English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  (E)-1-(2-Hydroxy-5-methoxybenzylidene)thiosemicarbazide.

Ardakani, A. A., Kargar, H., Kia, R., & Tahir, M. N. (2012). (E)-1-(2-Hydroxy-5-methoxybenzylidene)thiosemicarbazide. Acta Crystallographica Section E, 68(2), o324-o325. doi:10.1107%2FS1600536811056182.

Item is

Files

show Files
hide Files
:
2366895.pdf (Publisher version), 451KB
Name:
2366895.pdf
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-
:
2366895_Suppl_1.cif (Supplementary material), 16KB
Name:
2366895_Suppl_1.cif
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
text/plain / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-
:
2366895_Suppl_2.hkl (Supplementary material), 132KB
Name:
2366895_Suppl_2.hkl
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
text/plain / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-
:
2366895_Suppl_3.cml (Supplementary material), 5KB
Name:
2366895_Suppl_3.cml
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/xml / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-
:
2366895_Suppl_4.html (Supplementary material), 129KB
Name:
2366895_Suppl_4.html
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/xhtml+xml / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-

Locators

show

Creators

show
hide
 Creators:
Ardakani, A. A., Author
Kargar, H., Author
Kia, R.1, Author           
Tahir, M. N., Author
Affiliations:
1Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for Biophysical Chemistry, Max Planck Society, ou_578564              

Content

show
hide
Free keywords: -
 Abstract: In the title mol­ecule, C9H11N3O2S, an intra­molecular O—H⋯N hydrogen bond generates an S(6) ring motif. In the crystal, mol­ecules are linked via pairs of N—H⋯S inter­actions, forming inversion dimers with R 2 2(8) ring motifs. These dimers are further linked via N—H⋯S and N—H⋯O hydrogen bonds, forming a two-dimensional network lying parallel to (100). The crystal structure is further stabilized by inter­molecular π–π inter­actions [centroid–centroid distance = 3.7972 (9) Å].

Details

show
hide
Language(s): eng - English
 Dates: 2012-01-112012-02-01
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1107%2FS1600536811056182
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Acta Crystallographica Section E
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 68 (2) Sequence Number: - Start / End Page: o324 - o325 Identifier: -