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81.
Reactions of various halogenated peroxyl radicals with guanine, uric acid, xanthine, hypoxanthine and ascorbic acid in a quaternary microemulsion consisting of sodium lauryl sulfate/water/1-pentanol/cyclohexane have been studied using the technique of pulse radiolysis. For all purine derivatives and ascorbic acid, formation of the respective radical cations have been observed. Variation in biomolecular rate constant values for the reactions of peroxyl radicals with the above-mentioned compounds has been discussed in terms of diffusion of radicals. 相似文献
82.
Chromatographia - Ivermectin injectable product is widely used as a parasiticide for the treatment and control of internal and external parasites of cattle and swine. A reversed-phase high... 相似文献
83.
S. D. Adhikari R. Balasubramanian F. Pappalardi P. Rath 《Proceedings Mathematical Sciences》2008,118(2):183-188
For an abelian group G, the Davenport constant D(G) is defined to be the smallest natural number k such that any sequence of k elements in G has a nonempty subsequence whose sum is zero (the identity element). Motivated by some recent developments around the notion
of Davenport constant with weights, we study them in some basic cases. We also define a new combinatorial invariant related
to (ℤ/nℤ)
d
, more in the spirit of some constants considered by Harborth and others and obtain its exact value in the case of (ℤ/nℤ)2 where n is an odd integer. 相似文献
84.
Jing Li Suan Shi Maobing Tu Brain Via Fubao Fuelbio Sun Sushil Adhikari 《Applied biochemistry and biotechnology》2018,186(3):662-680
Bioconversion of lignocellulose to biofuels suffers from the degradation compounds formed during pretreatment and acid hydrolysis. In order to achieve an efficient biomass to biofuel conversion, detoxification is often required before enzymatic hydrolysis and microbial fermentation. Prehydrolysates from ethanol organosolv-pretreated pine wood were used as substrates in butanol fermentation in this study. Six detoxification approaches were studied and compared, including overliming, anion exchange resin, nonionic resin, laccase, activated carbon, and cysteine. It was observed that detoxification by anion exchange resin was the most effective method. The final butanol yield after anion exchange resin treatment was comparable to the control group, but the fermentation was delayed for 72 h. The addition of Ca(OH)2 was found to alleviate this delay and improve the fermentation efficiency. The combination of Ca(OH)2 and anion exchange resin resulted in completion of fermentation within 72 h and acetone–butanol–ethanol (ABE) production of 11.11 g/L, corresponding to a yield of 0.21 g/g sugar. The cysteine detoxification also resulted in good detoxification performance, but promoted fermentation towards acid production (8.90 g/L). The effect of salt on ABE fermentation was assessed and the possible role of Ca(OH)2 was to remove the salts in the prehydrolysates by precipitation. 相似文献
85.
86.
87.
Panchanan Puzari Biplab Sarkar Satrajit Adhikari 《International journal of quantum chemistry》2005,105(3):209-224
The time‐dependent discrete variable representation (TDDVR) of a wave function with grid points defined by the Hermite part of the Gauss–Hermite (G‐H) basis set introduces quantum corrections to classical mechanics. The grid points in this method follow classical trajectory and the approach converges to the exact quantum formulation with sufficient trajectories (TDDVR points) but just with a single grid point; only classical mechanics performs the dynamics. This newly formulated approach (developed for handling time‐dependent molecular quantum dynamics) has been explored to calculate vibrational transitions in the inelastic scattering processes. Traditional quantum mechanical results exhibit an excellent agreement with TDDVR profiles during the entire propagation when enough grid points are included in the quantum‐classical dynamics. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2005 相似文献
88.
Selective Control of HOD photodissociation has been investigated using simple field profiles. Initial results indicate that preferential dissociation of O–H bond may be achieved from the ground vibrational state and that the O–D bond can be selectively dissociated using only the fundamental excitation in this mode. Dissociation from 2 quanta of excitation in the O–D mode produces 82.8% products with O–D bond dissociation. Preferential maximization of O–D dissociation vis-à-vis O–H bond may also be achieved from the ground vibrational state using a combination of two lasers with carrier frequencies 54920 cm−1 and 52203 cm−1. The use of Field Optimized Initial STate (FOIST) based scheme to enhance selective control of HOD photodissociation provides additional 6 − 8% H–O + D products compared to those obtained without FOIST. 相似文献
89.
[reaction: see text] A new synthesis of enantiopure 3,3-disubstituted oxindoles by stereoselective Mukaiyama aldol reaction of 3-substituted 2-siloxyindoles and chiral, enantiopure aldehydes having nitrogen or oxygen substituents at the alpha carbon is described. When the C3 substituent of the prochiral nucleophile is aryl or heteroaryl, stereoselectivity is high (10-80:1). 相似文献