Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Study of three solvates of sulfamethazine
Synthesis and Solid State Pharmaceutical Centre, Department of Chemical Sciences, Bernal Institute, University of Limerick, Castletroy, Co., Limerick, Ireland.
Synthesis and Solid State Pharmaceutical Centre, Department of Chemical Sciences, Bernal Institute, University of Limerick, Castletroy, Co., Limerick, Ireland.
Synthesis and Solid State Pharmaceutical Centre, Department of Chemical Sciences, Bernal Institute, University of Limerick, Castletroy, Co., Limerick, Ireland.ORCID iD: 0000-0003-1790-2310
2017 (English)In: CrystEngComm, ISSN 1466-8033, E-ISSN 1466-8033, Vol. 19, no 43, p. 6481-6488Article in journal (Refereed) Published
Abstract [en]

Three novel solvates of sulfamethazine (SMT), an anti-microbial and anti-infective sulfonamide drug with the solvents-dimethylacetamide, dimethylformamide and dimethyl sulfoxide have been identified and characterized by analytical techniques including differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction and Raman spectroscopy. All three are 1:1 solvates. Crystal structure analysis revealed N-H-O type intermolecular hydrogen bonding interactions between SMT and the solvent imparting stability to the solvate structure. Thermal analysis measurements for the stoichiometry of the solvates were in good agreement with the single crystal data. The solubility of the solvates in their respective solvents at 25 °C has been determined. © 2017 The Royal Society of Chemistry.

Place, publisher, year, edition, pages
Cambridge, England, 2017. Vol. 19, no 43, p. 6481-6488
National Category
Chemical Sciences
Research subject
Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-260108DOI: 10.1039/c7ce01610gISI: 000414494700010Scopus ID: 2-s2.0-85033212627OAI: oai:DiVA.org:kth-260108DiVA, id: diva2:1355939
Note

Cited By :7; Export Date: 25 September 2019; Article

QC20191004

Available from: 2019-09-30 Created: 2019-09-30 Last updated: 2019-10-04Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopushttps://www2.scopus.com/inward/record.uri?eid=2-s2.0-85033212627&doi=10.1039%2fc7ce01610g&partnerID=40&md5=5cf5a0938c843442b2d593dee38b6593

Search in DiVA

By author/editor
Rasmuson, Åke Christoffer
In the same journal
CrystEngComm
Chemical Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 3 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf