イリタニ コウヘイ
Iritani Kohei
入谷 康平 所属 工学部 応用化学科 職種 助教 |
|
言語種別 | 英語 |
発行・発表の年月 | 2019/10 |
形態種別 | 学術論文 |
査読 | 査読あり |
標題 | Electrostatically Driven Guest Binding in Self-Assembled Molecular Network of Hexagonal Pyridine Macrocycle at the Liquid/Solid Interface: Symmetry Breaking Induced by Coadsorbed Solvent Molecules |
執筆形態 | 共著 |
掲載誌名 | Langmuir |
掲載区分 | 国外 |
出版社・発行元 | American Chemical Society |
巻・号・頁 | 35(47),pp.15051-15062 |
著者・共著者 | Kohei Iritani, Hiroshi Takeda, Michael Kather, Masahiko Yokoi, Magali Moeglen, Motoki Ikeda, Yusuke Otsubo, Yu Ozawa, Kazukuni Tahara, Keiji Hirose, Steven De Feyter, Yoshito Tobe |
概要 | We present here the construction of a self-assembled two-dimensional (2D) porous monolayer bearing a highly polar 2D space to study guest co-adsorption through electrostatic interactions at the liquid/solid interface. For this purpose, a dehydrobenzo[12]annulene (DBA) derivative, DBA-TeEG, having tetraethylene glycol (TeEG) groups at the end of the three alternating alkoxy chains connected by p-phenylene linkers was synthesized. As a reference host molecule, DBA-C10, having nonpolar C10 alkyl chains at three alternating terminals, was employed. As guest molecules, hexagonal phenylene–ethynylene macrocycles (PEMs) attached by triethylene glycol (TEG) ester and hexyl ester groups, PEM-TEG and PEM-C6, respectively, at each vertex of the macrocyclic periphery were used. Scanning tunneling microscopy observations at the 1,2,4-trichlorobenzene/highly oriented pyrolytic graphite interface revealed that PEM-TEG was immobilized in the pores formed by DBA-TeEG at higher probability because of electrostatic interactions such as dipole–dipole and hydrogen bonding interactions between oligoether units of the host and guest, in comparison to PEM-C6 with nonpolar groups. These observations are discussed based on molecular mechanics simulations to investigate the role of the polar functional groups. When a nonpolar host matrix formed by DBA-C10 was used, however, only phase separation and preferential adsorption were observed; virtually no host–guest complexation was discernible. This is ascribed to the strong affinity between the guest molecules which form by themselves densely packed van der Waals networks on the surface. |