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61.
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63.
Maruyama T Yamamura H Hiraki M Kemori Y Takata H Goto M 《Colloids and surfaces. B, Biointerfaces》2008,66(1):119-124
We investigated DNA-directed aggregation of vesicles using DNA-surfactants. Following tethering of single-stranded DNA oligonucleotides to vesicles using DNA-surfactant, the tethered vesicles were assembled with other vesicles bearing complementary strands. The vesicle aggregation was strongly affected by the salt concentration and by temperature according to the characteristics of DNA hybridization. Restriction enzyme, which can hydrolyze the double-stranded DNA used in the present study, dissociated the vesicle aggregates. Exploration using fluorescently labeled vesicles suggested that the DNA-directed vesicle aggregation took place in a sequence-specific manner through DNA-duplex formation. Interestingly, the DNA-directed aggregation using short DNA-surfactant induced the fusion of vesicles to produce giant vesicles, resulting in an enzymatic reaction in the giant vesicle. 相似文献
64.
Li WS Yamamoto Y Fukushima T Saeki A Seki S Tagawa S Masunaga H Sasaki S Takata M Aida T 《Journal of the American Chemical Society》2008,130(28):8886-8887
For tailoring solution-processable optoelectronic thin films, a rational strategy with amphiphilic molecular design is proposed. A donor-acceptor dyad consisting of an oligothiophene and C60, when modified with a hydrophilic wedge on one side and a paraffinic wedge on the other (1Amphi), forms over a wide temperature range a photoconducting smectic A liquid crystal having bicontinuous arrays of densely packed donor and acceptor units. In contrast, when modified with only paraffinic wedges (1Lipo), the dyad forms a smectic A liquid crystalline mesophase, which however is poorly conductive. As indicated by an absorption spectral feature along with a synchrotron radiation small-angle X-ray scattering profile, 1Lipo in the lamellar structure does not adopt a uniform head/tail orientation. Such defective donor and acceptor arrays likely contain a large number of trapping sites, leading to short-lived charge carriers, as observed by a flash photolysis time-resolved microwave conductivity study. 相似文献
65.
Sakurai T Shi K Sato H Tashiro K Osuka A Saeki A Seki S Tagawa S Sasaki S Masunaga H Osaka K Takata M Aida T 《Journal of the American Chemical Society》2008,130(42):13812-13813
A triply fused copper porphyrin dimer, when site-specifically modified on its periphery with hydrophobic and hydrophilic wedges (1C12/TEG), self-assembles into a columnar liquid crystalline (LC) mesophase over a wide-temperature range from -17 to 99 degrees C but gives rise to an amorphous solid when modified with only hydrophobic (1C12/C12) or hydrophilic wedges (1TEG/TEG). A LC film of 1C12/TEG displays at 16 degrees C a top-class one-dimensional electron mobility (0.27 cm2/V x s), as evaluated from its maximum flash-photolysis time-resolved microwave conductivity. 相似文献
66.
67.
Kohara S Takata M Matsumoto K Hagiwara R Suzuya K Morita H Siewenie JE Benmore CJ 《The Journal of chemical physics》2008,129(1):014512
The structure of liquid Cs(FH)(2.3)F was revealed using a combination of high-energy x-ray and neutron diffraction measurements. We found that the strongest intermolecular H-F hydrogen bonds at an average distance of 1.36 A are accompanied by the formation of a high degree of bending of the oligomer chain in the melt, with [angle]FHF=150 degrees . A reverse Monte Carlo simulation showed that the average number of atoms per chain is 4.4. A detailed chain analysis of the atomic configuration revealed that (FH)(2)F(-) oligomer chains are the major entities in the liquid, and asymmetrical FHF(-) are formed owing to the strong H-F hydrogen bonds. The results suggest that an average of one or two HF molecules bond to each of the 11 fluorine atoms surrounding a cesium ion. 相似文献
68.
Asymmetric Induction by a Nitrogen 14N/15N Isotopomer in Conjunction with Asymmetric Autocatalysis 下载免费PDF全文
Dr. Arimasa Matsumoto Hanae Ozaki Shunya Harada Kyohei Tada Tomohiro Ayugase Hitomi Ozawa Prof. Dr. Tsuneomi Kawasaki Prof. Dr. Kenso Soai 《Angewandte Chemie (International ed. in English)》2016,55(49):15246-15249
Chirality arising from isotope substitution, especially with atoms heavier than the hydrogen isotopes, is usually not considered a source of chirality in a chemical reaction. An N2,N2,N3,N3‐tetramethyl‐2,3‐butanediamine containing nitrogen (14N/15N) isotope chirality was synthesized and it was revealed that this isotopically chiral diamine compound acts as a chiral initiator for asymmetric autocatalysis. 相似文献
69.
Dr. Kenichi Kato Dr. Hidetaka Kasai Dr. Akihiro Hori Prof. Dr. Masaki Takata Prof. Dr. Hiroshi Tanaka Prof. Dr. Susumu Kitagawa Akira Kobayashi Dr. Nobuki Ozawa Prof. Dr. Momoji Kubo Dr. Hidekazu Arikawa Prof. Dr. Tatsuya Takeguchi Dr. Masaaki Sadakiyo Prof. Dr. Miho Yamauchi 《化学:亚洲杂志》2016,11(10):1537-1541
The layered P2‐NaxMO2 (M: transition metal) system has been widely recognized as electronic or mixed conductor. Here, we demonstrate that Co vacancies in P2‐NaxCoO2 created by hydrogen reductive elimination lead to an ionic conductivity of 0.045 S cm?1 at 25 °C. Using in situ synchrotron X‐ray powder diffraction and Raman spectroscopy, the composition of the superionic conduction phase is evaluated to be Na0.61(H3O)0.18Co0.93O2. Electromotive force measurements as well as molecular dynamics simulations indicate that the ion conducting species is proton rather than hydroxide ion. The fact that the Co‐stoichiometric compound Nax(H3O)yCoO2 does not exhibit any significant ionic conductivity proves that Co vacancies are essential for the occurrence of superionic conductivity. 相似文献
70.
Inside Cover: Superionic Conduction in Co‐Vacant P2‐NaxCoO2 Created by Hydrogen Reductive Elimination (Chem. Asian J. 10/2016) 下载免费PDF全文
Dr. Kenichi Kato Dr. Hidetaka Kasai Dr. Akihiro Hori Prof. Dr. Masaki Takata Prof. Dr. Hiroshi Tanaka Prof. Dr. Susumu Kitagawa Akira Kobayashi Dr. Nobuki Ozawa Prof. Dr. Momoji Kubo Dr. Hidekazu Arikawa Prof. Dr. Tatsuya Takeguchi Dr. Masaaki Sadakiyo Prof. Dr. Miho Yamauchi 《化学:亚洲杂志》2016,11(10):1465-1465