Skip to main content
Erschienen in: Cellulose 6/2009

01.12.2009

Syntheses of 6-O-ethyl/methyl-celluloses via ring-opening copolymerization of 3-O-benzyl-6-O-ethyl/methyl-α-d-glucopyranose 1,2,4-orthopivalates and their structure–property relationships

verfasst von: Hiroshi Kamitakahara, Toshihiro Funakoshi, Shinji Nakai, Toshiyuki Takano, Fumiaki Nakatsubo

Erschienen in: Cellulose | Ausgabe 6/2009

Einloggen

Aktivieren Sie unsere intelligente Suche, um passende Fachinhalte oder Patente zu finden.

search-config
loading …

Abstract

6-O-Alkyl-celluloses with well-defined ratio of ethyl and methyl groups at position 6 were prepared by ring-opening copolymerization of 6-O-ethyl and 6-O-methyl glucose 1,2,4-orthopivalate derivatives. An aqueous solution of 6-O-ethyl-cellulose having no methyl group was found to be thermo-responsive to be turbid at ~70 °C. An aqueous solution of 6-O-ethyl-cellulose with higher molecular weight showed endothermic and exothermic peaks in the heating and cooling curves of DSC measurements, respectively. However, 6-O-alkyl-cellulose having 10% methyl group lost its thermo-responsive character. 6-O-Alkyl-celluloses having more than ten percent of ethyl group at position 6 became water-soluble, though 6-O-methyl-cellulose is insoluble in water. Thus, 6-O-ethyl group was found to be of importance for the water solubility of regioselective 6-O-alkyl-celluloses. Furthermore, a small amount of methyl group introduced at C6 position was found to affect some of physical properties of 6-O-alkyl-celluloses such as thermo responsive property.

Sie haben noch keine Lizenz? Dann Informieren Sie sich jetzt über unsere Produkte:

Springer Professional "Technik"

Online-Abonnement

Mit Springer Professional "Technik" erhalten Sie Zugriff auf:

  • über 67.000 Bücher
  • über 390 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Maschinenbau + Werkstoffe




 

Jetzt Wissensvorsprung sichern!

Springer Professional "Wirtschaft+Technik"

Online-Abonnement

Mit Springer Professional "Wirtschaft+Technik" erhalten Sie Zugriff auf:

  • über 102.000 Bücher
  • über 537 Zeitschriften

aus folgenden Fachgebieten:

  • Automobil + Motoren
  • Bauwesen + Immobilien
  • Business IT + Informatik
  • Elektrotechnik + Elektronik
  • Energie + Nachhaltigkeit
  • Finance + Banking
  • Management + Führung
  • Marketing + Vertrieb
  • Maschinenbau + Werkstoffe
  • Versicherung + Risiko

Jetzt Wissensvorsprung sichern!

Literatur
Zurück zum Zitat Ifuku S, Nakai S, Kamitakahara H, Takano T, Tsujii Y, Nakatsubo F (2005) Preparation and characterization of monolayer and multilayer langmuir-blodgett films of a series of 6-O-alkylcelluloses. Biomacromolecules 6(4):2067–2073CrossRef Ifuku S, Nakai S, Kamitakahara H, Takano T, Tsujii Y, Nakatsubo F (2005) Preparation and characterization of monolayer and multilayer langmuir-blodgett films of a series of 6-O-alkylcelluloses. Biomacromolecules 6(4):2067–2073CrossRef
Zurück zum Zitat Kamitakahara H, Hori M, Nakatsubo F (1996) Substituent effect on ring-opening polymerization of regioselectively acylated α-d-glucopyranose 1, 2, 4-orthopivalate derivatives. Macromolecules 29(19):6126–6131CrossRef Kamitakahara H, Hori M, Nakatsubo F (1996) Substituent effect on ring-opening polymerization of regioselectively acylated α-d-glucopyranose 1, 2, 4-orthopivalate derivatives. Macromolecules 29(19):6126–6131CrossRef
Zurück zum Zitat Kamitakahara H, Nakatsubo F, Klemm D (2006) Block co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides as model compounds for methylcellulose and its dissolution/gelation behavior. Cellulose 13(4):375–392CrossRef Kamitakahara H, Nakatsubo F, Klemm D (2006) Block co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides as model compounds for methylcellulose and its dissolution/gelation behavior. Cellulose 13(4):375–392CrossRef
Zurück zum Zitat Kamitakahara H, Nakatsubo F, Klemm D (2007) New class of carbohydrate-based nonionic surfactants: diblock co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides. Cellulose 14(5):513–528CrossRef Kamitakahara H, Nakatsubo F, Klemm D (2007) New class of carbohydrate-based nonionic surfactants: diblock co-oligomers of tri-O-methylated and unmodified cello-oligosaccharides. Cellulose 14(5):513–528CrossRef
Zurück zum Zitat Kamitakahara H, Koschella A, Mikawa Y, Nakatsubo F, Heinze T, Klemm D (2008) Syntheses and comparison of 2, 6-di-O-methyl celluloses from natural and synthetic celluloses. Macromol Biosci 8(7):690–700CrossRef Kamitakahara H, Koschella A, Mikawa Y, Nakatsubo F, Heinze T, Klemm D (2008) Syntheses and comparison of 2, 6-di-O-methyl celluloses from natural and synthetic celluloses. Macromol Biosci 8(7):690–700CrossRef
Zurück zum Zitat Karakawa M (2003) Chemical synthesis of high-regioselectively methylated celluloses by a cationic ring-opening polymerization (Kyoto). Ph.D. Thesis, Kyoto University Karakawa M (2003) Chemical synthesis of high-regioselectively methylated celluloses by a cationic ring-opening polymerization (Kyoto). Ph.D. Thesis, Kyoto University
Zurück zum Zitat Nakatsubo F, Kamitakahara H, Hori M (1996) Cationic ring-opening polymerization of 3, 6-di-O-benzyl-α-d-glucose 1, 2, 4-orthopivalate and the first chemical synthesis of cellulose. J Am Chem Soc 118(7):1677–1681CrossRef Nakatsubo F, Kamitakahara H, Hori M (1996) Cationic ring-opening polymerization of 3, 6-di-O-benzyl-α-d-glucose 1, 2, 4-orthopivalate and the first chemical synthesis of cellulose. J Am Chem Soc 118(7):1677–1681CrossRef
Metadaten
Titel
Syntheses of 6-O-ethyl/methyl-celluloses via ring-opening copolymerization of 3-O-benzyl-6-O-ethyl/methyl-α-d-glucopyranose 1,2,4-orthopivalates and their structure–property relationships
verfasst von
Hiroshi Kamitakahara
Toshihiro Funakoshi
Shinji Nakai
Toshiyuki Takano
Fumiaki Nakatsubo
Publikationsdatum
01.12.2009
Verlag
Springer Netherlands
Erschienen in
Cellulose / Ausgabe 6/2009
Print ISSN: 0969-0239
Elektronische ISSN: 1572-882X
DOI
https://doi.org/10.1007/s10570-009-9339-4

Weitere Artikel der Ausgabe 6/2009

Cellulose 6/2009 Zur Ausgabe