O-H ... PI(ARENE) INTERMOLECULAR HYDROGEN-BONDING IN THE STRUCTURE OF 1,1,2-TRIPHENYLETHANOL

被引:31
作者
FERGUSON, G [1 ]
GALLAGHER, JF [1 ]
GLIDEWELL, C [1 ]
ZAKARIA, CM [1 ]
机构
[1] UNIV ST ANDREWS,SCH CHEM,ST ANDREWS KY16 9ST,FIFE,SCOTLAND
关键词
D O I
10.1107/S0108270193007164
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The 1,1,2-triphenylethanol molecule, Ph2(PhCH2)COH (1), forms centrosymmetric dimers in the solid state. The shortest O ... O separation, 5.837 (3) angstrom, is too long for any O-H ... O hydrogen-bond formation. Instead, there are O-H ... pi(arene) interactions between the hydroxyl group of one molecule and a phenyl group of a centrosymmetrically related molecule. The O ... C and H ... C distances between the hydroxyl group and the closest phenyl-ring C atom are 3.525 (4) and 2.73 (4) angstrom, respectively. These intermolecular contacts are the only driving force towards dimer formation in the solid state.
引用
收藏
页码:70 / 73
页数:4
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