TY - JOUR
T1 - Three N-2-benzoyloxybenzamidines: sheet structures built from hard and soft hydrogen bonds and aromatic pi-pi stacking interactions
AU - Carvalho, C E M
AU - Wardell, S M S V
AU - Wardell, J L
AU - Skakle, J M S
AU - Low, J N
AU - Glidewell, C
PY - 2004/1
Y1 - 2004/1
N2 - Molecules of the title compounds N-2-( benzoyloxy) benzamidine, C14H12N2O2, ( I), N-2-( 2- hydroxybenzoyloxy) benzamidine, C14H12N2O3, ( II), and N-2- benzoyloxy- 2- hydroxybenzamidine, C14H12N2O3, ( III), all have extended chain conformations, with the aryl groups remote from one another. In ( I), the molecules are linked into chains by a single N - H ... N hydrogen bond [H ... N = 2.15 Angstrom, N ... N = 3.029 (2) Angstrom and N - H ... N = 153degrees] and these chains are linked into sheets by means of aromatic pi - pi stacking interactions. There is one intramolecular O - H ... O hydrogen bond in ( II), and a combination of one three-centre N - H ...( N, O) hydrogen bond [H ... N = 2.46 Angstrom, H ... O = 2.31 Angstrom, N ... N = 3.190 ( 2) Angstrom, N ... O = 3.146 ( 2) Angstrom, N - H ... N = 138degrees and N - H ... O = 154degrees] and one two- centre C - H ... O hydrogen bond [H ... O = 2.46 Angstrom, C ... O = 3.405 (2) Angstrom and C - H ... O = 173degrees] links the molecules into sheets. In ( III), an intramolecular O H H ... N hydrogen bond and two N - H ... O hydrogen bonds [H ... O = 2.26 and 2.10 Angstrom, N ... O = 2.975 ( 2) and 2.954 ( 2) Angstrom, and N - H ... O = 138 and 163degrees] link the molecules into sheets.
AB - Molecules of the title compounds N-2-( benzoyloxy) benzamidine, C14H12N2O2, ( I), N-2-( 2- hydroxybenzoyloxy) benzamidine, C14H12N2O3, ( II), and N-2- benzoyloxy- 2- hydroxybenzamidine, C14H12N2O3, ( III), all have extended chain conformations, with the aryl groups remote from one another. In ( I), the molecules are linked into chains by a single N - H ... N hydrogen bond [H ... N = 2.15 Angstrom, N ... N = 3.029 (2) Angstrom and N - H ... N = 153degrees] and these chains are linked into sheets by means of aromatic pi - pi stacking interactions. There is one intramolecular O - H ... O hydrogen bond in ( II), and a combination of one three-centre N - H ...( N, O) hydrogen bond [H ... N = 2.46 Angstrom, H ... O = 2.31 Angstrom, N ... N = 3.190 ( 2) Angstrom, N ... O = 3.146 ( 2) Angstrom, N - H ... N = 138degrees and N - H ... O = 154degrees] and one two- centre C - H ... O hydrogen bond [H ... O = 2.46 Angstrom, C ... O = 3.405 (2) Angstrom and C - H ... O = 173degrees] links the molecules into sheets. In ( III), an intramolecular O H H ... N hydrogen bond and two N - H ... O hydrogen bonds [H ... O = 2.26 and 2.10 Angstrom, N ... O = 2.975 ( 2) and 2.954 ( 2) Angstrom, and N - H ... O = 138 and 163degrees] link the molecules into sheets.
U2 - 10.1107/S0108270103025435
DO - 10.1107/S0108270103025435
M3 - Article
SN - 1600-5759
VL - 60
JO - Acta Crystallographica Section C-Crystal Structure Communications
JF - Acta Crystallographica Section C-Crystal Structure Communications
ER -