TY - JOUR
T1 - Neutron and X-ray diffraction, inelastic neutron scattering, and solid-state 13C NMR investigations of polymorphic p-chlorophenylformamide
T2 - Absence of proton transfer along the intermolecular N-H⋯O hydrogen bond
AU - Tam, Cheok N.
AU - Cowan, John A.
AU - Schultz, Arthur J.
AU - Young, Victor G.
AU - Trouw, Frans R.
AU - Sykes, Andrew G.
PY - 2003/8/7
Y1 - 2003/8/7
N2 - Neutron and X-ray crystal structures of p-chlorophenylformamide (ClC 6H4NHCHO, 1) have been determined after recrystallization from methanol and acetone solvents. Acetone and methanol grown samples are polymorphic, where the central layer of a three layer asymmetric unit is partially (0.37:0.63) reversed within the acetone grown crystal. All structures reveal that the formamide group is essentially coplanar with the chlorophenyl ring. The possibility of hydrogen atom transfer between amide and iminol tautomers has been ruled out on the basis of crystallographic results and additional 13C CPMAS NMR and inelastic neutron scattering investigations. Only infinite chains of hydrogen-bonded formamide units are found in the crystal. Compound 1 crystallizes from methanol in the orthorhombic space group P212121 (Mo Kα radiation; 173 K; Z = 4; a = 6.1356(2) Å, b = 9.5362(3) Å, c = 11.8990(4) Å; V = 696.2 Å3) and (neutron radiation; 20 K; Z = 4; a = 6.0873(10) Å, b = 9.5095(15) Å, c = 11.814(5) Å; V= 683.9 Å3). From acetone, a supercell is observed for crystalline 1, where 3a = c (P212121; Mo Kα radiation; 173 K; Z = 12; a = 9.5704(2) Å, b = 11.9479(1) Å, c = 18.4555(2) Å; V= 2110.3 Å3).
AB - Neutron and X-ray crystal structures of p-chlorophenylformamide (ClC 6H4NHCHO, 1) have been determined after recrystallization from methanol and acetone solvents. Acetone and methanol grown samples are polymorphic, where the central layer of a three layer asymmetric unit is partially (0.37:0.63) reversed within the acetone grown crystal. All structures reveal that the formamide group is essentially coplanar with the chlorophenyl ring. The possibility of hydrogen atom transfer between amide and iminol tautomers has been ruled out on the basis of crystallographic results and additional 13C CPMAS NMR and inelastic neutron scattering investigations. Only infinite chains of hydrogen-bonded formamide units are found in the crystal. Compound 1 crystallizes from methanol in the orthorhombic space group P212121 (Mo Kα radiation; 173 K; Z = 4; a = 6.1356(2) Å, b = 9.5362(3) Å, c = 11.8990(4) Å; V = 696.2 Å3) and (neutron radiation; 20 K; Z = 4; a = 6.0873(10) Å, b = 9.5095(15) Å, c = 11.814(5) Å; V= 683.9 Å3). From acetone, a supercell is observed for crystalline 1, where 3a = c (P212121; Mo Kα radiation; 173 K; Z = 12; a = 9.5704(2) Å, b = 11.9479(1) Å, c = 18.4555(2) Å; V= 2110.3 Å3).
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U2 - 10.1021/jp034271i
DO - 10.1021/jp034271i
M3 - Article
AN - SCOPUS:0042233533
SN - 1520-6106
VL - 107
SP - 7601
EP - 7606
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 31
ER -