TY - JOUR
T1 - Development of a C60-fullerene bonded open-tubular capillary using a photo/thermal active agent for liquid chromatographic separations by π-π interactions
AU - Kubo, Takuya
AU - Murakami, Yoshiki
AU - Tominaga, Yuichi
AU - Naito, Toyohiro
AU - Sueyoshi, Kenji
AU - Yan, Mingdi
AU - Otsuka, Koji
N1 - Funding Information:
This research was partly supported by the Grant-in Aid for Scientific Research (No. 25620111 and 24350039 ) from the Japan Society for the Promotion of Science . This development was partly supported by SENTAN from the Japan Science and Technology Agency . Takuya Kubo thanks for Research Grant Program of The Asahi Glass Foundation .
PY - 2014/1/3
Y1 - 2014/1/3
N2 - This short communication describes a newly developed open-tubular capillary which was coated with C60-fullerene by a covalent bonding via a photo/thermal active agent. We utilized perfluorophenyl azide (PFPA) as an active agent, which can be used for the "photo click" coupling of the carbon materials. The inner wall of a fused silica capillary was treated with silane conjugated PFPA, and then C60-fullerene was chemically modified by a photoreaction or a thermal reaction. Through evaluations of the capillaries by liquid chromatography, the separation characteristics of three polycyclic aromatic hydrocarbons (PAHs) were confirmed in both capillaries. With comparison of the retention behavior to a commonly used C18 column, the prepared capillaries showed the specific separation ability based on the π-π stacking by C60-fullerene. The capillary prepared by the thermal reaction provided the base line separation of phenanthrene, triphenylene, and benz[a]pyrene within 3min at 18.8cm capillary length.
AB - This short communication describes a newly developed open-tubular capillary which was coated with C60-fullerene by a covalent bonding via a photo/thermal active agent. We utilized perfluorophenyl azide (PFPA) as an active agent, which can be used for the "photo click" coupling of the carbon materials. The inner wall of a fused silica capillary was treated with silane conjugated PFPA, and then C60-fullerene was chemically modified by a photoreaction or a thermal reaction. Through evaluations of the capillaries by liquid chromatography, the separation characteristics of three polycyclic aromatic hydrocarbons (PAHs) were confirmed in both capillaries. With comparison of the retention behavior to a commonly used C18 column, the prepared capillaries showed the specific separation ability based on the π-π stacking by C60-fullerene. The capillary prepared by the thermal reaction provided the base line separation of phenanthrene, triphenylene, and benz[a]pyrene within 3min at 18.8cm capillary length.
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U2 - 10.1016/j.chroma.2013.10.097
DO - 10.1016/j.chroma.2013.10.097
M3 - Article
C2 - 24280614
AN - SCOPUS:84890791300
VL - 1323
SP - 174
EP - 178
JO - Journal of Chromatography A
JF - Journal of Chromatography A
SN - 0021-9673
ER -