Format

Send to

Choose Destination
Chemistry. 2018 Jan 9;24(2):478-486. doi: 10.1002/chem.201704714. Epub 2017 Dec 4.

Dendritic and Core-Shell-Corona Mesoporous Sister Nanospheres from Polymer-Surfactant-Silica Self-Entanglement.

Author information

1
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, P.R. China.
2
Laboratoire de chimie, Ecole Normale Supérieure de Lyon, Institut de Chimie de Lyon, Université de Lyon, 46 Allée d'italie, 69364, Lyon cedex 07, France.

Abstract

Mesoporous nanospheres are highly regarded for their applications in nanomedicine, optical devices, batteries, nanofiltration, and heterogeneous catalysis. In the last field, the dendritic morphology, which favors molecular diffusion, is a very important morphology known for silica, but not yet for carbon. A one-pot, easy, and scalable co-sol-gel route by using the triphasic resol-surfactant-silica system is shown to yield the topologies of dendritic and core-shell-corona mesoporous sister nanospheres by inner radial phase speciation control on a mass-transfer-limited process, depending on the relative polycondensation rates of the resol polymer and silica phases. The trick was the use of polyolamines with different catalytic activities on each hard phase polycondensation. The self-entanglement of phases is produced at the {O- , S+ , I- } organic-surfactant-inorganic interface. Mono- and biphasic mesoporous sister nanospheres of carbon and/or silica are derivatized from each mother nanospheres and called "syntaxic" because of similar sizes and mirrored morphologies. Comparing these "false twins", or yin and yang mesoporous nanospheres, functionalized by sulfonic groups provides evidence of the superiority of the dendritic topologies and the absence of a shell on the diffusion-controlled catalytic alkylation of m-cresol.

KEYWORDS:

mesoporous materials; nanoparticles; organic-inorganic hybrid composites; self-assembly; synthesis design

PMID:
29105872
DOI:
10.1002/chem.201704714

Supplemental Content

Loading ...
Support Center