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41.
The exponential cells ofBacillus cereus immobilized in calcium alginate and spun into microcylindrical particles were used in a fluidized-bed reactor for continuous
synthesis of thermostable α-amylase. The reactor was operated over a period of 30 d with a dilution rate of 0.33 h-1, producing 1000–1200 U/mL of enzyme. The productivity of the reactor was in the range of 330–396 kU/h. A 20-fold increase
in the productivity with respect to batch fermentation with free cells was attained. 相似文献
42.
Manish Kumar Jeengar Mallesh Kurakula Poonam Patil Ashwini More Ramakrishna Sistla Deepti Parashar 《Molecules (Basel, Switzerland)》2022,27(4)
Chikungunya is an infectious disease caused by mosquito-transmitted chikungunya virus (CHIKV). It was reported that NS1 and E2 siRNAs administration demonstrated CHIKV inhibition in in vitro as well as in vivo systems. Cationic lipids are promising for designing safe non-viral vectors and are beneficial in treating chikungunya. In this study, nanodelivery systems (hybrid polymeric/solid lipid nanoparticles) using cationic lipids (stearylamine, C9 lipid, and dioctadecylamine) and polymers (branched PEI-g-PEG -PEG) were prepared, characterized, and complexed with siRNA. The four developed delivery systems (F1, F2, F3, and F4) were assessed for stability and potential toxicities against CHIKV. In comparison to the other nanodelivery systems, F4 containing stearylamine (Octadecylamine; ODA), with an induced optimum cationic charge of 45.7 mV in the range of 152.1 nm, allowed maximum siRNA complexation, better stability, and higher transfection, with strong inhibition against the E2 and NS1 genes of CHIKV. The study concludes that cationic lipid-like ODA with ease of synthesis and characterization showed maximum complexation by structural condensation of siRNA owing to high transfection alone. Synergistic inhibition of CHIKV along with siRNA was demonstrated in both in vitro and in vivo models. Therefore, ODA-based cationic lipid nanoparticles can be explored as safe, potent, and efficient nonviral vectors overcoming siRNA in vivo complexities against chikungunya. 相似文献
43.
Nagi Reddy Vanga Anudeep Kota Ramakrishna Sistla Mallavadhani Uppuluri 《Molecular diversity》2017,21(2):273-282
44.
H.S.S. Ramakrishna Matte A.K. Cheetham C.N.R. Rao 《Solid State Communications》2009,149(23-24):908-910
Hybrid organic–inorganic framework compounds constitute an important class of materials whose properties, especially paired ones, have not been adequately investigated hitherto. In this communication, we report the non-linear optical properties of hybrid compounds exhibiting interesting magnetic properties. 相似文献
45.
The catalytic role of various inert solid supports on acceleration of alcohol fermentation by Saccharomyces cerevisiae was investigated. The enhanced rate of alcohol production was dependent on the nature of the support as well as on the amount
used. Among all the tested supports, chitosan flakes showed the maximum yield of alcohol (93% of theoretical yield). This
higher rate of alcohol production was associated with the twofold increase in the activity of alcohol dehydrogenase over control.
Our results suggest that the addition of a small fraction of solids in submerged fermentations to facilitate cell anchorage
for enhanced metabolic activity is easier and more economical compared to cell immobilization processes.
IICT Communication No. 4266. Some of the results in this article are covered under a patent. 相似文献
46.
M. C. Reddy B. P. Nagi Reddy K. R. Sridharan J. Ramakrishna 《Magnetic resonance in chemistry : MRC》1984,22(7):464-467
From consideration of 1H–1H vicinal coupling constants and 13C? 1H long-range coupling constants in a series of amino acid derivatives, the precise values of 13C component vicinal coupling constants have been calculated for the three minimum energy staggered rotamers for the C(α)H? C(β)H2 side-chains of amino acids. 相似文献
47.
