ISSN:
1572-8854
Keywords:
5,7-Dioxo-1,4,8,11-tetraazacyclotetradecane
;
2,6-dihydoxyanthraquinone
;
hydrogen bonding
;
supramolecular network
Source:
Springer Online Journal Archives 1860-2000
Topics:
Geosciences
,
Physics
Notes:
Abstract A complex of 5,7-dioxo-1,4,8,11-tetraazacyclotetradecane (dioxocyclam) and 2,6-dihydoxyanthraquinone (anthraflavic acid) has been obtained. The complex (crystals grown from water-ethanol solution) has a stoichiometry dioxocyclam-anthraflavic acid 1:1:5. C31H32N4O8, chemical formula weight 588.61, triclinic, P − 1, a = 10.542(3) Å, b = 11.936(2) Å, c = 12.206(2) Å, α = 104.00(1)°, β = 92.68(2)°, γ = 103.64(2)°, V = 1439.4 (5) Å3, Z = 2, Dx = 1.358 g cm−3. Only one of the two amine N-atoms of the macrocycle is protonated due to very weak acidic properties of 2,6-dihydoxyanthraquinone. Due to the rather poor quality of the crystals and structure refinement, reliable determination of H-bonds is complicated. Nevertheless, several types of H-bonding responsible for the formation of a developed supramolecular network can be suggested: between the protonated amino groups and macrocycle's C=O moieties; between non-protonated amino groups and macrocycle's C=O moieties; between protonated and non-protonated amino groups; between the amide NH and C=O groups of anthraflavic acid; and between protonated and deprotonated hydroxy groups of the acid. Two types of anthraflavic components can be distinguished in the lattice: those having a parallel orientation with respect to the macrocyclic fragments and forming hydrogen bonds with the latter, and those lying in an approximately perpendicular plane and not involved in H-bonding with the macrocycles.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1023/A:1009539316291
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