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151.
Functionalized platinum(II) terpyridyl alkynyl complexes as colorimetric and luminescence pH sensors 总被引:1,自引:0,他引:1
A series of platinum(II) terpyridyl alkynyl complexes that have been derivatized with basic amino functionalities, [Pt(tpy)(C[triple bond]C-C6H4-NR2-4]X (X = OTf-, R = CH3 1, R = CH2CH2OCH3 2, R = H 3; X = Cl-, R = CH3 4, R = CH2CH2OCH3 5, R = H 6) (tpy = 2,2':6',2' '-terpyridine), have been synthesized and characterized. Their photophysical responses at various acid concentrations were studied. The abilities of the complexes to function as colorimetric and luminescence pH sensors were demonstrated with dramatic color changes and luminescence enhancement upon introduction of acid. 相似文献
152.
Ab initio molecular orbital theory using basis sets up to 6-311G* *, with electron correlation incorporated via configuration interaction calculations with single and double substitutions, has been used to study the structures and energies of the C3H2 monocation and dication. In agreement with recent experimental observations, we find evidence for stable cyclic and linear isomers of [C3H2]+ ˙. The cyclic structure (, a) represents the global minimum on the [C3H2]+ ˙ potential energy surface. The linear isomer (, b) lies somewhat higher in energy, 53 kJ mol?1 above a. The calculated heat of formation for [HCCCH]+ ˙ (1369 kJ mol?1) is in good agreement with a recent experimental value (1377 kJ mol?1). For the [C3H2]2+ dication, the lowest energy isomer corresponds to the linear [HCCCH]2+ singlet (h). Other singlet and triplet isomers are found not to be competitive in energy. The [HCCCH]2+ dication (h) is calculated to be thermodynamically stable with respect to deprotonation and with respect to C? C cleavage into CCH+ + CH+. The predicted stability is consistent with the frequent observation of [C3H2]2+ in mass spectrometric experiments. Comparison of our calculated ionization energies for the process [C3H2]+ ˙ → [C3H2]2+ with the Qmin values derived from charge-stripping experiments suggests that the ionization is accompanied by a significant change in structure. 相似文献
153.
A group of symmetrically substituted 2,3-diaryloxiranes have been studied as photoprecursors for carbonyl ylides. The stereochemistry of the adducts obtained upon interception of these 4n pi-transient systems with a variety of dipolarophiles provides information on the mode(s) of electrocyclic opening of the oxiranes to carbonyl ylides, as well as the mechanism of the 4n + 2 cycloaddition process. The stereochemistry of the dipolarophiles is preserved in the cycloadducts, which is consistent with a concerted addition process; however, solvent effects, steric hindrance, and possibly secondary orbital overlap factors all may play a role in determining the product distribution. 相似文献
154.
Amarante D Cherian C Catapano A Adams R Wang MH Megehee EG 《Inorganic chemistry》2005,44(24):8804-8809
Five new mixed diimine 1,1'-dithiolate or dithiocarbamate ligand complexes of the form [Rh(bpy)2(SS)][PF6]n, where bpy = 2,2'-bipyridine and SS = various substituted dialkyldithiocarbamates or 1,1'-dithiolates, were synthesized from cis-[Rh(bpy)2(OTf)2][OTf]. The triflate ligands are easily displaced by other ligands and allow these syntheses to proceed in high yields (80-90% overall) under relatively mild reaction conditions and to give high purity products. Electrochemistry shows irreversible two-electron reduction of Rh(III) to Rh(I) and a concomitant loss of one bipyridine ligand; this is followed by reversible one-electron reduction of the remaining 2,2'-bipyridine ligand. The electronic characterizations of these complexes are consistent with significant delocalization of the sulfur electron density onto the empty metal d orbitals. The 1,1'-dithiolate ligands induce larger red shifts in the absorption and emission spectra than the dithiocarbamates as the 1,1'-dithiolates have a more extensive conjugation system. 相似文献
155.
An intraindividual study of the characteristics of erythema induced by bath and oral methoxsalen photochemotherapy and narrowband ultraviolet B 总被引:1,自引:0,他引:1
We compared the characteristics of psoralen and ultraviolet A (PUVA) erythema in skin photosensitized by bath or oral methoxsalen in 20 subjects. Erythema was assessed visually and with a reflectance instrument at 24 h intervals for 7 days. In addition, narrowband ultraviolet B (TL-01 UVB) erythema was examined in 19 of these subjects at 4, 8, 12, 24, 48 and 72 h and in another nine subjects at 12, 15, 18, 21 and 24 h. Both bath and oral PUVA exhibited broad erythemal peaks beyond 72 h. For topical PUVA the lowest minimal phototoxic dose (MPD) occurred at 120 and 144 h (P = 0.01 and 0.03 compared with 72 h). Oral PUVA erythema peaked earlier at 96 h: the MPD was significantly lower at 96, 120 and 144 h compared with 72 h (P = 0.001, 0.01 and 0.02, respectively). At 120 h, bath PUVA had a significantly steeper slope compared with oral PUVA. The TL-01 UVB minimal erythema dose was significantly lower at 12 h compared with 24 h (P = 0.019). The majority of subjects were at maximal erythema at 12 h (22 of 28) and 15 h (eight of nine). Our results suggest that peak erythema for bath PUVA, oral PUVA and TL-01 UVB occurs at 120, 96 and 12-15 h, respectively. 相似文献
156.
