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91.
Abul K. Mallik 《European Polymer Journal》2009,45(6):1811-1819
Poly(octadecyl acrylate)-grafted silicas were prepared by surface-initiated atom transfer radical polymerization (ATRP). Initially, undecyl ester and allyl ester-based ATRP initiators were synthesized and then immobilized on silica. The surface-initiated ATRP of octadecyl acrylate was carried out from the initiator-grafted silicas using copper(I) bromide and N,N,N′,N′,N′′-pentamethyldiethylenetriamine as catalyst precursors to produce poly(octadecyl acrylate)-grafted silicas, Sil-C11-ODAn (obtained from undecyl ester) and Sil-C3-ODAn (originated from allyl ester), respectively. Both Sil-C11-ODAn and Sil-C3-ODAn were characterized by DRIFT, suspension-state 1H NMR, solid-state 13C CP/MAS NMR spectroscopies, thermogravimetric analysis (TGA), elemental analysis and differential scanning calorimetry (DSC) measurements. Suspension-state 1H NMR, solid-state 13C CP/MAS NMR and DSC analyses suggest that Sil-C11-ODAn demonstrated more ordered structure than Sil-C3-ODAn. In this paper, it is also described that for ordering of the polymer phase is accompanied by the selectivity increase for the separation of poly cyclic aromatic hydrocarbons (PAHs) in RP-HPLC. 相似文献
92.
Sodium borohydride reduction of E-3-benzylidenechromanone epoxides in dry methanol has afforded 3(S*), 4(S*)-dihydroxy-3-[α(R*)-methoxybenzyl]chromans as an interesting class of products, the structures of which have been assigned mainly from spectral data and consideration of the mechanistic aspects. X-ray diffraction study of one of them, 3-[4-bromo-α(R*)-methoxybenzyl]-6-chloro-3(S*),4(S*)- dihydroxychroman, is performed. The title compound crystallizes in the monoclinic sp. gr. P21/n, with a = 13.336(6) Å, b = 10.866(5) Å, c = 27.166(11) Å, β = 95.193(6)°, V = 3920(3) Å3, and Z = 8. Supramolecular construction of the compound involves O–H···O intermolecular hydrogen bonds as well as three other types of non-covalent interactions which are responsible for crystal packing. Density functional theory was applied for geometry optimization, molecular orbital calculations, and prediction of UV spectral features. The geometric parameters (bond lengths, bond angles, and dihedral angles) for the representative compound obtained from density functional theory with B3LY6-31G basis set were in good agreement with experimental values. 相似文献
93.
U.N. Roy K. Mallik L.M. Kukreja 《Applied Physics A: Materials Science & Processing》1998,67(2):259-261
0 ) in the reflectivity spectra has been found to be blue-shifted with respect to that for bulk CdS. The appearance of the E1(A) peak at about 5 eV is evidence for the hexagonal nature of the particles with the c axis normal or nearly normal to the
plane of the film. This suggests the epitaxial nature of the grown particulate films. Another reflectivity peak has been observed
at about 320 nm. However, its origin is not yet clear.
Received: 26 May 1998/Accepted: 28 May 1998 相似文献
94.
Reduction of the indole-1-carboxaldehydes (-) with borane /THF gives the 1-methylindoles () in 42-91-% yields together with the di(indolylmethyl)ethers (), the indolyl-methyl indolines (), the unsymmetric ether() and the indolenine () as the minor products, except . This appears to be the first report on the formation of symmetric ethers in the borane/THF reduction of an oxygen function. The formation of and from and implies that electrophilic substitution takes place primarily at position 3 of 3-substituted indoles, did not form the corresponding probably because of steric hindrance. These results are discussed in relation to the mechanisms of borane/THF reduction, origin of the different products and electrophilic substitution in 3-substituted indoles. 相似文献
95.
Mallik B Thander A Sanyal MK 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,61(3):485-490
The time-dependent changes in absorbance in the case of ferrocene-doped poly(methyl methacrylate) thin films containing chloroform molecules have been investigated after photoexcitation in nitrogen atmosphere. Photoexcitations have been made by the monochromatic light (using Xe-source and a monochromator) in the UV range. An increase in absorbance associated with spectacular fluctuations in its value, has been noticed. The nature of the variation in the fluctuations has been studied as a function of time (duration) of photoexcitation, photoexcitation wavelength and concentration of ferrocene in the film. The observed results have been discussed considering the role of secondary reaction after photoexcitation as well as the diffusion of small chemical species in the polymer matrix. 相似文献
96.
