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T. Matsumoto, K. Mochizuki, K. Higuchi, M. Goto, and H.
Matsumoto, Structure
and Oxidation of Octakis(tert-butyldimethylsilyl)octasilacubane, J. Organomet. Chem., 685,
156–161 (2003). https://doi.org/10.1016/S0022-328X(03)00288-2
(81) M. Unno,
H. Masuda, and H. Matsumoto, Photo-initiated Bromination
of
Octakis(1,1,2-trimethylpropyl)octasilacubane
with
Tetrabromomethane, Silicon
Chem., 1,
377–381 (2002). https://doi.org/10.1023/B:SILC.0000025578.17683.2a
(82) K.
Yamada, M. Unno, K. Kobayashi, H. Oku, H. Yamamura, S. Araki,
H. Matsumoto, R.
Katakai, and M. Kawai, Stereochemistry of Protected Ornithine
Side Chains of
Gramicidin S Derivatives: X-ray Crystal Structure of the
Bis-Boc-tetra-N-methyl
Derivatives of Gramicidin S, J. Am. Chem. Soc., 124, 12684–12688 (2002). https://doi.org/10.1021/ja020307t
(83) R.
Tanaka, S. Kyushin, M. Unno, and H. Matsumoto, Chiral
crystallization of anti-dodecaisopropyltricyclo[4.2.0.02,5]octasilane,
Enantiomer, 7, 157–159 (2002). https://doi.org/10.1080/10242430212882
(84) M. Unno,
A. Suto, and H. Matsumoto, Pentacyclic Laddersiloxane, J. Am. Chem. Soc., 124,
1574–1575 (2002). https://doi.org/10.1021/ja0173876
(85) M. Unno,
Y. Kawai, and H. Matsumoto, Synthesis and Crystal Structures
of 2,4,6-Tri-tert-butylphenyltrichlorogermane
and
2,4,6-Tri-tert-butylphenylgermane,
Heteroatom Chem., 12, 238–243 (2001). https://doi.org/10.1002/hc.1038
(86) M. Unno,
T. Saito, and H. Matsumoto, Synthesis and Crystal Structures
of Silapericyclynes, Bull.
Chem. Soc. Jpn., 74,
2407–2413 (2001). https://doi.org/10.1246/bcsj.74.2407
(87) M. Unno,
K. Negishi, and H. Matsumoto, Extended Silapericyclynes, Chem. Lett., 30, 340–341
(2001). https://doi.org/10.1246/cl.2001.340
(88) M. Unno,
K. Higuchi, K. Furuya, H. Shioyama, S. Kyushin, M. Goto, and
H. Matsumoto, Synthesis,
Structure, and Reactions of
Octakis(1,1,2-trimethylpropyl)octagermacubane,
Bull. Chem.
Soc. Jpn., 73,
2093–2097 (2000). https://doi.org/10.1246/bcsj.73.2093
(89)
S. Kyushin, A. Meguro,
M. Unno, and H. Matsumoto, Photolysis of anti-Dodecaalkyltricyclo[4.2.0.02,5]octasilane:
Generation
and Reactions of Cyclotetrasilene, Chem. Lett., 29, 494–495 (2000).
https://doi.org/10.1246/cl.2000.494
(90)
H. Horiuchi, Y. Nakano,
T. Matsumoto, M. Unno, H. Matsumoto, and H. Hiratsuka,
Electronic Structure and
Photochemical Reaction Intermediates of Octakis(1,1,2-trimethylpropyl)octasilacubane,
Chem. Phys. Lett., 322, 33–40 (2000). https://doi.org/10.1016/S0009-2614(00)00357-2
(91)
M. Unno, K. Takada, and
H. Matsumoto, Formation of Supramolecule by Assembling of Two
Different
Silanols, Chem. Lett.,
29, 242–243 (2000). https://doi.org/10.1246/cl.2000.242
(92) M. Unno, A. Suto, K. Takada,
and H. Matsumoto, Synthesis
of Ladder and Cage
Silsesquioxanes from 1,2,3,4-Tetrahydroxycyclotetrasiloxane, Bull. Chem. Soc. Jpn.,
73, 215–220 (2000). https://doi.org/10.1246/bcsj.73.215
(93) M. Unno, D. Ishii, and H. Matsumoto, Kinetic Study of Thermal
Isomerization of the
“Double-decker”-type Sesquichalcogenides, (Thex2M2E2)2E2
(M=Si, Ge; E=S, Se), Bull. Chem. Soc. Jpn, 72, 2469–2473
(1999). https://doi.org/10.1246/bcsj.72.2469
(94) M. Unno,
T. Saito, and H. Matsumoto, Silapericyclyne, (Ph2SiCºC)6:
Spontaneous Conformational Resolution of Boat- and
Chair-'Exploded' Cyclohexane,
Chem. Lett., 28,
1235–1236
(1999). https://doi.org/10.1246/cl.1999.1235
(95) R.
