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  • 1
    ISSN: 1572-8935
    Keywords: Thermotropic liquid crystalline ; Poly(amide-ester) ; Direct polycondensation ; Thermal stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Four series of novel fully aromatic thermotropic liquid crystalline high molecular weight poly(amide-esters were prepared by direct polycondensation from terephthalic acid (TPA) and 2,6-naphthalene dicarboxlic acid with various aromatic diols and diamines in the presence of diphenyl chlorophosphate (DPCP), LiCl, and pyridine. The structures and thermal properties of the synthesized poly(amide-ester) s were examined by FTIR spectrum, wide angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), thermal optical polarized microscope and thermogravimetric analysis (TGA). The effects of the amounts and kinds of the aromatic diols and diamines (bisphenyl units, naphthalene and (un)substituted phenylene structures) on the molecular weight and thermal properties of the synthesized poly (amide-ester) s were investigated in this study. When a portion of the amide groups were replaced with the ester groups, most of the synthesized poly(amide-ester)s containing naphthalene or substituted hydroquinone units showed excellent mesophase and thermal stability, but the poly(amide-ester)s containing bisphenyl structures lost the mesophase behaviors. The P3 series of poly(amide-ester)s derived from TPA and 2,6-naphthalene dicarboxlic acid with phenylhydroquinone and various diamines possess liquid crystalline properties, even some of the diamines containing kink structures.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 551-560 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermosetting cholesteric oligocarbonates were prepared by polycondensation of mesogenic diphenols such as 4,4′-dihydroxybiphenyl (DHB) or hydroquinone 4-hydroxy-benzoate (HQHB; system. name: 4-hydroxyphenyl 4-hydroxybenzoate) with methylhy-droquinone and isosorbide. Trichloromethyl chloroformate served as condensing agent and propargyl alcohol (system. name of propargyl: 2-propynyl), 4-propargyloxybenzoyl chloride or 6-propargyloxy-2-napthoyl chloride served as chain stoppers. Most oligocar-bonates form a cholesteric phase over a broad temperature range. Depending on the mole fraction of isosorbide these oligocarbonates form Grandjean textures when sheared in the molten state.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 3039-3046 
    ISSN: 0887-624X
    Keywords: liquid crystalline poly(imide-carbonate)s ; melt polycondensation ; nematic phase ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two series of novel thermotropic liquid crystalline poly(imide-carbonate)s were prepared by melt polycondensation from various arylene or alkylene bis(phenylcarbonate)s by using N,N′-bis(hydroxyethyl)pyromellitimide and N,N′-bis(hydroxypropyl)pyromellitimide as monomers. Thermotropic liquid crystalline properties were characterized by a polarizing microscope with a heating stage and a differential scanning calorimeter (DSC). Nematic melts were found for the synthesized aromatic poly(imide-carbonate)s. In order to investigate whether the pyromellitimide unit could be used as a mesogenic unit for preparing LC polymers, a series of aliphatic poly(imide-carbonate)s was prepared in this study. However, no significant LC textures were found under the observation by polarizing microscope. It was suggested that the aspect ratio of the pyromellitimide unit was too short to form liquid crystalline poly(imide-carbonate)s. In addition, it was interesting that the aliphatic poly(imide-carbonate)s with a longer spacer (n = 3) in the pyromellitimide unit showed better crystallinity. Thermostabilities of all synthesized poly(imide-carbonate)s were measured by thermogravimetric analysis (TGA). © 1994 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2465-2472 
    ISSN: 0887-624X
    Keywords: thermotropic liquid crystalline ; poly(imide-ester) ; mesophase ; even-odd effect ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three series of the thermotropic liquid crystalline copoly(imide-ester)s were prepared by direct polycondensation. The first two series of the copoly(imide-ester)s were synthesized from N-(4-carboxyphenyl) trimellitimide with N,N-di(hydroxypropyl) pyromellitic diimide and various aromatic diols. The third series of copoly(imide-ester)s were prepared by N-(4-carboxyphenyl) trimellitimide with various imide-diols (methylene spacer = 2-6) and phenyl hydroquinone. The structures and thermal properties of the synthesized poly(imide-ester)s were examined by FTIR spectrum, wide-angle