Banerjee AL Swanson M Roy BC Jia X Haldar MK Mallik S Srivastava DK 《Journal of the American Chemical Society》2004,126(35):10875-10883
We elaborate on a novel strategy for enhancing the binding affinity of an active-site directed inhibitor by attaching a tether group, designed to interact with the surface-exposed histidine residue(s) of enzymes. In this approach, we have utilized the recombinant form of human carbonic anhydrase-II (hCA-II) as the enzyme source and benzenesulfonamide and its derivatives as inhibitors. The steady-state kinetic and the ligand binding data revealed that the attachment of iminodiacetate (IDA)-Cu(2+) to benzenesulfonamide (via a triethylene glycol spacer) enhanced its binding affinity for hCA-II by about 40-fold. No energetic contribution of either IDA or triethylene glycol spacer was found (at least in the ground state of the enzyme-inhibitor complex) when Cu(2+) was stripped off from the tether group-conjugated sulfonamide derivative. Arguments are presented that the overall strategy of enhancing the binding affinities of known inhibitors by attaching the IDA-Cu(2+) groups to interact with the surface-exposed histidine residues will find a general application in designing the isozyme-specific inhibitors as potential drugs. 相似文献
97.
Roy BC Banerjee AL Swanson M Jia XG Haldar MK Mallik S Srivastava DK 《Journal of the American Chemical Society》2004,126(41):13206-13207
The enzyme inhibitors are usually designed by taking into consideration the overall dimensions of the enzyme's active site pockets. This conventional approach often fails to produce desirable affinities of inhibitors for their cognate enzymes. To circumvent such constraints, we contemplated enhancing the binding affinities of inhibitors by attaching tether groups, which would interact with the surface exposed amino acid residues. This strategy has been tested for the inhibition of human carbonic anhydrase II. Benzenesulfonamide serves as a weak inhibitor for the enzyme, but when it is conjugated to iminodiacetate-Cu2+ (which interacts with the surface-exposed His residues) via a spacer group, its binding affinity is enhanced by about 2 orders of magnitude. This "two-prong" approach is expected to serve as a general strategy for converting weak inhibitors of enzymes into tight-binding inhibitors. 相似文献
98.
Baltrusaitis RM Becker JJ Blaylock GT Brown JS Bunnell KO Burnett TH Cassell RE Coffman D Cook V Coward DH Dado S Dorfan DE Dubois GP Duncan AL Einsweiler KF Eisenstein BI Fabrizio R Gladding G Grancagnolo F Hamilton RP Hauser J Heusch CA Hitlin DG Köpke L Lockman WS Mallik U Mockett PM Mozley RF Nappi A Odian A Partridge R Perrier J Plaetzer SA Richman JD Roehrig J Russell JJ Sadrozinski HF Scarlatella M Schalk TL Schindler RH Seiden A Simopoulos C Sleeman JC Spadafora AL Stockdale IE 《Physical review letters》1986,56(20):2140-2143
99.
Adler J Becker JJ Blaylock GT Bolton T Brown JS Bunnell KO Burnett TH Cassell RE Coffman D Cook V Coward DH Dorfan DE Dubois GP Duncan AL Eigen G Einsweiler KF Eisenstein BI Freese T Gladding G Grab C Grancagnolo F Hamilton RP Hauser J Heusch CA Hitlin DG Izen JM Köpke L Li A Lockman WS Mallik U Matthews CG Mir R Mockett PM Mozley RF Nemati B Odian A Parrish L Partridge R Perrier J Pitman D Plaetzer SA Richman JD Sadrozinski HF Scarlatella M Schalk TL Schindler RH Seiden A Simopoulos C 《Physical review letters》1987,59(14):1527-1529
100.
Adler J Becker JJ Blaylock GT Bolton T Brown JS Bunnell KO Burnett TH Cassell RE Coffman D Cook V Coward DH Dorfan DE Dubois GP Duncan AL Eigen G Einsweiler KF Eisenstein BI Freese T Gladding G Grab C Grancagnolo F Hamilton RP Hauser J Heusch CA Hitlin DG Izen JM Köpke L Li A Lockman WS Mallik U Matthews CG Mir R Mockett PM Mozley RF Nemati B Odian A Parrish L Partridge R Perrier J Pitman D Plaetzer SA Richman JD Sadrozinski HF Scarlatella M Schalk TL Schindler RH Seiden A Simopoulos C 《Physical review letters》1988,60(14):1375-1378