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  • Chemistry  (8)
  • Polymer and Materials Science  (8)
  • Polyboranes  (1)
  • isotactic comb-like functional polyolefins  (1)
  • polyethylene copolymer  (1)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of inorganic and organometallic polymers and materials 1 (1991), S. 37-51 
    ISSN: 1572-8870
    Schlagwort(e): Polyboranes ; transitional metal catalysts ; isotactic comb-like functional polyolefins ; block copolymers ; alternating copolymers
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract This paper summarizes our research results on the synthesis of polyboranes and their applications in the functionalization of polyolefins. The method involves the borane monomers and transitional metal catalysts, such as Ziegler-Natta and metathesis catalysts. Our results show that most trialkylboranes are stable to a broad range of transitional metal catalysts. The borane-containing olefins can be homo- or copolymerized with olefins to the corresponding polyborane homo- and copolymers. The molecular weights of polyboranes are usually very high. Some of the reasons are attributed to the good solubility of polyboranes in hydrocarbon solutions during the polymerization processes. In turn, the borane groups in polymers are easily converted to other functional groups, such as hydroxyl groups, under mild conditions. Some high molecular weight functional polyolefins have been prepared with unique polymer structures, such as isotactic comb-like functional polymers, block copolymers, and alternating functional copolymers.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 3251-3261 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A wide range of functional diblock copolymers containing both functional polymer and hydrocarbon polymer, have been prepared by the combination of anionic polymerization and borane chemistry. The distinctive hydroboration reactivity between various polydienes enables us to selectively functionalize one polydiene segment in diblock copolymers which contain two different polydiene segments. In turn, the hydroborated polymers are valuable intermediate compounds which can be converted to a whole family of functional polymers with a variety of other functionalities under mild reaction conditions. The hydroxylated diblock copolymer is used as an example to demonstrate the chemistry. The two-phase nature of these copolymers is also shown by the observation of two distinctive glass transition temperatures associated with the individual polymer segments.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2759-2763 
    ISSN: 0887-624X
    Schlagwort(e): hydroxylated polypropylene ; high polymers ; hydroboration ; functionalization ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This article relates to functionalized polypropylene with high molecular weight and high crystallinity. The chemistry involves the hydroboration of poly(propylene-co-1,4-hexadiene) with borane reagents, such as diborane and 9-BBN. In turn, the borane-containing polymers are very versatile and can be easily converted to various functionalized polymers under mild reaction conditions. Despite the heterogeneous reaction conditions, both hydroboration and interconversion reactions were very effective using appropriate solvents. Apparently, the double bonds in the side chains are located in the amorphous phase and are ready for reaction with reagents. Overall, this functionalization process preserves the molecular weight and most of the crystallinity of poly(propylene-co-1,4-hexadiene). © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1017-1029 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This paper discusses the poly(ethylene-co-p-methylstyrene) copolymers prepared by metallocene catalysts, such as Et(Ind)2ZrCl2 and [C5Me4(SiMe2NtBu)]-TiCl2, with constrained ligand geometry. The copolymerization reaction was examined by comonomer reactivity (reactivity ratio and comonomer conversion versus time), copolymer microstructure (DSC and 13C-NMR analyses) and the comparisons between p-methylstyrene and other styrene-derivatives (styrene, o-methylstyrene and m-methylstyrene). The combined experimental results clearly show that p-methylstyrene performs distinctively better than styrene and its derivatives, due to the cationic coordination mechanism and spatially opened catalytic site in metallocene catalysts with constrained ligand geometry. A broad composition range of random poly(ethylene-co-p-methylstyrene)copolymers were prepared with narrow molecular weight and composition distributions. With the increase of p-methylstyrene concentration, poly(ethylene-co-p-ethylstyrene)copolymer shows systematical decrease of melting point and crystallinity and increase of glass transition temperature. At above 10 mol % of p-methylstyrene, the crystallinity of copolymer almost completely disappears. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1017-1029, 1998
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 505-514 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This paper presents an improved method to prepare divinylphenyl compounds which are a useful class of precursors in preparing difunctional organolithium initiators. In the past, most of the divinylphenyl compounds reported were prepared from reactions of phosphorus-substituted carbanions with aldehydes and ketones (Wittig reaction). The phosphorus by-product of the Witting reaction was difficult to be completely removed from the final products. In this paper, we apply the Peterson reaction (silane substituted carbanions) to the synthesis of divinylphenyl compounds. This reaction appears to be operationally simpler and cleaner than the Wittig reaction since the by-product of silane is easily removed by silica Gel chromatography. The syn-elimination of β-hydroxylsilane is complete and clean under NaH condition with no detectable isomers in the final product. The reaction of the divinylphenyl compound with S-butylithium forms a difunctional organolithium initiator which is used to prepare triblock copolymers with the desirable microstructure in each block.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 575-579 
    ISSN: 0887-624X
    Schlagwort(e): polyethylene copolymer ; functional polyolefin ; p-methylstyrene ; metallocene catalyst ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 0959-8103
    Schlagwort(e): polyethylene ; functionalization ; borane reagent ; metallocene catalyst ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A new method to prepare functionalized polyethylene involving borane intermediates and transition metal catalysts is described. Two processes, direct and post polymerizations, were employed to prepare borane-containing polyethylene (PE-B), which can be transformed to functionalized polyethylene (LLDPE-f) with various functional groups, such as —BR2, —OH, —NH2, —OSi(CH3)3. In the direct process, the PE-B copolymers were prepared in one step by copolymerization of ethylene with a borane monomer (ω-borane-α-olefin). The post polymerization process requires two steps: copolymerization of ethylene and 1,4-hexadiene, and subsequential hydroboration reaction of unsaturated PE. Three transition metal catalysts, including two homogeneous metallocene (Cp2ZrCl2 [bis(cyclopentadienyl) zirconium dichloride] and Et(Ind)2ZrCl2 [1,1′-ethylenedi-η5-indenyl-zirconium dichloride] with MAO (methylaluminoxane)) and one heterogeneous (TiCl3·AA/Et2AlCl) ones, were studied in the copolymerization reactions. The single site Et(Ind)2ZrCl2/MAO homogeneous catalyst, with a strained ligand geometry and opened active site, is by far the most effective system in the incorporation of high olefins into polyethylene structures.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 2 (1991), S. 545-552 
    ISSN: 1042-7163
    Schlagwort(e): Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: This article reviews recent advances in the synthesis of polar functional polymers via the mediation of organoborane monomers and polymers. Both direct polymerization and post-polymerization functionalization processes are described. Organoborane-assisted Ziegler-Natta, metathesis, and hydroboration (haloboration) polymerizations are presented. Moreover, the special problems and opportunities of polymer modification of olefin containing homo and copolymers by organoboranes are discussed.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 427-432 
    ISSN: 0360-6384
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 1239-1246 
    ISSN: 0098-1273
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The results of measurements of the optical absorption spectra, IR absorption spectra, thermogravimetric analysis, and elementary analysis of pyrolyzed polyacrilonitrile are presented as a function of the pyrolysis temperature Tp and of the duration of pyrolysis. At Tp ∼ 200°C, an intermediate phase was discovered, containing conjugated CN sequences and a completely unreacted carbon backbone. The optical absorption data imply that the resulting polymer is a semiconductor with a delocalized π-electron system and an energy gap Eg ⋍ 2.5 eV. For Tp 〉 260°C, the weight loss rapidly increases, and the absorption edge gradually broadens and shifts to lower energies. The resulting polymer (after higher-temperature pyrolysis) contains CN and C=C—C conjugation sequences, but appears to be a complex structure consisting of a mixture of different chemical species.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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