x-ray diffraction (WAXD), differential scanning calorimetry (DSC), thermal optical polarized microscope, and thermogravimetric analysis (TGA). The effects of the structures of the aromatic diols on the thermal properties of the resulting copoly(imide-ester)s were investigated. It was found that most of the copoly(imide-ester)s possessed excellent mesophase stabilities and thermostabilities. The mesophase stabilities of poly(imide-ester)s decreased with the increase of the size of lateral group, and the mesophase range increased with the increase of the amount of PhHQ. No significant odd-even effects were observed between the methylene spacer lengths and transition temperatures. © 1996 John Wiley & Sons, Inc.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 31 (1993), S. 2237-2243 
    ISSN: 0887-624X
    Keywords: fully aromatic polycarbonate ; melt birefringence ; thermotropic liquid crystalline polycarbonate ; mesophase transition ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four series of fully aromatic polycarbonates were prepared by using melt polycondensation from various novel phenylene diphenyl dicarbonates: 1,4-phenylenc diphenyl dicarbonate, 1,3-phenylene diphenyl dicarbonate, methyl-1,4-phenylene diphenyl dicarbonate, and chloro-1,4-phenylene diphenyl dicarbonate with various diols - 4,4′-biphenyl diol, hydroquinone, 2,7-naphthalene diol and 1,5-naphthalene diol, respectively. The thermotropic liquid crystalline properties of synthesized polycarbonates were investigated by: (1) examination of the melt birefringence and stir opalescence by a polarizing microscope equipped with a heating stage, (2) characterization by a differential scanning calorimeter (DSC), and (3) analysis of the wide angle x-ray diffraction. It was found that the 1,3-phenylene unit is compensated for the nonlinearity of the carbonate group, and polycarbonates which contain this bent shape unit showed excellent wide mesophase transition in this study. © 1993 John Wiley & Sons, Inc.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 2127-2133 
    ISSN: 0887-624X
    Keywords: liquid crystalline polyester elastomer ; direct polycondensation ; two-phase morphology ; smectic phase ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three series of novel thermotropic liquid crystalline polyester elastomers (TLCPEEs) were prepared by direct polycondensation from terephthalic acid, polyols (Mn = 1000 or 2000), and various diols. The structures and thermal properties of the synthesized TLCPEEs were examined by FTIR spectroscopy, differential scanning calorimetry, thermal optical polarized microscopy, thermogravimetric analysis, and wide-angle x-ray diffraction. The effects of kinds and amount of diols and the molecular weight of polyols on the thermal properties of TLCPEEs were studied. By introducing long flexible spacers (PE-1000 or PE-2000) into the polymer main chain, all polymers showed two-phase morphology under the thermal optical microscopic observation. All of the synthesized polymers, except polymer P1-BPA60 and P2-BPA60, which were prepared from BPA, exhibited thermotropic liquid crystalline properties that were in the smectic phase. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 2119-2125 
    ISSN: 0887-624X
    Keywords: thermotropic ; liquid crystalline poly(amide-ester) elastomer ; direct polycondensation ; two-phase morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three series of novel poly(amide-ester) (PAE) elastomers were prepared by direct poly-condensation from terephthalic acid (TPA), polyols (Mn = 1000 or 2000), and various diamines. The structures and thermal properties of the synthesized PAEs were examined by FTIR spectroscopy, wide angle X-ray diffraction (WAXD), differential scanning calo-rimetry (DSC), thermal optical polarized microscopy, thermogravimetric analysis (TGA), and dynamic mechanical analysis (DMA). The effects of kinds and amount of diamines and the molecular weight of polyols on the thermal properties of PAEs were studied. By introducing long flexible spacers (PE-1000 or PE-2000) into the polymer main chain, all polymers showed two-phase morphology under the thermal optical microscopic observation. It was interesting that most of the synthesized polymers exhibited only one melting transition corresponding to the soft segments. The melting transition of hard segments could not be detected due to decomposition of the soft segments. However, a thermotropic liquid crystalline PAE (TLCPAE) prepared from methylhydroquinone and 2-chloro-5-methyl-phenylenediamine with PE-1000 could be obtained by lowering the melting transition temperature of the hard segment. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 771-779 
