謝辞 (化学測定機器室が貢献した研究成果)
Acknowledgements of research results contributed by CIF



39 (We are also grateful to K. Oyama and R.Yamada for their technical support in spectroscopic measurements)
    "Photocatalytic CO2 Reduction Using an Osmium Complex as a Panchromatic Self-Photosensitized Catalyst:
    Utilization of Blue,Green, and Red Light"

    Kenji Kamada, Jieun Jung,* Chihiro Yamada, Taku Wakabayashi, Keita Sekizawa,
    Shunsuke Sato, Takeshi Morikawa, Shunichi Fukuzumi, and Susumu Saito*
    Angew. Chem. Int. Ed. 2024, e202403886      doi.org/10.1002/anie.202403886.

38 (We thank the Chemical Instrumentation Facility).
    "Development of PCR primers enabling the design of flexible sticky ends for efficient concatenation
    of long DNA fragments"

    Kohei Nomura, Kaoru Onda, Hirotaka Murase, Fumitaka Hashiya, Yukiteru Ono,
    Goro Terai, Natsuhisa Oka, Kiyoshi Asai, Daisuke Suzuki, Naho Takahashi,
    Haruka Hiraoka, Masahito Inagaki, Yasuaki Kimura, Yoshihiro Shimizu, Naoko Abe and Hiroshi Abe*
    RSC Chem. Biol., 2024, 5, 360–371.      DOI: 10.1039/d3cb00212h.

37 (We thank Dr. Kin-ichi OYAMA for mass spectrometry analysis of the synthesized OFMs.)
    "Molecules with a TEMPO-based head group as highperformance organic friction modifiers"
    Jinchi HOU, Masaki TSUKAMOTO, Seanghai HOR, Xingyu CHEN, Juntao YANG, Hedong ZHANG,*,
    Nobuaki KOGA, Koji YASUDA, Kenji FUKUZAWA, Shintaro ITOH, Naoki AZUMA
    Friction, 2023, 11, 316–332.      doi.org/10.1007/s40544-022-0610-0

36 (We are grateful for the support of the Chemical Instrumentation Facility).
    "Cap analogs with a hydrophobic photocleavable tag enable facile purification of fully
     capped mRNA with various cap structures "

    Masahito Inagaki, Naoko Abe, Zhenmin Li, Yuko Nakashima, Susit Acharyya,
    Kazuya Ogawa, Daisuke Kawaguchi, Haruka Hiraoka ,Ayaka Banno, Zheyu Meng, Mizuki Tada, Tatsuma Ishida,
    Pingxue Lyu, Kengo Kokubo, Hirotaka Murase, Fumitaka Hashiya, Yasuaki Kimura, Satoshi Uchida, Hiroshi Abe*
    Nature Communications, 2023, 14, 2657.      doi.org/10.1038/s41467-023-38244-8.

35 (We thank the Chemical Instrumentation Facility).
    "Complete Chemical Synthesis of Minimal Messenger RNA by Efficient Chemical Capping Reaction"
    Naoko Abe, Akihiro Imaeda, Masahito Inagaki, Zhenmin Li, Daisuke Kawaguchi, Kaoru Onda,
    Yuko Nakashima, Satoshi Uchida, Fumitaka Hashiya, Yasuaki Kimura, and Hiroshi Abe*
    ACS Chem. Biol. 2022, 17, 1308−1314.      doi/10.1021/acschembio.1c00996.

34 (We thank Dr. Kin-ichi Oyama for assistance with elemental analysis.)
    "Thermally Stable Array of Discrete C60s on a Two-Dimensional Crystalline Adlayer of Macrocycles
    both in Vacuo and under Ambient Pressure"

    Shin-ichiro Kawano,# Masato Nakaya,# Masaaki Saitow, Atsuki Ishiguro, Takeshi Yanai, Jun Onoe,
    and Kentaro Tanaka*
    J. Am. Chem. Soc. 2022, 144, 6749−6758.      DOI: 10.1021/jacs.1c13610

33 (We sincerely thank Prof. Susumu Saito and Dr. Kin-ichi Oyama (Nagoya University)
         for the CSI-MS measurements.)
    "Three-center-four-electron halogen bond enables non-metallic complex catalysis
    for Mukaiyama-Mannich-type reaction"

    Shunya Oishi, Takeshi Fujinami, Yu Masui, Toshiyasu Suzuki, Masayuki Kato, Naoya Ohtsuka, Norie Momiyama*
    iScience 2022, 25, 105220.      doi.org/10.1016/j.isci.2022.105220

32 (We thank Dr K. Oyama for elemental analysis.)
    "Mesogenic discrete metallofoldamer for columnar liquid crystal"
    Shin-ichiro Kawano, Kazutaka Narita, Yuka Ikemoto, Ako Sasaki, Kentaro Tanaka*
    Chem. Commun., 2022, 58, 3274–3277.      DOI: 10.1039/d2cc00310d


.

under construction

.


