Chain formation by disordered, but correlated, hydrogen bonds in cis-(2RS,4SR)-2-(thio­phen-2-yl)-2,3,4,5-tetra­hydro-1H-1-benzazepin-4-ol and cis-(2RS,4SR)-2-(5-methyl­thio­phen-2-yl)-2,3,4,5-tetra­hydro-1H-1-benz­azepin-4-ol

Blanco, M.C.; Palma, A.; Cobo, J.; Glidewell, C.

doi:10.1107/S0108270112003988

Acta Crystallographica Section C
Acta Crystallographica
Section C STRUCTURAL CHEMISTRY

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Figure 1
The molecular structures of the two independent molecules of (I)

, showing the atom-labelling schemes for (a) a molecule of type 1 and (b) a molecule of type 2, where the major and minor orientations of the thienyl substituent have occupancies of 0.856 (2) and 0.144 (2), respectively. The disordered hydroxy H atoms were modelled with an occupancy of 0.5, and displacement ellipsoids are drawn at the 30% probability level.

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

Volume 68| Part 3| February 2012| Pages o126-o130

doi:10.1107/S0108270112003988

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