研究業績（主なもの; 1995-2023)

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  1. S. Erten-Ela, C. Yavuz, R. Hasegawa, Y. Kubo, p-Type DSSCs by sensitizing a benzofuran[b]-fused BODIPY with cyanoacrylic acid, Next Materials, 2024, 3, 100177. DOI: 10.1016/j.nxmate.2024.100177
  2. K. Kawaguchi, N. Sugawara, M. Ito, Y. Kubo, Thermochromic Afterglow from Benzene-1,4-diboronic Acid-doped Co-crystals, Chem. Eur. J., 2024. DOI: 10.1002/chem.202303924
  3. S. Takegawa, M. Ito, Y. Kubo, Turn-on type afterglow probe for Hg2+ sensing by a PVA-mediated triplet sensitizer, New J. Chem., 2023, 47, 12554-12560. DOI: 10.1039/D3NJ01281F
  4. K. Kawaguchi, M. Ito, Y. Kubo, Chemometrics-assisted mechanism study of the room-temperature phosphorescence on nanoscopic boronate assemblies, Chem. Commun., 2023, 59, 3130-3133. DOI: 10.1039/D2CC07049A
  5. R. Hasegawa, M. Ito, Y. Kubo, Tuning triplet population of arylselanyl-BODIPY photosensitizers through substituents engineering for triplet-triplet annihilation photonupconversion with perylene, J Porphyr Phthalocyanines, 2023, 27, 757-764. DOI: 10.1142/S1088424623500037
  6. K. Omasa, M. Ito, Y. Kubo, Zn(II)-coordination-driven chiroptical and emissive sensing for chiral amines using a quaterphenyl-5'-carbaldehyde, New J. Chem., 2022, 46, 21845-21851. DOI: 10.1039/D2NJ04781K
  7. A. Koga, K. Kawagguchi, M. C. Maida, Y. Kubo, A ratiometric afterglow response of aluminium ions in methanol-water, Chem. Asian J., 2022, e2022000402. DOI: 10.1002/asia.202200402R1
  8. S. Iwakiri, R. Hasegawa, Y. Kubo, Near-infrared room-temperature phosphorescence in arylselanyl BODIPY-doped materials, ChemPhotoChem, 2022, 6, e202200073. DOI: 10.1002/cptc.202200073
  9. S. Farshbaf, K. Dey, W. Mochida, M. Kanakubo, R. Nishiyabu, Y. Kubo, and P. Anzenbacher Jr., Detection of phosphates in water utilizing a Eu3+- mediated relay mechanism, New J. Chem., 2022, 46, 1839-1844. DOI: 10.1039/d1nj04578d
  10. K. Kawaguchi, A. Moro, S. Kojima and Y. Kubo, Chiral recognition coupled with chemometrics using boronate ensembles containing D-π-A cyanostilbenes, Chem. Commun., 2021,57, 12952-12955. DOI:10.1039/D1CC05492A.
