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
Filter
  • 1960-1964  (4)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 29 (1964), S. 801-812 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 26 (1961), S. 625-626 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry 53 (1961), S. 7-9 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 2115-2125 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of polyesters of trans-1,4-cyclohexanedimethanol was prepared and the melting points compared with those of the analogous series of polyesters prepared from p-xylylene glycol. Only slight differences in melting points were noted between the corresponding pairs of polyesters prepared from a single aliphatic dicarboxylic acid and from the two glycols. However, polyesters derived from aromatic dibasic acids and trans-1,4-cyclohexanedimethanol melt at a higher temperature than the corresponding polymer from p-xylylene glycol. The probable molecular configuration of polyesters based on trans-1,4-cyclohexanedimethanol is discussed. It is suggested that the diol moiety in the polyester can adopt a slightly contracted conformation so that the oxygen-oxygen distance is less than in polyesters derived from p-xylylene glycol. This, together with the similar degree of rigidity and symmetry of the trans-1,4-cyclohexylene and p-phenylene ring systems, is employed to explain the observed melting points. Polyesters prepared from cis-1,4-cyclohexanedimethanol are also described. As expected from the lower degree of symmetry of the diol, these polyesters have lower melting points than the analogous compositions prepared from trans-1,4-cyclohexanedimethanol. Polyesters of cis-1,4-cyclohexanedimethanol and trimethylene glycol have similar melting points. It is suggested that a cis-1,4-cyclohexylene ring and a methylene group have a similar effect on the melting point of a polyester. Copolyesters of cis- and trans-1,4-cyclohexanedimethanol with terephthalic acid do not form a minimum melting composition. Instead, they show a continuous change of melting point from that of the polyester prepared from one stereoisomer to that of the polymer prepared from the other isomer.
    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...