31 (MS, FT-IR; Dr. K. Oyama).
    Tomoya Kanda,Asuka Naraoka,Hiroshi Naka
    J. Am. Chem. Soc. 2019, 141, 825-830      DOI: 10.1021/jacs.8b12877.


30 (Elemental analysis; Dr. K. Oyama).
    Haruki Inada, Masatoshi Shibuya,Yoshihiko Yamamoto
    Org. Lett. 2019, 21, 709-713      DOI: 10.1021/acs.orglett.8b03910.


29 (Chromatography; Dr. K. Oyama).
    Koichi Mimura, Riku Okada, Tamihito Nishida
    J. Chromatogr. A 2018, 1566, 118-123.      DOI: 10.1016/j.chroma.2018.06.051


28 (Elemental analysis; Dr. K. Oyama).
    Shin-ichiro Kawano, Tomoaki Fukushima, and Kentaro Tanaka
    Angew. Chem. Int. Ed. 2018, 57, 14827-14831.      DOI: 10.1002/anie.201809167


27 (MS; Dr. K. Oyama).
    Taizo Mori, Hiroyuki Tanaka, Amit Dalui, Nobuhiko Mitoma, Kengo Suzuki, Mutsuyoshi Matsumoto, Nikhil Aggarwal, Archita Patnaik, Somobrata Acharya, Lok Kumar Shrestha, Hirotoshi Sakamoto, Kenichiro Itami, and Katsuhiko Ariga
    Angew. Chem. Int. Ed. 2018, 57, 6979-9683.      DOI: 10.1002/anie.201803859


26 (MS; Dr. K. Oyama).
    Jianhua Qi, Lihong Cheng, Yujuan Sun, Yushi Hirata, Naoki Ushida, Zhonghua Ma, Hiroyuki Osada, Toshio Nishikawa, Lan Xiang
    Angew. Chem. Int. Ed. 2018, 57, 8100-8104.      DOI: 10.1002/anie.201803329


25 (Elemental analysis; Dr. K. Oyama).
    H. Hattori, S. Yokoshima, T. Fukuyama
    Angew. Chem. Int. Ed. 2017, 56, 6980-6983.      DOI: 10.1002/anie.201702204


24 (MS; Dr. K. Oyama).
    M. Naruto, S. Agrawal, K. Toda, S. Saito
    Sci, Rep. 2017, 7, 3425.      DOI: 10.1038/s41598-017-03436-y


23 (MS; Dr. K. Oyama).
    T. Miura, M. Naruto, K. Toda, T. Shimomura, S. Saito
    Sci, Rep. 2017, 7, 1586.      DOI: 10.1038/s41598-017-01645-z


22 (FT-IR, MS; Dr. K. Oyama).
    Qingcai Chen,Fumikazu Ikemori,Yuua Nakamura,Petr Vodicka,Kimitaka Kawamura,Michihiro Mochida
    AEnviron. Sci. Technol. 2017, 51, 8293-8303      DOI: 10.1021/acs.est.7b01630


21 (CD; Dr. K. Oyama).
    T. Tomura, S. Nagashima, S. Yamazaki, T. Iizuka, R. Fudou, M. Ojika
    Mar. Drugs 2017, 15, 109.

20 (Elemental analysis; Dr. K. Oyama).
    N. Mihara, Y. Yamada, H. Takaya, Y. Kitagawa, S. Aoyama, K. Igawa, K. Tomooka, K. Tanaka
    Chem. Eur. J. 2017, 23, 7508-7514.


19 (fluorescence, UV-vis, FT-IR; Dr. K. Oyama).
    Qingcai Chen,Fumikazu Ikemori,Yuua Nakamura,Petr Vodicka,Kimitaka Kawamura,Michihiro Mochida
    Environ. Sci. Technol. 2016, 50, 10859-10868      DOI: 10.1021/acs.est.6b02541


18 (MS, Elemental analysis; Dr. K. Oyama).
    S. Wakabayashi, Y. Hori, S. Komeda, Y. Shimizu, Y. Ohki, M. Horiuchi,T. Itoh, Y. Sugihara, K. Tatsumi
    J. Org. Chem. 2016, 81, 2399-2404.


