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Influence of Chain Architecture on Nanopore Accessibility in Polyelectrolyte Block‐Co‐Oligomer Functionalized Mesopores

Brilmayer, Robert ; Hess, Christian ; Andrieu‐Brunsen, Annette (2021)
Influence of Chain Architecture on Nanopore Accessibility in Polyelectrolyte Block‐Co‐Oligomer Functionalized Mesopores.
In: Small, 41 (15)
doi: 10.26083/tuprints-00019924
Artikel, Zweitveröffentlichung, Verlagsversion

Kurzbeschreibung (Abstract)

Functionalized ordered mesoporous silica materials are commonly investigated for applications such as drug release, sensing, and separation processes. Although, various homopolymer functionalized responsive mesopores are reported, little focus has been put on copolymers in mesopores. Mesoporous silica films are functionalized with responsive and orthogonally charged block-co-oligomers. Responsive 2-dimethylamino)ethyl methacrylate)-block-2-(methacryloyloxy)ethyl phosphate (DMAEMA-b-MEP) block-co-oligomers are introduced into mesoporous films using controlled photoiniferter initiated polymerization. This approach allows a very flexible charge composition design. The obtained block-co-oligomer functionalized mesopores show a complex gating behavior indicating a strong interplay between the different blocks emphasizing the strong influence of charge distribution inside mesopores on ionic pore accessibility. For example, in contrast to mesopores functionalized with zwitterionic polymers, DMAEMA-b-MEP block-co-oligomer functionalized mesopores, containing two oppositely charged blocks, do not show bipolar ion exclusion, demonstrating the influence of the chain architecture on mesopore accessibility. Furthermore, ligand binding–based selective gating is strongly influenced by this chain architecture as demonstrated by an expansion of pore accessibility states for block-co-oligomer functionalized mesopores as compared to the individual polyelectrolyte functionalization for calcium induced gating.

Typ des Eintrags: Artikel
Erschienen: 2021
Autor(en): Brilmayer, Robert ; Hess, Christian ; Andrieu‐Brunsen, Annette
Art des Eintrags: Zweitveröffentlichung
Titel: Influence of Chain Architecture on Nanopore Accessibility in Polyelectrolyte Block‐Co‐Oligomer Functionalized Mesopores
Sprache: Englisch
Publikationsjahr: 2021
Verlag: Wiley
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Small
Jahrgang/Volume einer Zeitschrift: 41
(Heft-)Nummer: 15
Kollation: 7 Seiten
DOI: 10.26083/tuprints-00019924
URL / URN: https://tuprints.ulb.tu-darmstadt.de/19924
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Herkunft: Zweitveröffentlichungsservice
Kurzbeschreibung (Abstract):

Functionalized ordered mesoporous silica materials are commonly investigated for applications such as drug release, sensing, and separation processes. Although, various homopolymer functionalized responsive mesopores are reported, little focus has been put on copolymers in mesopores. Mesoporous silica films are functionalized with responsive and orthogonally charged block-co-oligomers. Responsive 2-dimethylamino)ethyl methacrylate)-block-2-(methacryloyloxy)ethyl phosphate (DMAEMA-b-MEP) block-co-oligomers are introduced into mesoporous films using controlled photoiniferter initiated polymerization. This approach allows a very flexible charge composition design. The obtained block-co-oligomer functionalized mesopores show a complex gating behavior indicating a strong interplay between the different blocks emphasizing the strong influence of charge distribution inside mesopores on ionic pore accessibility. For example, in contrast to mesopores functionalized with zwitterionic polymers, DMAEMA-b-MEP block-co-oligomer functionalized mesopores, containing two oppositely charged blocks, do not show bipolar ion exclusion, demonstrating the influence of the chain architecture on mesopore accessibility. Furthermore, ligand binding–based selective gating is strongly influenced by this chain architecture as demonstrated by an expansion of pore accessibility states for block-co-oligomer functionalized mesopores as compared to the individual polyelectrolyte functionalization for calcium induced gating.

Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-199247
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Makromolekulare Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Physikalische Chemie
Hinterlegungsdatum: 19 Nov 2021 13:08
Letzte Änderung: 22 Nov 2021 06:27
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