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421.
Sarova GH Bokach NA Fedorov AA Berberan-Santos MN Kukushkin VY Haukka M Fraústo da Silva JJ Pombeiro AJ 《Dalton transactions (Cambridge, England : 2003)》2006,(31):3798-3805
The imidoylamidinate platinum(II) compounds [Pt{NH=C(R)NC(Ph)NPh}2] (R = CH2Ph 2, p-ClC6H43, Ph 4) were prepared by the reaction of the appropriate trans-[PtCl2(RCN)2] with 4 equiv of the amidine PhC(NH)NHPh giving 2-4 and 2 equivs of the salt PhC(=NH)NHPh.HCl. We also synthesized, by the double alkylation of 4 with MeOSO2CF3, complex [Pt{NH=C(Ph)N(Me)C(Ph)=NPh}2][CF3SO3]2 (5) which models the bis-protonated form of 4. The complexes were characterized by 1H, 13C NMR, and IR spectroscopies, FAB-MS and by C, H, N elemental analysis. The X-ray crystallography of 4.2CH2Cl2 enables the confirmation of the square planar coordination geometry of the metal center with almost planar imidoylamidine ligands, while in 5.2CHCl3 the planarity of the metallacycles is lost and and the central N atom is sp3-hybridized. The imidoylamidinate complexes represent a new family of Pt(II)-based luminescent complexes and they are emissive at room temperature both in solution and in the solid state, with an emission quantum yield ranging from 3.7 x 10(-4) to 6.2 x 10(-2) in methanol solution; the emission intensity is pH-dependent, being quenched at low pH. UV-visible and luminescence spectroscopies indicate that the lowest excited state of these compounds is 3MLCT or 3IL with significant MLCT character, with emission lifetimes of a few micros. A blue shift of both the absorption and emission with increasing solvent polarity and with decreasing pi-electron withdrawing properties of the ligand substituent was observed. 相似文献
422.
Luzyanin KV Kukushkin VY Kuznetsov ML Ryabov AD Galanski M Haukka M Tretyakov EV Ovcharenko VI Kopylovich MN Pombeiro AJ 《Inorganic chemistry》2006,45(5):2296-2306
The coupling between coordinated propiononitriles in trans-[PtCln(EtCN)2] (n = 2, 4) and the 1,2-hydroxylaminooximes HON(H)CMe2C(R)=NOH (R = Ph 1, Me 2) proceeds smoothly in CHCl(3) at ca. 40-45 degrees C and gives trans-[PtCln{NH=C(Et)ON(H)CMe2C(R)=NOH}2] (n = 2, R = Ph 5, Me 6; n = 4, R = Ph 7, Me 8) in 80-85% isolated yields. The reaction is highly regioselective, and both spectroscopic (IR; FAB+-MS; 1D 1H, 13C{1H}, and 195Pt NMR; and 2D 1H,13C HMQC, 1H,13C HMBC, and 1H,15N HMQC NMR) and X-ray data for 6-8 suggest that the addition proceeds exclusively via the hydroxylamine moiety of the 1,2-hydroxylaminooxime species; the existence of an oxime group remote from the nucleophile was also confirmed. Heating of 6 in air leads to its conversion to the unusual nitrosoalkane complex [PtCl2{HON=C(Me)C(Me)2N=O}] (9), whereas in the case of 5, only the metal-free salt [H3NC(Me)2C(Ph)=NOH]2(NO3)Cl.H2O (10) was isolated. To compare the kinetic aspects and trends in the addition of both types of nucleophiles (oximes and hydroxylamines; for the latter, see our recent work: Inorg. Chem. 2005, 44, 2944) to coordinated nitriles, a kinetic study of the addition of HON=C(CH2Ph)2 to [Ph3PCH2Ph][PtCl5(EtCN)] (11) to give [Ph(3)PCH(2)Ph][PtCl(5){NH=C(Et)ON=C(CH2Ph)2}] (12) was performed. The calculated rate constant k2 of 3.9 x 10(-6) M(-1) s(-1) at -20 degrees C for the addition of the oxime indicates that the hydroxylamine is, by a factor 1.7 x 10(4), more reactive toward the addition to nitriles than the oxime. Results of the synthetic, kinetic, and theoretical (at the B3LYP level of theory) studies have demonstrated that the high regioselectivity of the reactions of the 1,2-hydroxylaminooximes with ligated nitriles is both kinetically and thermodynamically controlled. 相似文献
423.
