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排序方式: 共有114条查询结果,搜索用时 328 毫秒
1.
Mikko Keränen Marcin Gnyba Paavo Raerinne Terho Kololuoma Arto Maaninen Juha T. Rantala 《Journal of Sol-Gel Science and Technology》2004,31(1-3):369-372
Sol–gel adhesive material for isostatic hotpressing lamination process was synthesized using 3-aminopropyltrimethoxysilane (APTES), 3-glycidyloxypropyltrimethoxysilane (GPTS) and methacryloxypropyltrimethoxysilane (MPTS) as precursors. Reaction dynamics between APTES and GPTS was followed on-line with Raman spectroscopy. The lamination process was optimized by varying hotpressing times and pressures at the constant temperature. Mechanical shear strength properties were found to be excellent for studied composition, 25–30 kg/cm2 at its best. One possible application of laminated polycarbonate (PC) structure is a soldier helmet visor. Therefore, the ballistic protection properties were tested by shooting with 1.1 gram standard fragment, and determining the v50 velocity value, which corresponds to 50% perforation. The laminated structure gave 5.7% better protection compared with the solid polycarbonate. The laminated components were found to have high optical transparency at the visible wavelengths as well as high environmental stability. 相似文献
2.
The selenium(IV) diimide AdN=Se=NAd (Ad = 1-adamantyl) adopts a monomeric structure with a Z,E configuration in the solid state whereas the seleninylamine OSe(mu-NBut)2SeO crystallizes as the cis-dimer. 相似文献
3.
Both (±)-17α-hydroxytacamonine (3) and its 17β-isomer (4) were synthesized in two steps (one-pot) from aldehyde mixture 5/6 via the cyanohydrin reaction. NMR spectral characterization of isomer 3 revealed it to be unidentical with natural 17-hydroxytacamonine, whereas spectral data of isomer 4 were in agreement with those published for the natural isomer. The configuration at C-17 was confirmed by NOE difference spectroscopy. 相似文献
4.
The synthesis of aldehyde intermediates suitable for the preparation of indole alkaloids of the tacamine ( 1 ) type is described. The four possible aldehydes 4–7 were prepared from methyl 5-ethylnicotinate ( 8 ) in a few simple steps using a base-catalyzed epimerization as the final step (Schemes 1 and 2). The key aldehyde 4 , which is an analogue of the important vincamine intermediate 3 (‘Oppolzer's aldehyde’), was finally converted into the indole alkaloid (±)-apotacamine ( 21 ). 相似文献
5.
Rajendran Arunachalam Eswaran Chinnaraja Arto Valkonen Kari Rissanen Palani S. Subramanian 《应用有机金属化学》2019,33(11)
The multidentate ligand H2 L upon complexation with Zn (II) and Cd (II) provide a one‐dimensional polymeric networks. These coordination polymers (CPs) CP‐1 and CP‐2 containing Zn (II) and Cd (II) metals respectively are well characterized. The single crystal structural analysis confirms the formation of one‐dimensional coordination polymer with zigzag fashion in CP‐1 and ladder chain CP‐2 . Both the CPs are applied as catalysts to synthesize various cyclic carbonates from epoxides and carbon dioxide. The catalysts are giving better conversion under solvent‐free and additive‐free condition using 10 bar CO2 and 100 °C as optimized pressure and temperature. The detailed kinetic experiments suggesting the first order kinetics, the energy of activation (Ea) is calculated for this catalytic conversion. 相似文献
6.
Nikolaos Pahimanolis Arto Salminen Paavo A. Penttilä Juuso T. Korhonen Leena-Sisko Johansson Janne Ruokolainen Ritva Serimaa Jukka Seppälä 《Cellulose (London, England)》2013,20(3):1459-1468
In this paper, nanofibrillated cellulose/carboxymethyl cellulose (CMC) composite films were prepared using tape casting. The obtained transparent films showed shear induced partial alignment of fibrils along the casting direction, resulting in birefringence in cross polarized light. The carboxyl groups of CMC could be further utilized to create ionic crosslinking by treatment with glycidyl trimethyl ammonium chloride (GTMA). The GTMA treated composite films had improved mechanical properties both in wet and dry state. The chemical composition and morphologies of composites were analyzed with X-ray photoelectron spectroscopy, elemental analysis, scanning electron microscopy and wide-angle X-ray scattering. 相似文献
7.
For very large proteins in the highest magnetic fields, the large chemical shift anisotropy (CSA) of carbonyl carbon deteriorates coherence transfer efficiency in experiments designed for unambiguous sequential backbone assignment. In this communication, coherence throughput of several TROSY experiments is evaluated. Two new experiments, MP-HNCA and HN(CO)CANH, are also introduced as attractive alternatives for sequential assignment purposes of large proteins with correlation time over 50 ns. Their theoretical coherence transfer efficiencies for the interresidual (13)C(alpha) correlations are significantly better than in recently introduced MP-CT-HNCA and sequential HNCA experiments. The improvement with the new experiments is observed already on 60.8 kDa homodimer of protein Cel6A at 800 (1)H MHz. 相似文献
8.
Thin films of polyelectrolyte/J aggregate dye bilayers with high absorption coefficient (6 nm thick with alpha approximately equal to 1.0 x 10(6) cm(-1)) inserted in an optical microcavity enable the cavity quantum electrodynamic strong coupling limit to be reached at room temperature with a coupling strength (Rabi splitting) of 265 +/- 15 meV. By embedding these films in a resonant cavity organic LED structure, we demonstrate the first emissive electrically pumped exciton-polariton device. 相似文献
9.
Perttu Permi Sami Heikkinen Ilkka Kilpelinen Arto Annila 《Journal of magnetic resonance (San Diego, Calif. : 1997)》1999,139(2):273
1H-detected two-dimensional double-/zero-quantum experiments are described for measurement of homonuclear 2JHH-couplings of NH2 or CH2 groups in proteins. These experiments utilize multiple-quantum coherence for determination of the size and the absolute sign of the geminal scalar and dipolar couplings in the presence of broad lines. Spectra are simplified by gradient selection and spin-state selective filters. 相似文献
10.
Kalle Rnkk Mathias Berner Reija Jokela Arto Tolvanen 《Journal of heterocyclic chemistry》2000,37(5):1145-1149
The total syntheses of 11‐methoxydeethyleburnamonines ( 4 ) and ( 13 ) were carried out with use of 6‐methoxytryptophyl bromide ( 5 ) as starting material. Compound 5 was converted in three steps to trans‐ester 8 . Acid‐catalysed epimerization of 8 , lithium aluminum hydride reduction of the ester group, tosylation and substitution with cyanide gave the cis‐nitrile 12 . Acid‐induced cyclization of 12 yielded mainly (±)‐trans‐11‐methoxydeethyleburnamonine ( 13 ), whereas base‐induced cyclization gave (±)‐cis‐11‐methoxydeethyleburnamonine ( 4 ). 相似文献