ナカライテスク株式会社

Cosmosil

COSMOSIL Buckyprep

  • HPLC/UHPLC

コスモシール Buckyprep は、フラーレン分離のスタンダードカラムです。特に高次フラーレンやフラーレン誘導体の分離に最適です。

特長
  • フラーレン分離のスタンダード
  • 誘導体化フラーレンや高次フラーレンの分離に最適
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製品説明

物性

充填剤名称 Buckyprep
シリカゲル 全多孔性球状高純度シリカゲル
平均粒子径(µm) 5
平均細孔径(nm) 12
比表面積(m2/g) 300
固定相構造 Buckyprep-kouzousiki.gif
化学結合基 ピレニルプロピル基
USP カテゴリー
結合形式 モノメリック
主な相互作用
エンドキャッピング あり
炭素含有率(%) 17
使用可能 pH 範囲 2 〜 7.5

製品使用例

分析例

高次フラーレン

10_a_1.gif
Conditions
Column

COSMOSIL Buckyprep
4.6 mm I.D. × 250 mm

Detection UV 312 nm
Mobilephase Toluene Sample C60, C70, C76, C84
Flow rate 1.0 mL/min
Temperature 30℃

酸化フラーレン

10_a_2.gif
Conditions
Column COSMOSIL Buckyprep
4.6 mm I.D. × 250 mm
Detection UV 312 nm
Mobilephase Toluene Sample C60, C60O
Flow rate 1.0 mL/min
Temperature 30℃

2 種類の移動相による高次フラーレンの分析

コスモシール Buckyprep カラムではフラーレンに対して強い保持力を示しますので、C70 以上の高次フラーレン(Higher Fullerenes)の溶出がトルエン移動相では困難になる場合があります。 トルエンよりも溶出力の強いクロロベンゼンを移動相として用いることによって、フラーレンの保持を約 1/3 にすることができます。

移動相 トルエン 移動相 クロロベンゼン
移動相 トルエン 移動相 クロロベンゼン
Conditions
Column COSMOSIL Buckyprep
4.6 mm I.D. × 250 mm
Temperature 30℃
Flow rate 1.0 mL/min Detection UV 285 nm

