全文获取类型
收费全文 | 145篇 |
免费 | 9篇 |
专业分类
化学 | 114篇 |
晶体学 | 1篇 |
数学 | 1篇 |
物理学 | 38篇 |
出版年
2024年 | 1篇 |
2023年 | 3篇 |
2022年 | 2篇 |
2021年 | 2篇 |
2020年 | 8篇 |
2019年 | 5篇 |
2018年 | 3篇 |
2017年 | 2篇 |
2016年 | 4篇 |
2015年 | 6篇 |
2014年 | 8篇 |
2013年 | 10篇 |
2012年 | 16篇 |
2011年 | 13篇 |
2010年 | 11篇 |
2009年 | 4篇 |
2008年 | 12篇 |
2007年 | 10篇 |
2006年 | 5篇 |
2005年 | 5篇 |
2004年 | 2篇 |
2003年 | 1篇 |
2000年 | 2篇 |
1999年 | 1篇 |
1998年 | 2篇 |
1994年 | 1篇 |
1992年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1983年 | 2篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1977年 | 3篇 |
1976年 | 1篇 |
排序方式: 共有154条查询结果,搜索用时 93 毫秒
21.
Mukherjee A Dateer RB Chaudhuri R Bhunia S Karad SN Liu RS 《Journal of the American Chemical Society》2011,133(39):15372-15375
We report two viable routes for the 1,2-difunctionalization of aminoalkynes using only oxidants. In the presence of a gold catalyst, nitrones enable the oxoamination of aminoalkynes 1 to form 2-aminoamides 2. With a suitable gold catalyst, nitrosobenzenes implement an alkyne/nitroso metathesis of the same substrates to give 2-oxoiminylamides 3. These two novel oxidations also provide 1,2-aminoalcohols with opposite regioselectivity via NaBH(4) reduction in situ. 相似文献
22.
23.
(NEt4)2[WIVO(S2C2(CN)2)2] (1), isolated by reaction of Na2 WO4, Na2S2C2(CN)2 (Na2mnt) in acidified (pH5.5) aqueous medium in the presence of excess of sodium dithionite and NEt4Br, reduces CO2/HCO
3
−
(pH 7.5) to yield HCOO− and (NEt4)2[WVIO2(S2C2(CN)2)2] (2) mimicking tungsten-formate dehydrogenase (W-FDH) activity. (1) reacts with Na2MoO4 in acidic medium to produce [MoIvO(S2C2(CN)2)2]2− implicating the displacement of tungsten by molybdenum from the cofactor complex in W-FDH. 相似文献
24.
Knowledge of the dynamical changes in molecular configurations in various amino acid structures over a wide range of time scales is important since such changes may influence the structural transformations and the diverse biological functionalities of proteins. Using the temperature dependence of the rotating-frame NMR spin-lattice relaxation times T(1rho) of protons as a probe, we have investigated the low-frequency (approximately 60-100 kHz) dynamics in the crystal structures of L-, D-, and DL- alanine (C(12)H(28)O(8)N(4)) polymorphs. The proton relaxation times T(1rho) were obtained from (13)C <-- (1)H and (15)N <-- (1)H cross-polarization magic-angle-spinning NMR experiments over a temperature range of 192-342 K. The data reveal that the time scales of these low-frequency dynamical processes are distinctly different from the localized, high-frequency rotational motion of methyl and amine groups. The strongly asymmetric T(1rho) versus temperature curves and the subtle dynamical differences between the DL-alanine and the L- and d-enantiomorphs indicate that these low-frequency processes are cooperative in nature and are sensitive to molecular packing. 相似文献
25.
Sabyasachi Kar Y.K. Ho 《Journal of Quantitative Spectroscopy & Radiative Transfer》2008,109(3):445-452
The effect of weakly coupled hot plasma environment on the oscillator strengths of the ultraviolet and visible series and the polarizabilities of helium has been investigated using variational highly correlated wave functions within the non-relativistic framework. The Debye shielding approach that admits a variety of plasma conditions is used to simulate the plasma effects. For each shielding parameter, dipole oscillator strengths are calculated for the 1 1S-n1P (n=2, 3), 2 1S-2 1P, 2 3S-n3P (n=2, 3) and 2 1,3P-n1,3D (n=3, 4) transitions. The dipole and quadrupole polarizabilities for the ground He (1s21S) state are also reported for each screening parameter. Results obtained are useful in plasma diagnostic purposes besides several other applications. 相似文献
26.
Molecular Diversity - In this study, an efficient and convenient domino Michael addition/intramolecular cyclization protocol is presented for the synthesis of biologically relevant... 相似文献
27.
28.
Two enantiomers of [Bu(4)N](3)[Cu(3)(mnt)(3)] () formed by Na(2)(mnt) (mnt = maleonitriledithiolate, [S(2)C(2)(CN)(2)](2-)) and CuCl in a 1 : 1 molar ratio react further with MCl (M = Cu or Ag) involving both the enantiomers of to produce the larger complex, [Bu(4)N](4)[Cu(6)M(2)(mnt)(6)] (M = Cu (2), Ag (3)) from which the capped Cu(+) or Ag(+) ion can readily be removed by Bu(4)NX (X = Cl, Br), reverting or back to . Such reversal does not work with non-coordinating anions like BF(4)(-), ClO(4)(-) and PF(6)(-). 相似文献
29.
Anna Chandrasekar Murali Prakash Nayak Shashwat Nayak Sabyasachi Das Dr. Satyaprasad P. Senanayak Prof. Krishnan Venkatasubbaiah 《Angewandte Chemie (International ed. in English)》2023,62(11):e202216871
Development of new n-type semiconductors with tunable band gap and dielectric constant has significant implication in dissociating bound charge carrier relevant for demonstrating high performance optoelectronic devices. Boron-β-thioketonates (MTDKB), analogues to boron-β-diketonates containing a sulfur atom in the framework of β-diketones were synthesized. Bulk transport measurement exhibited an outstanding bulk electron mobility of ≈0.003 cm2 V−1 s−1, which is among the best values reported till date in these class of semiconducting materials and correspondingly a single junction photo responsivity of upto 6 mA W−1 was obtained. This new family of O,S-chelated boron compounds exhibited luminescence in the far red/near-infrared region. The remarkable red shift of 89 nm (fluorescence) observed for 4 a in comparison with analogues boron-β-diketonate signifies the importance of sulfur in these molecules. MTDKBs with amine functionality have also been investigated as an ON/OFF fluorescent sensor. 相似文献
30.
A new electron precise, six-electron, sulfide-bicapped trinuclear cluster complex [Et4N]4[Mo(IV)3(mu3-S)2(mnt)6] (1) has been synthesized, where each Mo(IV) atom is seven coordinated. Identical reaction conditions yielded a dimeric complex, [PNP]2[W(V)2(mu2-S)2(mnt)4] (2) from the starting W(IV) analogue due to oxidation by sulfur formed by the auto-oxidation of H2S. Two stepwise reversible reductions and no oxidation of 2 as observed by cyclic voltammetry are correlated with the nonbonding nature of the lowest unoccupied molecular orbital and deeply buried highest occupied molecular orbital by theoretical calculations at the density-functional theory level. 相似文献