Cargando…

Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)

Reaction of CoCl(2)·6H(2)O with KNCSe and 4-meth­oxy­pyridine in water led to the formation of the title compound, [Co(NCSe)(2)(C(6)H(7)NO)(4)] or Co(NCSe)(2)(4-meth­oxy­pyridine)(2), which was characterized by single-crystal X-ray diffraction. Its asymmetric unit consists of one crystallographicall...

Descripción completa

Detalles Bibliográficos
Autores principales: Näther, Christian, Jess, Inke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993910/
https://www.ncbi.nlm.nih.gov/pubmed/36909984
http://dx.doi.org/10.1107/S2056989023001391
_version_ 1784902591823478784
author Näther, Christian
Jess, Inke
author_facet Näther, Christian
Jess, Inke
author_sort Näther, Christian
collection PubMed
description Reaction of CoCl(2)·6H(2)O with KNCSe and 4-meth­oxy­pyridine in water led to the formation of the title compound, [Co(NCSe)(2)(C(6)H(7)NO)(4)] or Co(NCSe)(2)(4-meth­oxy­pyridine)(2), which was characterized by single-crystal X-ray diffraction. Its asymmetric unit consists of one crystallographically independent Co cation, two seleno­cyanate anions and four 4-meth­oxy­pyridine coligands in general positions. In the crystal structure, the cobalt cations are sixfold coordinated by two terminal N-bonded seleno­cyanate anions and four 4-meth­oxy­pyridine coligands within a slightly distorted octa­hedral coordination. Between the complexes, weak C—H⋯Se inter­actions are found. IR spectroscopic investigations revealed that the CN stretching vibration of the anionic ligands is observed at 2068 cm(−1), which is in agreement with the presence of only terminally coordinated seleno­cyanate anions. PXRD measurements prove that a pure compound was obtained. Differential thermoanalysis coupled to thermogravimetry (DTA-TG) at different heating rates shows that the TG curves are poorly resolved. PXRD measurements of the residue obtained by a TG measurement prove that an amorphous compound was obtained.
format Online
Article
Text
id pubmed-9993910
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-99939102023-03-09 Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II) Näther, Christian Jess, Inke Acta Crystallogr E Crystallogr Commun Research Communications Reaction of CoCl(2)·6H(2)O with KNCSe and 4-meth­oxy­pyridine in water led to the formation of the title compound, [Co(NCSe)(2)(C(6)H(7)NO)(4)] or Co(NCSe)(2)(4-meth­oxy­pyridine)(2), which was characterized by single-crystal X-ray diffraction. Its asymmetric unit consists of one crystallographically independent Co cation, two seleno­cyanate anions and four 4-meth­oxy­pyridine coligands in general positions. In the crystal structure, the cobalt cations are sixfold coordinated by two terminal N-bonded seleno­cyanate anions and four 4-meth­oxy­pyridine coligands within a slightly distorted octa­hedral coordination. Between the complexes, weak C—H⋯Se inter­actions are found. IR spectroscopic investigations revealed that the CN stretching vibration of the anionic ligands is observed at 2068 cm(−1), which is in agreement with the presence of only terminally coordinated seleno­cyanate anions. PXRD measurements prove that a pure compound was obtained. Differential thermoanalysis coupled to thermogravimetry (DTA-TG) at different heating rates shows that the TG curves are poorly resolved. PXRD measurements of the residue obtained by a TG measurement prove that an amorphous compound was obtained. International Union of Crystallography 2023-02-21 /pmc/articles/PMC9993910/ /pubmed/36909984 http://dx.doi.org/10.1107/S2056989023001391 Text en © Näther and Jess 2023 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Communications
Näther, Christian
Jess, Inke
Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title_full Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title_fullStr Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title_full_unstemmed Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title_short Synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κN)tetra­kis­(4-meth­oxy­pyridine-κN)cobalt(II)
title_sort synthesis, crystal structure and properties of bis­(iso­seleno­cyanato-κn)tetra­kis­(4-meth­oxy­pyridine-κn)cobalt(ii)
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993910/
https://www.ncbi.nlm.nih.gov/pubmed/36909984
http://dx.doi.org/10.1107/S2056989023001391
work_keys_str_mv AT natherchristian synthesiscrystalstructureandpropertiesofbisisoselenocyanatokntetrakis4methoxypyridinekncobaltii
AT jessinke synthesiscrystalstructureandpropertiesofbisisoselenocyanatokntetrakis4methoxypyridinekncobaltii