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排序方式: 共有210条查询结果,搜索用时 31 毫秒
1.
Franca M. Cordero Francesco De Sarlo Alberto Brandi 《Monatshefte für Chemie / Chemical Monthly》2004,40(2):649-669
The review outlines the various different azaheterocycles available from 5-spirocyclopropane isoxazolidines. These compounds can be regarded as versatile direct precursors of tetrahydro-, dihydropyridone and azetidinone derivatives. The current scope and limitations, and the selectivity aspects of the different processes are discussed therein. 相似文献
2.
Giampiero Bettinetti Milena Sorrenti Laura Catenacci Franca Ferrari Silvia Rossi Ilaria Salvadeo Paolo Carraro 《Journal of inclusion phenomena and macrocyclic chemistry》2007,57(1-4):329-332
Triacetyl α-cyclodextrin, triacetyl β-cyclodextrin and triacetyl γ-cyclodextrin were tested as possible hydrophobic carriers
to prolong the release of hydrophilic teicoplanin (TCP). Physical–chemical characterization of individual components, drug-carrier
physical mixtures at 0.5, 0.67 and 0.75 mass fraction of carrier, and the respective interaction products by kneading or evaporative
crystallization under microwave irradiation was carried out using differential scanning calorimetry (DSC) and thermogravimetric
analysis (TGA). In vitro drug release in pH 7.4 phosphate buffer at 37 °C was determined by intrinsic dissolution rate (IDR)
measurements on non disintegrating compressed discs. Solid-state interactions of TCP with triacetyl α-cyclodextrin by evaporative
crystallization and kneading and with triacetyl β-cyclodextrin by evaporative crystallization (probably resulting in carrier
amorphization) were demonstrated. The role of carrier hydrophobicity, carrier mass fraction and preparation method of solid
drug-carrier combinations on solid-state drug-carrier interactions and slowing down of TCP release was assessed. Modulation
of drug release can be achieved using TCP-triacetyl γ-cyclodextrin combinations at 0.5 mass fraction of carrier. 相似文献
3.
Improta R Mele F Crescenzi O Benzi C Barone V 《Journal of the American Chemical Society》2002,124(26):7857-7865
The importance of vicinal and long-range interresidue effects in determining the stability of the collagen triple helix has been investigated by quantum mechanical (QM) and molecular mechanical (MM) computations on suitable model polypeptides, taking into account solvent effects by the polarizable continuum model (PCM). At the QM level, the PII conformation corresponds to an energy minimum for pentapeptide analogues incorporating the sequence Gly-Pro-Pro-Gly, irrespective of the down or up puckering of the pyrrolidine ring. However, our computations indicate that the alternation of down and up prolines characterizing collagen and collagen-like peptides is not due to an intrinsic preference of the Pro-Pro-Gly sequence. This result is confirmed by MM computations of longer polypeptides. Next, MM computations on model triple helices show that a better packing is obtained for specific values of backbone dihedrals, which, in turn, favor the alternation of down and up prolines along each chain. 相似文献
4.
Raffaele P. Bonomo Vincenzo Cucinotta Franca D' Allessandro Giuseppe Impellizzeri Giuseppe Maccarrone Enrico Rizzarelli Graziella Vecchio 《Journal of inclusion phenomena and macrocyclic chemistry》1993,15(2):167-180
The functionalized cyclodextrin 6-deoxy-6-[1-(2-amino)ethylamino]--cyclodextrin was synthesized, and an NMR, EPR, pH-metric, and calorimetric investigation was carried out in aqueous solution in order to ascertain its behaviour towards protonation and copper(II) complex formation. The thermodynamic parameters of the ternary complex formation with alanine, phenylalanine and tryptophan enantiomeric pairs were also determined (25° C andI=0.1 mol dm–3). No thermodynamic enantioselectivity was observed in these systems, while a chiral, though poor, discrimination was observed in LEC: c.d. spectra also show enantiomeric stereoselectivity. The results of the present investigation, compared with previously reported results, suggest the occurence of acis-complex trans-complex equilibrium in such systems. 相似文献
5.
D. Malferrari Maria Franca Brigatti Angela Laurora L. Medici S. Pini 《Journal of Thermal Analysis and Calorimetry》2006,86(2):365-370
The thermal behavior
of montmorillonite and organically modified montmorillonite, both treated
with heavy metal cations [Cu(II), Cd(II) and Hg(II)], was characterized via
thermal analyses (TG, DTG and DTA) combined with evolved species gas mass
spectrometry (MS-EGA), and X-ray diffraction at in situ controlled temperature
(HTXRD). The reactions involving Cu(II)- and Cd(II)-montmorillonite samples
are mostly related to H2O and OH loss, unlike Hg(II)-montmorillonite,
where effects associated to Hg(II) loss are also present. Finally reactions
related to dehydration, dehydroxylation and to organic matter decomposition
can be observed in montmorillonite samples treated with cysteine. 相似文献
6.
Willian Franca 《代数通讯》2018,46(7):2890-2898
Let R be a unital simple ring. Under some technical restrictions, we characterize m-linear mappings G:Rm→R satisfying [G(u,…,u),u]?=?0 for all unit u∈R. 相似文献
7.
Franca Martini 《Annali dell'Universita di Ferrara》1978,24(1):17-24
Riassunto In questo lavoro si generalizza la dualità di Poincaré a spazi topologici localmente omeomorfi con insiemi analitici realin-dimensionali con singolarità isolate; tali spazi non sono in generale orientabili, nè sono muniti di una struttura analitica
globale.