Tanaka, M. Unno, and H. Matsumoto, Synthesis and Molecular
Structures of Novel
Isopropyl-substituted Oligosilanes, Chem.
Lett., 28,
595–596 (1999). https://doi.org/10.1246/cl.1999.595
(96) M. Unno, R. Tanaka, S.
Kyushin, and H. Matsumoto, Synthesis
and Reactions of Hepta-t-butylcyclotetragermane,
Phosphorus,
Sulfur, Silicon Relat. Elem., 150/151, 167–176 (1999).
https://doi.org/10.1080/10426509908546382
(97) M. Unno, B. A. Shamsul,
M. Arai, K. Takada, R. Tanaka
and H. Matsumoto, Synthesis and Characterization of Cage and
Bicyclic
Silsesquioxanes via Dehydration of Silanols, Appl. Organomet. Chem., 13,
303-310 (1999). https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291099-0739%28199904%2913%3A4%3C303%3A%3AAID-AOC846%3E3.0.CO%3B2-%23
(98) M. Unno, K. Takada, and
H. Matsumoto, Synthesis,
Structure, and Reaction of the Tetrahydroxycyclotetrasiloxane
[(i-Pr)(OH)SiO]4,
Chem. Lett., 27, 489–490 (1998). https://doi.org/10.1246/cl.1998.489
(99) M. Unno,
H. Masuda, and H. Matsumoto,
1,2,3-Triphenyl-1,2,3-trithexylcyclotrisilanes:
Synthesis and Ring-Opening by Halogens, Bull. Chem. Soc. Jpn, 70,
2449–2458 (1997). https://doi.org/10.1246/bcsj.71.2449
(100)
M. Unno, R. Tanaka,
T. Kuribara, M. Saito, and H. Matsumoto, Synthesis,
Structures, and Reactions
of 1,2,3-Tris(diethylamino)-1,2,3,4-tetrakis-(1,1,2-trimethylpropyl)cyclotetrasilanes,
Bull. Chem. Soc. Jpn,
70, 2749–2756
(1997). https://doi.org/10.1246/bcsj.70.2749
(101)
K. Kobayashi, T.
Kato, M. Unno, and S. Masuda, Asymmetric Synthesis of
Organosilicon Compounds
Using a C2
Chiral
Auxiliary, Bull. Chem.
Soc. Jpn, 70,
1393–1401 (1997). https://doi.org/10.1246/bcsj.70.1393
(102)
M. Unno, Y. Kawai,
H. Shioyama, and H. Matsumoto, Syntheses, Structures, and
Properties of Tricyclo[5.1.1.13,5]tetrasilachalcogenanes
(Thex2Si2E2)2E2
(E = S, Se) and Tricyclo[5.1.1.13,5]tetragermachalcogenanes
(Thex2Ge2E2)2E2
(E = S, Se), Organometallics,
16, 4428–4434
(1997). https://doi.org/10.1021/om970432r
(103) M. Unno, H. Shioyama,
and H. Matsumoto, Synthesis and
Structures of Tetrasilsesquisulfides, Phosphorus,
Sulfur, Silicon Relat. Elem., 120/121, 377–378 (1997).
https://doi.org/10.1080/10426509708545556
(104)
M. Unno, T. Yokota,
and H. Matsumoto, Oxaoctasilahomocubane and
Dioxaoctasilabishomocubane: Novel
Silicon Ring System, J.
Organomet. Chem.,
521, 409–411
(1996). https://doi.org/10.1016/0022-328X(96)06421-2
(105)
M. Unno, B. A.
Shamsul, H. Saito, and H. Matsumoto, Synthesis of
Hexasilsesquioxanes Bearing
Bulky Substituents:
Hexakis(1,1,2-trimethylpropylsilsesquioxane) and Hexakis(tert-butylsilsesquioxane),
Organometallics, 15, 2413–2414 (1996). https://doi.org/10.1021/om950737a
(106) M. Unno, H. Shioyama, M.
