Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography

Kiyokatsu Jinno, Hatsuichi Ohta, Yoshihiro Saito, Takashi Uemura, Hideo Nagashima, Kenji Itoh, Yung Lin Chen, Gary Luehr, Jim Archer, John C. Fetzer, Wilton R. Biggs

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Fullerenes were separated using three chemically bonded phases, dimethoxyphenylpropyl (DMP), monomeric octadecyl and polymeric octadecyl modified silicas (ODS), with n-hexane as the mobile phase. DMP and the monomeric ODS are the best choices for the separation of C60 and C70 compounds, while DMP is the only phase that has high temperature stability while maintaining the resolution. For the separation of higher fullerenes, DMP offers faster analysis at higher temperatures while maintaining its high resolution, whereas ODS phases cannot provide similar run times while offering the same resolution. In conclusion, DMP is the most suitable and promising stationary phase for fullerenes analysis because of the short run time and its superior separation efficiency.

Original languageEnglish
Pages (from-to)71-77
Number of pages7
JournalJournal of Chromatography A
Volume648
Issue number1
DOIs
Publication statusPublished - Oct 1 1993
Externally publishedYes

Fingerprint

Fullerenes
High performance liquid chromatography
Silicon Dioxide
High Pressure Liquid Chromatography
Temperature

All Science Journal Classification (ASJC) codes

  • Analytical Chemistry
  • Biochemistry
  • Organic Chemistry

Cite this

Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography. / Jinno, Kiyokatsu; Ohta, Hatsuichi; Saito, Yoshihiro; Uemura, Takashi; Nagashima, Hideo; Itoh, Kenji; Chen, Yung Lin; Luehr, Gary; Archer, Jim; Fetzer, John C.; Biggs, Wilton R.

In: Journal of Chromatography A, Vol. 648, No. 1, 01.10.1993, p. 71-77.

Research output: Contribution to journalArticle

Jinno, K, Ohta, H, Saito, Y, Uemura, T, Nagashima, H, Itoh, K, Chen, YL, Luehr, G, Archer, J, Fetzer, JC & Biggs, WR 1993, 'Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography', Journal of Chromatography A, vol. 648, no. 1, pp. 71-77. https://doi.org/10.1016/0021-9673(93)83288-4
Jinno, Kiyokatsu ; Ohta, Hatsuichi ; Saito, Yoshihiro ; Uemura, Takashi ; Nagashima, Hideo ; Itoh, Kenji ; Chen, Yung Lin ; Luehr, Gary ; Archer, Jim ; Fetzer, John C. ; Biggs, Wilton R. / Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography. In: Journal of Chromatography A. 1993 ; Vol. 648, No. 1. pp. 71-77.
@article{882cedc9611742e9bb9540659d22c9f9,
title = "Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography",
abstract = "Fullerenes were separated using three chemically bonded phases, dimethoxyphenylpropyl (DMP), monomeric octadecyl and polymeric octadecyl modified silicas (ODS), with n-hexane as the mobile phase. DMP and the monomeric ODS are the best choices for the separation of C60 and C70 compounds, while DMP is the only phase that has high temperature stability while maintaining the resolution. For the separation of higher fullerenes, DMP offers faster analysis at higher temperatures while maintaining its high resolution, whereas ODS phases cannot provide similar run times while offering the same resolution. In conclusion, DMP is the most suitable and promising stationary phase for fullerenes analysis because of the short run time and its superior separation efficiency.",
author = "Kiyokatsu Jinno and Hatsuichi Ohta and Yoshihiro Saito and Takashi Uemura and Hideo Nagashima and Kenji Itoh and Chen, {Yung Lin} and Gary Luehr and Jim Archer and Fetzer, {John C.} and Biggs, {Wilton R.}",
year = "1993",
month = "10",
day = "1",
doi = "10.1016/0021-9673(93)83288-4",
language = "English",
volume = "648",
pages = "71--77",
journal = "Journal of Chromatography",
issn = "0021-9673",
publisher = "Elsevier",
number = "1",

}

TY - JOUR

T1 - Dimethoxyphenylpropyl bonded silica phase for higher fullerenes separation by high-performance liquid chromatography

AU - Jinno, Kiyokatsu

AU - Ohta, Hatsuichi

AU - Saito, Yoshihiro

AU - Uemura, Takashi

AU - Nagashima, Hideo

AU - Itoh, Kenji

AU - Chen, Yung Lin

AU - Luehr, Gary

AU - Archer, Jim

AU - Fetzer, John C.

AU - Biggs, Wilton R.

PY - 1993/10/1

Y1 - 1993/10/1

N2 - Fullerenes were separated using three chemically bonded phases, dimethoxyphenylpropyl (DMP), monomeric octadecyl and polymeric octadecyl modified silicas (ODS), with n-hexane as the mobile phase. DMP and the monomeric ODS are the best choices for the separation of C60 and C70 compounds, while DMP is the only phase that has high temperature stability while maintaining the resolution. For the separation of higher fullerenes, DMP offers faster analysis at higher temperatures while maintaining its high resolution, whereas ODS phases cannot provide similar run times while offering the same resolution. In conclusion, DMP is the most suitable and promising stationary phase for fullerenes analysis because of the short run time and its superior separation efficiency.

AB - Fullerenes were separated using three chemically bonded phases, dimethoxyphenylpropyl (DMP), monomeric octadecyl and polymeric octadecyl modified silicas (ODS), with n-hexane as the mobile phase. DMP and the monomeric ODS are the best choices for the separation of C60 and C70 compounds, while DMP is the only phase that has high temperature stability while maintaining the resolution. For the separation of higher fullerenes, DMP offers faster analysis at higher temperatures while maintaining its high resolution, whereas ODS phases cannot provide similar run times while offering the same resolution. In conclusion, DMP is the most suitable and promising stationary phase for fullerenes analysis because of the short run time and its superior separation efficiency.

UR - http://www.scopus.com/inward/record.url?scp=0027366467&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0027366467&partnerID=8YFLogxK

U2 - 10.1016/0021-9673(93)83288-4

DO - 10.1016/0021-9673(93)83288-4

M3 - Article

VL - 648

SP - 71

EP - 77

JO - Journal of Chromatography

JF - Journal of Chromatography

SN - 0021-9673

IS - 1

ER -