Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability

Size control has been successfully achieved in inorganic materials, but it remains a challenge in polymer nanomaterials due to their polydispersity. Here, we report a facile approach to tailor the diameters of polyurethane (PU) nanoparticles (490 nm, 820 nm and 2.1 µm) via perylene bisimide (PBI) as...

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Main Authors: Xiaoxiao Zhang, Tingyuan Gong, Hong Chi, Tianduo Li
Format: Article
Language:English
Published: The Royal Society 2018-01-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.171686
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author Xiaoxiao Zhang
Tingyuan Gong
Hong Chi
Tianduo Li
author_facet Xiaoxiao Zhang
Tingyuan Gong
Hong Chi
Tianduo Li
author_sort Xiaoxiao Zhang
collection DOAJ
description Size control has been successfully achieved in inorganic materials, but it remains a challenge in polymer nanomaterials due to their polydispersity. Here, we report a facile approach to tailor the diameters of polyurethane (PU) nanoparticles (490 nm, 820 nm and 2.1 µm) via perylene bisimide (PBI) assisted self-assembly. The formed morphologies such as spindle, spherical and core–shell structures depend on the ratio of PBI and polymer concentrations. It is shown that the formation of PU nanoparticles is directed by π–π stacking of PBI and the morphology transition is not only affected by the amount of PBI incorporated, but also influenced by solvent, which controls the initial evaporation balance. Furthermore, the prepared PUs exhibit retained optical stability and enhanced thermal stability. The PUs, designed to have conjugated PBI segments in backbones, were synthesized via ring-opening and condensation reactions. Compared with the neat PU, gel permeation chromatography shows narrower molecular weight distribution. Fluorescence spectra and ultraviolet–visible spectra indicate retained maximum emission wavelength of PBI at 574 nm and 5.2% quantum yields. Thermo-gravimetric analysis and differential scanning calorimetry reveal 79°C higher decomposition temperature and 22°C higher glass transition temperature. This study provides a new way to fabricate well-defined nanostructures of functionalized PUs.
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spelling doaj.art-d00001b3bc7c4701a8a0fd9075400cdd2022-12-21T19:22:11ZengThe Royal SocietyRoyal Society Open Science2054-57032018-01-015310.1098/rsos.171686171686Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stabilityXiaoxiao ZhangTingyuan GongHong ChiTianduo LiSize control has been successfully achieved in inorganic materials, but it remains a challenge in polymer nanomaterials due to their polydispersity. Here, we report a facile approach to tailor the diameters of polyurethane (PU) nanoparticles (490 nm, 820 nm and 2.1 µm) via perylene bisimide (PBI) assisted self-assembly. The formed morphologies such as spindle, spherical and core–shell structures depend on the ratio of PBI and polymer concentrations. It is shown that the formation of PU nanoparticles is directed by π–π stacking of PBI and the morphology transition is not only affected by the amount of PBI incorporated, but also influenced by solvent, which controls the initial evaporation balance. Furthermore, the prepared PUs exhibit retained optical stability and enhanced thermal stability. The PUs, designed to have conjugated PBI segments in backbones, were synthesized via ring-opening and condensation reactions. Compared with the neat PU, gel permeation chromatography shows narrower molecular weight distribution. Fluorescence spectra and ultraviolet–visible spectra indicate retained maximum emission wavelength of PBI at 574 nm and 5.2% quantum yields. Thermo-gravimetric analysis and differential scanning calorimetry reveal 79°C higher decomposition temperature and 22°C higher glass transition temperature. This study provides a new way to fabricate well-defined nanostructures of functionalized PUs.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.171686polyurethaneperylene bisimideself-assemblyfluorescencethermal stability
spellingShingle Xiaoxiao Zhang
Tingyuan Gong
Hong Chi
Tianduo Li
Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
Royal Society Open Science
polyurethane
perylene bisimide
self-assembly
fluorescence
thermal stability
title Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
title_full Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
title_fullStr Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
title_full_unstemmed Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
title_short Nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
title_sort nanostructured polyurethane perylene bisimide ester assemblies with tuneable morphology and enhanced stability
topic polyurethane
perylene bisimide
self-assembly
fluorescence
thermal stability
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.171686
work_keys_str_mv AT xiaoxiaozhang nanostructuredpolyurethaneperylenebisimideesterassemblieswithtuneablemorphologyandenhancedstability
AT tingyuangong nanostructuredpolyurethaneperylenebisimideesterassemblieswithtuneablemorphologyandenhancedstability
AT hongchi nanostructuredpolyurethaneperylenebisimideesterassemblieswithtuneablemorphologyandenhancedstability
AT tianduoli nanostructuredpolyurethaneperylenebisimideesterassemblieswithtuneablemorphologyandenhancedstability