Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-beta-D-thiogalactopyranoside

C  Glidewell; J N  Low; J L  Wardell

Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-beta-D-thiogalactopyranoside

C Glidewell, J N Low, J L Wardell

School of Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

In the title compound, C12H15NO7S, the molecular conformation shows a concerted disrotatory twist of the nitro group and the galactose fragment out of the plane of the aryl ring. The molecules are linked by O-H . . .O hydrogen bonds [O . . .O range 2.725 (2)-3.024 (2) Angstrom and O-H . . .O range 155-175 degrees] to form a three-dimensional framework.

Original language	English
Pages (from-to)	1465-1467
Number of pages	3
Journal	Acta Crystallographica Section C-Crystal Structure Communications
Volume	56
Publication status	Published - Dec 2000

Cite this

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title = "Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-beta-D-thiogalactopyranoside",

abstract = "In the title compound, C12H15NO7S, the molecular conformation shows a concerted disrotatory twist of the nitro group and the galactose fragment out of the plane of the aryl ring. The molecules are linked by O-H . . .O hydrogen bonds [O . . .O range 2.725 (2)-3.024 (2) Angstrom and O-H . . .O range 155-175 degrees] to form a three-dimensional framework.",

author = "C Glidewell and Low, {J N} and Wardell, {J L}",

year = "2000",

month = dec,

language = "English",

volume = "56",

pages = "1465--1467",

journal = "Acta Crystallographica Section C-Crystal Structure Communications",

issn = "1600-5759",

publisher = "International Union of Crystallography",

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TY - JOUR

T1 - Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-beta-D-thiogalactopyranoside

AU - Glidewell, C

AU - Low, J N

AU - Wardell, J L

PY - 2000/12

Y1 - 2000/12

N2 - In the title compound, C12H15NO7S, the molecular conformation shows a concerted disrotatory twist of the nitro group and the galactose fragment out of the plane of the aryl ring. The molecules are linked by O-H . . .O hydrogen bonds [O . . .O range 2.725 (2)-3.024 (2) Angstrom and O-H . . .O range 155-175 degrees] to form a three-dimensional framework.

AB - In the title compound, C12H15NO7S, the molecular conformation shows a concerted disrotatory twist of the nitro group and the galactose fragment out of the plane of the aryl ring. The molecules are linked by O-H . . .O hydrogen bonds [O . . .O range 2.725 (2)-3.024 (2) Angstrom and O-H . . .O range 155-175 degrees] to form a three-dimensional framework.

M3 - Article

SN - 1600-5759

VL - 56

SP - 1465

EP - 1467

JO - Acta Crystallographica Section C-Crystal Structure Communications

JF - Acta Crystallographica Section C-Crystal Structure Communications

ER -

Conformational preferences and supramolecular aggregation in 2-nitrophenylthiolates: 2-nitrophenyl-beta-D-thiogalactopyranoside

Abstract

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