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111.
Kim H Ralph J Lu F Ralph SA Boudet AM MacKay JJ Sederoff RR Ito T Kawai S Ohashi H Higuchi T 《Organic & biomolecular chemistry》2003,1(2):268-281
Peroxidase/H2O2-mediated radical coupling of 4-hydroxycinnamaldehydes produces 8-O-4-, 8-5-, and 8-8-coupled dehydrodimers as has been documented earlier, as well as the 5-5-coupled dehydrodimer. The 8-5-dehydrodimer is however produced kinetically in its cyclic phenylcoumaran form at neutral pH. Synthetic polymers produced from mixtures of hydroxycinnamaldehydes and normal monolignols provide the next level of complexity. Spectral data from dimers, oligomers, and synthetic polymers have allowed a more substantive assignment of aldehyde components in lignins isolated from a CAD-deficient pine mutant and an antisense-CAD-downregulated transgenic tobacco. CAD-deficient pine lignin shows enhanced levels of the typical benzaldehyde and cinnamaldehyde end-groups, along with evidence for two types of 8-O-4-coupled coniferaldehyde units. The CAD-downregulated tobacco also has higher levels of hydroxycinnamaldehyde and hydroxybenzaldehyde (mainly syringaldehyde) incorporation, but the analogous two types of 8-O-4-coupled products are the dominant features. 8-8-Coupled units are also clearly evident. There is clear evidence for coupling of hydroxycinnamaldehydes to each other and then incorporation into the lignin, as well as for the incorporation of hydroxycinnamaldehyde monomers into the growing lignin polymer. Coniferaldehyde and sinapaldehyde (as well as vanillin and syringaldehyde) co-polymerize with the traditional monolignols into lignins and do so at enhanced levels when CAD-deficiency has an impact on the normal monolignol production. The implication is that, particularly in angiosperms, the aldehydes behave like the traditional monolignols and should probably be regarded as authentic lignin monomers in normal and CAD-deficient plants. 相似文献
112.
A reductive transmetalation of the pi-allylpalladium(II) complexes, generated in situ from a catalytic amount of a palladium(0) complex and a variety of allylic substrates, with indium(I) salts proceeded smoothly in various solvents, providing a new route for allylindium(III) reagents. 相似文献
113.
1.5-mum emissions from Nd:YAG, Nd:YVO(4), and LiNdP(4) O>(12) microchip lasers pumped by laser diodes have been observed. These coherent emissions are attributed to the effect of high-energy modified lattice vibration owing to the existence of Nd ions as well as to stimulated intracavity Raman scattering enhanced by the microchip configuration. A four-wave mixing process involving two lasing fields and a Stokes field was identified as the generator of new adjacent 1.5-mu;m emission. 相似文献
114.
A.K.M. Akther Hossain K. Khirul Kabir T. Kawai 《Journal of Physics and Chemistry of Solids》2007,68(10):1933-1939
Structural, AC and DC magnetic properties of polycrystalline Zn1−xCoxFe2O4 (x=0.2, 0.4) samples sintered at various temperatures (1100-1300 °C), and various dwell times (0.2-15 h) have been investigated thoroughly. The bulk density of the Zn0.60Co0.40Fe2O4 samples increases as the sintering temperature (Ts) increases from 1100 to 1250 °C, and above 1250 °C the bulk density decreases slightly. The Zn0.80Co0.20Fe2O4 samples show similar behavior of changes to that of Zn0.60Co0.40Fe2O4 samples except that the bulk density is found to be highest at 1200 °C. The DC magnetization as a function of temperature curves show that the Zn0.60Co0.40Fe2O4 sample is ferrimagnetic at room temperature while the Zn0.80Co0.20Fe2O4 sample is paramagnetic at room temperature. The Tc of Zn0.80Co0.20Fe2O4 sample is found to be 170 K from DC magnetization measurement. Separate measurement (AC magnetization), initial permeability as a function of temperature shows that the Tc of the Zn0.60Co0.40Fe2O4 sample is 353 K. Slight variation of Tc is observed depending on sintering condition. The initial permeability for the Zn0.60Co0.40Fe2O4 composition sintered at 1250 °C is found to be maximum. 相似文献
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116.
Kazuaki Yanagisawa Deborah E. Cutler 《Journal of Radioanalytical and Nuclear Chemistry》2011,287(3):879-886
Bibliometric analysis was carried out for champion data comparisons among prestigious nuclear research institutes (PNRI) existed
in Japan, the U. S., France, and Germany. The analysis was relied on database INIS (IAEA), ECD (DOE), WOS (Thomson), and SCOPUS
(Elsevier). INIS is advanced, key ex-post evaluating tool for determining general research paper-based champion. Over the
30-year time span of research paper publication, the world champion among 11 PNRI is JAERI confirmed by INIS but ORNL confirmed
by ECD, WOS, and SCOPUS, the latter two collected journal submitted research paper. Five years ago JAERI is the 3rd ranked
institutes following ORNL and ANL. INIS database results revealed that CEA/Grenoble is the French domestic champion regarding
research paper publication. Five years ago it was CEA/Saclay. Results from analytical tools used in bibliometric studies should
be viewed with careful consideration to learn of any influencing factors because different characteristics exhibited by individual
databases can sometimes generate conflicting bibliometric results. This was true among INIS, ECD, WOS, and SCOPUS when looking
at trends especially between 5-year periods. 相似文献
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120.
Kazunori Nakano Kazuaki Aburaya Ichiro Hisaki Norimitsu Tohnai Mikiji Miyata 《Chemical record (New York, N.Y.)》2009,9(2):124-135
We have systematically investigated structures and properties of inclusion crystals of bile acids and their derivatives. These steroidal compounds form diverse host frameworks having zero‐, one‐ and two‐dimensional cavities, causing various inclusion behaviors towards many organic compounds. The diverse host frameworks exhibit the following guest‐dependent flexibility. First, the frameworks mainly depend on the included guests in size and shape. The size‐dependence is quantitatively estimated by the parameter PCcavity, which is the volume ratio of a guest molecule to a host cavity. The resulting values of PCcavity lie in the range of 42–76%. Second, each of the host frameworks has its own range of the values. Some guests can employ two different frameworks with the boundary values, explaining formation of polymorphic crystals. Third, the host frameworks are selected by host–guest interactions through weak hydrogen bonds, such as NH/π and CH/O. The weak hydrogen bonds play an important role for various selective inclusion processes. Fourth, the host frameworks are dynamically exchangeable, resulting in intercalation and polymerization in the cavities. These static and dynamic structures of the frameworks demonstrate great potential of crystalline organic inclusion compounds as functional materials. © 2009 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 9: 124–135; 2009: Published online in Wiley InterScience ( www.interscience.wiley.com ) DOI 10.1002/tcr.20171 相似文献