Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. One-Step Conversion of Cellobiose to C<sub>6</sub>-Alcohols Using a Ruthenium Nanocluster Catalyst
 
research article

One-Step Conversion of Cellobiose to C6-Alcohols Using a Ruthenium Nanocluster Catalyst

Yan, N  
•
Zhao, C
•
Luo, C
Show more
2006
Journal of the American Chemical Society

The one-step conversion of cellulose to C6-alcs. via green and energy efficient approaches has, as far as we are aware, not been reported. Such a process presents a considerable challenge, the two key problems being (1) finding a suitable solvent that dissolves the cellulose, and (2) the development of advanced catalytic chem. for selective cleavage of the C-O-C bonds (glycosidic bonds) connecting glucose residues. The dissoln. of cellulose has been recently realized by using ionic liqs. as green solvents; there is still no efficient method, such as selective hydrogenation, for the precise C-O-C cleavage under mild conditions, however. Cellobiose is a glucose dimer connected by a glycosidic bond and represents the simplest model mol. for cellulose. We disclose in this communication that the one-step conversion of cellobiose to C6-alcs. can be realized by selectively breaking the C-O-C bonds via selective hydrogenation using a water-sol. ruthenium nanocluster catalyst under 40 bar H2 pressure.

  • Files
  • Details
  • Metrics
Loading...
Thumbnail Image
Name

ja062468t.pdf

Access type

restricted

Size

93.54 KB

Format

Adobe PDF

Checksum (MD5)

01f35ef374dd22fa4d787a7cebb98798

Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés