首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   99篇
  免费   1篇
  国内免费   1篇
化学   58篇
晶体学   12篇
力学   3篇
数学   10篇
物理学   18篇
  2022年   3篇
  2021年   2篇
  2019年   7篇
  2018年   3篇
  2017年   1篇
  2016年   5篇
  2015年   1篇
  2014年   3篇
  2013年   5篇
  2012年   7篇
  2011年   10篇
  2010年   11篇
  2009年   6篇
  2008年   7篇
  2007年   9篇
  2006年   7篇
  2005年   1篇
  2004年   8篇
  2003年   1篇
  2002年   1篇
  1999年   2篇
  1996年   1篇
排序方式: 共有101条查询结果,搜索用时 375 毫秒
1.
We calculate here the Brillouin frequencies of the L-mode [010], [001] and [100] of NaNO2 for the phase transitions from the paraelectric phase to the sinusoidal anti-ferroelectric phase near the Neel temperature (TN = 437.7 K) and to the ferroelectric phase near the critical temperature (TC = 436.3 K) in this crystalline system. For calculating the frequencies. we use the thermal expansivity data for the phase regions considered, under the assumption that the mode Gruneisen parameter determined for each mode remains constant across the phase transitions. Our calculated frequencies agree well with the observed frequencies for the modes studied in NaNO2.  相似文献   
2.
The surface area of kaolinite-benzamide (K-Bz)6.62 m2 g–1, whichis noticeably lower than that of kaolinite-dimethyl sulphoxide (K-DMSO) 14.61m2 g–1, the co-perturbationof the inner-surface hydroxyl features at 3697 and 3650 cm–1,and the increase of d(001) value by 7.44 Å are all related to the benzamidespecies inserted into the kaolinite structure through the replacement of theK-DMSO composites. Disappearance of the DMSO reflections and emergence ofwell-defined features at 6.04(2θ) and 11.16(2θ), 001 and 002 reflectionswith d values of 14.62 and 7.92 Å, respectively point out that the DMSOspecies were substituted efficiently by benzamide molecules. The thermal stabilityof the K-Bz derivative up to 300°C can be attributed to the slightly tiltedaromatic ring keying into the gibbsitic sheets via the –NH2groups.  相似文献   
3.
An approach to investigation of catalytical behaviors of Co (II) and Cu (II) phthalocyanines is reported that is based on changing any parameter to effect these behaviors. Towards this end, new anthracene substituted Co (II) and Cu (II) phthalocyanines were prepared and characterized spectroscopic methods. New cobalt (II) and copper (II) phthalocyanines were used as catalyst for oxidation of different phenolic compounds (such as 2,3‐dichlorophenol, 4‐methoxyphenol, 4‐nitrophenol, 2,3,6‐trimethylphenol) with different oxidants. Then, electrochemical characterization of cobalt (II) and copper (II) phthallocyanines were determined by using cyclic voltammetry (CV) and square wave voltammetry (SWV) techniques. Although copper (II) phthalocyanine showed similar Pc based electron transfer processes, cobalt (II) phthalocyanine showed metal and ligand based reduction reactions as expected.  相似文献   
4.
5.
Research on Chemical Intermediates - N-Heterocyclic carbene (NHC)-linked PEPPSI-type palladium complexes have recently been used in the direct C-H bond arylation of heteroarenes. However, in most...  相似文献   
6.
At present, CNT supported catalysts were prepared by two different methods as NaBH4 reduction and dendrimer templated NaBH4 reduction method to observe the effect of preparation method on the sensitivity and activity of H2O2 reduction. Then, CNT supported PdxAuy bimetallic nanocatalysts having various atomic ratio were synthesized via novel dendrimer templated NaBH4 reduction method. The resulting materials were characterized employing XRD and TEM. Crystallite size of 10 %Pd0.7Au0.3/CNTdendrimer was obtained from XRD 17.1 nm and mean particle size obtained from TEM is about 15 nm. Moreover, the electrochemical behavior of these catalysts was characterized by cyclic voltammetry (CV) and chronoamperometry (CA) techniques. PdxAuy bimetallic nanocatalysts have excellent electrocatalytic properties and great potential for applications in electrochemical detection. The sensitivity and the limit of detection values for the prepared sensor with monometallic 10 % Pd/CNTdendrimer catalysts are 219.78 μA mM?1cm?2 and 2.6 μM, respectively. However, the sensor constructed with 10 %Pd0.7Au0.3/CNTdendrimer modified electrode has a very high sensitivity of 316.89 μA mM?1 cm?2 with a quick response time of 2 s and a wide linear range of 0.001–19.0 mM. In addition, the interference experiment indicated that the 10 % Pd0.7Au0.3/CNTdendrimer nanoparticles have good selectivity toward H2O2.  相似文献   
7.
Undoped and manganese doped ZnO (ZnO:Mn) films were prepared by sol gel method using spin coating technique. The effect of Mn incorporation on the structural and optical properties of the ZnO film has been investigated. The crystalline structure and orientation of the films have been investigated by using their X-ray diffraction spectra. The films exhibit a polycrystalline structure. Mn incorporation led to substantial changes in the structural characteristics of the ZnO film. The scanning electron microscopy (SEM) images of the films showed that the surface morphology of the ZnO film was affected by the Mn incorporation. The transparency of the ZnO film decreased with the Mn incorporation. The optical band gap and Urbach energy values of the ZnO and ZnO:Mn films were found to be 3.22, 3.19 eV and 0.10, 0.23 eV, respectively. The optical constants of these films, such as refractive index, extinction coefficient and optical dielectric constants were determined using transmittance and reflectance spectra. The refractive index dispersion curve of the films obeys the single oscillator model with dispersion parameters. The oscillator energy, E o , and dispersion energy, E d, of the films were determined 5.30 and 16.26 eV for ZnO film and 5.80 and 12.14 eV for ZnO:Mn film, respectively.  相似文献   
8.

