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61.
Takashi Fujita Takao Yoshioka 《Journal of polymer science. Part A, Polymer chemistry》1982,20(6):1639-1647
Copolymerization of N-oxyl biradical with α-chloro-p-xylylene was carried out by varying the feed ratio of α,α′-dichloro-p-xylene which was the precursor of α-chloro-p-xylylene. The structures of the obtained copolymers were determined spectroscopically. The results that the N-oxyl attacked the carbon-bearing chlorine atom of α-chloro-p-xylylene suggest a nucleophilic reactivity of N-oxyl radical. The copolymerization process was also discussed. 相似文献
62.
The hydrogenation of benzaldehyde and cinnamaldehyde has been studied with a 5% Pt/C catalyst in compressed CO(2). The effect of CO(2) pressure on the total conversion was found to be different between the two aldehydes. The total conversion of benzaldehyde merely decreases with increasing CO(2) pressure, while that of cinnamaldehyde shows a maximum at a certain pressure. High-pressure FTIR measurements indicate the existence of interactions of CO(2) with the aldehydes. The absorption of nu(C=O) red-shifts at increasing CO(2) pressure, and this red-shift is more significant for cinnamaldehyde than for benzaldehyde, indicating that the C=O bond of the former becomes more reactive than the latter. The difference in the mode of interactions of CO(2) with these aldehydes has also been indicated by changes of nu(C=O) of CO(2). Thus, the conversion of benzaldehyde will decrease with increasing CO(2) pressure because of a simple dilution by introducing a larger quantity of CO(2). For cinnamaldehyde, the conversion will increase at low pressures because of increasing interactions with CO(2) molecules (increasing the reactivity of the C=O bond) but decrease at high pressures because of the simple dilution effect, similar to the case of benzaldehyde. The dense CO(2) molecules are not likely to change the catalytic activity of supported Pt particles, which was previously suggested from optical absorption of supported fine metal (Au) particles in a compressed CO(2) medium. 相似文献
63.
Silylcarbenes are generated by the pyrolysis of 1,1-bis(trimethylsilyl)-1-alkanols with elimination of trimethylsilanol. 相似文献
64.
Summary The “chemical” relaxation of stress either in Amilan (6-Nylon) or polyvinyl alcohol caused by penetration of water vapor was
studied at 40% R. H. and temperatures 15, 30, and 50° C. A theory was presented of the chemical relaxation in a polymer which
comprises penetrant-sensitive bonds as the crosslinkages between the molecular chains. This theory assumes the diffusion coefficient
of penetrant in the polymer to he independent of concentration and any other factors. It was found that the system Amilan-water
behaves in exact conformity with the theory over the ranges of elongation and temperature studied. The diffusion coefficient,D, of water in Amilan could thus be evaluated from the chemical relaxation data, using the theory presented, as functions of
elongation and temperature. An ordinary sorption experiment was carried out for this system at 40% R. H. and 16.8° C and demonstrated
that the diffusion of water in Amilan was Fickian with a constant diffusion coefficient. Both diffusion coefficients from
the chemical relaxation data and the sorption. data were found to agree quite well when the former was extrapolated to zero-strain.
The chemical relaxation behavior in the system polyvinyl alcohol-water was markedly different from that expected from the
theory, suggesting primarily that the diffusion coefficient of water in this polymer was not constant. A parallel evidence
for this fact was obtained from sorption measurements on this system, which demonstrated the diffusion in this system to be
dependent both on concentration and time.
From these results it may be concluded that the chemical relaxation technique, when combined properly with an adequate theory,
can be used not only to evaluate the diffusion coefficient of penetrant in a given polymer solid but also to investigate,
at least qualitatively, the type of sorption behavior characteristic of the system under given experimental conditions.
