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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 7 (1984), S. 171-199 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Some key concepts available to the macromolecular engineer have been outlined. In addition to useful ultimate properties the macromolecular engineer has also to consider convenient processing characteristics. The way toward these objectives is by combining of elementary events, by exploiting the mechanistic understanding of controlled ion generation cationation/propagation and termination. Figure 14 outlines and combines some of the elements considered, and shows some representative structures that can be synthesized by utilizing carbocationic macromolecular engineering concepts.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 16 (1981), S. 123-197 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mono- and di-ended linear and three-arm star allyl-telechelic polyisobutylenes, PIB—A, A—PIB—A and (where A = —CH2—CH=CH2) have been prepared by a rapid economical one-pot polymerization-functionalization process. The process involves the living polymerization of isobutylene (IB) by mono-, di-, or tri-functional initiating systems, specifically by allphatic and aromatic tert-ester and -ether/TiCl4 combinations, followed by electrophilic functionalization of the living sites with allyl-trimethylsilane (ATMS). Structural characterization by 1H-NMR spectroscopy and end group titration with m-chloroperbenzoic acid (m-CPBA) indicate quantitative end allylation even with relatively slowly initiating systems like DiOAcTMH7/TiCl4. Detailed kinetic analysis of the latter system indicates, unexpetedly, cationation to be rate determining. Quantitative derivatizations of the allyl termini have yielded mono-, di-, and tri-epoxy- and -hydroxy-telechelic PIBs. Strong rubbery networks have been made by curing the epoxy-telechelic PIBs with triethylene tetramine and by reacting the hydroxy-telechelic PIBs with MDI.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2825-2834 
    ISSN: 0887-624X
    Keywords: carbocationic polymerization ; living polymerization ; poly(isobutyl vinyl ether) ; polyisobutylene ; block copolymers ; titanium tetrachloride ; common ion salt ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The MeCH(O-i-Bu)Cl/TiCl4/MeCONMe2 initiating system was found to induce the rapid living carbocationic polymerization (LC⊕Pzn) of isobutyl vinyl ether (IBuVE) at -100°C. Degradation by dealcoholation which usually accompanies the polymerization of alkyl vinyl ethers by strong Lewis acids is “frozen out” at this low temperature and poly(isobutyl vinyl ether)s (PIBuVEs) with theoretical molecular weights up to ca. 40,000 g/mol (calculated from the initiator/monomer input) and narrow molecular weight distributions (M̄w/M̄n ≤ 1.2) are readily obtained. According to 13C-NMR spectroscopy, PIBuVEs prepared by living polymerization at -100°C are not stereoregular. The MeCH(O-i-Bu)Cl/TiCl4 combination induces the rapid LC⊕Pzn of IBuVE even in the absence of N,N-dimethylacetamide (DMA). The addition of the common ion salt, n-Bu4NCl to the latter system retards the polymerization and meaningful kinetic information can be obtained. The kinetic findings have been explained in terms of TiCl4. IBuVE and TiCl4 · IBuVE and TiCl4 · PIBuVE complexes. The HCl (formal initiator)/TiCl4/DMA combination is the first initiating system that can be regarded to induce the LC⊕Pzn of both isobutylene (IB) and IBuVE. Polyisobutylene (PIB)-PIBuVE diblocks were prepared by sequential monomer addition in “one pot” by the 2-chloro-2,4,4-trimethylpentane (TMP-Cl)/TiCl4/DMA initiating system. Crossover efficiencies are, however, below 35% because the PIB⊕ + IBuVE → PIB-b-PIBuVE⊕ crossover is slow. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0887-624X