Ida, and H. Matsumoto,
Reductive dehalogenation of 4,8-Dihalooctakis(1,1,2-trimethylpropyl)tetracyclo-[3.3.0.02,7.03,6]octasilanes
with
Sodium, Organometallics,
14, 4004–4009
(1995). https://doi.org/10.1021/om00008a054
(107)
M. Unno, M. Saito,
and H. Matsumoto, Synthesis, Structure, and Properties of
Novel Aminodisilanes
Bearing Bulky Substituents:
1,2-bis(1,1,2-trimethylpropyl)-1,1,2,2-tetrakis(diethylamino)disilane
and
1,2-di-(tert-butyl)1,1,2,2-tetrakis(diethylamino)disilane,
J. Organomet. Chem., 499, 221–228 (1995).
https://doi.org/10.1016/0022-328X(95)00314-G
(108)
M. Unno, K.
Higuchi, M. Ida, H. Shioyama, S. Kyushin, M. Goto, and H.
Matsumoto,
Ring-Opening Reaction of Octakis(1,1,2-trimethylpropyl)octasilacubane,
Organometallics, 13, 4633–4635 (1994). https://doi.org/10.1021/om00023a075
(109)
B. Imperiali, K. L.
Shannon, M. Unno, and K. W. Rickert, A Mechanistic Proposal
for
Asparagine-Linked Glycosylation, J. Am.
Chem. Soc., 114,
7944–7945
(1992). https://doi.org/10.1021/ja00046a069
(110) L. T.
Scott and M. Unno, Novel Heterocycles Comprising Alternating
Phosphorus Atoms
and Alkyne Units, J. Am. Chem. Soc., 112, 7823–7825
(1990). https://doi.org/10.1021/ja00177a069
(111) R.
Okazaki, M. Unno, and N. Inamoto, Estimation of Bulkiness of a
Highly
Sterically Demanding
2,4,6-Tris[bis(trimethylsilyl)methyl]-phenyl Group, Chem. Lett., 18, 791–792 (1989). https://doi.org/10.1246/cl.1989.791
(112) R.
Okazaki, M. Unno, G. Yamamoto, and N. Inamoto, A
Conformational Study on Highly
Crowded 1,3,5-Tris[bis(trimethylsilyl)methyl]benzene
Derivatives. Chem.
Lett. 18,
493–496 (1989). https://doi.org/10.1246/cl.1989.493
(113) R.
Okazaki, M. Unno, and N. Inamoto, 2,4,6-Tris[bis(Trimethylsilyl)methyl]phenyl,
a New Sterically Demanding Group for Kinetic Stabilization of
Unstable
Compounds, Chem. Lett.,
16, 2293–2294
(1987). https://doi.org/10.1246/cl.1987.2293
(114) R.
Okazaki, M. Unno, and N. Inamoto, A New synthesis
of 1,3-thiazine
derivatives bearing a dithiolane
ring and their reductive
cleavage with sodium cyanoborohydride, Heterocycles,
25, 183–190 (1987).
https://doi.org/10.3987/S-1987-01-0183
[Review,
Proceedings]
(1) 海
野雅史, ヤ
ヌスキューブ(ヤヌス分子)の合成と応用展開,ファインケミカル, 48, 3,
38–48 (2019).
https://www.cmcbooks.co.jp/products/detail.php?product_id=5607
(2) 海
野雅史,シランカップリング剤のメカニズムと将来展開,色材協会誌,88,5,143–147
(2015). https://doi.org/10.4011/shikizai.88.143
(3) M. Unno, A.
Suto,
and T. Matsumoto, "Laddersiloxanes— Silsesquioxanes with
defined ladder
structure", Russ. Chem.
