A STEROID DERIVATIVE THAT CRYSTALLIZES WITH 3 MOLECULES IN THE ASYMMETRIC UNIT

Citation
Cp. Brock et al., A STEROID DERIVATIVE THAT CRYSTALLIZES WITH 3 MOLECULES IN THE ASYMMETRIC UNIT, Acta crystallographica. Section C, Crystal structure communications, 50, 1994, pp. 434-438
Citations number
14
Categorie Soggetti
Crystallography
ISSN journal
01082701
Volume
50
Year of publication
1994
Part
3
Pages
434 - 438
Database
ISI
SICI code
0108-2701(1994)50:<434:ASDTCW>2.0.ZU;2-X
Abstract
Crystals of (20R,23S,24R)-5alpha-dinosteran-29-ol, C30H54-O, grow as b lades elongated in the direction of hydrogen-bonded chains of OH group s and thin in the direction of the 50 angstrom c axis. There are three independent molecules in the unit cell. Hydrogen-bonding requirements dictate that the OH group of each molecule be within a few angstroms of two other OH groups, but the bulk and shape of the rest of the mole cule preclude the three being related by crystallographic symmetry ele ments. The local symmetry of the hydrogen-bonded chains is approximate ly 3(1), but the only crystallographic symmetry parallel to the chains is translation. A survey of the Cambridge Structural Database shows t hat hydrocarbons with a single OH substituent commonly crystallize wit h more than one molecule in the asymmetric unit, or in space groups wi th three- or fourfold axes.