  11. K. Makino, T. I, and Y. Kubo, A benzofuran[b]-fused BODIPY as an efficient sensitizer for photocatalytic hydrogen production, Sustain. Energy Fuels, 2021, 5, 3676-3686. DOI: 10.1039/D1SE00387A
  12. M. Pushina, S. Farshbaf, W. Mochida, M. Kanakubo, Ryuhei Nishiyabu, Yuji Kubo, and P. Anzenbacher, Jr., A fluorescence sensor array based on zinc(II)-carboxyamidoquinolines: Toward quantitative detection of ATP, Chem. Eur. J., 2021, 27, 1-9. DOI: 10.1002/chem.202100896
  13. R. Hasegawa, S. Iwakiri, Y. Kubo, Synthesis and triplet sensitization of bis(arylselanyl)BOPHYs; potential application in triplet-triplet annihilation upconversion, New J. Chem., 2021, 45, 6091-6099.DOI: 10.1039/D1NJ00721A
  14. M. Kanakubo, Y. Yamamoto, Y. Kubo, Room-temperature phosphorescence of thiophene boronate ester-cross linked polyvinyl alcohol; a triplet-to-singlet FRET-induced multi-color afterglow luminescence with Sulforhodamine B, Bull. Chem. Soc. Japan., 2021, 94, 1204-1209.DOI: 10.1039/D1NJ00721A
  15. Y. Kubo, T. Nozawa, K. Maeda, Y. Hashimoto, Asymmetrical benzo[a]-fused N2O2-boron-chelated BODIPYs as red to near-infrared absorbing chromophores: Synthesis, characteristics and device applications for opto-electronics, Mater. Adv., 2021, 2, 1059-1071.DOI: 10.1039/D0MA00910E
  16. T. Arai, Y. Kubo, Chemical stimulus-responsive tricyanopyrroline-based ICT chromophore as a potential environment-sensitive probe, Dyes and Pigments., 2021, 185, 108927.DOI: 10.1016/j.dyepig.2020.108927
  17. Y. Sasaki, S. Kojima, V. Hamedpour, R. Kubota, S. Takizawa, I. Yoshikawa, H. Houjou, Y. Kubo and T. Minami, Accurate chiral pattern recognition for amines, albeit a single chemosensor, Chem. Sci., 2020, 11, 3790-3796.DOI: 10.1039/D0SC00194E
  18. M. Hoshi, R. Nishiyabu, Y. Hayashi, S. Yagi and Y. Kubo, Room-temperature phosphorescence-active boronate particles: characterization and ratiometric afterglow-sensing behavior via surface grafting of Rhodamine B, Chem. Asian J., 2020, 15, 787-795.DOI: 10.1002/asia.201901740
  19. R. Nishiyabu, Y. Takahashi, T. Yabuki, S. Gommori, Y. Yamamoto, H. Kitagishi and Y. Kubo, Boronate sol–gel method for one-step fabrication of polyvinyl alcohol hydrogel coatings by simple cast- and dip-coating techniques. RSC Adv., 2020, 20, 86-94. DOI: 10.1039/C9RA08208E
  20. Y. Kubo, T. Shimada, K. Maeda and Y. Hashimoto, Thieno[1,3,2]oxazaborinine-containing aza-BODIPYs with near infrared absorption bands: synthesis, photophysical properties, and device application. New J. Chem., 2020, 44, 29-37. DOI: 10.1039/C9NJ04612G
  21. Y. Higashino, S. Erten-Ela, Y. Kubo, π-Expanded dibenzo-BODIPY with near-infrared light absorption: investigation of photosensitizing properties of NiO-based p-type dye-sensitized solar cells. Dyes and Pigments, 2019, 170, 107613. DOI: 10.1016/j.dyepig.2019.107613
  22. O, Suryani, Y. Higashino, H. Sato and Y. Kubo, Visible-to-Near-Infrared Light-Driven Photocatalytic Hydrogen Production Using Dibenzo-BODIPY and Phenothiazine Conjugate as Organic Photosensitizer. ACS Appl. Energy Mater., 2019, 2, 448-458. DOI: 10.1021/acsaem.8b01474
  23. M. Hoshi, N. Kaneko, R. Nishiyabu and Y. Kubo, Formation of emissive nanoparticles from tetraphenylethylene-containing boronate macrocycles: preparation, characterization and functionalization. J. Mater. Chem. C, 2018, 6, 11052-11062. DOI: 10.1039/C8TC03748E
