全文获取类型
收费全文 | 82篇 |
免费 | 0篇 |
专业分类
化学 | 61篇 |
晶体学 | 2篇 |
数学 | 6篇 |
物理学 | 13篇 |
出版年
2023年 | 2篇 |
2022年 | 4篇 |
2021年 | 2篇 |
2020年 | 2篇 |
2017年 | 1篇 |
2014年 | 6篇 |
2013年 | 1篇 |
2012年 | 5篇 |
2011年 | 2篇 |
2010年 | 2篇 |
2008年 | 5篇 |
2007年 | 4篇 |
2006年 | 5篇 |
2005年 | 3篇 |
2004年 | 3篇 |
2003年 | 5篇 |
2001年 | 1篇 |
1999年 | 4篇 |
1997年 | 2篇 |
1996年 | 1篇 |
1993年 | 2篇 |
1992年 | 2篇 |
1985年 | 1篇 |
1983年 | 3篇 |
1980年 | 5篇 |
1973年 | 1篇 |
1967年 | 2篇 |
1965年 | 1篇 |
1964年 | 1篇 |
1962年 | 1篇 |
1933年 | 2篇 |
1931年 | 1篇 |
排序方式: 共有82条查询结果,搜索用时 15 毫秒
1.
2.
Zusammenfassung Die Darstellung sämtlicher am mittleren Benzolkern p-substitutierten Verbindungen (C6H5)2
MC6H4
M(C6H5)2 mitM=N, P, As, Sb und Bi wird beschrieben. Für die bereits bekannte Stickstoff-bzw. Arsen-Verbindung konnte ein neuer Darstellungs-weg mit guten Ausbeuten gefunden werden, während die Antimon-und Wismutverbindung erstmals beschrieben werden. Durch Dipolmomentmessungen, UV- und IR-Aufnahmen ist ein Vergleich mit den einfachen Triphenylderivaten der genannten Elemente möglich.
Herrn Prof. Dr.F. Wessely zum 70. Geburtstag gewidmet. 相似文献
The compounds p-(C6H5)2 MC6H4 M(C6H5)2,M=N, P, As, Sb, and Bi, were prepared. New methods for the preparation of the N and As compound with good yields were found. The Sb and Bi compound were synthesized for the first time. Dipole moments, IR- and UV-spectra of these compounds were compared with those of the triphenyl derivates.
Herrn Prof. Dr.F. Wessely zum 70. Geburtstag gewidmet. 相似文献
3.
4.
Characterization of modified low density lipoprotein subfractions by capillary isotachophoresis 总被引:4,自引:0,他引:4
Zorn U Haug C Celik E Wennauer R Schmid-Kotsas A Bachem MG Grünert A 《Electrophoresis》2001,22(6):1143-1149
Oxidative modification of low density lipoproteins (LDLs) is an important pathogenetic factor in atherosclerosis. The various steps in oxidative modifications of LDL can be monitored using different methodologies with varying degrees of complexity. In this study, we propose capillary isotachophoresis (CITP) as a suitable tool to detect and measure the degree of oxidation of LDL. LDL was isolated from pooled plasma of healthy volunteers by sequential ultracentrifugation, and oxidation was performed in vitro as well as in cell culture experiments. Native LDL and oxidatively modified LDL were characterized by apo B-100 fluorescence and conjugated diene formation. Samples were separated by CITP combined with sudan black B staining. To underline the inherent advantages of this approach, CITP was compared with classical lipoprotein electrophoresis using agarose gel. We demonstrate the CITP method to be highly sensitive, as changes in peak area of the separated LDL subfractions were detected after only 2 h of oxidation. The leading LDL peaks increased, while the terminating LDL peaks decreased in parallel throughout the duration of oxidation. The LDL samples, oxidized for 4-24 h, also exhibited an increased migration velocity of the fractions. In summary, we present the first study investigating LDL-subfractions separated by CITP and the alterations of these LDL-subfractions after gradual in vitro oxidation and after oxidative modification by monocyte-derived macrophages and vascular smooth muscle cells. 相似文献
5.
