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991.
Castillo CE Davies DL Klair AK Singh K Singh S 《Dalton transactions (Cambridge, England : 2003)》2012,41(2):628-635
Reactions of [Ir(C^N)(2)Cl](2) [HC^N = 2-(3-R-phenyl)pyridine, 2-(3-R-phenylpyrazole) R = H, Me] with Me(2)-phencat give luminescent complexes [Ir(C^N)(2)(Me(2)-phencat)][PF(6)] (Me(2)-2a, b, c)[PF(6)]. Deprotection of the methoxy groups with BBr(3) is problematic as simultaneous bromination of the cyclometallated phenyl groups occurs. However, deprotection of Me(2)-phencat with BBr(3) followed by complexation with [Ir(C^N)(2)Cl](2) gives luminescent complexes [Ir(C^N)(2)(H(2)-phencat)][PF(6)] (H(2)-3a, c)[PF(6)], which are luminescent sensors for molybdate. 相似文献
992.
Eçik ET Beşli S Çiftçi GY Davies DB Kılıç A Yuksel F 《Dalton transactions (Cambridge, England : 2003)》2012,41(22):6715-6725
Nucleophilic substitution reactions of N(3)P(3)Cl(4)[O(CH(2))(2)NCH(3)], (1) with the sodium salts of mono- and di-functional alcohols [methanol (2), phenol (3), tetraethyleneglycol (4) and 1,3-propanediol (5)] were carried out in order to investigate a possible directing effect of the spiro O-moiety on the formation of mono-substituted (2a, 3a), non-geminal di-substituted (2c, 3c) and ansa (4a, 5a) derivatives. Compounds isolated from the reactions were characterized by elemental analysis, mass spectrometry, (1)H and (31)P NMR spectroscopy and X-ray crystallographic analysis showed that the substituent OR in compounds (2a, 3a and 2c, 3c) and the ansa-ring in compounds (4a, 5a) formed cis to the P-O moiety of the exocyclic [O(CH(2))(2)NCH(3)] spiro ring. The formation of products (2a-d, 3a-d, 4a, 5a and 5b) was quantified from the (31)P NMR spectra of the reaction mixtures, which showed an overwhelming preference for derivatives (2a, 3a, 2c, 3c, 4a, 5a) with the substituent cis to the P-O moiety of the exocyclic spiro ring (2a, 3a, 2c, 3c, 4a, 5a), except for reaction with 1,3-propanediol where the six-membered ring spiro derivative (5b) was about three times more abundant than the eight-membered ring ansa-derivative (5a). Overwhelming formation of products with the substituent cis to the exocyclic P-O moiety is proof that the cation-assisted mechanism is responsible for the stereo-selectivity in the reactions with alkoxides. 相似文献
993.
Dominika Bratkowska Arlene Davies Núria Fontanals Peter A.G. Cormack Francesc Borrull David C. Sherrington Rosa M. Marcé 《Journal of separation science》2012,35(19):2621-2628
Two novel high‐specific surface area polymeric sorbents (HXLPP‐SAXa and HXLPP‐SAXb) were synthesised and evaluated as solid‐phase extraction sorbents. The novel sorbents under study are based on hypercrosslinked polymer microspheres and designed specifically to offer ion‐exchange properties; the specific polymers of interest in the current work have been chemically modified in such a way as to impart a tuneable level of strong anion‐exchange character onto the sorbents. The novel sorbents were applied as strong anion‐exchange sorbents in solid‐phase extraction studies, with the goal being to selectively extract a group of acidic compounds from complex environmental samples in an efficient manner. Out of two HXLPP‐SAX resins evaluated in this study, it was found that the sorbent with the lower ion‐exchange capacity (HXLPP‐SAXa) gave rise to the best overall performance characteristics and, indeed, was found to compare favourably to the solid‐phase extraction performance of commercial strong anion‐exchange sorbents. When the HXLPP‐SAXa sorbent was applied to the solid‐phase extraction of environmental water samples, the result showed quantitative and selective extraction of low levels of acidic pharmaceuticals from 500 mL of river water and 100 mL of effluent wastewater. 相似文献
994.
L Zhou H Ishizaki M Spitzer KL Taylor ND Temperley SL Johnson P Brear P Gautier Z Zeng A Mitchell V Narayan EM McNeil DW Melton TK Smith M Tyers NJ Westwood EE Patton 《Chemistry & biology》2012,19(7):883-892
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995.