    Keywords: isobutylene polymerization ; living carbocationic ; conventional carbocationic ; proton trap ; mechanism ; kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of the proton trap, 2,6hyphen;di-tert-butylpyridine (DtBP), on the polymerization of isobutylene (IB) induced by the “HX”/TiCl4 (“HX” = protoic impurity) intiating system has been studied. Significantly, in the presence of a large (∼ 40 molar) excess of DtBP relative to “HX”, free proton-induced chain transfer-dominated conventional IB polymerization is converted to living polymerization. In the absence of the proton trap the kinetics are dominated by rapid proton-induced processs which overwhelm the relatively slower living polymerization. These investigations also led to a quantitative assessment of the concentration of initiating species: [“HX”] = 1.46 × 10-4 mol/L. The polymerizations are first-order in monomer and the apparent rate constants of propagation drop precipituously with increasing DtBP concentration until a constant low value is reached. The rate of formation of propagating living chains has been expressed quantitatively. Chain transfer is bimolecular and first order in monomer, and kinetic investigations led to a quantitative description of the effect of proton trap concentration on the apparent first order chain transfer constant. The results have been explained in terms of a simple mechanistic scheme. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3341-3347 
    ISSN: 0887-624X
    Keywords: styrene polymerization ; p-chlorostyrene polymerization ; p-methylstyrene polymerization ; living carbocationic ; common ion effect ; kinetics ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of common anion producing salt, tetrabutylammonium chloride (n-Bu4NCl), on the livingness and kinetics of styrene (St), p-chlorostyrene (pClSt), and p-methylstyrene (pMeSt) polymerization initiated by the 2-chloro-2,4,4-trimethylpentane (TMPCl)/TiCl4 system has been investigated. Uncontrolled (conventional) carbocationic polymerization of St and p MeSt can be converted to living polymerization by the use of n-Bu4NCl. Under similar conditions the polymerization of p ClSt is living even in the absence of n-Bu4NCl, although the molecular weight distribution (MWD) of the polymer becomes narrower in the presence of this salt. The apparent rates of polymerizations decrease in the presence of n-Bu4NCl in proportion with the concentration of the salt. The rate of living polymerization of p ClSt is noticeably lower than that of St, while that of p MeSt is higher. The apparent rate constants, kpA, of these polymerizations have been determined, and the effects of the electron donating p Me- and electron withdrawing p Cl-substituents relative to the rate of St polymerization have been analyzed. [For part LXI, see J. Si and J. P. Kennedy, Polym. Bull., 33, 651 (1994)]. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3341-3347, 1997
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and characterization of novel thermoplastic elastomers consisting of multiple polystyrene-b-polyisobutylene (PSt-b-PIB) arms emanating from cyclosiloxane cores is described. The synthesis involved the sequential living cationic block copolymerization of styrene (St) and isobutylene (IB), followed by quantitative allylic end-functionalization of the living PSt-b-PIB+ to produce PSt-b-PIB—CH2— CH=CH2 prearms, and finally linking by hydrosilation of these prearms with Si—H-containing cyclosiloxanes (e.g., 2,4,6,8,10,12-hexamethylcyclohexasiloxane, DH6). Two types of star-blocks, namely primary and higher-order star-blocks, were prepared: Primary star-blocks containing 3-9 PSt-b-PIB arms were obtained by using various cyclosiloxanes (DH6 to DH12) and a close to exact stoichiometry between the Si—H and allyl groups, [Si—H]/[C=C] ∼ 1, in the essential absence of moisture ([H2O] ∼ 100 ppm). Higher-order star-blocks consisting of 13-24 PSt-b-PIB arms radiating from complex coupled cyclosiloxanes were prepared by the use of Si—H/allyl ratios significantly larger than unity ([Si—H]/[C=C] = 2-3) in the presence of controlled amounts of moisture ([H2O] ∼ 600 ppm). Reaction conditions (temperature, concentration, stoichiometry, solvent nature, catalyst concentration, etc.) for efficient syntheses have been developed. The products were characterized by 200 and 600 MHz 1H-NMR spectroscopy and triple-detector (RI, UV, LLS) GPC. The microstructure of the condensed cores in the higher-order star-blocks was studied by 2D-NMR (HMQC) spectroscopy, and the number of cyclosiloxane rings in the cores (i.e., the content (wt %) of cores in the star-blocks) was determined. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 2997-3012, 1998
