Issue 37, 2013

Synthon polymorphs of sulfacetamide–acetamide cocrystal based on N–H⋯O[double bond, length as m-dash]S and N–H⋯O[double bond, length as m-dash]C hydrogen bonding

Abstract

A rare case of polymorphism in SO2–NH–C[double bond, length as m-dash]O containing molecules is reported in the 1 : 1 cocrystal of sulfacetamide (SACT) and acetamide (ACT). The R44(16) ring motif in polymorph 1 is assembled via N–H⋯O[double bond, length as m-dash]S and N–H⋯O[double bond, length as m-dash]C H-bonds whereas a similar hydrogen-bonded ring motif made of N–H⋯O[double bond, length as m-dash]C H-bonds only is present in form 2.

Graphical abstract: Synthon polymorphs of sulfacetamide–acetamide cocrystal based on N–H⋯O [[double bond, length as m-dash]] S and N–H⋯O [[double bond, length as m-dash]] C hydrogen bonding

Supplementary files

Article information

Article type
Communication
Submitted
19 Jun 2013
Accepted
11 Jul 2013
First published
15 Jul 2013

CrystEngComm, 2013,15, 7456-7461

Synthon polymorphs of sulfacetamide–acetamide cocrystal based on N–H⋯O[double bond, length as m-dash]S and N–H⋯O[double bond, length as m-dash]C hydrogen bonding

N. R. Goud and A. Nangia, CrystEngComm, 2013, 15, 7456 DOI: 10.1039/C3CE41179F

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