Rev., 82,
289–302 (2013). https://doi.org/10.1070/RC2013v082n04ABEH004360
(4) 海野雅史, 超
分子から構造規制次世代材料まで—シラノールが築く新しい化学—, 有
機合成化学協会誌, 69,
413–425 (2011). https://doi.org/10.5059/yukigoseikyokaishi.69.413
(5) 海野雅史,近
未来材料のシルセスキオキサン, 化学, 65, 10,
68–69 (2010). https://www.kagakudojin.co.jp/book/b73488.html
(6) 海野雅史, ケ
イ素化合物の優れた結合能を利用した表面処理ならびに増感色素への応用, ファインケミカル, 39, 3,
5–12 (2010). https://www.cmcbooks.co.jp/products/detail.php?product_id=3528
(7) 海野雅史, 花
屋実, ケイ素を利用した新規色素増感太陽電池の設計, ケミカルエンジニヤリング, 53, 9,
687–693
(2008). http://www.kako-sha.co.jp/2008contentschem.htm
(8) M.
Unno, Laddersiloxanes: silsesquioxanes with
defined ladder structure. Materials Research Society Symposium
Proceedings 1007-S01-05
(2007),. https://doi.org/10.1557/PROC-1007-S01-05
(9) 海野雅史, シ
ラノールの水素結合を利用したナノサイズ超分子の形成, ナノ学会会報, 5, 47–51 (2007). http://www.ac-square.co.jp/nano/journal_01.html
(10) M. Unno,
K. Takada, Y. Kawaguchi, and H. Matsumoto, Supramolecular aggregates of
silanols and solid-state synthesis of
siloxanes, Mol. Cryst. Liq.
Cryst., 440, 259–264
(2005). https://doi.org/10.1080/15421400590958584
(11) 海野雅史, 松
本英之, オクタシラキュバンの化学, 有機合成化学協会誌, 62, 107–115 (2004).
https://doi.org/10.5059/yukigoseikyokaishi.62.107
(12) K. Yamada,
M. Unno, K. Kobayashi, H. Oku, H. Yamamura, H. Matsumoto, R.
Katakai, and K.
Masao, Stereochemistry of protected ornithine side chains of
gramicidin S
derivatives: X-ray crystal structure of N-methylated
derivative of gramicidin, Peptide Science,
2002, 39th, 305–308 (2003).
(13) 海野雅史, フ
ラーレン化学合成12年の歩み〜L. T.
Scott研究室, ケイ素化学協会誌, No.16, pp.12-15 (2002).
(14) H.
Matsumoto, S. Kyushin, M. Unno, and R. Tanaka, Synthesis,
Structures, and
Properties of Ladder Oligosilanes and Ladder Oligogermanes, J. Organomet. Chem. 611, 52–63 (2000). https://doi.org/10.1016/S0022-328X(00)00299-0
(15) 海野雅史, 松
本英之, ケイ素原子を持つ超分子,科学と工業 (大阪), 74, 489–494 (2000).
(16) 海野雅史, ヘテロ原子化学+有機金属化学, ケイ素化学協会誌, No.12, pp.11-14 (2000).
(17) 海野雅史, Tbt基が生まれた頃−When Tbt was born, ケイ素化学協会誌, No.11, pp.45-46 (1999).
(18) 海野雅史, 松本英之, シ
ルセスキオキサン類の化学−かご状化合物を中心に, ケイ素化学協会誌, No.8, pp.16-22 (1997).
[Books]
(1) 海野雅史(分担), シランカップリング剤の最新技術
動向(第6章第1節)次世代シランカップリング剤,シーエムシー出版,pp.216–223 (2020).
(2) 海野雅史(分担), シランカップリング剤の使い方と
応用事例(第9章第1節)シルセスキオキサンの種類・構造,合成方法,サイエ
ンス&テクノロジー,pp.313–321
(2020).
(3) 海野雅史(分担), 添加剤の最適使用法(第8節 シ
ランカップリング剤の種類,反応,使用方法),R&Dリサーチセン
ター,pp.129–135 (2020).
(4)
M. Unno and
H. Endo, “Silanols as Building Blocks for Nanomaterials” in
Novel Nanoscale Hybrid
Materials, Ed. Bhanu P. S. Chauhan, John Wiley & Sons,
Inc., New York, pp.
1–31 (2018). https://doi.org/10.1002/9781119156253.ch1
(5)
M. Unno and
R. Tanaka, “Silanols and Silsesquioxanes” in Efficient Methods
for Preparing
Silicon Compounds, Ed. H. W. Roesky, Academic Press, London,
pp. 399–440 (2016).
https://doi.org/10.1016/B978-0-12-803530-6.00032-9
(6) シランカップリング剤の使いこなし
ノウハウ集, 第1章「シランカップリング剤の反応メカニズム」,技術情報協会
(2016). ISBN 978-4-86104-610-0
(7)
M. Unno, "Substituted Polyhedral Silicon
and Germanium
Clusters", in Functional Molecular Silicon Compounds II, Ed.
