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121.
Tibor Cserháti Barna Bordás Attila Kis-Tamás Gyula Mikite József Szejtli Éva Fenyvesi 《Journal of inclusion phenomena and macrocyclic chemistry》1986,4(1):55-59
Cyclodextrin complexation decreases the apparent lipophilicity of hydrophobic guest molecules. A higher complex stability results in a larger decrease of lipophilicity as determined by reversed-phase thin-layer chromatography. The method was applied to study the complex formation of 33 nitrostyrene derivatives with a water soluble cross linked -cyclodextrin polymer (weight average molecular weight: 4300). The substituents in thepara position of the benzene ring had a higher impact on the complex stability than those in themeta andortho positions. The substituents on the alkyl side chain influenced the complex stability to the same extent as those on the benzen ring. 相似文献
122.
Gyula v. Sz. Nagy 《Monatshefte für Mathematik》1948,51(1):59-62
Ohne Zusammenfassung 相似文献
123.
Soma Papp Gyula Jágerszki Prof. Róbert E. Gyurcsányi 《Angewandte Chemie (International ed. in English)》2018,57(17):4752-4755
We report the synthesis and analytical application of the first Cu2+‐selective synthetic ion channel based on peptide‐modified gold nanopores. A Cu2+‐binding peptide motif (Gly‐Gly‐His) along with two additional functional thiol derivatives inferring cation‐permselectivity and hydrophobicity was self‐assembled on the surface of gold nanoporous membranes comprising of about 5 nm diameter pores. These membranes were used to construct ion‐selective electrodes (ISEs) with extraordinary Cu2+ selectivities, approaching six orders of magnitude over certain ions. Since all constituents are immobilized to a supporting nanoporous membrane, their leaching, that is a ubiquitous problem of conventional ionophore‐based ISEs was effectively suppressed. 相似文献
124.
János Wölfling Ágota Szájli László Vörös Mónika Gáspár Gyula Schneider 《Monatshefte für Chemie / Chemical Monthly》2006,137(8):1099-1107
Summary. 3β-Hydroxy-16,17-seco-13α-androsta-5,16-dien-17-al was obtained from 3β-acetoxyandrost-5-en-17-one in six steps with a Grob fragmentation as the key step. This seco-steroid, containing a formyl group and an unsaturated side-chain in a sterically favourable cis position, is a useful synthon
for the synthesis of novel heterocycles condensed to the 3β-hydroxy-13α-androst-5-en-17-one skeleton. 相似文献
125.
Under weak UV irradiation (flux: 2.4 mmol hv/h) the activity of the hydrogenation catalyst IrCl(CO)(PPh3)2 is increased by a factor up to 40. Reactive intermediates are formed in reversible and irreversible steps. Once the active intermediate is produced in the irreversible step fast hydrogenation can be carried out even in the dark. 相似文献
126.
127.
Kubícek V Havlícková J Kotek J Tircsó G Hermann P Tóth E Lukes I 《Inorganic chemistry》2010,49(23):10960-10969
Given the practical advantages of the (68)Ga isotope in positron emission tomography applications, gallium complexes are gaining increasing importance in biomedical imaging. However, the strong tendency of Ga(3+) to hydrolyze and the slow formation and very high stability of macrocyclic complexes altogether render Ga(3+) coordination chemistry difficult and explain why stability and kinetic data on Ga(3+) complexes are rather scarce. Here we report solution and solid-state studies of Ga(3+) complexes formed with the macrocyclic ligand 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid, (DOTA)(4-), and its mono(n-butylamide) derivative, (DO3AM(Bu))(3-). Thermodynamic stability constants, log K(GaDOTA) = 26.05 and log K(GaDO3AM(Bu)) = 24.64, were determined by out-of-cell pH-potentiometric titrations. Due to the very slow formation and dissociation of the complexes, equilibration times of up to ~4 weeks were necessary. The kinetics of complex dissociation were followed by (71)Ga NMR under both acidic and alkaline conditions. The GaDOTA complex is significantly more inert (τ(1/2) ~12.2 d at pH = 0 and τ(1/2) ~6.2 h at pH = 10) than the GaDO3AM(Bu) analogue (τ(1/2) ~2.7 d at pH = 0 and τ(1/2) ~0.7 h at pH = 10). Nevertheless, the kinetic inertness of both chelates is extremely high and approves the application of Ga(3+) complexes of such DOTA-like ligands in molecular imaging. The solid-state structure of the GaDOTA complex, crystallized from a strongly acidic solution (pH < 1), evidenced a diprotonated form with protons localized on the free carboxylate pendants. 相似文献
128.
