共查询到20条相似文献,搜索用时 15 毫秒
1.
Joseph P. Kennedy Kenneth F. Castner 《Journal of polymer science. Part A, Polymer chemistry》1979,17(7):2039-2054
The reaction between tert-butylchloride (t-BuCl) and dimethylcyclopentadienylaluminum (Me2AlCPD) was studied as a model for initiation by the tert-butyl cation (t-Bu⊕) and termination by cyclopentadienylation by the Me2Al(CPD)Cl? counteranion of isobutylene polymerization. All reaction products formed in this model system have been identified and quantitatively determined. A comprehensive scheme that indicates pathways to these products was developed (scheme III). It is proposed that the predominant product, tert-butylcyclopentadiene (t-BuCPD), arises in the collapse of the t-Bu⊕-Me2Al(CPD)Cl? ion pair, mainly by CPD? transfer to the tert-butyl cation. The minor products are neopentane (t-BuMe) and isobutylene (i-C4H8), which are probably formed, respectively, by Me? transfer to and proton loss from the t-butyl cation. Cyclopentadienylation selectivity increases by lowering the temperature and extrapolation of results suggests 100% cyclopentadienylation at ?55°C. The t-BuCl/Me2AlCPD ratio strongly influences the overall reaction pathway. The reaction is first order in t-BuCl with ΔEa of ca. 7 kcal/mole (1,2-dichloroethane or chlorobenzene solvents, +24 to ?29°C). Indirect evidence indicates that the kinetic product of cyclopentadienylation is 5-t-BuCPD and that this isomer cannot be tert-butylated; that is, the initiation of 5-t-BuCPD polymerization by t-Bu⊕ is sterically unfavorable. Detailed analysis of the chemistry and kinetics of the t-BuCl/Me2AlCPD model system holds important clues to the controlled polymerization of olefins leading to macromolecules with cyclopentadiene (CPD) termini. 相似文献
2.
The stepwise addition polymerization reactions of bisazlactones [bis(2-oxazolin-5-one)s] and a variety of 4,4′-bisphenols have been studied for the purpose of making thermally reversible linear polymers. Thus polymerization occurs at or near room temperature, while depolymerization yielding the two monomer species occurs at elevated temperatures. The synthesis of oligomers in solution without the use of catalyst occurs for the reaction of bisazlactones with bisphenols containing an electron-withdrawing moiety between the two phenol groups of the bisphenol. These oligomers regenerate the bisphenol and bisazlactone monomers upon heating to 165–200°C for several hours under dry box conditions. In many cases, these reactions follow the same patterns of reactivity observed in model studies. This chemistry may be useful for forming degradable or recyclable polymers, where shortchain prepolymers, or macromonomers, endcapped with azlactone and phenol moieties could be used to form high molecular weight polymers that are thermoreversible. Such a reaction system might also be used for preventing reactions of bisphenols and/or bisazlactones at low temperatures, with the desired reaction initiated by formation of the reactive species at elevated temperatures. Envisioned uses in this case might be thermally triggered crosslinking or polymerization reactions, or temperature controlled drug release. © 1993 John Wiley & Sons, Inc. 相似文献
3.
Xiaonong Chen Eli Ruckenstein 《Journal of polymer science. Part A, Polymer chemistry》1999,37(23):4390-4401
A novel crosslinker for thermally reversible covalent (TRC) linking of halide-containing polymers is suggested. Chlorine-containing polymers such as chloromethylstyrene copolymers, chlorinated polypropylene, polyvinylchloride, chlorinated polyisoprene, and polyepichlorohydrin were crosslinked with potassium dicyclopentadienedicarboxylate (KDCPDCA). The crosslinker was prepared by reacting potassium ethoxide with dicyclopentadienedicarboxylic acid. Because of the low solubility of KDCPDCA in organic solvents, a phase transfer catalyst, benzyltrimethyl-ammonium bromide, was employed for the crosslinking reaction. The crosslinking reaction occurred at a higher rate in a polar solvent, such as dimethylformamide, than in a nonpolar one, such as toluene, and was affected by the nature of the chlorine-containing polymer. Some of the polymers crosslinked even at room temperature. The chain-extending reaction between KDCPDCA and a α,ω-dihalide compound such as α,α′-dichloro-p-xylene, 1,4-dichlorobutane, or 1,4-dibromobutane also was carried out to obtain linear oligomers. The IR spectra indicated that the crosslinking and chain-extending reactions were based on the esterification between the halide carbon bonds of the polymer and the COOK groups of KDCPDCA. The flowability at 195 °C and solubility on heating in a dichlorobenzen-maleic compound mixture of the crosslinked polymers indicated that the TRC crosslinking occurred via the reversible Diels–Alder cyclopentadiene/dicyclopentadiene conversion as long as the polymer was thermally stable and did not contain olefinic CC bonds. The TRC linking also was confirmed by the rapid decrease of the specific viscosity of the obtained linear oligomers on heating. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 4390–4401, 1999 相似文献
4.
