which correspond to 95–550 fmol per injection. The intra‐ and inter‐day precisions of typical, highly polar carboxylic acids were all <9.0%. The developed method was successfully applied to the comprehensive analysis of carboxylic acids in various samples, which included fruit juices, red wine and media from cultured tumor cells. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
974.
975.
Yoshihisa Kurasawa Kiminari Yoshida Naoki Yamazaki Kotoji Iwamoto Yoshihiko Hamamoto Eisuke Kaji Kenji Sasaki Yoshito Zamami 《Journal of heterocyclic chemistry》2012,49(6):1323-1331
The 4‐quinolone‐2‐carboxylates 4a,b were converted into the 4‐quinolone‐2‐carbohydrazides 5a,b , hydrazones 6,7,10 , and related compounds 8,9,11 . The 4‐methoxyquinoline‐2‐carboxylate 12 was also transformed into the 4‐methoxyquinoline‐2‐carbohydrazide 13 , which was modified to the hydrazone 14 and related compound 15 . The antimicrobial activities of compounds 6b and 14 are described together with the 4‐oxo and 4‐hydroxy tautomers of compounds 4‐11 in deuteriodimethyl sulfoxide and deuteriotrifluoroacetic acid. 相似文献
976.
Isoryanodane diterpenoids possess a densely oxygenated and intricately fused pentacycle (ABCDE-ring), although its unique ring system has not yet been assembled chemically. The 6/5/7-membered BCD-rings of isoryanodanes differ from the 5/6/6-membered rings of the structurally-related ryanodanes. We previously achieved the total synthesis of ryanodine and five other ryanodane diterpenoids by employing the common ABDE-tetracyclic intermediate 1. Herein, we report a new strategy for constructing isoryanodane ABCDE-ring structure 3 from 1 via a combination of the oxy-Cope rearrangement and SmI2-mediated transannular cyclization. 相似文献
977.
Saidatul Iva Akihiro Tanabe Takaaki Maeda Hideki Funamizu Yoshihisa Aizu 《Optical Review》2014,21(3):353-358
We developed a new type of three-layered skin tissue phantom using silicone material. This phantom maintains its optical properties in a certain period of time, typically about three months, which is much longer than about 30 min with our previous agar-type phantom. Experiments on spectral reflectance measurements and color analysis indicate the possibility of silicone-type skin tissue phantom. 相似文献
978.
979.
Symmetry‐Driven Strategy for the Assembly of the Core Tetracycle of (+)‐Ryanodine: Synthetic Utility of a Cobalt‐Catalyzed Olefin Oxidation and α‐Alkoxy Bridgehead Radical Reaction
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Dr. Masanori Nagatomo Dr. Koji Hagiwara Kengo Masuda Masaki Koshimizu Takahiro Kawamata Yuki Matsui Dr. Daisuke Urabe Prof. Dr. Masayuki Inoue 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(1):222-229
Ryanodine ( 1 ) is a potent modulator of intracellular calcium release channels, designated as ryanodine receptors. The exceptionally complex molecular architecture of 1 comprises a highly oxygenated pentacyclic system with eleven contiguous stereogenic centers, which makes it a formidable target for organic synthesis. We identified the embedded C2‐symmetric tricyclic substructure within 1 . This specific recognition permitted us to design a concise synthetic route to enantiopure tricycle 9 by utilizing a series of pairwise functionalizations. The four tetrasubstituted carbon centers of 9 were effectively constructed by three key reactions, a dearomatizing Diels–Alder reaction, the kinetic resolution of the obtained racemic 14 through asymmetric methanolysis, and the transannular aldol reaction of the eight‐membered diketone 10 . A new combination of cobalt‐catalyzed hydroperoxidation and NfF‐promoted elimination enabled conversion of the hindered olefin of 9 into the corresponding ketone, thus realizing the desymmetrization. Finally, the tetrasubstituted carbon was stereospecifically installed by utilizing the α‐alkoxy bridgehead radical to deliver the core tetracycle 7 with the six contiguous tetrasubstituted carbon centers. Consequently, the present work not only accomplishes efficient assembly of four out of the five fused rings of 1 , but also develops two new powerful methodologies: two‐step ketone formation and bridgehead radical reaction. 相似文献
980.
Yoshihisa Kakuta Naoyuki Masuda Michihiro Kurushima Takashi Hashimoto Daisuke Yoshioka Hiroshi Sakiyama Yuya Hiraoka Makoto Handa Masahiro Mikuriya 《Chemical Papers》2014,68(7):923-931
The template reaction of salicylaldehyde and its substituted derivatives and 2-hydroxy-5-bromobenzylamine or 2-hydroxy-5-chlorobenzylamine with copper(II) acetate in dimethyl sulphoxide (dmso) afforded eight dinuclear Cu(II) complexes, [Cu2(L)2(dmso)2] (H2 L = N-salicylidene-2-hydroxy-5-bromobenzylamine, N-salicylidene-2-hydroxy-5-chlorobenzylamine and their 5-bromo, 5-nitro and 5-methyl-substituted salicylidene derivatives). These Cu(II) complexes were characterised by IR and UV-VIS-NIR spectroscopy, electric conductivity, cyclic voltammetry, and temperature dependence of magnetic susceptibilities (4.5–300 K). In the THF solution, the complexes are nonelectrolytes and exhibit a characteristic CT band due to phenoxido-bridging at 360–384 nm. In the cyclic voltammograms, an irreversible reduction process was observed at ?1.18–1.54 V vs Fc/Fc+. Single-crystal X-ray crystallography revealed that two Cu(II) ions were bridged by the two phenoxido-oxygen atoms of the two Schiff-base ligands with axial coordination of dmso molecules forming a square pyramid with a Cu-Cu distance of 3.0628(8)–3.0931(6) °A. In accordance with the crystal structures, the magnetic interaction between the two Cu(II) ions is relatively anti-ferromagnetic with ?2J value of 386–575 cm?1. The axial coordination effect of the dmso molecule was discussed in relation to the correlation between the Cu-O-Cu angle and the ?2J value. 相似文献