Encapsulation of Homogeneous Catalysts in Porous Polymer Nanocapsules Produces Fast-Acting Selective Nanoreactors
Author(s) -
Sergey A. Dergunov,
А.Т. Khabiyev,
Sergey N. Shmakov,
Mariya D. Kim,
Nasim Ehterami,
Mary Clare Weiss,
Vladimir B. Birman,
Eugene Pinkhassik
Publication year - 2016
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.6b06735
Subject(s) - nanocapsules , nanoreactor , catalysis , polymer , materials science , chemical engineering , monomer , kinetics , polymerization , nanochemistry , polymer chemistry , nanoparticle , chemistry , nanotechnology , organic chemistry , composite material , physics , quantum mechanics , engineering
Nanoreactors were created by entrapping homogeneous catalysts in hollow nanocapsules with 200 nm diameter and semipermeable nanometer-thin shells. The capsules were produced by the polymerization of hydrophobic monomers in the hydrophobic interior of the bilayers of self-assembled surfactant vesicles. Controlled nanopores in the shells of nanocapsules ensured long-term retention of the catalysts coupled with the rapid flow of substrates and products in and out of nanocapsules. The study evaluated the effect of encapsulation on the catalytic activity and stability of five different catalysts. Comparison of kinetics of five diverse reactions performed in five different solvents revealed the same reaction rates for free and encapsulated catalysts. Identical reaction kinetics confirmed that placement of catalysts in the homogeneous interior of polymer nanocapsules did not compromise catalytic efficiency. Encapsulated organometallic catalysts showed no loss of metal ions from nanocapsules suggesting stabilization of the complexes was provided by nanocapsules. Controlled permeability of the shells of nanocapsules enabled size-selective catalytic reactions.
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