    ISSN: 0887-624X
    Keywords: polyurethane elastomers ; liquid crystalline ; mesogenic unit ; chain extender ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four series of thermotropic polyurethane elastomers (TPUEs) were synthesized in this study. The hard segments were formed by using 4,4′-methylenedicyclohexyl diisocyanate (H12MDI) reacted with various mesogenic units, such as benzene-1,4-di(4-iminophenoxy-n-hexanol), benzene-1,4-di(4-iminophenol), and 3,3′-(4,4′-biphenylene)dipropanol, which also acted as the chain extender. Poly(oxytetramethylene)glycols (PTMEGs), PTMEG-2000 (Mn 2,000) and PTMEG-1000 (Mn 1,000) were used as a soft segment. The structures of all synthesized thermotropic liquid crystalline polyurethanes (TLCPUs) were characterized by FTIR spectroscopy. The effects of mesogenic units on the LC properties and elastic behaviors of LCPUs were studied. It was difficult to show LC behaviors for the PU elastomers derived from the mesogenic units with a lower aspect ratio, such as 3,3′-(4,4′-biphenylene)dipropanol, or the long soft segments, PTMEG-2000. In addition, these PU elastomers show better elastic properties by using a higher aspect ratio mesogenic unit as the chain extender, such as benzene-1,4-di(4-iminophenoxy-n-hexanol and benzene-1,4-di(4-imino-phenol)). The thermal properties were investigated by DSC measurements, thermal optical polarized microscopy, wide angle X-ray diffraction, dynamic mechanical analysis, and thermogravimetric analysis. The mechanical properties were measured by a tensilemeter. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 787-796 
    ISSN: 0887-624X
    Keywords: liquid crystalline polyurethane elastomers ; mesogenic unit ; mesophase ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three series of novel thermotropic liquid crystalline polyurethane elastomers (TLCPUEs) were studied. Hard segments were formed by using hexamethylene diisocyanate (HDI) reacted with a mesogenic unit, benzene-1,4-di(4-iminophenoxy-n-hexanol), which also acted as a chain extender. Three diols: 1,10-decanediol,poly(oxytetramethylene) glycol (PTMEG) Mn = 1000 and PTMEG Mn = 2000 were used as the soft segments. The effects of soft segments of polyurethanes on the liquid crystalline behavior were studied. Higher molecular weight TLCPUEs were obtained by adding 30-50 mol % of mesogenic segments to diisocyanates. In contrast to a conventional chain extender such as 1,2-ethylene glycol or 1,4-butyl glycol, the synthesized polyurethane elastomers exhibited a mesophase transition by using a mesogenic unit as the chain extender. Mesophase was found for all synthesized LC polyurethanes except of polymers H2-A-12 and H2-A-7. The structures and the thermal properties of all synthesized TLCPUEs were studied by using FTIR spectroscopy, wide-angle x-ray diffraction (WAXD) and DSC measurements, a polarizing microscope equipped with a heating stage, dynamic mechanical analysis (DMA), and thermogravimetric analysis (TGA). Mechanical properties were also examined by using a tensilemeter. © 1995 John Wiley & Sons, Inc.
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  • 10
    ISSN: 0887-624X
    Keywords: photosetting polycarbonates ; isosorbide ; 4,4′-dihydroxychalcone ; cholesteric phase ; Grandjean texture ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Numerous polycarbonates were prepared by means of “diphosgene” in pyridine using hydroquinone 4-hydroxybenzoate (HQHB) as mesogenic diphenol. In addition to the homopolycarbonate, binary copolycarbonates of HQHB and 4,4′-dihydroxychalcone (DHC) with varying molar composition were prepared. A series of ternary copolycarbonates were obtained by incorporation of isosorbide. Furthermore, an alternating copolycarbonate of HQHB and isosorbide was synthesized. All polycarbonates were characterized by inherent viscosities, elemental analyses, IR-, 1H-NMR, and 13C NMR spectroscopy, by WAXS powder patterns DSC measurements, and optical microscopy with crossed polarizers. The homopolycarbonate of HQHB and most binary copolycarbonates were semicrystalline materials forming an enantiotropic nematic melt. Particularly noteworthy is the finding that the alternating copolycarbonate of HQHB and isosorbide forms a broad cholesteric phase despite the unfavorable stereochemistry of isosorbide. The ternary copolycarbonates containing isosorbide formed a cholesteric melt and a Grandjean texture upon shearing. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1611-1619, 1997
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