Zusammenfassung Die chemische Spannungsrelaxation in Amilan (6-Nylon) und Polyvinylalkohol, verursacht durch Eindringen von Wasserdampf, wurde bei 40% r. F. und Temperaturen von 15, 30 und 50° C untersucht. Es wird eine Theorie der chemischen Relaxation von Polymeren vorgelegt, die als empfindliche Bindungen auf das eindringende Niedermolekulare die Vernetzungen zwischen den molekularen Ketten betrachtet. Diese Theorie setzt voraus, da? der Diffusionskoeffizient im Polymeren für die eindringende Substanz unabh?ngig von Konzentration und anderen Faktoren ist. Das System Amilan-Wasser benimmt sich vollkommen entsprechend dieser Theorie in den studierten Verstreckungs- und Temperaturbereiche. Der Diffusionskoeffizient von Wasser in Amilan konnte daher aus der chemischen Relaxation als Funktion von Dehnung und Temperatur ausgewertet werden. Ein normales Quellungsexperiment wurde für das System bei 40% r. F. und 16,8° C ausgeführt und zeigte, da? die Diffusion von Wasser in Amilan dem Fickschen Gesetz mit konstantem Diffusionskoeffizienten folgt. Beide Diffusionskoeffizienten, der aus chemischer Relaxation und der aus Quellungsdaten gewonnene, stimmten sehr gut überein, falls der erstere auf die Dehnung 0 extrapoliert wurde. Die chemische Relaxation des Systems Polyvinylalkohol-Wasser war merklich anders als nach der Theorie erwartet und lie? in erster Linie vermuten, da? der Diffusionskoeffizient von Wasser in diesem Polymeren nicht konstant ist. Eine entsprechende Andeutung wurde aus Quellungsmessungen an diesem System erhalten. Die Diffusion h?ngt von Konzentration und Zeit ab. Aus diesen Resultaten kann gefolgert werden, da? die Technik der Untersuchungen der chemischen Relaxation unter Verwendung einer geeigneten Theorie nicht nur dazu angewendet werden kann, Diffusionskoeffizienten von kleinen Molekülen in einem gegebenen festen Polymeren zu messen, sondern zumindest auch qualitativ den Typ des Quellungsverhaltens festzustellen, der das System unter den gegebenen experimentellen Bedingungen charakterisiert.相似文献
65.
Yoshizawa M Nagao M Umemoto K Biradha K Fujita M Sakamoto S Yamaguchi K 《Chemical communications (Cambridge, England)》2003,(15):1808-1809
Despite their structural similarity, triangular tetradentate ligands 2b and 2c experience different assembly pathways on complexation with (en)Pd(NO3)2 to give M8L4 tetrahedral (3) and open cone (4) structures, respectively, due to steric restriction by side chains at the corner or on the edge of the ligands. 相似文献
66.
Shin-Ichi Hirano Toshinobu Yogo Ko-Ichi Kikuta Wataru Sakamoto 《Journal of Sol-Gel Science and Technology》1994,2(1-3):329-334
The sol-gel processing is one of promising methods to fabricate well-derived integrated thin films at relatively low temperature. Ferroelectric niobates films do afford the possibilities for adding the values by the hybridization with semiconductor and/or electro-optic systems. The molecular level designing of the precursor solution was stressed as well as the control of key processing factors. The advantages of this sol-gel have been extended to prepare the ferroelectric Pb(Mg, Nb)O3-PbTiO3 solid solution films integrated on Si wafers. The crystallization of the films with desired crystal structure could be promoted by the controlled partial hydrolysis of designed alkoxide solution in the intermediate state and the pre-heated treatment of alkoxide-derived films in flow of water vapor and oxygen gas mixture. 相似文献
67.
