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Star Polymers SIGNED

When Soft Matter Goes Really Soft – A New Paradigm for Star Polymer Self-Assembly

Total Cost €

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EC-Contrib. €

0

Partnership

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 Star Polymers project word cloud

Explore the words cloud of the Star Polymers project. It provides you a very rough idea of what is the project "Star Polymers" about.

equilibrium    stringent    prevent    tools    physical    structures    ordered    directional    solvophilic    interactions    block    electron    limited    biologic    scattering    supramolecular    emergence    comprise    reconfigurability    spontaneous    domains    self    solvophobic    macroscopic    segments    mechanical    propensity    drive    orientations    envisioned    encountered    synthetic    trapped    soft    undesired    crystalline    simulation    cores    fluctuations    located    colloidal    assemblies    situ    reconfigure    background    adaptability    absent    guide    complementing    building    superstructure    photonic    imprint    paradigm    analytic    complexes    flexible    geometric    core    resolved    porous    man    capsids    class    adverse    particle    optimum    pioneering    metastable    assembly    place    fail    prevents    freedom    periphery    locked    made    patch    arms    blocks    form    micro    flexibility    separation    structural    hard    complexity    criterion    lack    polymer    polymers    deformability    particles    patchy    linked    unprecedented    introducing    ing    lattices    multiprotein    microscopy    relaxes    time    quasi    uniformity    attached    grafted    virus    conformational    patches   

Project "Star Polymers" data sheet

The following table provides information about the project.

Coordinator
TECHNISCHE UNIVERSITEIT EINDHOVEN 

Organization address
address: GROENE LOPER 3
city: EINDHOVEN
postcode: 5612 AE
website: www.tue.nl/en

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Netherlands [NL]
 Total cost 175˙572 €
 EC max contribution 175˙572 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-01-13   to  2022-01-12

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITEIT EINDHOVEN NL (EINDHOVEN) coordinator 175˙572.00

Map

 Project objective

Biologic supramolecular assemblies, e.g., virus capsids and multiprotein complexes, show unprecedented complexity compared to man-made structures. A key feature of the building blocks facilitating the emergence of this structural complexity is their deformability. This enables them to reconfigure during assembly to find optimum orientations within the superstructure. Here, I propose to exploit the concept of reconfigurability as design criterion for developing a new class of colloidal building blocks. Where currently available hard particles fail to form macroscopic structures due to lack of building block uniformity and undesired metastable states encountered during assembly, introducing flexibility will prevent these adverse characteristics. The envisioned building blocks are based on polymer grafted cores, where the attached polymers arms comprise solvophilic and solvophobic blocks. The limited number of arms have significant conformational freedom, a feature absent in traditional hard particles. The solvophobic segments, located at the particle’s periphery, drive spontaneous polymer micro-phase separation into patchy domains which are then locked into place. These patches imprint directional interactions to guide self-assembly and are linked to the core via flexible solvophilic polymers, enabling patch fluctuations. The resulting patch adaptability prevents the system from getting trapped in non-equilibrium states and relaxes stringent requirements on geometric uniformity, promoting the formation of long-range ordered assemblies. Following simulation studies, these soft particles should have propensity to order into ‘open’ (quasi)crystalline lattices providing unique photonic, mechanical and porous characteristics. Complementing my physical/polymer synthetic background with pioneering analytic tools, e.g. time-resolved scattering and in situ electron microscopy, this project will detail a new paradigm for self-assembly and the importance of patch flexibility.

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The information about "STAR POLYMERS" are provided by the European Opendata Portal: CORDIS opendata.

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