TY - JOUR
T1 - Magnetically separable chiral periodic mesoporous organosilica nanoparticles
AU - Omar, Suheir
AU - Abu-Reziq, Raed
N1 - Publisher Copyright:
© 2020 by the authors.
PY - 2020/9
Y1 - 2020/9
N2 - We describe, for the first time, a successful strategy for synthesizing chiral periodic mesoporous organosilica nanoparticles (PMO NPs). The chiral PMO nanoparticles were synthesized in a sol-gel process under mild conditions; their preparation was mediated by hydrolysis and condensation of chiral-bridged organo-alkoxysilane precursor compounds,(OR')3Si-R-Si(OR')3, in the presence of cetyltrimethylammonium bromide (CTAB) surfactant. The resulting nanoparticles were composed merely from a chiral- bridged organo-alkoxysilane monomer. These systems were prepared by applying different surfactants and ligands that finally afforded monodispersed chiral PMO NPs consisting of 100% bridged-organosilane precursor. In addition, the major advancement that was achieved here was, for the first time, success in preparing magnetic chiral PMO NPs. These nanoparticles were synthesized by the co-polymerization of 1,1'-((1R,2R)-1,2- diphenylethane-1,2-diyl)bis(3-(3-(triethoxysilyl) propyl) urea) chiral monomer by an oil in water (o/w) emulsion process, to afford magnetic chiral PMO NPs with magnetite NPs in their cores. The obtained materials were characterized with high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray (EDX) spectroscopy, powder X-ray diffraction (XRD), solid-state NMR analysis, circular dichroism (CD) analysis, and nitrogen sorption analysis (N2-BET).
AB - We describe, for the first time, a successful strategy for synthesizing chiral periodic mesoporous organosilica nanoparticles (PMO NPs). The chiral PMO nanoparticles were synthesized in a sol-gel process under mild conditions; their preparation was mediated by hydrolysis and condensation of chiral-bridged organo-alkoxysilane precursor compounds,(OR')3Si-R-Si(OR')3, in the presence of cetyltrimethylammonium bromide (CTAB) surfactant. The resulting nanoparticles were composed merely from a chiral- bridged organo-alkoxysilane monomer. These systems were prepared by applying different surfactants and ligands that finally afforded monodispersed chiral PMO NPs consisting of 100% bridged-organosilane precursor. In addition, the major advancement that was achieved here was, for the first time, success in preparing magnetic chiral PMO NPs. These nanoparticles were synthesized by the co-polymerization of 1,1'-((1R,2R)-1,2- diphenylethane-1,2-diyl)bis(3-(3-(triethoxysilyl) propyl) urea) chiral monomer by an oil in water (o/w) emulsion process, to afford magnetic chiral PMO NPs with magnetite NPs in their cores. The obtained materials were characterized with high-resolution scanning electron microscopy (HR-SEM), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive X-ray (EDX) spectroscopy, powder X-ray diffraction (XRD), solid-state NMR analysis, circular dichroism (CD) analysis, and nitrogen sorption analysis (N2-BET).
KW - Chiral materials
KW - Magnetic nanoparticles
KW - Nanoparticles
KW - Periodic mesoporous organosilica
UR - http://www.scopus.com/inward/record.url?scp=85090214553&partnerID=8YFLogxK
U2 - 10.3390/app10175960
DO - 10.3390/app10175960
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AN - SCOPUS:85090214553
SN - 2076-3417
VL - 10
JO - Applied Sciences (Switzerland)
JF - Applied Sciences (Switzerland)
IS - 17
M1 - 5960
ER -