全文获取类型
收费全文 | 1149篇 |
免费 | 27篇 |
国内免费 | 6篇 |
专业分类
化学 | 723篇 |
晶体学 | 8篇 |
力学 | 3篇 |
数学 | 198篇 |
物理学 | 250篇 |
出版年
2023年 | 6篇 |
2022年 | 17篇 |
2021年 | 20篇 |
2020年 | 11篇 |
2019年 | 8篇 |
2018年 | 13篇 |
2017年 | 10篇 |
2016年 | 32篇 |
2015年 | 26篇 |
2014年 | 41篇 |
2013年 | 60篇 |
2012年 | 55篇 |
2011年 | 54篇 |
2010年 | 38篇 |
2009年 | 36篇 |
2008年 | 53篇 |
2007年 | 51篇 |
2006年 | 50篇 |
2005年 | 49篇 |
2004年 | 38篇 |
2003年 | 34篇 |
2002年 | 33篇 |
2001年 | 19篇 |
2000年 | 26篇 |
1999年 | 14篇 |
1998年 | 18篇 |
1996年 | 13篇 |
1995年 | 9篇 |
1994年 | 16篇 |
1993年 | 7篇 |
1992年 | 19篇 |
1991年 | 19篇 |
1990年 | 19篇 |
1989年 | 11篇 |
1988年 | 9篇 |
1987年 | 15篇 |
1986年 | 9篇 |
1985年 | 18篇 |
1984年 | 14篇 |
1983年 | 11篇 |
1982年 | 14篇 |
1981年 | 10篇 |
1980年 | 15篇 |
1979年 | 9篇 |
1978年 | 14篇 |
1977年 | 13篇 |
1976年 | 15篇 |
1973年 | 9篇 |
1970年 | 5篇 |
1936年 | 6篇 |
排序方式: 共有1182条查询结果,搜索用时 15 毫秒
11.
The present state of a long term program is reviewed. It was started to elaborate a remote controlled automated radiochemical
processing system for the neutron activation analysis of biological materials. The system is based on wet ashing of the sample,
followed by reactive desorption of some volatile components. The distillation residue is passed through a series of columns
filled with selective ion screening materials to remove the matrix activity. The solution is thus “stripped” from the interfering
radioions, and it is processed to single-elements through group separations using ion-exchange chromatographic techniques.
Some special problems concerning this system are treated. (a) General aspects of the construction of a (semi)automated radiochemical
processing system are discussed; (b) Comparison is made between various technical realizations of the same basic concept;
(c) Some problems concerning the “reconstruction” of an already published processing system are outlined. 相似文献
12.
Tuoto C. V. Regina A. Nagy J. B. Nastro A. 《Journal of Thermal Analysis and Calorimetry》1998,54(3):891-899
DSC, TG and quadrupole mass spectrometer data concerning methylquinuclidinium iodide (MeQ1), dried precursor gel, and crystalline
levyne-type zeolite are discussed together with the thermal degradation of MeQ1 mixed with single inorganic components of
the gel.
It is shown that MeQ+ions play a role in the organization of the gel structure.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
13.
14.
The fluorescence lifetime of Nile Red (NR) is not sensitive to dielectric solvent–solute interactions but markedly decreases with the increase of the hydrogen bond donating ability in alcohols because vibrations associated with hydrogen bonding are involved in the deactivation process. The negligible viscosity effect indicates that twisting of the diethylamino moiety of NR does not play significant role in the dissipation of the excitation energy. 相似文献
15.
Radoslav D. Mii Radmila P. Marinkovi-Neduin Zoltán Schay István Nagy Jelena S. Kiurski Ern E. Kiss 《Reaction Kinetics and Catalysis Letters》2007,91(1):85-92
Investigations of a commercial NiMo/Al2O3 hydrodesulfurization (HDS) catalyst are directed towards optimization of the activation procedure of HDS catalyst concerning
active phase formation and thermal stability. Structural and textural data obtained with XRD, IR-FTIR, XPS and LTNA reveal
that the optimal temperature for the formation of active species on the catalyst surface and an appropriate pore structure
is 300°C. 相似文献
16.
