(R)-1-Phenylethanaminium–(S,S)-2,3-dibromosuccinate–(R,R)-2,3-dibromosuccinic acid–water (2/1/1/2)
2006 ◽
Vol 62
(4)
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pp. o1281-o1283
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From an aqueous solution of racemic 2,3-dibromosuccinic acid and (R)-1-phenylethanamine, crystals of the title compound, C8H12N+·0.5C4H2Br2O4 2−·0.5C4H4Br2O4·H2O, were obtained in almost quantitative yield. The structure contains both enantiomers of the starting material, dibromosuccinic acid. The S,S enantiomer is present as a dianion and the R,R enantiomer as the neutral acid; both of these components lie on twofold rotation axes. The structure features a complex two-dimensional network of hydrogen bonds.
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2014 ◽
Vol 70
(8)
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pp. o875-o876
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2013 ◽
Vol 69
(11)
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pp. o1632-o1632
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2015 ◽
Vol 71
(10)
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pp. o719-o720
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2006 ◽
Vol 62
(4)
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pp. o1360-o1361
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2012 ◽
Vol 68
(8)
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pp. o2561-o2561
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2015 ◽
Vol 71
(7)
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pp. o519-o520
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2006 ◽
Vol 62
(7)
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pp. o2965-o2966
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2006 ◽
Vol 62
(5)
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pp. o1735-o1737
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