Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 193 (1992), S. 1723-1728 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Oxidative polymerization of aniline using the H2O2-FeSO4 system gave polyaniline under mild conditions. The prepared powdery emeraldine base, a form of polyaniline, is blue black and shows high solubility in organic solvents (e.g., ca. 200 mg/mL in N-methylpyrrolidone). The number-average molecular weight (Mn) of the polymer obtained was 1,3-1,7 · 104 (via gel permeation chromatography vs. polystyrene) and Mw/Mn = 1,6-2,2. Poly(2-ethylaniline) and poly-(2-propylaniline) with high molecular weights were also synthesized by this procedure in high yield.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 194 (1993), S. 3149-3155 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reduction of the emeraldine base form of polyaniline (PEM) by N,N-diethylhydroxylamine, sodium tetrahydroborate, sodium dithionite, and hydrazine monohydrate proceeds smoothly at room temperature to give the leucoemeraldine base form of polyaniline (PLM). The reduction of PEM to PLM with these reducing agents obeys a pseudo-first-order kinetics with respect to the concentration of PEM. The pseudo-first order rate constants, k, of the reduction with hydrazine monohydrate (5,0 · 10-1 mol · L-1), N,N-diethylhydroxylamine (6,2 · 10-2 mol · L-1), and NaBH4 (1,13 · 10-3 mol · L-1) are 1,46 · 10-4 S-1, and 2,50 · 10-4 s-1, and 1,7 · 10-3 s-1 at 20°C, respectively. In the case of sodium dithionite, which has a higher reducing ability, the reduction proceeds very rapidly at room temperature. Plot of In(k/[reductant]) against the electrochemically measured half-wave potential E1/2 affords a linear correlation with a slope of 20 V-1.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 1649-1654 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ni-catalyzed dehalogenation polycondensation of 3-formyl-, 3-hydroxyiminomethyl- and 3-cyano-2,5-dibromothiophene with zinc affords oligo(3-formyl-2,5-thienylene) (2a), oligo-(3-hydroxyiminomethyl-2,5-thienylene) (2b), and oligo(3-cyano-2,5-thienylene) (2c). Electrochemical polymerization of 3-methoxythiophene and 3,4-dimethoxythiophene give blueblack films of oligo(3-methoxy-2,5-thienylene) (2d) and poly(3,4-dimethoxy-2,5-thienylene) (2e). Iodine adducts of 2a-2c show electrical conductivity values between 1,8 · 10-11 and 8,8 · 10-8 S · cm-1. Doped 2d shows electrical conductivity of 2 · 10-1 S · cm-1, whereas doped 2e exhibits an electrical conductivity between 1,5 and 30 S · cm-1. Doping of undoped 2d and 2e causes profound changes in their IR and NMR spectra, colour, and electrical conductivity properties.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0887-624X
    Keywords: polycondensation ; palladium-catalyzed ; π-conjugated polymer ; copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2821-2825 
    ISSN: 0887-624X
    Keywords: end-capped polyester ; SmI2 ; Tishchenko-type polyaddition ; dialdehydes ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: SmI2-catalyzed polyaddition of 1,12-dodecanedial followed by treatment with benzaldehyde gives a polyester (1) containing three structural units, [OCH2—(CH2)10—CH2O], [OCH2—(CH2)10—CO], and [CO—(CH2)10—CO], in the main chain and an OCH2Ph end-capping group. GPC analysis of 1 shows molecular weights of Mn = 5.5 × 103 and Mw = 14 × 103. The 1H-NMR spectrum reveals the polymer structure with the COOCH2Ph end group as well as the Mn value (2.6 × 103) calculated based on an amount of the end-capping group and lower than that estimated from GPC. Mixtures of terephthalaldehyde and 1,12-dodecanedial in several molar ratios undergo similar polyaddition catalyzed by SmI2 to give the corresponding copolyesters after treatment with benzaldehyde. Increase in the ratio of 1,12-dodecanedial causes increase in yield and molecular weight of the copolymer. Terephthalaldehyde shows a tendency to give alcohol-side —O—R—O— unit in the polyester, whereas 1,12-dodecanedial is mostly incorporated as the acid-side —CO—R′—CO— unit. Terminal aldehyde group derived from dodecanedial is capped effectively by benzaldehyde to give the COOCH2Ph end group. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2821-2825, 1997
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 0887-624X
