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91.
Gabyshev N Abe K Abe K Adachi I Aihara H Asano Y Aulchenko V Aushev T Bahinipati S Bakich AM Balagura V Barberio E Bartel W Bay A Bedny I Bitenc U Bizjak I Bondar A Bozek A Bracko M Browder TE Chen A Chen WT Cheon BG Chistov R Choi Y Chuvikov A Cole S Dalseno J Danilov M Dash M Drutskoy A Eidelman S Garmash A Gershon T Gokhroo G Golob B Haba J Hayasaka K Hayashii H Hazumi M Hokuue T Hoshi Y Hou S Hou WS Hsiung YB Ikado K Imoto A Inami K Itoh R Iwasaki M Iwasaki Y Kang JH Kawasaki T Khan HR 《Physical review letters》2006,97(20):202003
We report the first measurements of the doubly charmed baryonic B decays B --> Lambda c+ Lambda c- K. The B+ --> Lambda c+ Lambda c- K+ decay is observed with a branching fraction of (6.5(-0.9)(+1.0)+/-1.1+/-3.4)x10(-4) and a statistical significance of 15.4sigma. The B0 --> Lambda c+ Lambda c- K0 decay is observed with a branching fraction of (7.9(-2.3)(+2.9)+/-1.2+/-4.1)x10(-4) and a statistical significance of 6.6sigma. The branching fraction errors are statistical, systematic, and the error resulting from the uncertainty of the Lambda c+ --> pK- pi+ decay branching fraction. The analysis is based on 357 fb(-1) of data accumulated at the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+ e- collider. 相似文献
92.
Chistov R Abe K Abe K Adachi I Aihara H Anipko D Aulchenko V Aushev T Bakich AM Balagura V Barberio E Bay A Bedny I Belous K Bitenc U Bizjak I Blyth S Bondar A Bozek A Bracko M Brodzicka J Browder TE Chang MC Chao Y Chen A Chen KF Chen WT Cheon BG Choi Y Choi YK Chuvikov A Cole S Dalseno J Danilov M Dash M Dragic J Drutskoy A Eidelman S Epifanov D Gabyshev N Garmash A Gershon T Go A Gokhroo G Golob B Gorisek A Ha H Haba J Hara T Hayasaka K Hayashii H Hazumi M Heffernan D Hokuue T Hoshi Y Hou S 《Physical review letters》2006,97(16):162001
We report the first observation of two charmed strange baryons that decay into Lambda(c)(+)Kappa(-)pi(+). The broader of the two states is measured to have a mass of 2978.5+/-2.1+/-2.0 MeV/c2 and a width of 43.5+/-7.5+/-7.0 MeV/c2. The mass and width of the narrow state are measured to be 3076.7+/-0.9+/-0.5 MeV/c;{2} and 6.2+/-1.2+/-0.8 MeV/c2, respectively. We also perform a search for the isospin partner states that decay into Lambda(c)(+)Kappa(0)/(s)pi(-) and observe a significant signal at the mass of 3082.8+/-1.8+/-1.5 MeV/c2. The data used for this analysis were accumulated at or near the Upsilon(4S) resonance, using the Belle detector at the e+ e- asymmetric-energy collider KEKB. The integrated luminosity of the data sample used is 461.5 fb(-1). 相似文献
93.
M. Galamboš V. Paučová J. Kufčáková O. Rosskopfová P. Rajec R. Adamcová 《Journal of Radioanalytical and Nuclear Chemistry》2010,284(1):55-64
The physical and chemical properties of illitic clay minerals from Slovak deposit suitable for application in engineering
barriers for high level radioactive waste repositories and spent nuclear fuels were studied. The isolation of spent nuclear
fuels and high level radioactive wastes from the outer environment in a deep repository is gained by means of a system of
multiple engineering and natural sealing barriers. Vital segments in a multiple barrier system are clay rocks, of which bentonites
represent the most suitable clay material. Cs-adsorption on fine fractions of adsorbents (bentonites from three Slovak deposits:
Jelšovy potok J15, Kopernica K15, Lieskovec L15 and montmorillonite K10) has been studied with using batch of radiometric
techniques. Adsorption parameters have been determined for adsorbent-cesium solution system as a function of contact time
and adsorbate concentration. The influences of pH change, the effect of competitive cations, complex-forming organic chelating
agents on the adsorption of Cs have also been studied. 相似文献
94.
