TY - JOUR
T1 - New cyrhetrenyl and ferrocenyl sulfonamides
T2 - Synthesis, characterization, X-ray crystallography, theoretical study and anti-Mycobacterium tuberculosis activity
AU - Quintana, Cristóbal
AU - Silva, Gisella
AU - Klahn, A. Hugo
AU - Artigas, Vania
AU - Fuentealba, Mauricio
AU - Biot, Christophe
AU - Halloum, Iman
AU - Kremer, Laurent
AU - Novoa, Néstor
AU - Arancibia, Rodrigo
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/9/25
Y1 - 2017/9/25
N2 - A new series of cyrhetrenyl and ferrocenyl sulfonamides were designed, synthesized and characterized. The reactions of organometallic amines (P2 and P3) with the corresponding arylsulfonyl chlorides produced cyrhetrenyl (2a-c) and ferrocenyl (3a-c) sulfonamide derivatives. All the compounds were characterized by conventional spectroscopic techniques (FT-IR, 1H and 13C NMR and mass spectrometry). The proposed molecular structures of 2a and 3a were confirmed by single-crystal X-ray crystallography. Theoretical calculations at the DFT level were also carried out as an approximation to rationalize the influences of the electronic natures of the organometallic fragments into the sulfonamide skeleton. All the complexes were screened in vitro against Mycobacterium tuberculosis and exhibited only modest activities in the micromolar range.
AB - A new series of cyrhetrenyl and ferrocenyl sulfonamides were designed, synthesized and characterized. The reactions of organometallic amines (P2 and P3) with the corresponding arylsulfonyl chlorides produced cyrhetrenyl (2a-c) and ferrocenyl (3a-c) sulfonamide derivatives. All the compounds were characterized by conventional spectroscopic techniques (FT-IR, 1H and 13C NMR and mass spectrometry). The proposed molecular structures of 2a and 3a were confirmed by single-crystal X-ray crystallography. Theoretical calculations at the DFT level were also carried out as an approximation to rationalize the influences of the electronic natures of the organometallic fragments into the sulfonamide skeleton. All the complexes were screened in vitro against Mycobacterium tuberculosis and exhibited only modest activities in the micromolar range.
KW - Anti-Mycobacterium tuberculosis activity
KW - Cyrhetrene
KW - DFT calculations
KW - Ferrocene
KW - Organometallic sulfonamide
UR - http://www.scopus.com/inward/record.url?scp=85021431826&partnerID=8YFLogxK
U2 - 10.1016/j.poly.2017.06.015
DO - 10.1016/j.poly.2017.06.015
M3 - Article
AN - SCOPUS:85021431826
VL - 134
SP - 166
EP - 172
JO - Polyhedron
JF - Polyhedron
SN - 0277-5387
ER -