A sensitive spectrophotometric method for the determination of carbon monoxide is described, based on the reduction of palladium(II) by carbon monoxide. The resulting elemental palladium is reacted with iodate in acidic medium in the presence of chloride, to produce an ICl(-)(n) species that is readily extracted as an ion-pair with Pyronine-G into benzene. Measurement of the absorbance of the extract at 535 nm permits the determination of carbon monoxide down to 1 mul/l. in air. The effect of interfering gases is discussed. The method is suitable for determination of carbon monoxide in motor vehicle exhaust gases and ambient air. 相似文献
48.
Singh AK Mondal JA Ramakrishna G Ghosh HN Bandyopadhyay T Palit DK 《The journal of physical chemistry. B》2005,109(9):4014-4023
The dynamics of ultrafast photoinduced intermolecular electron transfer (ET) from the excited singlet (S1) state of perylene (Pe) to an electron-accepting cationic surfactant molecule, N-cetylpyridinium chloride (CPC), in aqueous micellar solutions has been investigated using the femtosecond transient absorption spectroscopic technique with temporal resolution of 120 fs. The Pe molecule is localized at or near the micellar surface, where it coexists with the pyridinium moieties (headgroups of the micelle) of the surfactant molecule. Following photoexcitation of Pe, an electron is transferred to the neat and geometrically restricted headgroup of the micelle. Dynamics of the forward ET process as well as the geminate recombination or back ET (BET) process have been followed by monitoring the temporal evolution of the S1 state of Pe and the cation radical of Pe (Pe*+), respectively. The multiexponential forward ET process indicates that the ET dynamics is highly correlated with the spatial distributions of the micellar headgroups around a donor Pe molecule and thus dependent on the donor-acceptor distance. The distance-dependent ET and BET rates have been calculated following the method of Weidemaier and Fayer (J. Chem. Phys. 1995, 102, 3820) to get the best fit parameters for the multiexponetial temporal profiles for the S1 state of Pe as well as Pe*+. Because the acceptor is a constituent of the neat micellar medium, their confinement on the surface of the microheterogeneous medium provides a very large concentration such that, even though the forward transfer rate is 0.06 ps(-1) at the distance of closest approach, the ET process is complete within a 200-ps time domain. If the concepts of distribution of ET distances are utilized, the possible role of material diffusion on the kinetics of forward ET is ruled out. This is an experimental study to show, for the first time, the ultrafast distance-dependent light-induced ET dynamics following both the excited state of the donor and the cation radical formed in an ET process using the transient absorption spectroscopic technique in a self-reactive restrictive environment. 相似文献
49.
Majeti BK Singh RS Yadav SK Bathula SR Ramakrishna S Diwan PV Madhavendra SS Chaudhuri A 《Chemistry & biology》2004,11(4):427-437
Herein, we report enhanced intravenous mouse lung transfection using novel cyclic-head-group analogs of usually open-head cationic transfection lipids. Design and synthesis of the new cyclic-head lipid N,N-di-n-tetradecyl-3,4-dihydroxy-pyrrolidinium chloride (lipid 1) and its higher alkyl-chain analogs (lipids 2-4) and relative in vitro and in vivo gene transfer efficacies of cyclic-head lipids 1-4 to their corresponding open-head analogs [lipid 5, namely N,N-di-n-tetradecyl-N,N-(2-hydroxyethyl)ammonium chloride and its higher alkyl-chain analogs, lipids 6-8] have been described. In stark contrast to comparable in vitro transfection efficacies of both the cyclic- and open-head lipids, lipids 1-4 with cyclic heads were found to be significantly more efficient (by 5- to 11-fold) in transfecting mouse lung than their corresponding open-head analogs (5-8) upon intravenous administration. The cyclic-head lipid 3 with di-stearyl hydrophobic tail was found to be the most promising for future applications. 相似文献
50.
[reaction: see text] Commercially available 1-bromobenzocyclobutene is a potentially useful synthon particularly with the application of organometallic methodology. Here we show that it is readily converted into Cp(2)Zr(benzocyclobutadiene), which couples with alkynes or nitriles giving five-membered zirconacycles. Treatment of these alkyne- or nitrile-derived zirconacycles with CuCl yields substituted naphthalenes, isoquinolines, or in the presence of MeO(2)C-CC-CO(2)Me, a 3-benzazocine containing an eight-membered ring [corrected]. 相似文献