D.
Scheschkewitz, Springer, Heidelberg, pp.49-84 (2014). https://doi.org/10.1007/430_2013_99
(8) 現代ケイ素化学(分担),第22章「シリコーンの応用」,吉良満夫,玉尾皓平編,化学同人 pp.349-360(2013).
(9) シルセスキオキサン材料の化学と応用展開, 伊藤真樹
監修, 第4章「かご型および精密合成ラダーシルセスキオキサン」, シーエムシー出版 pp. 37-48
(2013).
(10) 最強エレメント ケイ素の不思議(分担) , 海野雅史編, 海
野雅史他著, 上毛新聞社,pp.9-11, 19-21 (2011).
(11) シランカップリング剤の反応メカニズムと処理条件の最適化, 第
1章「シランカップリング剤の基本的メカニズム」, 第5章「シランカップ
リング剤への新規機能性の付与」, 技術情報協会pp.1-20, 88-105 (2010).
(12) シルセスキオキサン材料の最新技術と応用, 伊藤真樹
監修, 第4章「かご型および精密合成ラダーシルセスキオキサン」, シーエムシー出版 (2007).
(13) 新時代への視点 −群馬大学研究室から−(分担),群馬大学地域連携推進室編,上毛新聞社,pp.
186-188 (2006).
(14)
M. Unno and
H. Matsumoto, "Reactions of Octasilacubane", in Organosilicon
Chemistry VI,Eds.
N. Auner and J. Weis, WILEY-VCH Verlag,
Weinheim, pp. 373–380 (2005). https://doi.org/10.1002/9783527618224.ch2c
(15) 10年使える有機スペクトル解析(分担),新津隆士,海野雅史,鍵裕之著,三共出版,第1章,第2章 (2005).
(16) 21世紀の有機ケイ素化学—機能性物質科学の宝庫(分
担),玉尾皓平監修,シーエムシー(2004).
(17) プロフェショナル英和辞典スペッドテラ 物質・工学編(分担),堀内克明、蟹江幸博編,小学館 (2004).
(18) キラキラわくわく化学(分担)上毛新聞社,pp.50-53
(2003).
(19) 有機ケイ素材料科学の新展開 (分担),櫻井英樹監修,シーエムシー,pp.146-156
(2001)
(20) 化合物の辞典 (分担), 稲本直樹ら編, 朝
倉書店
(1998).
(21) 気軽に化学 (分担), 上毛新聞社,pp.168-169,172-173
(1996).
[Patents]
(1)
特願2016-232998、海野雅史、江川泰暢、島田茂、佐藤一彦、「反応性置換基を有
するシルセスキオキサンの製造方法」、国立大学法人群馬大学、独立行政法人産業技術総合研究所、平成28年11月30日.
(2)
特願2015-204578、海野雅史、江川泰暢、島田茂、佐藤一彦、「異なる置換基を対
面に4つずつ有するかご型シルセスキオキサン」、国立大学法人群馬大学、独立
行政法人産業技術総合研究所、平成27年10月16日.
(3)
特開2014-093158、
神谷正人、齋藤平、寺島純平、鳶島真一、森本英行、海野雅史、「リチウムイオン二次電池」、ト
ヨタ自動車株式会社、国立大学法人群馬大学、平成26年5月19日.
(4)
特開2014-053097、神谷正人、齋藤平、鳶島真一、森本英行、海野雅史、
「リチウム二次電池およびその製造方法」、国立大学法人群馬大学、トヨタ自動車株式会社、平成26年3月20日.
(5)
特願2014-76446、海野雅史、佐藤一彦、島田茂、五十嵐正安、「シロキサン化合物
の製造方法」、国立大学法人群馬大学、独立行政法人産業技術総合研究所、平成26年4月2日.
(6)
特開2013-241497、小熊武美、渡辺淳、海野雅史、「ポリシルセスキオキサン化合
物、光素子封止材及びその用途」、国立大学法人群馬大学、電気化学工業株式会社、平成25年12月5日.
(7)
WO 2012137568, M.
Hanaya, K. Kakiage, M. Unno, Y. Aoyama, T. Yano, D.