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3255-3265 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Essentially quantitative allylation of linear and three-arm star tert-chloro capped polyisobutylenes [tCl-PIB-Clt and PIB(Clt)3] has been achieved by the use of allyltrimethylsilane (AllylSiMe3) and Friedel-Crafts acids. Quantitative allylation occurs under suitable conditions, e.g., slight molar excess of TiCl4 and AllySiMe3 polar media, -70°C. These conditions have been developed from quantitative model allylation experiments using 2,4,4-trimethyl-2-chloropentane. Essentially quantitative allylation occurs with long-chain or “once fired” tert-chloro-end groups. Complete allylation can also be effected in a “one-pot two-step” synthesis, i.e., by first preparing the tert-chloro-ended PIB by the inifer method and without isolating the product, completing the synthesis by allylation in the same reactor. Extensive but not quantitative allylation can also be obtained in situ, i. e., during polymerization, by the use of the AllylSiMe3/cumyl chloride/BCI3/isobutylene combination. While allylation proceeds with great ease under the mildest conditions, e.g., -70°C, vinylation with vinyltrimethylsilane could not be achieved even under more forcing conditions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 3153-3160 
    ISSN: 0887-624X
    Keywords: polyisobutylene ; 2-sulfoethyl methacrylate ; copolymer ; network ; synthesis ; characterization ; swelling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of environmentally sensitive amphiphilic networks consisting of 2-sulfoethyl methacrylate (SEMA) chains linked by methacrylate-ditelechelic polyisobutylene (MA-PIB-MA) chains have been prepared and characterized. Network composition was determined after sequential solvent extraction by elemental analysis. These networks are two-phase microheterogeneous systems containing hydrophobic rubbery PIB domains (Tg ∼ -60°C) and hydrophilic poly(2-sulfoethyl methacrylate) domains (Tg ∼ -15°C). They exhibit large contact-angle hysteresis in water which is due to surface segmental mobility and microheterogeneity. By increasing the SEMA content of the networks the contact-angle hysteresis increases. This phenomenon is due to an increase in the advancing contact angle most likely caused by the migration of the nonpolar PIB domains toward the surface and concomitant decrease of the receding contact angle. These amphiphilic networks exhibit non-Fickian swelling in n-heptane, as well as in water, and show pH-sensitive swelling in aqueous media. They rapidly and reversibly swell and deswell in response to increasing or decreasing the pH of the media (cycling between pH = 2 and 12). © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1891-1899 
    ISSN: 0887-624X
    Keywords: polyisobutylene ; poly(dimethylsiloxane) ; hydrosilation ; bicomponent networks ; molecular weight between crosslinks ; network functionality ; sol fraction ; extractables ; model networks ; end-linking ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of novel polyisobutylene (PIB)/poly(dimethylsiloxane) (PDMS) bicomponent networks is described. The synthesis strategy (see Figure 1) was to prepare well-defined and -characterized allyl-tritelechelic polyisobutylenes [φ(PIB - C - C=C)3] and SiH-ditelechelic poly(dimethylsiloxanes) (HSi-PDMS-SiH) and then crosslink these moieties by hydrosilation. The φ(PIB - C - C=C)3 was prepared by living isobutylene polymerization followed by end-quenching with allyltrimethylsilane, whereas the HSi-PDMS-SiH was obtained by equilibrium polymerization of octamethylcyclotetrasiloxane and tetramethyldisiloxane. The detailed structures of the starting polymers were characterized by GPC and 1H-NMR spectroscopy. A series of PIB/PDMS bicomponent networks of varying compositions and average molecular weights between crosslinks (Mc) of ∼ 20,000 g/mol were assembled. Optimum crosslinking conditions were defined in terms of H2PtCl6 catalyst concentration, nature of solvent, time, temperature, and stoichiometry of ∼ CH2CH=CH2/∼SiH groups, allowing for the convenient synthesis of well-defined model bicomponent networks. Swelling studies and elemental analysis confirm the correctness of the synthetic strategy. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1891-1899, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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