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The Structure and Conformation of Lignin as Judged by X-ray Crystallographic Investigations of Lignin Model Compounds: Arylglycerol β-Syringyl Ethers

Knut Lundquist (Institutionen för kemi- och bioteknik, Skogsindustriell kemiteknik) ; Vratislav Langer (Institutionen för kemi- och bioteknik, Oorganisk miljökemi) ; Jim Parkås
Proceedings of the10th EUROPEAN WORKSHOP ON LIGNOCELLULOSICS AND PULP, EWLP 2008; KTH Royal institute of Technology, Stockholm, Sweden 25-28 August 2008 p. 308-311. (2008)
[Konferensbidrag, refereegranskat]

Structural elements of the arylglycerol β-syringyl ether type are very frequent in hardwood lignins. A variety of crystalline dimeric lignin models representing different diastereomeric forms of structural elements in lignin of this type have been studied using X-ray crystallography. Bond distances and bond angles in the model compounds are in all probability nearly identical with those of the corresponding structural elements in lignins. Based on X-ray crystallographic data from four compounds a sequence of units (5 aromatic rings, 8 chiral Catoms) attached to each other by β-syringyl ether linkages was constructed. The appearance of the resulting oligomer illustrates that stereoisomerism can be expected to influence the shape of the lignin molecules to a great extent. The constructed oligomer constitutes one of 256 possible stereoisomers (128 racemates).

Denna post skapades 2008-11-04. Senast ändrad 2008-11-11.
CPL Pubid: 76826


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Institutioner (Chalmers)

Institutionen för kemi- och bioteknik, Skogsindustriell kemiteknik (2005-2014)
Institutionen för kemi- och bioteknik, Oorganisk miljökemi (2005-2014)


Organisk kemi

Chalmers infrastruktur