17 (MS; Dr. K. Oyama).
    J.-I. Ito, S. Ubukata, S. Muraoka, H. Nishiyama
    Chem. Eur. J. 2016, 22, 16801-16804.


16 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, T. Kato, K. Tanaka
    Chem. Eur. J. 2016, 22, 12371-12380.


15 (Elemental analysis; Dr. K. Oyama).
    A. Alexandrov, T. Asada, A. Buonaura, L. Consiglio, N. D窶僊mbrosio,
    G. De Lellis, A. Di Crescenzo, N. Di Marco, M.L. Di Vacri, S. Furuya, G. Galati,
    V. Gentile, T. Katsuragawa, M. Laubenstein, A. Lauria, P.F. Loverre, S. Machii,
    P. Monacelli, M.C. Montesi, T. Naka, F. Pupilli, G. Rosa, O. Sato,
    P. Strolin, V. Tioukov, A. Umemoto, M. Yoshimoto
    Astroparticle Physics 2016, 80, 16-21.


14 (MS; Dr. K. Oyama).
    A. Matsuoka, T. Isogawa, Y. Morioka, B. R. Knappett, A. E. H. Wheatley, S. Saito, H. Naka
     RSC Adv., 2015, 5, 12152-12160.      DOI: 10.1039/C4RA15682J


13 (Elemental analysis; Dr. K. Oyama).
    S. Kawano, Y. Ishida, K. Tanaka
    J. Am. Chem. Soc. 2015, 137, 2295-2302.      DOI: 10.1021/ja510585u


12 (MS; Dr. K. Oyama).
    Y. Takada, S. W. Foo, Y. Yamazaki, S. Saito
     RSC Adv., 2014, 4, 50851-50857.      DOI: 10.1039/C4RA09609F


11 (MS; Dr. K. Oyama).
    H. Shirouzu, H. Morita, M. Tsukamoto
     Tetrahedron 2014, 70, 3635-3639.      DOI:10.1016/j.tet.2014.03.013


10 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, S. Matsumoto, K. Yamada, T. Nishino, N. Mihara, K. Sugimoto, K. Tanaka
    Chem. Lett. 2014, 43, 1377-1379.      DOI: 10.1246/cl.140392


9 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, T. Kubota, M. Nishino, K. Tanaka
    J. Am. Chem. Soc. 2014, 136, 6505-6509.      DOI: 10.1021/ja502898t


8 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, N. Mihara, S. Shibano, K. Sugimoto, K. Tanaka
    J. Am. Chem. Soc. 2013, 135, 11505-11508.      DOI: 10.1021/ja405963t

7 (Elemental analysis; Dr. K. Oyama).
    Y. Yamada, N. Mihara, S. Shibano, K. Sugimoto, K. Tanaka
    Dalton Trans., 2013, 42, 15873-15876.      DOI: 10.1039/C3DT51043C


6 (MS; Dr. K. Oyama).
    S. Wakabayashi, M. Uchida, R. Tanaka, Y. Habata, M. Shimizu,
     Asian J. Org. Chem. 2013, 2, 786 -791.      DOI: 10.1002/ajoc.201300131


5 (MS; Dr. K. Oyama).
    Y. Yamamoto, S. Yamada, H. Nishiyama,
     Chem. Eur. J. 2012, 18, 3153-3156.      DOI: 10.1002/chem.201103697


4 (MS; Dr. K. Oyama).
    H. Takaba, H. Omachi, Y. Yamamoto, J. Bouffard, K. Itami,
     Angew. Chem. Int. Ed. 2009, 48, 6112-6116.      DOI:10.1002/anie.200902617


.

under construction

.


3 (MS; Dr. K. Oyama).
    C. A. Sandoval, T. Ohkuma, K. Muniz, R. Noyori,
     J. Am. Chem. Soc. 2003, 125, 13490-13503.      DOI:10.1021/ja030272c


2 (MS; K. Oyama).
    N. Momiyama, H. Yamamoto,
     Org. Lett. 2002, 4, 3579-3582.      DOI: 10.1021/ol026443k


1 (MS; K. Oyama).
    N. Momiyama, H. Yamamoto,
     Angew. Chem. Int. Ed. 2002, 41, 2986-2988.      DOI: 10.1002/anie.200902617








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