Existence of Two‐Dimensional Physical Gels even at Zero Surface Pressure at the Air/Water Interface: Rheology of Self‐Assembled Domains of Small Molecules

Films of mesoscopic domains self‐assembled from fluorocarbon/hydrocarbon diblock copolymers (FnHm) at the air/water interface were found to display highly elastic behavior. We determined the interfacial viscoelasticity of domain‐patterned FnHm Langmuir monolayers by applying periodic shear stresses....

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Veröffentlicht in:Angewandte Chemie 2017-10, Vol.129 (41), p.12777-12781
Hauptverfasser: Veschgini, Mariam, Habe, Taichi, Mielke, Salomé, Inoue, Shigeto, Liu, Xianhe, Krafft, Marie Pierre, Tanaka, Motomu
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container_issue 41
container_start_page 12777
container_title Angewandte Chemie
container_volume 129
creator Veschgini, Mariam
Habe, Taichi
Mielke, Salomé
Inoue, Shigeto
Liu, Xianhe
Krafft, Marie Pierre
Tanaka, Motomu
description Films of mesoscopic domains self‐assembled from fluorocarbon/hydrocarbon diblock copolymers (FnHm) at the air/water interface were found to display highly elastic behavior. We determined the interfacial viscoelasticity of domain‐patterned FnHm Langmuir monolayers by applying periodic shear stresses. Remarkably, we found the formation of two‐dimensional gels even at zero surface pressure. These monolayers are predominantly elastic, which is unprecedented for surfactants, exhibiting gelation only at high surface pressures. Systematic variation of the hydrocarbon (n=8; m=14, 16, 18, 20) and fluorocarbon (n=8, 10, 12; m=16) block lengths demonstrated that subtle changes in the block length ratio significantly alter the mechanics of two‐dimensional gels across one order of magnitude. These findings open perspectives for the fabrication of two‐dimensional gels with tuneable viscoelasticity via self‐assembly of mesoscale, low‐molecular‐weight materials. Gelbildung organischer Monoschichten: Hochelastische zweidimensionale Gele können bei einem Oberflächendruck von 0 mN m−1 aus mesoskopischen Oberflächendomänen von Fluorkohlenstoff/Kohlenwasserstoff‐Diblockcopolymeren (FnHm) erhalten werden. Die Grenzflächenviskoelastizität der FnHm‐Monoschichten wurde durch Anwendung periodischer Scherspannung bestimmt.
doi_str_mv 10.1002/ange.201707009
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We determined the interfacial viscoelasticity of domain‐patterned FnHm Langmuir monolayers by applying periodic shear stresses. Remarkably, we found the formation of two‐dimensional gels even at zero surface pressure. These monolayers are predominantly elastic, which is unprecedented for surfactants, exhibiting gelation only at high surface pressures. Systematic variation of the hydrocarbon (n=8; m=14, 16, 18, 20) and fluorocarbon (n=8, 10, 12; m=16) block lengths demonstrated that subtle changes in the block length ratio significantly alter the mechanics of two‐dimensional gels across one order of magnitude. These findings open perspectives for the fabrication of two‐dimensional gels with tuneable viscoelasticity via self‐assembly of mesoscale, low‐molecular‐weight materials. Gelbildung organischer Monoschichten: Hochelastische zweidimensionale Gele können bei einem Oberflächendruck von 0 mN m−1 aus mesoskopischen Oberflächendomänen von Fluorkohlenstoff/Kohlenwasserstoff‐Diblockcopolymeren (FnHm) erhalten werden. 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subjects Chemistry
Elasticity
Fabrication
Gelation
Gele
Gels
Hydrocarbons
Langmuir-Blodgett films
Monolayers
Mud-water interfaces
Perfluorocarbons
Pollutants
Polymere
Pressure
Rheological properties
Rheology
Scherrheologie
Selbstorganisation
Self-assembly
Surfactants
Viscoelasticity
Viskoelastizität
title Existence of Two‐Dimensional Physical Gels even at Zero Surface Pressure at the Air/Water Interface: Rheology of Self‐Assembled Domains of Small Molecules
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