TY - JOUR
T1 - 1,4-Di-n-heptyloxy-2,5-dinitrobenzene
AU - Blackburn, Octavia A.
AU - Coe, Benjamin J.
AU - Futhey, Robert
AU - Helliwell, Madeleine
PY - 2010
Y1 - 2010
N2 - The complete molecule of the title compound, C20H 32N2O6, is generated by crystallographic inversion symmetry. The two mutually trans nitro substituents are hence in fully eclipsed conformation and also twisted by 43.2 (2)° with respect to the phenyl ring plane. The benzene-connected portions of the alkoxy substituents lie almost coplanar with the ring [C-O-C-C torsion angle = 2.0 (2)°]. In the crystal, weak C-H⋯O interactions link the molecules.
AB - The complete molecule of the title compound, C20H 32N2O6, is generated by crystallographic inversion symmetry. The two mutually trans nitro substituents are hence in fully eclipsed conformation and also twisted by 43.2 (2)° with respect to the phenyl ring plane. The benzene-connected portions of the alkoxy substituents lie almost coplanar with the ring [C-O-C-C torsion angle = 2.0 (2)°]. In the crystal, weak C-H⋯O interactions link the molecules.
U2 - 10.1107/S160053680905123X
DO - 10.1107/S160053680905123X
M3 - Article
SN - 1600-5368
VL - 66
SP - o36
JO - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
IS - 1
ER -