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21.
Amine‐Responsive Adaptable Nanospaces: Fluorescent Porous Coordination Polymer for Molecular Recognition 下载免费PDF全文
Ritesh Haldar Prof. Ryotaro Matsuda Prof. Susumu Kitagawa Prof. Subi J. George Prof. Tapas Kumar Maji 《Angewandte Chemie (International ed. in English)》2014,53(44):11772-11777
Flexible and dynamic porous coordination polymers (PCPs) with well‐defined nanospaces composed of chromophoric organic linkers provide a scaffold for encapsulation of versatile guest molecules through noncovalent interactions. PCPs thus provide a potential platform for molecular recognition. Herein, we report a flexible 3D supramolecular framework {[Zn(ndc)(o‐phen)]?DMF}n (o‐phen=1,10‐phenanthroline, ndc=2,6‐napthalenedicarboxylate) with confined nanospaces that can accommodate different electron‐donating aromatic amine guests with selective turn‐on emission signaling. This system serves as a molecular recognition platform through an emission‐readout process. Such unprecedented tunable emission with different amines is attributed to its emissive charge‐transfer (CT) complexation with o‐phen linkers. In certain cases this CT emission is further amplified by energy transfer from the chromophoric linker unit ndc, as evidenced by single‐crystal X‐ray structural characterization. 相似文献
22.
Chakraborty T Holm AI Hvelplund P Nielsen SB Poully JC Worm ES Williams ER 《Journal of the American Society for Mass Spectrometry》2006,17(12):1675-1680
Electron capture by both bare and microsolvated small peptide dications was investigated by colliding these ions with sodium vapor in an accelerator mass spectrometer to provide insight into processes that occur on the microsecond time frame. Survival of the intact peptide monocation after electron capture depends strongly on molecular size. For dipeptides, no intact reduced species were observed; the predominant ions correspond to loss of hydrogen and ammonia. In contrast, the intact reduced species was observed for larger peptides. Calculated structures indicate that the diprotonated dipeptide ions form largely extended structures with low probability of internal ionic hydrogen bonding (i.e., charge solvation) whereas internal ionic H-bonding occurs extensively for larger peptide dications. Solvation of the peptide ions with between one to seven methanol molecules reduces the total extent of H loss even for dipeptides where intact reduced species can survive more than a microsecond after electron capture. The yield of ions corresponding to cleavage of NCalpha bonds (c+ and z+* ions) does not depend strongly on peptide size but decreases with the extent of microsolvation for the dipeptide dications. H-bonding appears to play an important role for the survival of the intact reduced ions but less so for the formation of c+ and z+* ions. Our results indicate that electron capture predominantly occurs at the ammonium groups (at least 70 to 80%), and provides important new insights into the electron capture dissociation process. 相似文献
23.
New phenylethanoid glycosides from Bacopa monniera 总被引:1,自引:0,他引:1
Chakravarty AK Sarkar T Nakane T Kawahara N Masuda K 《Chemical & pharmaceutical bulletin》2002,50(12):1616-1618
Three new phenylethanoid glycosides, viz. monnierasides I-III (1-3) along with the known analogue plantainoside B were isolated from the glycosidic fraction of Bacopa monniera. Their structures were elucidated mainly on the basis of two dimensional (2D) NMR spectral analyses. 相似文献
24.
Subhashis Ghosal Jayanta K. Ghosh Tapas Samanta 《Annals of the Institute of Statistical Mathematics》1999,51(3):479-497
We consider a family of models that arise in connection with sharp change in hazard rate corresponding to high initial hazard rate dropping to a more stable or slowly changing rate at an unknown change-point . Although the Bayes estimates are well behaved and are asymptotically efficient, it is difficult to compute them as the posterior distributions are generally very complicated. We obtain a simple first order asymptotic approximation to the posterior distribution of . The accuracy of the approximation is judged through simulation. The approximation performs quite well. Our method is also applied to analyze a real data set. 相似文献
25.
Surajit?Dasgupta Neven?Bilic Tapas?K.?DasEmail author 《General Relativity and Gravitation》2005,37(11):1877-1890
We demonstrate that a spherical accretion onto astrophysical black holes, under the influence of Newtonian or various post-Newtonian
pseudo-Schwarzschild gravitational potentials, may constitute a concrete example of classical analogue gravity naturally found
in the Universe. We analytically calculate the corresponding analogue Hawking temperature as a function of the minimum number
of physical parameters governing the accretion flow. We study both the polytropic and the isothermal accretion. We show that
unlike in a general relativistic spherical accretion, analogue white hole solutions can never be obtained in such post-Newtonian
systems. We also show that an isothermal spherical accretion is a remarkably simple example in which the only one information–the
temperature of the fluid, is sufficient to completely describe an analogue gravity system. For both types of accretion, the
analogue Hawking temperature may become higher than the usual Hawking temperature. However, the analogue Hawking temperature
for accreting astrophysical black holes is considerably lower compared with the temperature of the accreting fluid. 相似文献
26.
Tapas PaulDebabrata Mukherjee 《Tetrahedron letters》2003,44(27):4985-4988
Stereocontrolled total syntheses of the bridged tricyclic ketones (±)-clovan-3-one (5) and (±)-epi-clovan-3-one (6) and a facile total synthesis of the tricyclic sesquiterpene (±)-pseudoclovene-A (3) have been successfully accomplished involving participation of an aryl intramolecular cyclisation of the bromophenol 11 as a key step. 相似文献
27.
28.
A variety of olefins have been shown to undergo conversion to the corresponding α-bromo/iodoketones when reacted with NBS/NIS and IBX in DMSO at room temperature. While the reaction is found to occur rapidly with e-rich arylolefins leading to the corresponding haloketones in 65-95% yields in 0.3-3.0 h, those containing e-withdrawing groups are found to yield diketones concomitantly, such that the latter are the exclusive products over extended duration of the reactions. 相似文献
29.
Vadapalli Chandrasekhar Palani Sasikumar Puja Singh Ramalingam Thirumoorthi Tapas Senapati 《Journal of Chemical Sciences》2008,120(1):105-113
Organostannoxane cages and aggregates of well-defined composition and structure can be prepared by the reactions of organotin
oxides or organotin oxide-hydroxides with protic acids. The utility of this strategy for the preparation of dendrimer-like
molecules containing a stannoxane core and a functional periphery is described. 相似文献
30.
Hydrothermal treatment of a mixture of ethylene diamine, phosphoric acid and citric acid under ambient pressure generates fluorescent carbon dots that are co-doped with phosphorus and nitrogen. These have features such as (a) both green fluorescence (peaking at 430 nm; 30% quantum yield) and red fluorescence (peaking at 500 nm, quantum yield 78%), (b) wavelength-dependent emission peaks, and (c) insensitivity to changes of pH values, dot concentration and ionic strength. The C-dots are useful for both fluorescent (FL) and photoacoustic (PA) imaging of living tissue. PA imaging warrants better spatial resolution and allows deeper tissues to be imaged compared to most optical imaging techniques. It is essential to assign a photoacoustic contrast agent as most of the diseases do not show a natural photoacoustic contrast in their early stage. The dually emitting C-dots are shown to be a useful contrast agent for PA and FL imaging of mice tumors. Intravenous administration of the C-dots resulted in strong signals in both PA and FL imaging. 相似文献