As an approach to replacing islets of Langerhans in an implanted biohybrid artificial pancreas, thermally reversible polymers based on N-isopropylacrylamide were synthesized and then evaluated as an extracellular matrix for islets in an immunoprotecting membrane pouch. A high molecular weight poly(N-isopropylacrylamide-co-acrylic acid (2 mole % in feed)) demonstrated gelation at 37°C and became a solution below 30°C. This polymer exhibited minimum syneresis (water separation) upon gelation from a solution state when the temperature was raised from room temperature to 37°C, while poly(N-isopropylacrylamide) exhibited considerable syneresis under the same conditions. These properties influence the efficiency of islet entrapment. The copolymer was able to entrap rat islets almost 100%, but the homopolymer entrapped less than 50%. The static insulin secretion of the islets in the copolymer matrix at high glucose concentration (16.5 mM) was comparable to that of control islets, however, the entrapped islets showed prolonged viability in vitro. These results indicate the potential of developing a rechargeable biohybrid pancreas using thermally reversible polymer gels. 相似文献
5.
Thermally reversible formation of microspheres through non-covalent polymer cross-linking 总被引:3,自引:0,他引:3
Thibault RJ Hotchkiss PJ Gray M Rotello VM 《Journal of the American Chemical Society》2003,125(37):11249-11252
Bis-thymine units were used to noncovalently cross-link a complementary diamidopyridine-functionalized copolymer. Upon combination in noncompetitive solvents, discrete micron-scale spherical aggregates were formed arising from specific three-point polymer-cross-linker hydrogen bonding interactions. The diameter of these microspheres could be controlled through spacer structure. The cross-linking process was fully thermally reversible, with complete dissolution observed at 50 degrees C and reformation of the aggregates upon return to ambient temperature. This process could be repeated multiply, with lower particle dispersity observed arising from the annealing process. 相似文献
6.
Howard C. Haas Robert D. Moreau Norman W. Schuler 《Journal of Polymer Science.Polymer Physics》1967,5(5):915-927
The homopolymer and many of the copolymers of N-acrylylglycinamide yield thermally reversible gels in water. These systems are uniquely suitable for studying synthetic photographic gelatin substitutes and for understanding the mechanism of the gelation process. Polymerization of N-acrylylglycinamide has been studied under a variety of conditions. The homopolymer is aggregated in dilute aqueous solution and probably molecularly dispersed in 2M thiocyanate solution. At concentrations of several per cent, in water, thermally reversible gels are formed whose melting points rise with increasing concentration and increasing molecular weight. The heat of gelation crosslinking has been calculated to be ?8.8 kcal./mole of crosslinks. Introduction of small amounts of carboxyl groups into the polymer raises the melting points of the aqueous gels. The effect of various organic and inorganic reagents on gelation is presented. The ability to prepare copolymers which can be flocculated has been demonstrated as well as the usefulness of the monomer in certain types of photoresist systems. Copolymerization with acrylic acid and β-aminoethyl vinyl ether has been studied, and the r1 and r2 values for these systems have been calculated as well as Q and e values for N-acrylylglycinamide. 相似文献
7.