Sawamoto, H. Osada, “Aromatic
amines bearing hydrocarbyloxysilyl
groups, supports containing supported them, and
photoelectric converters”,
Adeka Corporation, Oct. 11, 2012.
(8)
WO 2012036010, M. Hanaya,
K. Kakiage, M. Unno, T. Yano, K. Akimoto, K. Sakamaki, “Production of pyridine
derivative additive
for electrolytic composition of dye-sensitized solar cell”,
Adeka
Corporation, Sep. 5, 2011.
(9)
特開2011-202057、海野雅史、小熊武美、村田弘、「ポリシルセスキオキサン化合
物、光素子封止材及びその用途」、電化化学工業株式会社、国立大学法人群馬大学,平成22年3月26日.
(10) 特開2009-249455(特願2008-097235)、
濱田光祥、永井晃、海野雅史、山村正樹、「封止用エポキシ樹脂成形材料及び電子部品装置」、日立化成工業株式会社、平成21年10月29日.
(11) 特開2009-249312(特願2008-097236)、
濱田光祥、永井晃、加藤木茂樹、杜暁黎、海野雅史、「シラン化合物」、日立化成工業株式会社、平成21年10月29日.
(12) 特開2007-197723(特願2006-356289)、
濱田光祥、永井晃、松本英之、海野雅史、「封止用エポキシ樹脂成形材料及び電子部品装置」、日立化成工業株式会社、平成19年8月9日.
(13) 特開2008-63390(特願2006-240428)、
海野雅史,花屋実,「色素増感太陽電池用色素及びこの色素を用いた光電変換素子並びに色素増感太陽電池」,国立大学法人群馬大学,平
成18年9月5日.
(14) 特開2006-016580(特願2004-198515)、
濱田光祥、永井晃、松本英之、海野雅史、「接着剤組成物、それを用いたフィルム状接着剤及び回路接続材料、並びに回路部材の接続構造
及びその製造方法」、日立化成工業株式会社、平成18年1月19日.
(15) 特開2006-016370(特願2004-198509)、
佐藤和也、湯佐正己、小林隆伸、藤縄貢、塚越功、松本英之、海野雅史、「シラン化合物」、日立化成工業株式会社、平成18年1月19日.
(16) 特開2006-016369(特願2004-198508)、
佐藤和也、湯佐正己、小林隆伸、藤縄貢、塚越功、松本英之、海野雅史、「シラン化合物の製造方法及びシラン化合物」、日立化成工業株
式会社、平成18年1月19日.
(17) 特開2004-315428(特願2003-111608)、
松本英之、海野雅史、田中陵二、「ハロゲン化アリール置換環状テトラシロキサンの製法」、独立行政法人
科学技術振興機構、2004年11月11日.
新聞発表等
1) 新物質「ヤヌスキューブ」群馬大大学院が新合成法, 日本経済新聞,
2016/05/28.
2) 群馬大が新合成法 新物質「ヤヌスキューブ」, 日本経済新聞, 電子
版,
2016/05/28.
3) エコタイヤの性能向上 化合物の合成法開発, 産
経新聞,
2016/05/28.
4) エコタイヤの性能向上に期待 群大院が「ヤヌスキュー
ブ」合成, 産経新聞電子版,
2016/05/28.
5) エコタイヤの性能向上に期待 群大院が「ヤヌスキュー
ブ」合成法開発, Yahooニュース,
2016/05/28.
6) ヤヌスキューブ簡便合成法 産総研群馬大 有機ケイ素部
材に有用, 化学工業日報,
2016/05/30.
7) ヤヌスキューブの簡易合成法を発見 エコタイヤ性能向上
期待,
上毛新聞, 2016/05/30.
8) ヤヌスキューブ効率的に合成
群馬大と産総研, 日刊工業新聞,
2016/06/02.
9) ヤヌスキューブ 簡便な合成法開発 詳細な分子構造も解
明, 桐生タイムス,
2016/06/02.
10) 「究極のエコタイヤ」へ新手法 ヤヌスキューブ材料の化
合物合成効率化, 読売新聞,
2016/06/03
11) ヤヌスの立方体,
有機化学美術館・分館, 2016/06/06.
12) カゴ型シルセスキオキサン「ヤヌスキューブ」合成と構造
決定, Chem-Stationスポットライトサーチ, 2016/06/10.
13) ヤヌスキューブ合成
科学新聞社電子版, 2016/06/17.