Masahiko Okada Keigo Aoi Wataru Mizuno Shinji Ito 《Journal of polymer science. Part A, Polymer chemistry》1993,31(5):1135-1140
New polyesters 6a–6c consisting of 2,4-linked tetrahydrofuran rings were synthesized by bulk polycondensation of methyl trans- and cis-4-hydroxytetrahydrofuran-2-carboxylates ( 5a and 5b ) and a stereoisomeric mixture of methyl 4-hydroxy-5-methyltetrahydrofuran-2-carboxylate ( 5c ) at high temperature. These monomers were prepared from methyl glycolate or methyl lactate and diethyl maleate through a four-step reaction sequence. The polycondensation was carried out without solvent at different temperatures ranging from 150 to 220°C. Titanium isopropoxide was most effective among the catalysts examined, giving polyesters with number-average molecular weights up to 2 × 104. Polyester 6a consisting of trans-2,4-linked tetrahydrofuran rings was soluble in trifluoroacetic acid and a mixed solvent of chloroform and methanol (10/1, v/v). Polyester 6b composed of cis-2,4-linked tetrahydrofuran rings was soluble in dimethyl sulfoxide and dimethylformamide in addition to the two solvents for 6a . Polyester 6c with 5-methyl-substituted tetrahydrofuran rings was composed of a mixture of stereoisomeric units and thus was soluble in a variety of solvents including chloroform, tetrahydrofuran, acetonitrile, dimethyl sulfoxide, and dimethylformamide. The glass transition temperatures of 6a, 6b , and 6c determined by DSC were 109, 88, and 66°C. These polyesters were found to be very slowly hydrolyzed in a neutral phosphate buffer solution at ambient temperature. © 1993 John Wiley & Sons, Inc. 相似文献
68.
Urata S Irisawa J Takada A Shinoda W Tsuzuki S Mikami M 《The journal of physical chemistry. B》2005,109(36):17274-17280
The membranes of a perfluorosulfonic acid polymer swollen in 10-80 wt % methanol solution were investigated to elucidate the methanol effect on their morphologies, such as size of the solvent cluster, solvent location, and polymer structure, by using isothermal-isobaric molecular dynamics simulations. In higher methanol concentrations, we found less-spherical solvent aggregation and a more spread polymer structure because of the ampholytic nature of methanol. The partial radial distribution functions between solvent oxygen and fluorocarbons, which are composed of the main chain, clearly show that methanol is located closer to the polymer matrix than water. On the other hand, water is preferentially located in the vicinity of an acidic headgroup, SO(3)(-), compared with methanol, although both have similar attractive interaction energies to the acidic group. Furthermore, we discussed solvent dynamics and hydrogen bonding between sulfonic oxygen and solvent O-H groups. 相似文献
69.
Sbin-Ichi Nagai Taisei Ueda Akito Nagatsu Keiko Nakaoka Nobutoshi Murakami Jinsaku Sakakibara Michiko Fujita Yoshihiro Hotta 《Journal of heterocyclic chemistry》1998,35(2):329-332
5,8-Methanoquinazolines fused with imidazoles 4a-4b , thiadiazoles 5–6 , pyrimidines 7, 9, 11 and 12 , and 1,3,5-triazine 13 were prepared starting from (5R,8S)-2-amino-8,9,9-trimethyl-5,6,7,8-tetrahydro-5,8-methanoquinazoline 3 . Most compounds possessed central nervous system stimulant activities. 相似文献
70.
Tomoko Sotomatsu Yoshiyuki Murata Toshio Fujita 《Journal of computational chemistry》1991,12(1):135-138
The AM1 calculation was done for ortho-substituted toluenes (o-X-C6H4-CH3) and ortho-substituted tert-butylbenzenes (o-X-C6H4-t-Bu). The difference in the calculated heat of formation between o-X-C6H4-CH3 and o-X-C6H4-t-Bu was used as a theoretical steric index for ortho-X. The correlation of this theoretical steric index with the empirical steric parameter sets such as our recently defined Es(AMD) and the Taft–Kutter–Hansch (TKH) Es was examined. In spite of the simplicity of the model system, the theoretical index was linear with the Es(AMD) constant with a correlation coefficient of r = 0.972 for 17 substituents of various structures. Including the phenyl group, the correlation with the TKH Es constant was r = 0.948. The theoretically calculated index was shown to serve as a measure of the ortho steric effect. 相似文献