Replaceable sieving polymers are the fundamental component for high‐resolution nucleic acids separation in CE. The choice of polymer and its physical properties play significant roles in influencing separation performance. Recently, reversible addition fragmentation chain transfer (RAFT) polymerization has been shown to be a versatile polymerization technique capable of yielding well‐defined polymers previously unattainable by conventional free‐radical polymerization. In this study, a high molecular weight poly‐(N,N‐dimethylacrylamide) (PDMA) at 765 000 gmol?1 with a polydispersity index of 1.55 was successfully synthesized with the use of chain transfer agent—2‐propionic acidyl butyl trithiocarbonate in a multistep sequential RAFT polymerization approach. This study represents the first demonstration of RAFT polymerization for synthesizing polymers with the molecular weight range suitable for high‐resolution DNA separation in sieving electrophoresis. Adjustment of pH in the reaction was found to be crucial for the successful RAFT polymerization of high molecular weight polymer as the buffered condition minimizes the effect of hydrolysis and aminolysis commonly associated with trithiocarbonate chain transfer agents. The separation efficiency of 2‐propionic acidyl butyl trithiocarbonate PDMA was found to have marginally superior separation performance compared to a commercial PDMA formulation, POP?‐CAP, of similar molecular weight range. 相似文献
8.
The water permeability K1 [which is related to water flux J1 per unit membrane area by J1 = K1(Δp ? ΔII)/ΔX, where Δp is the pressure difference, ΔII is the osmotic pressure of feed solution, and ΔX is the membrane thickness] of homogeneous ionic polymer membranes in reverse osmosis and their salt rejection Rs [which is given by Rs ≡ 1 ? (C2″/C2′), where C2′ is the concentration of the salt in feed solution, and C2″ is the concentration of salt in effluent] were examined with cationic and anionic membranes of block and graft copolymers. For ionic membranes, Rs and K1 are related by K1 = A exp { ? BRs}, where A and B are constants. This equation was found to be independent of the ion charge, the chemical nature of the polymer, and film morphology. The principle of salt rejection by ionic membranes was explained by the difference in the transport volumes (volume elements available for transport) for mobile co-ions and water. The electric repulsive force between a fixed ion and a mobile co-ion decreases the transport volume of the latter, thus creating a transport depletion of salt flux relative to water transport. This transport depletion is governed by the amount of water sorbed by a fixed ionic site, which also determines the water flux. Consequently, Rs and K1 for ionically charged membranes are related as described above. This relation significantly differs from that found between Rs and K1 for nonionic polymer membranes, where the size and the solubility of ions in the membrane are mainly responsible for the transport depletion. The decline of Rs with increasing K1 is much less in ionic membranes than in nonionic ones; however, in the high Rs region, K1 for both ionic and nonionic membranes become similar as the dominant mode of water transport changes from flow to diffusion. 相似文献
9.
Large photocurrents have been observed in films of some simple polymers (containing no π-orbitals), of which poly(vinyl fluoride) is a typical example. Not only are the currents large (up to 10?5 A/cm2) but also they are capable of being excited by light in the visible wavelength region where absorption by the polymer is too low to be detectable. The results indicate that the effects are electronic, rather than ionic, in nature. 相似文献
10.
Kenneth A. Kun 《Journal of polymer science. Part A, Polymer chemistry》1966,4(4):847-857
A series of redox polymers was prepared by the addition of different redox groups to preformed, chloromethylated macroreticular styrene–divinylbenzene copolymers. These polymers contained the hydroquinone, hydroquinonesulfonic acid, methylhydroquinone, 2,5-dimethylhydroquinone, 2,5-dimethylhydroquinonesulfonic acid, 2,3,5-trimethylhydroquinone, tert-butylhydroquinone, chlorohydroquinone, benzyl mercaptan, anthraquinone, and the pyrogallol redox groups. Thus, a set of redox polymers is available having redox potentials that may range from approximately 150 to 700 mv. 相似文献
11.
Pietro Maravigna 《Journal of polymer science. Part A, Polymer chemistry》1988,26(9):2475-2485
Polycondensation of bisphenol A, hydroquinone, or dihydroxynaphthalenes with glyoxal using methane sulphonic acid as condensing agent leads to polymeric materials having linear and ladder structure and high thermal stability. These polymers were characterized by NMR and TG. Oligomers (from dimer to tetramer) were isolated by GPC and their structures characterized. 相似文献
12.