Zorn G Baio JE Weidner T Migonney V Castner DG 《Langmuir : the ACS journal of surfaces and colloids》2011,27(21):13104-13112
Biointegration of titanium implants in the body is controlled by their surface properties. Improving surface properties by coating with a bioactive polymer is a promising approach to improve the biological performance of titanium implants. To optimize the grafting processes, it is important to fully understand the composition and structure of the modified surfaces. The main focus of this study is to provide a detailed, multitechnique characterization of a bioactive poly(sodium styrene sulfonate) (pNaSS) thin film grafted from titanium surfaces via a two-step procedure. Thin titanium films (~50 nm thick with an average surface roughness of 0.9 ± 0.2 nm) prepared by evaporation onto silicon wafers were used as smooth model substrates. X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) showed that the titanium film was covered with a TiO(2) layer that was at least 10 nm thick and contained hydroxyl groups present at the outermost surface. These hydroxyl groups were first modified with a 3-methacryloxypropyltrimethoxysilane (MPS) cross-linker. XPS and ToF-SIMS showed that a monolayer of the MPS molecules was successfully attached onto the titanium surfaces. The pNaSS film was grafted from the MPS-modified titanium through atom transfer radical polymerization. Again, XPS and ToF-SIMS were used to verify that the pNaSS molecules were successfully grafted onto the modified surfaces. Atomic force microscopy analysis showed that the film was smooth and uniformly covered the surface. Fourier transform infrared spectroscopy indicated that an ordered array of grafted NaSS molecules were present on the titanium surfaces. Sum frequency generation vibration spectroscopy and near edge X-ray absorption fine structure spectroscopy illustrated that the NaSS molecules were grafted onto the titanium surface with a substantial degree of orientational order in the styrene rings. 相似文献
6.
Schönhals A Goering H Schick Ch Frick B Zorn R 《The European physical journal. E, Soft matter》2003,12(1):173-178
The glassy dynamics of poly(propylene glycol) (PPG) and poly(dimethyl siloxane) (PDMS) confined to a nanoporous host system revealed by dielectric spectroscopy, temperature-modulated DSC and neutron scattering is compared. For both systems the relaxation rates estimated from dielectric spectroscopy and temperature-modulated DSC agree quantitatively indicating that both experiments sense the glass transition. For PPG the segmental dynamics is determined by a counterbalance of adsorption and confinement effect. The former results form an interaction of the confined macromolecules with the internal surfaces. A confinement effect originates from an inherent length scale on which the underlying molecular motions take place. The increment of the specific-heat capacity
at the glass transition vanishes at a finite length scale of 1.8 nm. Both results support the conception that a characteristic length scale is relevant for glassy dynamics. For PDMS only a confinement effect is observed which is much stronger than that for PPG. Down to a pore size of 7.5 nm, the temperature dependence of the relaxation times follows the Vogel-Fulcher-Tammann dependence. At a pore size of 5 nm this changes to an Arrhenius-like behaviour with a low activation energy. At the same pore size
vanishes for PDMS. Quasielastic neutron scattering experiments reveal that also the diffusive character of the relevant molecular motions --found to be characteristic above the glass transition-- seems to disappear at this length scale. These results gives further strong support that the glass transition has to be characterised by an inherent length scale of the relevant molecular motions.Received: 1 January 2003, Published online: 14 October 2003PACS:
64.70.Pf Glass transitions - 77.22.Gm Dielectric loss and relaxation - 61.25.Hq Macromolecular and polymer solutions; polymer melts; swelling 相似文献
7.