Gbor Nray-Szab Gyrgy Kramer Pter Nagy Sndor Kugler 《Journal of computational chemistry》1987,8(4):555-561
Computer programs have been developed or are under development for the IBM personal computer that enable their users to get information on atomic charges, electrostatic potentials, conformational and other properties of molecular systems containing H, C, N, O, F, Si, P, S, or Cl atoms. The zero-order wavefunction is constructed of strictly localized molecular orbitals with fixed atomic orbital coefficients. The wave function can be refined by optimizing these coefficients, i.e., considering inductive effects via a coupled set of 2 × 2 secular equations within the CNDO /2 approximation. Delocalization and exchange effects are accounted for by expanding the wavefunction on a basis of the aforementioned strictly localized orbitals, instead of conventional atomic orbitals, and solving the corresponding SCF equations. Our method has been applied to the study of large systems. We calculated the electrostatic field of the complex of β-trypsin and basic pancreatic trypsin inhibitor and it has been found that strong field regions more or less coincide with hydration sites. A further potential application of protein electrostatic fields is in NMR spectroscopy. We found a linear correlation between CαH or backbone NH proton chemical shifts and the protein field at the site of the corresponding proton. At last, we propose a simple method to mimic the bulk around atomic clusters modeling crystalline and amorphous silicon. Based on this method we found a linear correlation between atomic net charges and bond angle distortions in silicon clusters with 35 atoms. 相似文献
17.
Hanna Nagy Kovacs Alvin D. Delman Bernard B. Simms 《Journal of polymer science. Part A, Polymer chemistry》1970,8(4):869-884
The effects of incorporating a p-phenylene- (or m-phenylene)-1,3,4-oxadiazole fragment into the backbone of poly[1,4-phenylene(diphenylsilyl)-1,4-phenylene-2,5-(1,3,4-oxadiazole)], which was developed by the authors, was investigated. Bis[(p-carbohydrazidophenyl)]diphenylsilane was copolymerized with dipentachlorophenyl terephthalate or isophthalate to produce the prepolymers poly[N-(p-diphenylsilylbenzoyl)-N′N″-(terephthaloyl)-N″′-(p-benzoyl)dihydrazide] and poly[N-(p-diphenylsilylbenzoyl)-N′,-N″-(isophthaloyl)-N″′-p-(benzoyl) dihydrazide], respectively. The polyhydrazides were converted by thermal dehydration into poly[1,4-phenylene(diphenylsilyl)-1,4-phenylene-(1,3,4-oxadiazole-2,5-diyl)-1,4-phenylene-2,5-(1,3,4-oxadiazole)] and poly[1,4-phenyl-ene(diphenylsilyl)-1,4-phenylene-(1,3,4-oxadiazole-2,5-diyl)-1,3,4-(oxadiazole)]. The new polymers were soluble in organic solvents. Films cast from these solutions exhibited good adhesion to glass and metal surfaces. Thermal analysis showed that the heat stability of all these polymers was about the same and that they were resistant to decomposition when heated in air to about 400°C. The results also indicated that these polymers were somewhat less heat-resistant than samples of poly-[1,4-phenylene(diphenylsilyl)-1,4-phenylene-2,5-]1,3,4-(oxadiazole) synthesized from bis(p-carbohydrazidophenyl)diphenylsilane and bis-(p-carbopentachlorophenoxy-phenyl)diphenylsilane. 相似文献
18.
M. Nagy 《Colloid and polymer science》1985,263(3):245-265
19.
Földvári M. Kovács-Pálffy P. Nagy N. M. Kónya J. 《Journal of Thermal Analysis and Calorimetry》1998,53(2):547-558
Various cation-exchanged montmorillonites (Li+, Na+, Ba2+, Mg2+, Ca2+, Mn2+, Co2+, Cu2+, Ag+, Cd2+, Hg2+, Al3+, Pb2+ and NH4+)
were prepared from calcium montmorillonite and their properties were studied by means of X-ray diffraction and thermal analysis.
The two methods give information on the cation exchange in the interlayer space only. X-ray diffraction studies at room temperature
are mainly suitable for estimation of the exchange of cations of different valencies. At 500°C, when the structure is completely
collapsed, the d value of montmorillonite depends on the non-hydrated ionic radius of the interlayer cation, but the measurement
interval is limited for fine interpretation. The thermoanalytical method is suitable for a better distinction of different
exchangeable cations of higher hydration energy on the basis of the DTG or DDTG curve.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
20.
Agnes G. Nagy 《Journal of organometallic chemistry》1985,291(3):335-340
Polarizations, polarization ranges and ratios of polarization ranges for vinylene groups in seven series, namely chalcone derivatives, ferrocene analogues of chalcone, stilbene derivatives, ferrocene analogues of stilbene, and styrene derivatives, were studied. The polarization ranges spanning the intervals between 13C NMR chemical shifts of the derivatives substituted by p-NO2 and p-NMe2 groups are compared in these related compounds. The influence of the side-chain groups in the vinylene moiety and of the sign of the polarization on the substituent-effect are discussed. 相似文献