Serguei Skorokhodov 《Macromolecular Symposia》1998,128(1):145-154
An approach to the synthesis of potentially thermotropic liquid crystalline polymers based on parallel investigation of their molecular mobility was realized. The initial idea was provoked by the observation that there exists some correspondence of molecular mobility data and the ability of a polymer to form a liquid crystalline phase. Previously this phenomenon was demonstrated on the example of a series of thermotropic main chain polymers with flexible dimethylsiloxane spacers of variable length. The relation between the structure of the main chain and local molecular mobility of different fragments was investigated in a series of regular polysiloxane-silarylenes containing rigid aromatic sequences. Molecular mobility was studied by dielectric spectroscopy in solution and in solid state. The structure of the main chain has been changed by variation of the repeated fragments' length, substituents and joint groups. The data of molecular mobility and their conformity with the chain structure were used for directed synthetic search of desired mesogenic polymers. 相似文献
13.
14.
H. X. Xiao K. C. Frisch H. L. Frisch 《Journal of polymer science. Part A, Polymer chemistry》1984,22(5):1035-1042
Interpenetrating polymer networks (IPNs) with opposite charge groups (tertiary amine and carboxyl groups) made from polyurethanes and methacrylate polymers have been synthesized and their properties and morphology, studied. With increasing carboxyl group concentration the mechanical properties and compatibility between the component networks were significantly improved, possibly because of the negative (or zero) free energy produced by the interaction contribution between the tertiary amine groups in the polyurethanes and the carboxyl groups in the methacrylate polymers determined by differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The improved molecular mixing in these IPNs was thought to be due to the influence of the opposite charge groups in these systems. 相似文献
15.
Gunther E. Molau Henno Keskkula 《Journal of polymer science. Part A, Polymer chemistry》1966,4(6):1595-1607
A mechanism for the formation of rubber particles in the polymerization of solutions of rubber in vinyl monomers is presented. A polymeric oil-in-oil emulsion is formed in the first phase of the polymerization. This polymeric oil-in-oil emulsion is transtormed into a solid dispersion of rubber in vinyl polymer in the second phase of the polymerization. A phase inversion takes place in the emulsion in the first phase of the polymerization. Rubber solution droplets are formed at the phase inversion point. These droplets harden as the polymerization proceeds and are gradually transformed into the solid, crosslinked rubber particles of the final polymer. 相似文献
16.
Walther Burchard 《Macromolecular Symposia》1990,39(1):179-195
The forward scattering of light allows determination of the osmotic modulus (=inverse osmotic compressibility), which in good solvents is a measure of repulsive forces among the particles in solution but also depends on the molar mass of the particle. The osmotic modulus increases with concentration if the particle weight remains constant. The increase differs for particles of different architecture and can for c < 3c* be described by structure specific g-factors, where g is defined through A3=gA22 Mw with A2 and A3 being the 2nd and 3rd virial coefficients. For associating systems in a good solvent also the particle weight increases with c. A procedure is suggested which allows within limits a correction of the measured apparent molar mass M̄app (c) for the true molar mass M̄w (c) at the concentration c. Three examples are discussed in detail. 相似文献
17.