Bratlie KM Montano MO Flores LD Paajanen M Somorjai GA 《Journal of the American Chemical Society》2006,128(39):12810-12816
Sum frequency generation (SFG) vibrational spectroscopy and high-pressure scanning tunneling microscopy (HP-STM) have been used in combination for the first time to study a catalytic reaction. These techniques have been able to identify surface intermediates in situ during benzene hydrogenation on a Pt(111) single-crystal surface at Torr pressures. In a background of 10 Torr of benzene, STM is able to image small ordered regions corresponding to the c(2 radical3 x 3)rect structure in which each molecule is chemisorbed at a bridge site. In addition, individual benzene molecules are also observed between the ordered regions. These individual molecules are assumed to be physisorbed benzene on the basis of the SFG results showing both chemisorbed and physisorbed molecules. The surface becomes too mobile to image upon addition of hydrogen but is determined to have physisorbed and chemisorbed benzene present by SFG. It was spectroscopically determined that heating the platinum surface after poisoning with CO displaces benzene molecules. The high-coverage pure CO structure of (radical19 x radical19)R23.4 degrees imaged with STM is a verification of spectroscopic measurements. 相似文献
424.
Ryhänen SJ Säily VM Parry MJ Luciani P Mancini G Alakoskela JM Kinnunen PK 《Journal of the American Chemical Society》2006,128(26):8659-8663
While much is known about the self-assembly of lipids on nanoscale, our understanding of their biologically relevant mesoscale organization remains incomplete. Here, we show for a cationic gemini lipid a sharp and reversible transition from small vesicles with an average diameter of approximately 40 nm to giant vesicles (GVs) with an average diameter of approximately 11 microm. This transition is dependent on proper [NaCl] and specific temperature. Below this transition and in the vicinity of the air/water interface, a series of mesoscale morphological transitions was observed, revealing complex structures resembling biological membranes. On the basis of microscopy experiments, a tentative [NaCl] versus temperature shape/size phase diagram was constructed. To explain this unprecedented transition, we propose a novel mechanism whereby a specific interaction of Cl(-) counterion with the cationic gemini surfactant initiates the formation of a commensurate solute counterion lattice with low spontaneous curvature. In keeping with the high bending rigidity of NaCl crystal, this tightly associated ionic lattice enslaves membrane curvature and the mesoscale 3-D organization of this lipid. 相似文献
425.
Alexander Kamyshny Matti Ben‐Moshe Shai Aviezer Shlomo Magdassi 《Macromolecular rapid communications》2005,26(4):281-288
Summary: Two types of ink‐jet inks are presented: ink containing an aqueous dispersion of silver nanoparticles and an oil‐in‐water microemulsion‐based ink. The metallic ink contains nanoparticles of silver, which are formed in the presence of an ionic polymeric stabilizer. Sintering of the printed image obtained with the use of such silver‐based inks at temperatures as low as 300 °C results in formation of patterns possessing noticeable conductivity. The microemulsion inks are based on a thermodynamically stable microemulsion, in which the dispersed oil phase is a volatile solvent containing a water‐insoluble colorant. After contact of the jetted ink droplets with a substrate, nanodroplets of the microemulsion are converted into nanoparticles of the solubilized colorant. In some cases, it was found that the evaporation of microemulsion ink droplets leads to formation of rings composed of ordered nanoparticles.