Rispetto ad un analogo risultato diL. Kaup ([6]), il nostro Teorema 2 si dimostra a prescindere dall'esistenza di normalizzazioni topologiche (nel senso di [6]).
Lavoro eseguito come borsista del C.N.R. nell'ambito del G.N.S.A.G.A. 相似文献
Summary In this paper we generalize Poincaré duality to topological spaces locally homeomorphic with real analyticn-dimensional sets with isolated singularities; these spaces are in general neither orientable nor globally analytic. Compared with a similar result ofL. Kaup ([6]), our Theorem 2 is proved without supposing the existence of a topological normalization (in the sense of [6]).
Lavoro eseguito come borsista del C.N.R. nell'ambito del G.N.S.A.G.A. 相似文献
8.
Canevali C Mari CM Mattoni M Morazzoni F Nodari L Ruffo R Russo U Scotti R 《The journal of physical chemistry. B》2005,109(15):7195-7202
The mechanism of NO interaction with nanosized Ru(Pd,Pt)-doped SnO(2) was studied by electron paramagnetic resonance, M?ssbauer, and electric resistance measurements. Three steps were proposed for the reaction between the semiconductor oxide and the gaseous component: (i) the formation of bielectronic oxygen vacancies (V(o)) in SnO(2); (ii) their single-ionization (V(o)(*)) with injection of electrons into the SnO(2) conduction band; (iii) the subsequent transfer of electrons from V(o)(*) to [Ru(Pd,Pt)](4+). The last process induces the formation of further oxygen vacancies which reduce the transition metal centers to lower oxidation states; the redox processes is enhanced and the electrical resistance in transition metal-doped SnO(2) is stronger modified with respect to the undoped material. 相似文献
9.
Franca Graiff 《Meccanica》1967,2(2):69-74
Summary When relativistic theory amalgamates space and time into event, other magnitudes of classical mechanics merge or superimpose. In special relativity it is still easy to find them again by referring to the inertial frame of reference, but general relativity presents them to us as already identified in the curvatures of the Riemannian universe, which admits of no inertial frames, except local ones. It is a search for particular magnitudes and relations (such as momentum and conservation laws), physically interpretablein the classical sense, which specifies a privileged frame. Starting from this frame of reference, the present Note sets out to define the energy-momentum density and super-potentials that give rise, in the same frame, to the known integral results due to the Einstein and Freud psendotensors. Thus the snags arising out of the transformation laws of these pseudotensors are eliminated at the same time.
Study conducted under the auspices of the mathematical teams of the Consiglio Nazionale delle Ricerche. 相似文献
Sommario Quando, nelle teorie relativistiche, si sostituisce alle grandezze spazio e tempo la loro fusione nell'evento, altre grandezze della meccanica classica si fondono e sovrappongono. Nella relatività ristretta è ancora agevole ritrovarle, riferendosi all'osservatore inerziale; ma la Relatività generale ce le presenta già fuse nelle curvature dell'Universo riemanniano, che non ammette osservatori inerziali, se non locali. E' la ricerca di particolari grandezze e relazioni, (come la quantità di moto e le leggi di conservazione), fisicamente interpretabili nel senso classico, che precisa un riferimento privilegiato. Valendosi di questo riferimento, vengono definiti, nella presente Nota, densità di energia-quantità di moto e superpotenziali che danno luogo, nello stesso riferimento, ai noti risultati integrali dovuti agli pseudo-tensori di Einstein e Freud. Risultano così eliminati, nello stesso tempo, gli inconvenienti dovuti alle leggi di trasformazione di questi pseudo-tensori.
Study conducted under the auspices of the mathematical teams of the Consiglio Nazionale delle Ricerche. 相似文献
10.
Organocatalytic,Asymmetric Eliminative [4+2] Cycloaddition of Allylidene Malononitriles with Enals: Rapid Entry to Cyclohexadiene‐Embedding Linear and Angular Polycycles 下载免费PDF全文
Dr. Nicoletta Brindani Dr. Gloria Rassu Dr. Luca Dell'Amico Dr. Vincenzo Zambrano Dr. Luigi Pinna Dr. Claudio Curti Dr. Andrea Sartori Prof. Dr. Lucia Battistini Prof. Dr. Giovanni Casiraghi Prof. Dr. Giorgio Pelosi Dr. Daniela Greco Prof. Dr. Franca Zanardi 《Angewandte Chemie (International ed. in English)》2015,54(25):7386-7390
A direct aminocatalytic synthesis has been developed for the chemo‐, regio‐, diastereo‐, and enantioselective construction of densely substituted polycyclic carbaldehydes containing fused cyclohexadiene rings. The chemistry utilizes, for the first time, remotely enolizable π‐extended allylidenemalononitriles as electron‐rich 1,3‐diene precursors in a direct eliminative [4+2] cycloaddition with both aromatic and aliphatic α,β‐unsaturated aldehydes. The generality of the process is demonstrated by approaching 6,6‐, 5,6‐, 7,6‐, 6,6,6‐, and 6,5,6‐fused ring systems, as well as biorelevant steroid‐like 6,6,6,6,5‐ and 6,6,6,5,6‐rings. A stepwise reaction mechanism for the key [4+2] addition is proposed as a domino bis‐vinylogous Michael/Michael/retro‐Michael reaction cascade. The utility of the malononitrile moiety as traceless activating group of the dicyano nucleophilic substrates is demonstrated. 相似文献