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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.

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

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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