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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. €

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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.

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

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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