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DTSTAMP:20261028T105920Z
SUMMARY:Programming COF organization across length scales: from polymer-gui
 ded crystallization to hierarchical assemblies
DESCRIPTION:<p><strong>IN-PERSON EVENT - REGISTER <a href="https://forms.cl
 oud.microsoft/Pages/ResponsePage.aspx?id=7y7ItE2bfUi-qg79NXo6WxH4jECG9S9Km
 yGb2KoqlQpUQVozQ0FLTTZUSTc3T1VIUzYwMVdFOU45MyQlQCN0PWcu">HERE</a></strong>
 <a href="https://forms.cloud.microsoft/Pages/ResponsePage.aspx?id=7y7ItE2b
 fUi-qg79NXo6WxH4jECG9S9KmyGb2KoqlQpUQVozQ0FLTTZUSTc3T1VIUzYwMVdFOU45MyQlQC
 N0PWcu"><strong>&nbsp\;</strong></a>to attend</p>\n<p>By Dr&nbsp\;<strong>
 Gaëlle Le Fer\,&nbsp\;</strong>University of Lille\, CNRS\, INRAE\, Lille
 \, France</p>\n<p><strong>Abstract:&nbsp\; </strong></p>\n<p>Covalent orga
 nic frameworks (COFs) are crystalline porous materials whose topology and 
 pore size can be precisely programmed through the molecular design of thei
 r building blocks.<sup>1\,2</sup> A central challenge is to extend this mo
 lecular programmability to larger length scales\, where crystal orientatio
 n\, particle architecture and collective organization determine how the in
 trinsic properties of COFs can be translated into functional materials.<su
 p>3</sup></p>\n<p>Our approach combines reticular chemistry and macromolec
 ular chemistry\, using linear polymers as active vectors of supramolecular
  organization. Rather than simply acting as additives\, the polymers inter
 act with COF building blocks\, modulating nucleation\, crystal growth\, an
 d the assembly of crystalline domains. Through these interactions\, they c
 an shape COF organization across multiple length scales\, from local molec
 ular organization to crystal orientation and particle morphology. This app
 roach has enabled us to access different COF particle architectures\, incl
 uding raspberry-like particles with radial crystal orientation<sup>4</sup>
  and hollow spheres with porous membranes.<sup>5</sup> These hollow archit
 ectures provide a direct link between structure and function: their porous
  membranes can regulate molecular transport\, allowing the particles to op
 erate as size-selective microreactors. We also highlighted the potential o
 f these hollow COF particles to reorganize within polymer gels into elonga
 ted micrometer-scale tubular structures\, revealing a new level of hierarc
 hical organization.</p>\n<p>Overall\, these results show how polymers can 
 guide COF organization from crystal growth to particle assembly. More broa
 dly\, they show that COFs are not only static porous solids\, but can also
  behave as dynamic systems capable of evolving and reorganizing in respons
 e to their environment. This dynamic behavior opens new opportunities for 
 COF-based materials with adaptive properties.</p>\n<p>References:</p>\n<ol
 >\n<li>Cote\, A. P.\, Benin\, A. I.\;\,Ockwig\, N. W.\, O'Keeffe\, M.\, Ma
 tzger\, A. J.\,Yaghi\, O. M. Porous\, crystalline\, covalent organic frame
 works. <em>Science </em><strong>2005</strong>\, <em>310</em> (5751)\, 1166
 .</li>\n<li>Bisbey\, R. P.\, Dichtel\, W. R. Covalent organic frameworks a
 s a platform for multidimensional polymerization. <em>ACS central science 
 </em><strong>2017</strong>\, <em>3</em> (6)\, 533.</li>\n<li>Dey\, K.\; Mo
 hata\, S.\; Banerjee\, R. Covalent organic frameworks and supramolecular n
 ano-synthesis. <em>ACS Nano </em><strong>2021</strong>\, <em>15</em> (8)\,
  12723.</li>\n<li>Salaün\, P.\, Fadel A.\, Pelaez‐Fernandez\, M.\, Moul
 oud\, B.‐\, Tahon\, J.-F.\, Volkringer\, C.\, Addad\, A.\, Woisel\, P.\,
  Le Fer\, G. Cooperative synthesis of raspberry‐like covalent organic fr
 amework‐polymer particles with a radial single‐crystal grain orientati
 on\, <em>Small</em> <strong>2023</strong>\, <em>19</em> (49)\, 2303697.</l
 i>\n<li>Salaün\, P.\, Mouloud\, B.-E.\, Richard\, E. \,Mariani\, V. Tahon
 \, J.-F.\, Addad\, A.\, Grazon\, C.\, Woisel\, P.\, Le Fer\, G. Polymer-dr
 iven self-templated synthesis of boronate-COF hollow spheres: toward the d
 evelopment of nanoreactors\, <em>ACS Applied Materials and Interfaces</em>
  <strong>2026</strong>\, DOI:1021/acsami.6c06835.</li>\n</ol>\n<p><strong>
 Short bio</strong>:</p>\n<p>Gaëlle Le Fer is a CNRS researcher since 2020
 \, in the “Unité Matériaux et Transformations” (UMR 8207) in Lille\,
  France. In 2015\, she obtained a PhD in chemistry (Université Paris-Est)
  at the Institut de Chimie et des Matériaux Paris-Est (UMR 7182). Her PhD
  thesis was focused on the development of polymer nanoparticles. Following
  her interest in polymer self-assembly\, she joined the group of Prof. Sé
 bastien Lecommandoux at the Laboratoire de Chimie des Polymères Organique
 s (UMR 5629) for a 2-year post-doctorate. Then\, she moved to the Prof. Ma
 tthew Becker’s group at the University of Akron\, USA\, for a second 2-y
 ear postdoc. She designed and characterized 3D-printed porous shape-memory
  materials. Currently\, she is developing her own topic on materials combi
 ning both COFs and polymers. She supervised three PhD students and four po
 stdocs\, was the coordinator of one ANR\, one international chair with Ghe
 nt University (Belgium) and one CNRS-Emergence project.</p>\n<p><strong>Ho
 sted by</strong>&nbsp\;ICREA Prof. Daniel Maspoch\, Group Leader\, <a href
 ="/en/supramolecular-nanochemistry-and-materials-group/daniel-maspoch">Sup
 ramolecular Nanochemistry ans Materials</a>&nbsp\;group at ICN2.</p>\n<p s
 tyle="text-align: justify\;">&nbsp\;</p>
DTSTART:20261030T110000
DTEND:20261030T225959
LOCATION:UAB Sala Graus Facultad de Ciències i Biociències
CATEGORIES:ICN2 Seminars
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