Sergey Dergunov

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Name: Dergunov, Sergey
Organization: University of Connecticut , USA
Department:
Title: (PhD)
Co-reporter:Mariya D. Kim, Sergey A. Dergunov, and Eugene Pinkhassik
Langmuir August 8, 2017 Volume 33(Issue 31) pp:7732-7732
Publication Date(Web):July 5, 2017
DOI:10.1021/acs.langmuir.7b01706
This work addresses the challenge of creating hollow nanocapsules with a controlled quantity of encapsulated molecules. Such nanocontainers or nanorattle-like structures represent an attractive platform for building functional devices, including nanoreactors and nanosensors. By taking advantage of the electrostatic attraction between oppositely charged cargo molecules and the surface of the templating bilayer of catanionic vesicles, formed by mixing single-tailed cationic and anionic surfactants, we were able to achieve a substantial increase in the local concentration of molecules inside the vesicle-templated nanocapsules. Control of electrostatic interactions through changes in the formulation of catanionic vesicles or the pH of the solution enabled fine tuning of the encapsulation efficiency in capturing ionic solutes. The ability to control the quantity of entrapped molecules greatly expands the application of nanocontainers in the creation of functional nanodevices.
Co-reporter:Sergey A. DergunovAlibek T. Khabiyev, Sergey N. Shmakov, Mariya D. KimNasim Ehterami, Mary Clare Weiss, Vladimir B. Birman, Eugene Pinkhassik
ACS Nano 2016 Volume 10(Issue 12) pp:
Publication Date(Web):November 15, 2016
DOI:10.1021/acsnano.6b06735
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.Keywords: homogenous catalysis; immobilization; nanopores; nanoreactors; polymer nanocapsules; vesicles;
2,5,8,9-Tetraaza-1-phosphabicyclo[3.3.3]undecane,2,8,9-tris(1-methylethyl)-
1,2-dimyristoyl-sn-glycero-3-phospho-choline monohydrate