排序方式: 共有23条查询结果,搜索用时 15 毫秒
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E. Berl K. Hofmann R. Bemmann E. G. Belmann L. N. Markwood G. H. W. Lucas L. Chalkey Jr. H. Tramm F. W. Horst F. Heinrich H. Bach L. R. Bryant A. W. Francis A. Simon F. Fehèr L. Köhler H. Mendel M. Schlesinger Z. Blaszkowska E. R. Caley J. B. Brown D. F. Othmer König H. Wollenberg Greiner & Freidrichs H. Liesegang B. A. Soule F. C. Mathers A. Karsten K. Hickmann und F. L. Robeson 《Fresenius' Journal of Analytical Chemistry》1930,81(5-7):216-227
Ohne Zusammenfassung 相似文献
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W. Hempel C. Paal W. Hartmann G. A. Burrell G. G. Oberfell O. Brunck Mathers J. E. Lee J. W. Robertson F. M. Seibert P. Lebeau A. Damiens O. Brunck L. A. Levy F. St. Sinnatt B. J. Cramer E. H. Weiskopf J. I. Graham Th. F. Winmill F. Haber F. Löwe O. Mohr R. L. von Klemperer O. Wolft E. Müller E. Reinhardt J. N. Pring Juan Calafat y Leon M. Guichard R. Nowicki John J. Griffin A. Sons L. Hamburger H. Filippo Izn Ch. Moureau G. Lunge und A. Rittener 《Fresenius' Journal of Analytical Chemistry》1915,54(10):504-509
Ohne Zusammenfassung 相似文献
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W. Hempel C. Paal W. Hartmann G. A. Burrell G. G. Oberfell O. Brunck Mathers J. E. Lee J. W. Robertson F. M. Seibert P. Lebeau A. Damiens O. Brunck L. A. Levy F. St. Sinnatt B. J. Cramer E. H. Weiskopf J. I. Graham Th. F. Winmill F. Haber F. Löwe O. Mohr R. L. von Klemperer O. Wolft E. Müller E. Reinhardt J. N. Pring Juan Calafat y Leon M. Guichard R. Nowicki John J. Griffin A. Sons L. Hamburger H. Filippo Izn Ch. Moureau G. Lunge A. Rittener 《Analytical and bioanalytical chemistry》1915,54(10):504-509
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A. Kisliuk R. T. Mathers A. P. Sokolov 《Journal of Polymer Science.Polymer Physics》2000,38(21):2785-2790
Light scattering spectra of two polymers, polyisobutylene (PIB) and polystyrene (PS), were analyzed in the broad frequency range at temperatures above the glass transition (Tg ). At high temperatures, the spectra followed the qualitative scenario suggested by mode‐coupling theory (MCT) of the glass transition. The crossover temperature (Tc ) was defined to be approximately 1.35 Tg in PIB and approximately 1.15 Tg in PS. At lower temperatures (T < Tc ), the light scattering spectra deviated strongly from the idealized MCT scenario. Different signs of the dynamic transition around Tc are discussed. The difference between the suggested interpretation and an old idea of the liquid–liquid transition in polymeric liquids is stressed: we describe the transition as purely dynamic in nature. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 2785–2790, 2000 相似文献
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Paul W.C CrossGeorge J Ellames Jennifer S GibsonJohn M Herbert William J KerrAlan H McNeill Trevor W Mathers 《Tetrahedron》2003,59(18):3349-3358
A series of iridium-based complexes formed in situ, containing pyridine, phosphines, triphenylarsine, triphenylstibine, and triphenylamine as ligands, has been screened for ability to mediate ortho-exchange of hydrogen in a series of model substrates. Improved incorporation into a number of substrate classes has been achieved. The electronic properties and number of ligands at the metal centre are instrumental in determining which catalysts are best suited to exchange in any given substrate. 相似文献
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Roderic P. Quirk Tae-Hee Cheong Kevin Jiang Deanna L. Gomochak Taejun Yoo Keith T. Andes Robert T. Mathers 《Macromolecular Symposia》2003,195(1):69-74
Recent results for the preparation of chain-end functionalized polymers using alkyllithium-initiated anionic polymerization are described. Termination with 4-chloro-1,1,1-trimethoxybutane has been used to prepare trimethoxy ortho ester (carboxyl)-functionalized polymers. Functionalization with the oxiranes, glycidoxypropyltrimethoxysilane, 3,4-epoxy-1-butene and 1,1,1-trifluoro-2,3-epoxypropane, has been investigated to prepare trimethoxysilyl-functionalized polymers, 1,3-diene-functionalized macro monomers and trifluoromethyl-functionalized polymers, respectively. Secondary amine-functionalized polymers have been prepared by termination with N-(benzylidene)methylamine and also using an N-benzyl tertiary amine-functionalized alkyllithium initiator followed by hydrogenolysis of the benzyl group. 相似文献
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This highlight discusses the recent progress aimed at maximizing the potential of biomass for commodity monomers and polymers. These efforts are no longer solely academic issues. In recent years, a variety of alkene, diene, aromatic, and condensation type monomers have utilized renewable resources, such as cellulose, lignin, plant oils, starches, and monoterpenes in commercial polymers. Generally, these multifaceted efforts involve pretreatment of biomass with thermal, chemical, or physical methods followed by a catalyst sequence that entails a combination of acid‐catalysis, bio‐catalysis, or metal‐based catalysis. In this regard, synthesis strategies for ethylene, propylene, α‐olefins, methylmethacrylate, 1,3‐butadiene, 1,3‐cyclohexadiene, isoprene, 1,3‐propanediol, 1,4‐butanediol, and terephthalic acid are discussed as well as opportunities for other renewable‐based monomers. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
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Justin M. Delancey Matthew D. Cavazza Matthew G. Rendos Cory J. Ulisse Susan G. Palumbo Robert T. Mathers 《Journal of polymer science. Part A, Polymer chemistry》2011,49(17):3719-3727
Renewable resources have been utilized to control the degree of crosslinking during ring‐opening metathesis polymerizations (ROMP). In this regard, the addition of monoterpenes to thermosets created a sustainable method for adjusting the physical properties and thermal stability. A number of monoterpenes with alkenes were examined as monofunctional reactants. The presence of these monoterpenes, such as β‐pinene, during the ROMP of dicyclopentadiene altered the degree of crosslinking and plasticized the thermoset. The resulting physical properties were tailored to obtain desired modulus and glass transition (Tg) temperatures. The influence of time, temperature, weight percent β‐pinene, and different metathesis catalysts was examined by dynamic mechanical analysis, thermogravimetric analysis, and FTIR spectroscopy. A comparison of β‐pinene with other monoterpenes, such as carvone, limonene oxide, myrcene, and d‐limonene, resulted in a reactivity profile for this general method. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
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