Crystal structures of the recreational drug N -(4-meth-oxy-phen-yl)piperazine (MeOPP) and three of its salts
Crystal structures are reported for -(4-meth-oxy-phen-yl)piperazine (MeOPP), (I), and for its 3,5-di-nitro-benzoate, 2,4,6-tri-nitro-phenolate (picrate) and 4-amino-benzoate salts, (II)-(IV), the last of which crystallizes as a monohydrate. In MeOPP, C H N O, (I), the 4-meth-oxy-phenyl group is near...
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Published in: | Acta crystallographica. Section E, Crystallographic communications Vol. 76; no. Pt 4; pp. 488 - 495 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
International Union of Crystallography
01-04-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | Crystal structures are reported for
-(4-meth-oxy-phen-yl)piperazine (MeOPP), (I), and for its 3,5-di-nitro-benzoate, 2,4,6-tri-nitro-phenolate (picrate) and 4-amino-benzoate salts, (II)-(IV), the last of which crystallizes as a monohydrate. In MeOPP, C
H
N
O, (I), the 4-meth-oxy-phenyl group is nearly planar and it occupies an equatorial site on the piperazine ring: the mol-ecules are linked into simple
(10) chains by N-H⋯O hydrogen bonds. In each of the salts,
, C
H
N
O
·C
H
N
O
, (II), C
H
N
O
·C
H
N
O
, (III), and C
H
N
O
·C
H
NO
·H
O, (IV), the effectively planar 4-meth-oxy-phenyl substituent again occupies an equatorial site on the piperazine ring. In (II), two of the nitro groups are disordered over two sets of atomic sites and the bond distances in the anion indicate considerable delocalization of the negative charge over the C atoms of the ring. The ions in (II) are linked by two N-H⋯O hydrogen bonds to form a cyclic, centrosymmetric four-ion aggregate; those in (III) are linked by a combination of N-H⋯O and C-H⋯π(arene) hydrogen bonds to form sheets; and the components of (IV) are linked by N-H⋯O, O-H⋯O and C-H⋯π(arene) hydrogen bonds to form a three-dimensional framework structure. Comparisons are made with the structures of some related compounds. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2056-9890 2056-9890 |
DOI: | 10.1107/S2056989020002844 |