Aaij R Abellan Beteta C Adeva B Adinolfi M Adrover C Affolder A Ajaltouni Z Albrecht J Alessio F Alexander M Alkhazov G Alvarez Cartelle P Alves AA Amato S Amhis Y Anderson J Appleby RB Aquines Gutierrez O Archilli F Arrabito L Artamonov A Artuso M Aslanides E Auriemma G Bachmann S Back JJ Bailey DS Balagura V Baldini W Barlow RJ Barschel C Barsuk S Barter W Bates A Bauer C Bauer T Bay A Bediaga I Belogurov S Belous K Belyaev I Ben-Haim E Benayoun M Bencivenni G Benson S Benton J Bernet R 《Physical review letters》2012,108(16):161801
First observations of the Cabibbo-suppressed decays B(0) → D(+)K(-)π(+)π(-) and B(-) → D(0)K(-)π(+)π(-) are reported using 35 pb(-1) of data collected with the LHCb detector. Their branching fractions are measured with respect to the corresponding Cabibbo-favored decays, from which we obtain B(B(0) → D(+)K(-)π(+)π(-))/B(B(0) → D(+)π(-)π(+)π(-))=(5.9±1.1±0.5)×10(-2) and B(B(-) → D(0)K(-)π(+)π(-))/B(B(-) → D(0)π(-)π(+)π(-))=(9.4±1.3±0.9)×10(-2), where the uncertainties are statistical and systematic, respectively. The B(-) → D(0)K(-)π(+)π(-) decay is particularly interesting, as it can be used in a similar way to B(-) → D(0)K(-) to measure the Cabibbo-Kobayashi-Maskawa phase γ. 相似文献
95.
Aaij R Abellan Beteta C Adeva B Adinolfi M Adrover C Affolder A Ajaltouni Z Albrecht J Alessio F Alexander M Alkhazov G Alvarez Cartelle P Alves AA Amato S Amhis Y Anderson J Appleby RB Aquines Gutierrez O Archilli F Arrabito L Artamonov A Artuso M Aslanides E Auriemma G Bachmann S Back JJ Bailey DS Balagura V Baldini W Barlow RJ Barschel C Barsuk S Barter W Bates A Bauer C Bauer T Bay A Bediaga I Belogurov S Belous K Belyaev I Ben-Haim E Benayoun M Bencivenni G Benson S Benton J Bernet R 《Physical review letters》2012,108(18):181806
The angular distributions and the partial branching fraction of the decay B0 → K*0 μ+ μ- are studied by using an integrated luminosity of 0.37 fb(-1) of data collected with the LHCb detector. The forward-backward asymmetry of the muons, A(FB), the fraction of longitudinal polarization, F(L), and the partial branching fraction dB/dq2 are determined as a function of the dimuon invariant mass. The measurements are in good agreement with the standard model predictions and are the most precise to date. In the dimuon invariant mass squared range 1.00-6.00 GeV2/c4, the results are A(FB)=-0.06(-0.14)(+0.13)±0.04, F(L)=0.55±0.10±0.03, and dB/dq2=(0.42±0.06±0.03)×10(-7) c4/GeV2. In each case, the first error is statistical and the second systematic. 相似文献
96.
In a previous study, we analyzed the electronic structure of S = 3/2 [FeNO](7) model complexes [Brown et al. J. Am. Chem. Soc. 1995, 117, 715-732]. The combined spectroscopic data and SCF-X alpha-SW electronic structure calculations are best described in terms of Fe(III) (S = 5/2) antiferromagnetically coupled to NO(-) (S = 1). Many nitrosyl derivatives of non-heme iron enzymes have spectroscopic properties similar to those of these model complexes. These NO derivatives can serve as stable analogues of highly labile oxygen intermediates. It is thus essential to establish a reliable density functional theory (DFT) methodology for the geometry and energetics of [FeNO](7) complexes, based on detailed experimental data. This methodology can then be extended to the study of [FeO(2)](8) complexes, followed by investigations into the reaction mechanisms of non-heme iron enzymes. Here, we have used the model complex Fe(Me(3)TACN)(NO)(N(3))(2) as an experimental marker and determined that a pure density functional BP86 with 10% hybrid character and a mixed triple-zeta/double-zeta basis set lead to agreement between experimental and computational data. This methodology is then applied to optimize the hypothetical Fe(Me(3)TACN)(O(2))(N(3))(2) complex, where the NO moiety is replaced by O(2). The main geometric differences are an elongated Fe[bond]O(2) and a steeper Fe[bond]O[bond]O angle in the [FeO(2)](8) complex. The electronic structure of [FeO(2)](8) corresponds to Fe(III) (S = 5/2) antiferromagnetically coupled to O(2)(-) (S = 1/2), and, consistent with the extended bond length, the [FeO(2)](8) unit has only one Fe(III)-O(2)(-) bonding interaction, while the [FeNO](7) unit has both sigma and pi type Fe(III)-NO(-) bonds. This is in agreement with experiment as NO forms a more stable Fe(III)-NO(-) adduct relative to O(2)(-). Although NO is, in fact, harder to reduce, the resultant NO(-) species forms a more stable bond to Fe(III) relative to O(2)(-) due to the different bonding interactions. 相似文献
97.