Abstract  

Schiff base 4-[(2-hydroxy-3-methoxybenzylideneamino)-N-(5-methylisoxazol-3-yl)benzene-sulfonamide has been synthesized from the reaction of 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide(sulfamethoxazole) with 2-hydroxy-3-methoxybenzaldehyde. It has been characterized by elemental analysis, MS, IR, 1H NMR, 13C NMR, HETCOR and UV–Visible techniques. The structure of it also has been examined crystallographically. For the compound exist as dominant form of enol-imines in both the solid state and the solutions. It crystallizes in the monoclinic space group P21/c with a = 8.2694(7), b = 8.3453(5), c = 26.260(2) ?, β = 97.142(7) °, V = 1798.1(2) ?3, D x  = 1.431 g cm−3, R 1 = 0.0529 and wR 2 = 0.1370 [I > 2σ(I)], respectively.  相似文献   
9.

Abstract  

Schiff base (E)-2-[(benzo[d]thiazol-2-ylimino)methyl]phenol (1) has been synthesized from the reaction of 2-hydroxy-benzaldehyde with 2-aminobenzothiazole. The 2-[(benzo[d]thiazol-2-ylamino)methyl]phenol (2) was prepared reduction of the Schiff base 1 with sodium borohydride. The compounds 1 and 2 have been characterized by elemental analysis, FT-IR, 1H-NMR, 13C-NMR and UV–visible spectroscopic techniques. The structure of the compound 2 has also been examined crystallographically. The compound 2 crystallizes in the monoclinic space group P2/c. The unit cell parameters were found as a = 10.017(1), b = 11.725(1), c = 10.341(1) ?, V = 1208.1(1) ?3, D x = 1.409 g cm−3 and Z = 4. The crystal structure was solved by direct methods and refined by the full-matrix least squares method and found as R 1 = 0.0308 and wR 2 = 0.0818 for 2032 for the observed reflections [I > 2σ(I)].  相似文献   
10.

Abstract  

Some molecules having a molecular skeleton similar to that of stilbenes and azobenzenes show orientational disorder in the crystals due to pedal motion. Heretofore, the orientational disorder through pedal motion has been observed for the compounds containing only two aromatic rings in the absence of bulky substituent groups. Here we report that the pedal motion can be detected even in the presence of a bulky substituent group to which orientational disorder becomes invisible as a result of anchor effect arising from phenoxyphtalonitrile group. X-ray crystallographic analysis of the compound, C23H18N4O, reveals the existence of partially overlapped two pedal conformers. The compound crystallizes in the monoclinic space group P21/c with a = 12.9429(11) Å, b = 8.5075(5) Å, c = 21.063(2) Å and β = 123.155(6)°. Major pedal conformer is stabilized by weak C–H···O type hydrogen bond and C–H···π type edge-to-face interactions in solid state. Quantum chemical calculations at B3LYP/6-311G+(d,p) level suggest that the stabilization of the compound decreases with increasing deviation from the planar geometry of trans-azobenzene fragment.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号