Interfacial Raft‐Like Structures From Bottlebrush Polymers

D Dupyo Jeon (Polymer Science & Engineering Department, Conte Center for Polymer Research) Q Qi Pan S Sai Zhao H Hong‐Gyu Seong (Polymer Science and Engineering Department Conte Center for Polymer Research University of Massachusetts Amherst Massachusetts USA) K Kyoungwon Lee (Polymer Science & Engineering Department, Conte Center for Polymer Research) X Xuchen Gan (Polymer Science & Engineering Department, Conte Center for Polymer Research) C Carla Steppan (Polymer Science and Engineering Department Conte Center for Polymer Research University of Massachusetts Amherst Massachusetts USA) S Steve Granick (Polymer Science and Engineering Department, University of Massachusetts) T Todd Emrick (Polymer Science & Engineering Department, Conte Center for Polymer Research) T Thomas P. Russell (Polymer Science & Engineering Department, Conte Center for Polymer Research)

Abstract

ABSTRACT We investigated the interfacial behavior of amphiphilic random copolymer‐grafted bottlebrush polymers (RC‐BBPs) synthesized by copper‐catalyzed azide–alkyne cycloaddition in a grafting‐to approach. RC‐BBPs stabilize the fluid–fluid interface by forming laterally confined, “raft‐like” structures that anchor the side‐chains parallel to the interface. These envisaged raft‐like structures, when adsorbed to a fluid–fluid interface, are inferred to leave bare interfacial regions that are inaccessible to adsorption of additional rafts. As such, RC‐BBPs prohibit dense interfacial packing and yield higher interfacial tensions and lower interfacial areal densities than compositionally uniform bottlebrush statistical copolymers (BSCPs). This interfacial assembly of bottlebrush polymer (BBP) rafts offers distinct advantages, since inter‐raft gaps reflect a lack of close‐packing that offers routes to mass transport, seen in this work as a >6‐fold higher interfacial ion flux across RC‐BBP‐stabilized droplets relative to their BSCP counterparts. These results show that controlling the spatial distribution of BBPs via sequence randomness within the side‐chains—a previously overlooked structural parameter—produces a distinct, sparsely packed assembly of BBPs that preserves bare interfacial area to yield regulated, patchy, selective, or adaptive liquid–liquid interfaces.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

D

Dupyo Jeon

Polymer Science & Engineering Department, Conte Center for Polymer Research

Q

Qi Pan

S

Sai Zhao

H

Hong‐Gyu Seong

Polymer Science and Engineering Department Conte Center for Polymer Research University of Massachusetts Amherst Massachusetts USA

K

Kyoungwon Lee

Polymer Science & Engineering Department, Conte Center for Polymer Research

X

Xuchen Gan

Polymer Science & Engineering Department, Conte Center for Polymer Research

C

Carla Steppan

Polymer Science and Engineering Department Conte Center for Polymer Research University of Massachusetts Amherst Massachusetts USA

S

Steve Granick

Polymer Science and Engineering Department, University of Massachusetts

T

Todd Emrick

Polymer Science & Engineering Department, Conte Center for Polymer Research

T

Thomas P. Russell

Polymer Science & Engineering Department, Conte Center for Polymer Research