Altieri A Gatti FG Kay ER Leigh DA Martel D Paolucci F Slawin AM Wong JK 《Journal of the American Chemical Society》2003,125(28):8644-8654
A series of [2]rotaxanes containing succinamide and naphthalimide hydrogen-bonding stations for a benzylic amide macrocycle is described. Electrochemical reduction and oxidation of the naphthalimide group alters its ability to form hydrogen bonds to the macrocycle to such a degree that redox processes can be used to switch the relative macrocycle-binding affinities of the two stations in a rotaxane by over 8 orders of magnitude. The structure of the neutral [2]rotaxane in solution is established by (1)H NMR spectroscopy and shows that the macrocycle exhibits remarkable positional integrity for the succinamide station in a variety of solvents. Cyclic voltammetry experiments allow the simultaneous stimulation and observation of a redox-induced dynamic process in the rotaxane which is both reversible and cyclable. Model compounds in which various conformational and co-conformational changes are prohibited demonstrate unequivocally that the redox response is the result of shuttling of the macrocycle between the two stations. At room temperature in tetrahydrofuran the electrochemically induced movement of the macrocycle between the two stations takes approximately 50 micros. 相似文献
157.
Siu Kay Wong 《Accreditation and quality assurance》2005,10(8):409-414
Proficiency testing (PT) is an essential tool used by laboratory accreditation bodies to assess the competency of laboratories.
Because of limited resources of PT providers or for other reasons, the assigned reference value used in the calculation of
z-score values has usually been derived from some sort of consensus value obtained by central tendency estimators such as the
arithmetic mean or robust mean. However, if the assigned reference value deviates significantly from the ‘true value’ of the
analyte in the test material, laboratories’ performance will be evaluated incorrectly. This paper evaluates the use of consensus
values in proficiency testing programmes using the Monte Carlo simulation technique. The results indicated that the deviation
of the assigned value from the true value could be as large as 40%, depending on the parameters of the proficiency testing
programmes under investigation such as sample homogeneity, number of participant laboratories, concentration level, method
precision and laboratory bias. To study how these parameters affect the degree of discrepancy between the consensus value
and the true value, a fractional factorial design was also applied. The findings indicate that the number of participating
laboratories and the distribution of laboratory bias were the prime two factors affecting the deviation of the consensus value
from the true value. 相似文献
158.
Summary High molecular weight poly 2- and 4-vinyl pyridines were synthesized by ionic polymerisation and their flocculation efficiency tested against kaolin and silica dispersions at pH 3. Low additions of the polymers, around 3 parts per 103 parts solid, destabilize the dispersions and clarify silica dispersions to a remarkable extent; however, over-addition of polymer leads to partial restabilization. The flocculation efficiency improves with increase of solids content, especially with clay dispersions. Flocculation efficiency increases with polymer molecular weight, especially over the lower part of the range covered, but is relatively independent of pH in the range 2–4. Quaternization of poly(4-vinyl pyridine) with bromobutane produces a good flocculant for aqueous silica dispersions in which the degree of restabilization on over-dosing depends on the KCI content. TheN-oxide derivatives of the vinyl pyridine polymers do not affect the colloidal stability of silica dispersions. The observations are interpreted in terms of bridging flocculation by the cationic polymer molecules between anionic surface sites on the solid particles. 相似文献
159.
Zheng Z Xu X Fan X Lau WM Kwok RW 《Journal of the American Chemical Society》2004,126(39):12336-12342
A new synthetic approach for the formation of ultrathin polymer films with customizable properties was developed. In this approach, the kinematic nature of proton collisions with simple organic molecules condensed on a substrate is exploited to break C-H bonds preferentially. The subsequent recombination of carbon radicals gives a cross-linked polymer thin film, and the selectivity of C-H cleavage preserves the chemical functionalities of the precursor molecules. The nature and validity of the method are exemplified with theoretical results from ab initio molecular dynamics calculations and experimental evidence from a variety of characterization techniques. Its applicability is demonstrated by the synthesis of ultrathin polymer films with precursor molecules such as dotriacontane, docosanoic acid, poly(acrylic acid) oligomer, and polyisoprene. The approach is fundamentally different from conventional chemical synthesis as it involves an unusual mix of physical and chemical processes including charge exchange, projectile penetration, kinematics, collision-induced dissociation, inelastic energy transfer, chain transfer, and chain cross-linking. 相似文献
160.
[reaction: see text] Effective epoxidation of lipophilic alkenes using hydrogen peroxide was accomplished with the manganese sulfate/bicarbonate catalytic system in an ionic liquid at room temperature. 相似文献