A. Schönhals H. Goering C. Schick B. Frick M. Mayorova R. Zorn 《The European physical journal. Special topics》2007,141(1):255-259
The effect of a nanometer confinement on the molecular
dynamics of poly(methyl phenyl siloxane) (PMPS) was studied by
dielectric spectroscopy (DS), temperature modulated DSC (TMDSC) and
neutron scattering (NS). Nanoporous glasses with pore sizes of
2.5–20 nm have been used. DS and TMDSC experiments show that for
PMPS in 7.5 nm pores the molecular dynamics is faster than in the
bulk which originates from an inherent length scale of the
underlying molecular motions. For high temperatures the temperature
dependence of the relaxation rates for confined PMPS crosses that of
the bulk state. Besides finite states effects also the thermodynamic
state of nano-confined PMPS is different from that of the bulk. At a
pore size of 5 nm the temperature dependence of the relaxation
times changes from a Vogel/Fulcher/Tammann like to an Arrhenius
behavior where the activation energy depends on pore size. This is
in agreement with the results obtained by NS. The increment of the
specific heat capacity at the glass transition depends strongly on
pore size and vanishes at a finite length scale between 3 and 5 nm
which can be regarded as minimal length scale for glass transition
to appear in PMPS. 相似文献
8.
This work considers the global optimization of general nonconvex nonlinear and mixed-integer nonlinear programming problems with underlying polynomial substructures. We incorporate linear cutting planes inspired by reformulation-linearization techniques to produce tight subproblem formulations that exploit these underlying structures. These cutting plane strategies simultaneously convexify linear and nonlinear terms from multiple constraints and are highly effective at tightening standard linear programming relaxations generated by sequential factorable programming techniques. Because the number of available cutting planes increases exponentially with the number of variables, we implement cut filtering and selection strategies to prevent an exponential increase in relaxation size. We introduce algorithms for polynomial substructure detection, cutting plane identification, cut filtering, and cut selection and embed the proposed implementation in BARON at every node in the branch-and-bound tree. A computational study including randomly generated problems of varying size and complexity demonstrates that the exploitation of underlying polynomial substructures significantly reduces computational time, branch-and-bound tree size, and required memory. 相似文献
9.
T. Hannappel S. Visbeck K. Knorr J. Mahrt M. Zorn F. Willig 《Applied Physics A: Materials Science & Processing》1999,69(4):427-431
For the first time direct contamination-free transfer to UHV was achieved for the P-rich InP(100) surface that is the easiest
to prepare and control in the MOCVD environment. To avoid contamination during transfer a commercial MOCVD apparatus was modified
to allow for transfer of samples to the 10-9 mbar UHV range within a very short time (less than 20 s) [1]. Epitaxial InP(100) films were prepared with TBP (tertiarybutylphosphine)
and TMIn (trimethylindium) as precursors. In situ reflectance anisotropy spectroscopy (RAS) was carried out in the MOCVD environment.
After transfer of the sample to UHV the same RAS spectrum was recovered. Auger-electron spectra (AES) confirmed the P-termination
of the surface reconstructions suggested by RAS.
Received: 19 October 1998 / Accepted: 21 April 1999 / Published online: 14 July 1999 相似文献
10.
Anna‐Marie Zorn Christopher Barner‐Kowollik 《Journal of polymer science. Part A, Polymer chemistry》2012,50(12):2366-2377
In the present study, n‐butyl acrylate macromonomer (BAMM) (Mn = 1900 g mol?1; PDI = 1.96) has been synthesized via a high‐temperature polymerization process. Subsequently, the olefinic termini of the BAMM have been transformed into a diol via a dihydroxylation process using KMnO4 as an oxidizing agent. The OH‐terminated macroinitiator pBA(OH)2 has subsequently been employed for the ring‐opening polymerization (ROP) of ε‐caprolactone via various catalytic systems, that is, organo‐(1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene), metal (tin(II) 2‐ethylhexanoate), and enzymatic catalysis (Novozym® 435). The obtained pBA‐b‐pCL block copolymers and the initiation efficiency of the BAMM macroinitiator have been investigated via size exclusion chromatography (SEC), electrospray ionization–mass spectrometry (ESI‐MS) hyphenated with SEC and liquid chromatography at the critical conditions of both poly(ε‐caprolactone) (pCL) and pBA. The in vitro enzyme catalysis (eROP) approach proved to be the most efficient catalysis system due to minor transesterification side reactions during the polymerization process. However, side reactions such as transesterifications occur in each catalytic system and—while they cannot be suppressed—they can be minimized. The species generated during the eROP process include the desired block copolymer pBA‐b‐pCL as main species as well as pCL homopolymer and residual macroinitiator pBA(OH)2. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献