Acta Crystallographica Section B

Structural Science

Volume 56, Part 4 (August 2000)


research papers



Acta Cryst. (2000). B56, 682-689    [ doi:10.1107/S0108768100002329 ]

Crystal-to-crystal photodimerization of trans-cinnamamides

H. Hosomi, Y. Ito and S. Ohba

Abstract: In the crystals of trans-4-methylcinnamamide, C10H11NO (I), trans-4-chlorocinnamamide, C9H8ClNO (II), trans-3-(2-thienyl)acrylamide, C7H7NOS (III), and trans-cinnamamide, C9H9NO (IV), the shortest intermolecular C\cdotsC distances between the C=C double bonds are 3.670 (2), 3.632 (2), 3.762 (3) and 4.120 (2) Å, respectively, for the pair of molecules related by a center of symmetry. The structure analysis was also carried out for trans-2-(p-chlorophenyl)-cis-4-(p-chlorophenyl)-1-trans-3-diamidocyclobutane, C18H16Cl2N2O2 (V), which is the [alpha]-type photodimer of (II). The N-H\cdotsO hydrogen-bond networks in (I)-(III) are composed of two-dimensional pleated sheets, and those in (IV) and (V) of one-dimensional flat ribbons. The single crystals of (I), (II) and (IV) were photoirradiated with a 250 W ultra-high-pressure mercury lamp through a band-pass filter or a long-pass filter for 2-5 h. The photodimer was produced in each crystal with retention of the single-crystal form. The populations of the dimers were converged to 86.2 (4), 48.4 (6) and 4.5 (2)% in the refinement of the crystals after photoirradiation, (I^{\prime}), (II^{\prime}) and (IV^{\prime}), respectively. Although the intermolecular N-H\cdotsO hydrogen-bond network remained in (I^{\prime}) and (II^{\prime}), the network was partly broken in (IV^{\prime}) in the process of photoreaction.

 bibliographic record in  format

  Find reference:   Volume   Page   
  Search:     From   to      Advanced search

Copyright © International Union of Crystallography
IUCr Webmaster