Xiong L Fletcher AM Davies SG Norman SE Hardacre C Compton RG 《Chemical communications (Cambridge, England)》2012,48(46):5784-5786
The electrode potentials for the two one electron oxidations of 1,2-diferrocenylethylene (bisferrocene, BF) were studied relative to that of the one electrode oxidation of decamethylferrocene in a variety of RTILs. The difference in these potentials was found to be very sensitive to the anion component of the ionic liquid showing the scope of these solutes as 'designer media' to tune the thermodynamic properties of solutes dissolved in them. 相似文献
996.
D Valette Y Lian JP Haydek KI Hardcastle HM Davies 《Angewandte Chemie (International ed. in English)》2012,51(34):8636-8639
Siloxy group migration: A rhodium(II) carbenoid approach has been developed for the synthesis of alkynoates. This transformation combines the addition of enol ethers at the vinylogous position of β-siloxy-substituted vinyldiazo derivatives with a siloxy group migration to give the products as single diastereomers. 相似文献
997.
Nilson PM Davies JR Theobald W Jaanimagi PA Mileham C Jungquist RK Stoeckl C Begishev IA Solodov AA Myatt JF Zuegel JD Sangster TC Betti R Meyerhofer DD 《Physical review letters》2012,108(8):085002
Time-resolved K(α) spectroscopy has been used to infer the hot-electron equilibration dynamics in high-intensity laser interactions with picosecond pulses and thin-foil solid targets. The measured K(α)-emission pulse width increases from ~3 to 6 ps for laser intensities from ~10(18) to 10(19) W/cm(2). Collisional energy-transfer model calculations suggest that hot electrons with mean energies from ~0.8 to 2 MeV are contained inside the target. The inferred mean hot-electron energies are broadly consistent with ponderomotive scaling over the relevant intensity range. 相似文献
998.
999.
Weinstein JA Tierney MT Davies ES Base K Robeiro AA Grinstaff MW 《Inorganic chemistry》2006,45(11):4544-4555
A general route for synthesis of six structurally similar Pt(II) diimine thiolate/phenolates chromophores possessing bulky phenolate or thiolate ligands is reported. The Pt chromophores were characterized using an array of techniques including 1H, 13C, and 195Pt NMR, absorption, emission, (spectro)electrochemistry, and EPR spectroscopy. Systematic variation of the electronic structure of the Pt(II) chromophores studied was achieved by (i) changing solvent polarity; (ii) substituting oxygen for sulfur in the donor ligand; (iii) alternating donor ligands from bis- to di-coordination; and (iv) changing the electron donating/withdrawing properties of the ligand(s). The lowest excited state in these new chromophores was assigned to a [charge-transfer-to-diimine] transition from the HOMO of mixed Pt/S (or Pt/O) character on the basis of absorption and emission spectroscopy, UV/vis (spectro)electrochemistry, and EPR spectroscopy. One of the chromophores, Pt(dpphen)(3,5-di-tert-butyl-catecholate) represents an example of a Pt(II) diimine phenolate chromophore that possesses a reversible oxidation centered predominantly on the donor ligand. Results from EPR spectroscopy indicate participation of the Pt(II) orbitals in the HOMO. There is a dramatic difference in the photophysical properties of carborane complexes compared to other mixed-ligand Pt(II) compounds, which includes room-temperature emission and photostability. The charge-transfer character of the lowest excited state in this series of chromophores is maintained throughout. Moreover, the absorption and emission energies and the redox properties of the excited state can be significantly tuned. 相似文献
1000.
Bollen G Davies D Facina M Huikari J Kwan E Lofy PA Morrissey DJ Prinke A Ringle R Savory J Schury P Schwarz S Sumithrarachchi C Sun T Weissman L 《Physical review letters》2006,96(15):152501
The mass of the short-lived radio nuclide 38Ca (T(1/2) = 440 ms) has been measured with the 9.4-T Penning trap mass spectrometer of the Low-Energy Beam and Ion Trap Facility. A mass uncertainty of deltam = 280 eV has been achieved, corresponding to deltam/m = 8 x 10(-9). The result makes 38Ca, a superallowed beta emitter, a new candidate to test the conserved-vector-current hypothesis. The experiment is also the first demonstration that short-lived radioactive isotopes produced by projectile fragmentation of relativistic heavy-ion beams can be slowed down and prepared such that precision experiments of this kind are possible. 相似文献