Charge induced formation of crystalline network polymers

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Order in purely organic network polymers is hard to achieve, as reversible, dynamic covalent bond formation is required. Strategies have focused on thermodynamically controlled transformations, as kinetics would not seemingly favour reversibility. Herein, we report formation of crystalline network polymers under kinetically favoured conditions by using quaternary ammonium salt linked networks. Charged bulky bridges align, even under fast reaction times (20 minutes) if the rotational freedom is granted. Adding vicinal methyl substituents blocks the ordering, hence forming amorphous networks. Raman experiments and SEM images reveal stacking of 2D layers.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2014
Language
English
Article Type
Article
Keywords

COVALENT-ORGANIC FRAMEWORKS; INTRINSIC MICROPOROSITY PIMS; HYDROGEN STORAGE MATERIALS; CARBON-DIOXIDE; TARGETED SYNTHESIS; SYNTHETIC ZEOLITE; GREEN CHEMISTRY; SURFACE-AREA; CO2 CAPTURE; ADSORPTION

Citation

RSC ADVANCES, v.4, no.104, pp.59779 - 59784

ISSN
2046-2069
DOI
10.1039/c4ra10594j
URI
http://hdl.handle.net/10203/201185
Appears in Collection
EEW-Journal Papers(저널논문)
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