dc.contributor.author
Moosavi-Zare, Ahmad Reza
dc.contributor.author
Zolfigol, Mohammad Ali
dc.contributor.author
Khakyzadeh, Vahid
dc.contributor.author
Böttcher, Christoph
dc.contributor.author
Beyzavi, Mohammad Hassan
dc.contributor.author
Zare, Abdolkarim
dc.contributor.author
Hasaninejad, Alireza
dc.contributor.author
Luque, Rafael
dc.date.accessioned
2018-06-08T04:05:43Z
dc.date.available
2016-09-26T11:14:59.695Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/16565
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-20746
dc.description.abstract
We report a novel nanostructured organosalt, based on sulfonic acid
functionalized pyrazinium {[H-pyrazine–SO3H]Cl2} that was synthesized and
characterized by several techniques including Fourier transform infrared (FT-
IR) spectroscopy, X-ray diffraction (XRD), thermal gravimetric analysis (TGA),
differential thermal gravimetric (DTG) analysis, transmission electron
microscopy (TEM), mass spectrometry (MS), proton NMR (1H NMR), carbon-13 NMR
(13C NMR) and also electron diffraction (ED) patterns. Results proved that the
unprecedented sulfonated pyrizinium organosalt is indeed nanostructured and
highly crystalline as supported by TEM, ED and XRD studies, having an average
nanoparticle size of 50 nm according to TEM micrographs. The novel nano-
organocatalyst was proved to be an efficient catalyst in the synthesis of
1,2,4,5-tetrasubstituted imidazoles by a one-pot multi-component condensation
of benzil, a broad range of aldehydes, primary amines and ammonium acetate at
90 °C under solvent-free conditions.
en
dc.rights.uri
http://www.rsc.org/journals-books-databases/open-access/green-open-access/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie
dc.title
Facile preparation of a nanostructured functionalized catalytically active
organosalt
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Journal of Materials Chemistry A. -2 (2014), 3, S. 770-777
dcterms.bibliographicCitation.doi
10.1039/C3TA13484A
dcterms.bibliographicCitation.url
http://pubs.rsc.org/en/content/articlelanding/2014/ta/c3ta13484a#!divAbstract
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000025417
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000007107
dcterms.accessRights.openaire
open access