Xiaonong Chen Eli Ruckenstein 《Journal of polymer science. Part A, Polymer chemistry》2000,38(9):1662-1672
Alkali and earth‐alkali salts of dicyclopentadiene dicarboxylic acid (DCPDCA) were prepared and employed as monomers in the polyesterification with an α,ω‐dihalide monomer, such as 1,4‐dichlorobutane (DCB), 1,4‐dibromobutane (DBB), α,α′‐dichloro‐p‐xylene (DCX), and α,α′‐dibromo‐p‐xylene (DBX). Novel linear polymers that possessed repeating moieties of dicyclopentadiene ( DCPD ) in the backbone were thus prepared. The IR and NMR spectra indicated that poly(tetramethylene dicyclopentadiene dicarboxylate) (PTMDD) with a number‐average molecular weight (Mn ) of about 1× 104 and poly(p‐xylene dicyclopentadiene dicarboxylate) (PXDD) with a Mn of 4–6 × 103 were obtained with an yield of about 80% via the polyesterification of the alkali salts with DBB and DCX, respectively. The reaction was carried out in the presence of a phase transfer catalyst, such as BzMe3NBr or poly(ethylene glycol), in DMF at 100 °C for 4 h. Oligomers with a lower Mn (1–2 × 103) were obtained when the earth‐alkali salts were employed as salt monomers. Compared to the irreversible linear polymers, poly(p‐xylene terephthalate) (PXTP) and poly(p‐xylene maleate) (PXM), prepared through the reaction between DCX and the potassium salts of terephthalic and maleic acid, respectively, the specific viscosities (ηsp) of the new linear polymers increased abnormally with the decrease of the temperature from 200 °C to 100 °C. This occurred due to the thermally reversible dedimerization/redimerization of DCPD moieties of the backbone of the polymers via the catalyst‐free Diels–Alder/retro Diels–Alder cycloadditive reactions. The ratio of the ηsp at 100 °C and 200 °C of the reversible polymers was found to be much higher than that of PXTP and PXM, even when the heating/cooling cycle was carried out several times under a N2 atmosphere. The obtained results indicated that thermally reversible covalently bonded linear polymer can be obtained by introducing the DCPD structure into the backbone of the polymer through the polymerization of a monomer containing the DCPD moiety. The reversible natures of the polymers and oligomers might be useful in preparing easily processable and recyclable polymers and thermosensor materials. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 1662–1672, 2000 相似文献
18.
Temperature‐modulated differential scanning calorimetry can detect a certain amount of reversible latent heat in flexible macromolecules. In short, one can identify a reversible melting in such polymers earlier thought to exhibit only fully irreversible crystallization and melting. Details of the reversible melting of isotactic polypropylene and ethylene‐1‐octene copolymers of low and medium densities have newly been measured and linked to the crystallization, annealing, or melting temperature. It is possible to assign the experimental reversibility of melting to specific crystal fractions that ultimately melt irreversibly at higher temperatures; that is, it is suggested that reversible melting mainly occurs only between the temperatures of their formation and their zero‐entropy‐production melting temperature, at which they change to a melt of the same degree of metastability. This is supported by the almost complete absence of reversibility below the temperature of crystal formation and the observation of a distinct relationship between the amount of irreversibly by annealing reorganized material and reversibility in the case of isotactic polypropylene. A given crystal fraction, characterized by its formation temperature and zero‐entropy‐production melting temperature, has a specific reversibility of the melt‐to‐crystal transition, which is represented by the ratio of the reversible latent heat to the total enthalpy change when the crystal fraction of interest ultimately melts. This specific reversibility is, for ethylene‐1‐octene copolymers, at least 25% at temperatures in the primary crystallization range, and this indicates that the reversible contribution to the total of the melting processes is much larger than expected from simple calculations by the excess apparent reversible heat capacity being referred to the heat of fusion of the polymer, as is commonly done. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2039–2051, 2003 相似文献
19.
Leung KC Mendes PM Magonov SN Northrop BH Kim S Patel K Flood AH Tseng HR Stoddart JF 《Journal of the American Chemical Society》2006,128(33):10707-10715
Acid-base switchable supramolecular dendronized polyacetylenes (DPAs) with increasing steric bulk on going from generation one [G1] to three [G3], were constructed using multiple self-assembly processes between Fréchet-type [G1]-[G3]-dendritic dialkylammonium salts and a dibenzo[24]crown-8-containing polymer. The formation of the supramolecular systems is acid-base switchable to either an ON (rodlike dendronized polymers) or an OFF (flexible polymers) state. Thus, by controlling the superstructures of the supramolecular polymers with the [G1]-[G3] dendrons, it is possible to induce conformational changes within the polymer backbones. The supramolecular dendronized polymers, as well as their threading-dethreading properties, were characterized by (1)H NMR and UV absorption spectroscopies, gel permeation chromatography (GPC) and light scattering (LS). Independent measures of molecular weight (GPC, LS) indicate that DPAs behave as increasingly rigid macromolecules with each generation in solution. Molecular dynamics simulations of each DPA suggest that the lengths of the polymer backbones increase accordingly. Atomic force microscopy of the [G3]-dendronized polystyrene (DPS), as well as the DPAs, reveal surface morphologies indicative of aggregated superstructures. 相似文献