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Dr. Matuoka, Hideki
CV
Educational Carrier:
1981 B.D. Department of Polymer Chemistry, Kyoto University
1983 M.D. Department of Polymer Chemistry, Kyoto University
1987 Ph.D. Department of Polymer Chemistry, Kyoto University
Professional Carrier:
1983 Assistant Professor, Department of Polymer Chemistry, Kyoto University
1996- Associate Professor, Department of Polymer Chemistry, Kyoto University
Research Interests:
Polymers at Interfaces, Amphiphilic Polymers, Ionic Polymers
Polymer Micelle, Polymer Monolayer, Ionic Polymers, Polymer Brush,
Polymer Nanoparticles
Small-angle Scattering, Light Scattering, Reflectivity
Award: 1991,The Chemical Society of Japan Award For Young Chemists for 1991.
Social Activities:
1997-1998 Editor, "Koubunshi Ronbunshu" (高分子論文集)
The Society of Polymer Science, Japan
2001-2002 Editor in Chief, The Journal of the Japanese Society of Neutron Science.
2001- Executive Secretary, the Division of Colloid and Surface Chemistry,the Chemical Society of Japan
2007- Officer of the Division of Colloid and Surface Chemistry,the Chemical Society of Japan
2013- Vice Charman, he Division of Colloid and Surface Chemistry, the Chemical Society of Japan
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Presentation day
wednesday 11:30 AM
TITLE
Nanostructure and stimuli-responsibiilty of poly(betaine) brushes at the air/water interface
Abstract
Polybetaines are zwitterionic and they show quite different properties from simple
polyelectrolytes, i.e., polycations and polyanions. [1,2] In this study, nanostructure and its stimuliresponsibility
of zwitterionic polybetaine brush were investigated by X-ray reflectivity (XR). The fundamental
properties of betaine polymers were also studied by dynamic light scattering (DLS), static light scattering
(SLS), and zeta-potential measurements.
Amphiphilic diblock copolymers with zwitterionic polybetaine and hydrophobic blocks were synthesized by
RAFT method. Three different betaines, i.e., carboxybetaine[3], phosphobetaine, and sulfobetaine were
used (Fig.1). The diblock copolymers were spread on the water surface to form monolayer. In the
monolayer, polybetaine brush is formed at the hydrophobic layer/ water interface. Its nanostructure was
investigated by pai-A isotherm and XR. All betaines formed brushes and showed carpet-only/ carpet+brush
structure transition. Quite different from simple (i.e., anionic and cationic) ionic brushes, brush thickness, in
principle, increased by salt addition.[3] This might be, so called, anti-polyelectrolyte effect. However, it was
found that brush thickness was very sensitive to salt concentration under very low salt concentration
condition; it increased and decreased and this behaviour was different for three kinds of betaine brushes.
Similar characteristic behaviour was observed also for hydrodynamic radius and zeta potential of
polybetaine homopolymers in aqueous solutions. UCST behaviour of sulfobetaine and Ion-specific effect of
added salt were also examined.
Institution
Department of Polymer Chemistry, Kyoto University, Kyoto, Kyoto, Japan.
Literatures
-
Anomalous Surface Tension and Micellization Behavior of Ionic Amphiphlilc Diblock Copolymers in Seawater
Hideki Matsuoka; Yuko Kido; Masahiro Hachisuka
Chemistry Letters, 2015, in press,
DOI: 10.1246/cl.150783 -
Photocleavable amphiphilic diblock copolymer micelles bearing a nitrobenzene block
Saurabh Shrivastava; Hideki Matsuoka
submitted, 2015, -
Nanostructure and Salt Effect of Zwitterionic Carboxybetaine Brush at the Air/Water Interface
Hideki Matsuoka; Yuta Yamakawa; Arjun Ghosh; Yoshiyuki Saruwatari
Langmuir, 2015, 31, 17, 4827 - 4836
DOI: 10.1021/acs.langmuir.5b00637 -
Salt-dependent surface activity and micellization behaviour of zwitterionic amphiphilic diblock copolymers having carboxybetaine
Sivanantham Murugaboopathy; Hideki Matsuoka
Colloid and Polymer Science, 2015, 293, 5, 1317 - 1328
DOI: 10.1007/s00396-015-3503-1