TY - JOUR
T1 - Synthesis of secondary arylamine copolymers with Iron(II) clathrochelate units and their functionalization into tertiary Polyarylamines via Buchwald-Hartwig cross-coupling reaction
AU - Shetty, Suchetha
AU - Baig, Noorullah
AU - Al-Mousawi, Saleh
AU - Al-Sagheer, Fakhreia
AU - Alameddine, Bassam
N1 - Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/9/12
Y1 - 2019/9/12
N2 - We report the synthesis of three secondary arylamine copolymers bearing iron(II) clathrochelate units (CLP1-3). Three of the latter copolymers were post-modified into their tertiary arylamine moieties (PCLP1-3) using a mild palladium-catalyzed Buchwald-Hartwig cross-coupling reaction. Interestingly, the functionalization of the secondary arylamine groups has resulted in the formation of highly soluble target compounds PCLP1-3, which allowed for their simple isolation and full analysis via various techniques. It is noteworthy that a prototypical secondary arylamine iron(II) clathrochelate monomer CLM1 was synthesized and post-modified into its tertiary arylamine target compound CLM2. The current study discloses the first examples on making secondary arylamine copolymers with clathrochelate constituents, and proves the possible post-modification of the latter compounds into tertiary arylamine, which proves the modularity of iron(II) clathrochelate unit to make functional polymers. Formation of the monomers and copolymers was confirmed by 1H- and 13C- nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), Thermogravimetric Analysis (TGA), scanning electron microscopy (SEM), and UV–Vis absorption spectroscopy.
AB - We report the synthesis of three secondary arylamine copolymers bearing iron(II) clathrochelate units (CLP1-3). Three of the latter copolymers were post-modified into their tertiary arylamine moieties (PCLP1-3) using a mild palladium-catalyzed Buchwald-Hartwig cross-coupling reaction. Interestingly, the functionalization of the secondary arylamine groups has resulted in the formation of highly soluble target compounds PCLP1-3, which allowed for their simple isolation and full analysis via various techniques. It is noteworthy that a prototypical secondary arylamine iron(II) clathrochelate monomer CLM1 was synthesized and post-modified into its tertiary arylamine target compound CLM2. The current study discloses the first examples on making secondary arylamine copolymers with clathrochelate constituents, and proves the possible post-modification of the latter compounds into tertiary arylamine, which proves the modularity of iron(II) clathrochelate unit to make functional polymers. Formation of the monomers and copolymers was confirmed by 1H- and 13C- nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), Thermogravimetric Analysis (TGA), scanning electron microscopy (SEM), and UV–Vis absorption spectroscopy.
KW - C-N cross-coupling
KW - ESCA/XPS
KW - Functionalization of polymers
KW - Inorganic polymers
KW - Polyaniline
UR - http://www.scopus.com/inward/record.url?scp=85067681204&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2019.121606
DO - 10.1016/j.polymer.2019.121606
M3 - Article
AN - SCOPUS:85067681204
SN - 0032-3861
VL - 178
JO - Polymer
JF - Polymer
M1 - 121606
ER -