COSMOSIL_application_button.png

使用文献

  • Tyler T. Clikeman, Shihu H. M. Deng, Alexey A. Popov, Xue-Bin Wang, Steven H. Strauss and Olga V. Boltalina. Fullerene cyanation does not always increase electron affinity: an experimental and theoretical study. Phys. Chem. Chem. Phys.,, 17, 2015, 551-556.
  • U. Ritter, Yu. I. Prylutskyy, M. P. Evstigneev, N. A. Davidenko, V. V. Cherepanov, A. I. Senenko, O. A. Marchenko & A. G. Naumovets. Structural Features of Highly Stable Reproducible C60 Fullerene Aqueous Colloid Solution Probed by Various Techniques. Fullerenes, Nanotubes and Carbon Nanostructures , 23 (6), 2015, 530-534. 
  • Gabor Bortel, Eva Kovats, Emma Jakab & Sandor Pekker. Solvent-free Sc3N@C80-Ih and Its Precursor Cocrystal with Toluene. Fullerenes, Nanotubes and Carbon Nanostructures , 23 (6), 2015, 557-565.
  • Yoko Abe & Yutaka Matsuo. 1,8-Diazabicycloundecene-mediated Separation of Singly Bonded Fullerene Dimer and Application to Facile Preparation of C61H2. Fullerenes, Nanotubes and Carbon Nanostructures , 23 (3), 2015, 259-262.
  • Marina G. Apenova, Vladimir A. Akhmetov, Nikita M. Belov, Dr. Alexey A. Goryunkov, Dr. Ilya N. Ioffe, Dr. Natalia S. Lukonina, Dr. Vitaliy Yu. Markov and Prof.-Dr. Lev N. Sidorov. Alkali-Metal Trichloroacetates for Dichloromethylenation of Fullerenes: Nucleophilic Addition-Substitution Route. Chemistry - An Asian Journal, 9 (3), 2014, 915-923.
  • Tao Wei, Dr. Nadezhda B. Tamm, Prof.-Dr. Shangfeng Yang and Prof.-Dr. Sergey I. Troyanov. New Trifluoromethylated Derivatives of Metal Nitride Clusterfullerenes: Sc3N@Ih-C80(CF3)14 and Sc3N@D5h-C80(CF3)16. Chemistry - An Asian Journal, 9 (9), 2014, 2449-2452.
  • Nikita M. Belov, Marina G. Apenova, Alexey V. Rybalchenko, Eugenia V. Borkovskaya, Dr. Natalia S. Lukonina, Dr. Alexey A. Goryunkov, Dr. Ilya N. Ioffe, Prof.-Dr. Sergey I. Troyanov and Prof.-Dr. Lev N. Sidorov. Transalkylation of Higher Trifluoromethylated Fullerenes with C70: A Pathway to New Addition Patterns of C70(CF3)8. Chemistry - A European Journal, 20 (4), 2014, 1126-1133.
  • Andrea Carboni, Erik Emke, John R. Parsons, Karsten Kalbitz, Pim de Voogt. An analytical method for determination of fullerenes and functionalized fullerenes in soils with high performance liquid chromatography and UV detection. Analytica Chimica Acta, 807 (7), 2014, 159-165.
  • Ran Tao, Tomokazu Umeyama, Kei Kurotobi, and Hiroshi Imahori. Effects of Alkyl Chain Length and Substituent Pattern of Fullerene Bis-Adducts on Film Structures and Photovoltaic Properties of Bulk Heterojunction Solar Cells. ACS Appl. Mater. Interfaces , 6 (19), 2014, 17313-17322.
  • Bryon W. Larson, James B. Whitaker, Alexey A. Popov, Nikos Kopidakis, Garry Rumbles, Olga V. Boltalina, and Steven H. Strauss. Thermal [6,6] → [6,6] Isomerization and Decomposition of PCBM (Phenyl-C61-butyric Acid Methyl Ester). Chem. Mater.,, 26 (7), 2014, 2361-2367.
  • Jing Yang Xue, Koki Ikemoto, Norihisa Takahashi, Tomoo Izumi , Hideo Taka, Hiroshi Kita, Sota Sato, and Hiroyuki Isobe. Cyclo-meta-phenylene Revisited: Nickel-Mediated Synthesis, Molecular Structures, and Device Applications. J. Org. Chem., , 79 (20), 2014, 9735-9739.
  • Yutaka Matsuo, Keisuke Ogumi , Masashi Maruyama , and Takafumi Nakagawa. Divergent Synthesis and Tuning of the Electronic Structures of Cobalt-Dithiolene-Fullerene Complexes for Organic Solar Cells. Organometallics, 33 (3), 2014, 659-664.
  • Makoto Karakawa, Takabumi Nagai, Kenji Adachi, Yutaka Ie and Yoshio Aso. N-phenyl[60]fulleropyrrolidines: alternative acceptor materials to PC61BM for high performance organic photovoltaic cells. J. Mater. Chem. A, 2, 2014, 20889-20895.
  • Airat R. Tuktarov, Artur A. Khuzin, Natal'ya R. Popod'ko & Usein M. Dzhemilev. Synthesis and Tribological Properties of Sulfur-Containing Methanofullerenes. Fullerenes, Nanotubes and Carbon Nanostructures , 22 (4), 2014, 397-403.
  • Chao Liu, Yongjun Li, Dan Chi, Songhua Chen, Taifeng Liu, Jizheng Wang, Huibiao Liu & Yuliang Lic. A Facile Way for Synthesis of High Performance Electron Receptor MCB: A Promising Replacer of PCBM. Fullerenes, Nanotubes and Carbon Nanostructures , 22 (1-3), 2014, 289-298.
  • R. G. Bulgakov, Z. S. Kinzyabaeva. Synthesis of fullerene Γ-lactones by free radical reaction of C60 with ketones promoted by compounds of transition metals Cr(VI), Ce(IV). Russian Journal of Organic Chemistry, 50 (8), 2014, 1189-1193.
  • A. S. Pimenova, A. A. Kozlov, A. A. Goryunkov, V. Yu. Markov, P. A. Khavrel, S. M. Avdoshenko, I. N. Ioffe, S. G. Sakharov, S. I. Troyanov and L. N. Sidorov. Synthesis and characterization of difluoromethylene-homo[60]fullerene, C60(CF2). Chem. Commun, 2007, 374 - 376.
  • S. V. Prylutska, O. P. Matyshevska, I. I. Grynyuk, Yu. I. Prylutskyy, U. Ritter, P. Scharff. Biological Effects of C60 Fullerenes in vitro and in a Model System. Molecular Crystals and Liquid Crystals, 468(1), 2007, 265-274.
  • T. S. Papina, V. A. Luk’yanova, A. A. Goryunkov, I. N. Ioffe, I. V. Gol’dt, A. G. Buyanovskaya, N. M. Kabaeva and L. N. Sidorov. The enthalpy of formation of fullerene fluoride C60F18 and the C-F bond energy. Russian Journal of Physical Chemistry A, Focus on Chemistry, 81(10), 2007, 1560-1564.
  • A. A. Goryunkov, E. I. Dorozhkin, N. B. Tamm, D. V. Ignat’eva, S. M. Avdoshenko, L. N. Sidorov and S. I. Troyanov. Synthesis and molecular structure of 1,6,11,16,18,24,27,36-C60(CF3)8. Mendeleev Communications, 17(2), 2007, 110-112.

価格表

分析・分取カラム(粒子径 5 µm)
COSMOSIL Buckyprep

製品名 サイズ 製品番号 オンラインカタログへ
COSMOSIL Buckyprep Guard Column 4.6 mm l.D. × 10 mm 37983-71 e-Nacalai.jpg
10 mm l.D. × 20 mm 37984-61 e-Nacalai.jpg
20 mm l.D. × 50 mm 34374-41 e-Nacalai.jpg
28 mm l.D. × 50 mm 05871-21 e-Nacalai.jpg
COSMOSIL Buckyprep Packed Column 4.6 mm l.D. × 250 mm 37977-61 e-Nacalai.jpg
10 mm l.D. × 250 mm 37981-91 e-Nacalai.jpg
20 mm l.D. × 250 mm 37982-81 e-Nacalai.jpg
28 mm l.D. × 250 mm 34346-11 e-Nacalai.jpg

※価格表に記載のないカラムサイズをご要望の際はお問い合わせください。

COSMOSIL / コスモシールはナカライテスク株式会社の登録商標です。

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