    Keywords: poly(aryleneethynylene) ; palladium-catalyzed ; copolymer ; optical properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium-catalyzed polycondensation between 2,5-diiodo-3-hexylthiophene I-Th(Hex)-I with mixtures of p-diethynylbenzene HC≡C - Ph - C≡CH and α,ω-diethynylalkane HC≡C(CH2)lC≡CH (l = 3 or 8) gives poly(aryleneethynylene) PAE-type copolymers [C≡C(CH2)lC≡C - Th(Hex)]m[C≡C - Ph - C≡C - Th(Hex)]n containing the methylene unit. The copolymers have a molecular weight (Mn) of about 1.2 × 104 as determined by GPC (polystyrene standard) and are considered to possess essentially a random sequences in view of the  - C≡C(CH2)lC≡C -  and  - C≡C - Ph - C≡C -  units as judged from their UV-visible spectra. By the incorporation of the (CH2)l unit, the λmax position of the corresponding PAE homopolymer [C≡C - Ph - C≡C - Th(Hex)]n is shifted to a shorter wavelength. However, the copolymers give rise to a photoluminescence PL peak essentially agreeing with a PL peak of the homopolymer, suggesting occurrence of energy transfer in the copolymer. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2201-2207, 1998
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 997-1001 
    ISSN: 0887-624X
    Keywords: π-conjugated polymer ; n-type polymer ; reduction potential ; electron affinity ; linear relationship ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ease of reduction of π-conjugated poly(p-phenylene)-, poly(naphthalene-2,6-diyl)-, and poly(naphthalene-1,4-diyl)-type polymers is determined by the electron accepting properties of the recurring aromatic units. Linear relationships hold between reduction potentials (Ered) of the π-conjugated poly(arylene)s and electron affinities (EA) of the recurring arylene units: Ered = ρEA + a. A ρ value of 0.85 ± 0.02 is found for the three types of polymers investigated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 463-474 
    ISSN: 0887-624X
    Keywords: π-conjugated polymer ; polythiophene ; phenolic substituent ; hindered phenolic substituent ; nickel-promoted ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dehalogenation polycondensation of 3-(4-methoxyphenyl)-2,5-dibromothiophene with Mg and a zerovalent nickel complex as well as chemical oxidative polymerization of 3-(4-methoxyphenyl)thiophene with FeCl3 gives poly[3-(4-methoxyphenyl)thiophene-2,5-diyl] P3(4-MeOPh)Th. Treatment of soluble P3(4-MeOPh)Th with BBr3 converts the OCH3 group to an OH group and gives poly[3-(4-hydroxyphenyl)thiophene-2,5-diyl] P3(4-OHPh)Th. Oxidative polymerization of 3-[3,5-di-t-butyl-4-{(trimethylsilyl)oxy}phenyl]thiophene with FeCl3 in an aqueous medium directly affords another kind of polythiophene with a sterically hindered phenolic group, poly[3-(3,5-di-t-butyl-4-hydroxyphenyl)thiophene-2,5-diyl] P3(4-OH-3,5-tBu2Ph)Th. An organometallic dehalogenation polymerization using a nickel complex also affords P3(4-OH-3,5-tBu2Ph)Th. All the polymers described above show strong photoluminescence in a region of 500-600 nm. Oxidation of P3(4-OH-3,5-tBu2Ph)Th with PbO2 gives stable radical species as confirmed by IR and ESR spectroscopy. Electrochemical redox behavior of the polymers is compared with that of other polythiophenes. © 1997 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 1265-1273 
    ISSN: 0887-624X
    Keywords: ruthenium ; samarium ; polyaddition ; dialdehydes ; polyester ; Tishchenko type reactions ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: RuH2(PPh3)4 catalyzed Tishchenko type polyaddition of terephthal-aldehyde gives aromatic polyester (1), which contains three structural units, [OCH2—C6H4—CH2O] (1a), [OCH2—C6H4—CO] (1b), and [CO—C6H4—CO] (1c). 1H-NMR spectrum shows the presence of the three units in a 1 : 2 : 1 ratio. Isophthalaldehyde also undergoes similar polyaddition to give another aromatic polyester (2), while 1,12-dodecanedial gives an aliphatic polyester (3) containing the following structural units: [OCH2—(CH2)10—CH2O] (3a), [OCH2—(CH2)10—CO] (3b), and [CO—(CH2)10—CO] (3c). The above polymers have Mn of 2.7 × 103-5.4 × 103 and Mw of 4.3 × 103 - 9.7 × 103, respectively. Mixtures of terephthalaldehyde and 1,12-dodecanedial produce copolymers, which contain the units 1a-1c and 3a-3c in a random sequence. In the copolymerization, terephthalaldehyde shows a strong tendency to give 1c units, whereas 1,12-dodecanedial predominantly affords 3a units. SmI2 also catalyzes polyaddition of terephthalaldehyde to give the corresponding polyester with Mn of 1.7 × 103 and Mw of 3.7 × 103, respectively. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1265-1273, 1997
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1609-1611 
    ISSN: 0887-624X
    Keywords: copper(I) iodide ; p-xylylene dibromide ; potassium carbonate ; poly[(p-xylylene carbonate)-co-(p-xylylene oxide)] ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No abstract.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...