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Fischer, Andreas (2006) (R)-1-Phenylethanaminium–(S,S)-2,3-dibromosuccinate–(R,R)-2,3-dibromosuccinic acid–water (2/1/1/2) Acta Crystallographica Section E Structure Reports Online, 62 (4) doi:10.1107/s1600536806007628

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Reference TypeJournal (article/letter/editorial)
Title(R)-1-Phenylethanaminium–(S,S)-2,3-dibromosuccinate–(R,R)-2,3-dibromosuccinic acid–water (2/1/1/2)
JournalActa Crystallographica Section E Structure Reports Online
AuthorsFischer, AndreasAuthor
Year2006 (April 1)Volume62
Issue4
PublisherInternational Union of Crystallography (IUCr)
DOIdoi:10.1107/s1600536806007628Search in ResearchGate
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Mindat Ref. ID460671Long-form Identifiermindat:1:5:460671:4
GUID0
Full ReferenceFischer, Andreas (2006) (R)-1-Phenylethanaminium–(S,S)-2,3-dibromosuccinate–(R,R)-2,3-dibromosuccinic acid–water (2/1/1/2) Acta Crystallographica Section E Structure Reports Online, 62 (4) doi:10.1107/s1600536806007628
Plain TextFischer, Andreas (2006) (R)-1-Phenylethanaminium–(S,S)-2,3-dibromosuccinate–(R,R)-2,3-dibromosuccinic acid–water (2/1/1/2) Acta Crystallographica Section E Structure Reports Online, 62 (4) doi:10.1107/s1600536806007628
In(2006, April) Acta Crystallographica Section E Structure Reports Online Vol. 62 (4) International Union of Crystallography (IUCr)
Abstract/NotesFrom 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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