va Boros Ferenc Bertha Gbor Czira Antal Feller Jzsef Fetter Mria Kajtr‐Peredy Gyula Simig 《Journal of heterocyclic chemistry》2006,43(2):371-388
Two efficient methods have been developed for the synthesis of variously substituted 2‐aminomethylazetidine derivatives 5 by regioselective nucleophilic substitution of 4‐mesyloxymethylazetidin‐2‐ones 3 followed by reduction or by reduction of the appropriate 4‐oxo‐azetidine‐2‐carboxamides 7 . A novel ring transformation of 4‐oxoazetidine‐2‐carboxamides 7 into tetrahydroquinolines 16 by reaction with lithium aluminium hydride/aluminium trichloride has been investigated. 相似文献
129.
Lszl Pong Jzef Reiter Gyula Simig Bla gai Ferenc Faigl 《Journal of heterocyclic chemistry》2006,43(6):1539-1547
o‐Aroylarylacetone type 1,5‐diketone derivatives (5, 6) were synthesised from arylacetones (1) protected as 1,3‐dioxolanes (4) through directed ortho lithiation followed by acylation with aroyl chlorides. 8,9‐Dialkoxy‐2,3‐benzodiazepines 9 were obtained by cyclisation of diketones 6 with hydrazine. The reaction of diketones 6 with ammonia gave 7,8‐dialkoxyisoquinolines 11. Reaction of ketals 5 with hydrazine hydrochloride and hydroxylamine hydrochloride afforded N‐amino‐7,8‐dialkoxyisoquinolinium chlorides (10) and 7,8‐dialkoxyisoquinolinium oxides (12), respectively. 相似文献
130.
The protonation constants () of 3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid (PCTA) and stability constants of complexes formed between this pyridine-containing macrocycle and several different metal ions have been determined in 1.0 M KCl at 25 degrees C and compared to previous literature values. The first protonation constant was found to be 0.5-0.6 log units higher than the value reported previously, and a total of five protonation steps were detected (log = 11.36, 7.35, 3.83, 2.12, and 1.29). The stability constants of complexes formed between PCTA and Mg2+, Ca2+, Cu2+, and Zn2+ were also somewhat higher than those previously reported, but this difference could be largely attributed to the higher first protonation constant of the ligand. Stability constants of complexes formed between PCTA and the Ln3+ series of ions and Y3+ were determined by using an "out-of-cell" potentiometric method. These values ranged from log K = 18.15 for Ce(PCTA) to log K = 20.63 for Yb(PCTA), increasing along the Ln series in proportion to decreasing Ln3+ cation size. The rates of complex formation for Ce(PCTA), Eu(PCTA), Y(PCTA), and Yb(PCTA) were followed by conventional UV-vis spectroscopy in the pH range 3.5-4.4. First-order rate constants (saturation kinetics) obtained for different ligand-to-metal ion ratios were consistent with the rapid formation of a diprotonated intermediate, Ln(H(2)PCTA)(2+). The stabilities of the intermediates as determined from the kinetic data were 2.81, 3.12, 2.97, and 2.69 log K units for Ce(H(2)PCTA), Eu(H(2)PCTA), Y(H(2)PCTA), and Yb(H(2)PCTA), respectively. Rearrangement of these intermediates to the fully chelated complexes was the rate-determining step, and the rate constant (k(r)) for this process was found to be inversely proportional to the proton concentration. The formation rates (k(OH)) increased with a decrease in the lanthanide ion size [9.68 x 10(7), 1.74 x 10(8), 1.13 x 10(8), and 1.11 x 10(9) M(-1) s(-1) for Ce(PCTA), Eu(PCTA), Y(PCTA), and Yb(PCTA), respectively]. These data indicate that the Ln(PCTA) complexes exhibit the fastest formation rates among all lanthanide macrocyclic ligand complexes studied to date. The acid-catalyzed dissociation rates (k1) varied with the cation from 9.61 x 10(-4), 5.08 x 10(-4), 1.07 x 10(-3), and 2.80 x 10(-4) M(-1) s(-1) for Ce(PCTA), Eu(PCTA), Y(PCTA), and Yb(PCTA), respectively. 相似文献