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Crystal Structure, Infrared Spectra and DFT Study of Benzyl 2,3-Anhydro-β-D-Ribopyranoside

Eva Scholtzová ; Vratislav Langer (Institutionen för kemi- och bioteknik, Oorganisk miljökemi) ; Lubomír Smrcok ; Miroslav Koós ; Vlasta Sasinková ; Jan Hirsch
Journal of Chemical Crystallography (1074-1542). Vol. 41 (2011), 2, p. 167-174.
[Artikel, refereegranskad vetenskaplig]

The crystal structure of benzyl 2,3-anhydro-β-D-ribopyranoside is orthorhombic, P212121, Z = 4. The pyranose ring adopts the EO conformation distorted considerably to the 5HO direction. The molecules of the title compound are linked into infinite chains running along the a-axis by bifurcated O–H···O hydrogen bonds. Interaction energies of these hydrogen bonds are significantly different, ~−5.4 for the bond with the smaller and ~−1.1 kcal/mol for the bond with the larger O···O separation. The hydrogen-bond pattern is completed by the two weaker C–H···O intermolecular hydrogen bonds, aiming at the epoxy oxygen atom. IR vibrational spectrum was interpreted by means of comparison with the full list of vibrational modes predicted using DFT method in the solid state. While till 1495 cm−1 the individual bands can be reconciled with single calculated modes, the region below this limit is populated by heavily overlapped HCH, HCO, HOC, COC and HCC bending modes merged with few ν(CC) and ν(CO) modes. The respective “red” shifts of the positions of the ν(OH) bands correlate well with the size of the O···O separation.

Nyckelord: Benzyl 2,3-anhydro-β-D-ribopyranoside, DFT, Hydrogen bonding , IR vibrational spectra

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Denna post skapades 2011-01-25. Senast ändrad 2011-03-21.
CPL Pubid: 136078


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


Organisk kemi
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Medicinsk bioteknologi (med inriktning mot cellbiologi)

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