98.
Dr. Franck Bertorelle Dr. K. David Wegner Martina Perić Bakulić Hussein Fakhouri Clothilde Comby-Zerbino Dr. Amin Sagar Dr. Pau Bernadó Dr. Ute Resch-Genger Prof. Vlasta Bonačić-Koutecký Dr. Xavier Le Guével Dr. Rodolphe Antoine 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(39):e202200570
Atomically precise gold nanoclusters are a fascinating class of nanomaterials that exhibit molecule-like properties and have outstanding photoluminescence (PL). Their ultrasmall size, molecular chemistry, and biocompatibility make them extremely appealing for selective biomolecule labeling in investigations of biological mechanisms at the cellular and anatomical levels. In this work, we report a simple route to incorporate a preformed Au25 nanocluster into a model bovine serum albumin (BSA) protein. A new approach combining small-angle X-ray scattering and molecular modeling provides a clear localization of a single Au25 within the protein to a cysteine residue on the gold nanocluster surface. Attaching Au25 to BSA strikingly modifies the PL properties with enhancement and a redshift in the second near-infrared (NIR-II) window. This study paves the way to conrol the design of selective sensitive probes in biomolecules through a ligand-based strategy to enable the optical detection of biomolecules in a cellular environment by live imaging. 相似文献
99.
Pau Besalú-Sala Dr. Josep M. Luis Prof. Dr. Miquel Solà 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(63):14481-14487
In the last 30 years, fullerene-based materials have become popular building blocks for devices with a broad range of applications. Among fullerene derivatives, endohedral metallofullerenes (EMFs, M@Cx) have been widely studied owing to their unique properties and reactivity. For real applications, fullerenes and EMFs must be exohedrally functionalized. It has been shown that encapsulated metal cations facilitate the Diels–Alder reaction in fullerenes. Herein, the Bingel–Hirsch (BH) addition of ethyl bromomalonate over a series of ion-encapsulated M@C60 (M=Ø, Li+, Na+, K+, Mg2+, Ca2+, and Cl−; Ø@C60 stands for C60 without any endohedral metal) is quantum mechanically explored to analyze the effect of these ions on the BH addition. The results show that the incarcerated ion has a very important effect on the kinetics and thermodynamics of this reaction. Among the systems studied, K+@C60 is the one that leads to the fastest BH reaction, whereas the slowest reaction is given by Cl−@C60. 相似文献
100.
Anna V. Bay Keegan P. Fitzpatrick Rick C. Betori Prof. Karl A. Scheidt 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(23):9228-9233
As a key element in the construction of complex organic scaffolds, the formation of C−C bonds remains a challenge in the field of synthetic organic chemistry. Recent advancements in single-electron chemistry have enabled new methods for the formation of various C−C bonds. Disclosed herein is the development of a novel single-electron reduction of acyl azoliums for the formation of ketones from carboxylic acids. Facile construction of the acyl azolium in situ followed by a radical–radical coupling was made possible merging N-heterocyclic carbene (NHC) and photoredox catalysis. The utility of this protocol in synthesis was showcased in the late-stage functionalization of a variety of pharmaceutical compounds. Preliminary investigations using chiral NHCs demonstrate that enantioselectivity can be achieved, showcasing the advantages of this protocol over alternative methodologies. 相似文献