  24. M. Nakashima, K. Iizuka, M. Karasawa, K. Ishii and Y. Kubo, Selenium-containing BODIPY dyes as photosensitizers for triplet-triplet annihilation upconversion, J. Mater. Chem. C, 2018, 6, 6208-6215. DOI: 10.1039/C8TC00944A
  25. R. Nishiyabu, M. Tomura, T. Okade, and Y. Kubo, Boronic acids as molecular inks for surface functionalization of polyvinyl alcohol substrates, New J. Chem., 2018, 42, 7392-7398. DOI: 10.1039/C8NJ00992A
  26. Y. Kubo, S. Tobinaga, Y. Ueno, T. Aotake, H. Yakushiji, and T. Yamamoto, Near-infrared-absorbing Photodetectors Based on Naphtho[1,3,2]oxazaborinine-type Dibenzo-BODIPY Dyes, Chem. Lett., 2018, 47, 300-303. DOI: 10.1246/cl.171061
  27. I. Purnama Y. Kubo, and J. Y. Mulyana, A robust ruthenium complex with nonyl-substituted bpy ligand for dye-sensitized photoelectrochemical cell application, Inorg. Chim. Acta, 2018, 471, 467-474. DOI: 10.1016/j.ica.2017.11.052
  28. M. Kawai, A. Hoshi, R. Nishiyabu and Y. Kubo, Fluorescent chirality recognition by simple boronate ensembles with aggregation-induced emission capability, Chem. Commun., 2017, 53, 10144-10147. DOI: 10.1039/C7CC05784A
  29. S. Erten-Ela, Y. Ueno, T. Asaba and Y. Kubo, Synthesis of a dibenzo-BODIPY-incorporating phenothiazine dye as a panchromatic sensitizer for dye-sensitized solar cells, New. J. Chem., 2017, 41, 10367-10375. DOI: 10.1039/C7NJ01735A
  30. O. Suryani, Y. Higashino, J. Y. Mulyana, M. Kaneko, T. Hoshi, K. Shigaki and Y. Kubo, Near-infrared organic photosensitizer for use in dye-sensitized photoelectrochemical water splitting, Chem. Commun., 2017, 53, 6784-6787. DOI: 10.1039/C7CC02730C
  31. R. Nishiyabu, S. Iizuka, S. Minegishi, H. Kitagishi, and Y. Kubo, Surface modification of polyvinyl alcohol sponge with functionalized boronic acid to develop porous materials for multicolor emission, chemical sensing and 3D cell culture, Chem. Commun., 2017, 53, 3563-3566. DOI: 10.1039/C7CC00490G
  32. K. Sakakibara, Y. Takahashi, R. Nishiyabu and Y. Kubo, A Zn2+-coordinated boronate dipyrrin as a chemodosimeter toward hydrogen peroxide, J. Mater. Chem. C, 2017, 5, 3684-3691. (2017 Journal of Materials Chemistry C HOT Papers) DOi: 10.1039/C7TC00405B
  33. Y. Satta, R. Nishiyabu, T. D. James and Y. Kubo, A 1-hydroxy-2,3,1-benzodiazaborine-containing π-conjugated system: synthesis, optical properties and solvent-dependent response toward anions, Tetrahedron, 2017, 73, 2053-2061. DOI: 10.1016/j.tet.2017.02.050
  34. Y. Kubo and R. Nishiyabu, White-light emissive materials based on dynamic polymerization in supramolecular chemistry, Polymer, 2017, 128, 257-275. DOI: 110.1016/j.polymer.2016.12.082
  35. R. Nishiyabu and A. Shimizu, Boronic acid as an efficient anchor group for surface modification of solid polyvinyl alcohol, Chem. Commun., 2016, 52, 9765-9768. DOI: 10.1039/C6CC02782B (Inside back cover)
  36. T. Minamia, F. Emami, R. Nishiyabu, Y. Kubo and P. Anzenbacher, Jr., Quantitative analysis of the modeled ATP hydrolysis in water by a colorimetric sensor array, Chem. Commun., 2016, 52, 7838-7841. DOI: 10.1039/C6CC02923J
  37. S. Yamazawa, M. Nakashima, Y. Suda, R. Nishiyabu and Y. Kubo, 2,3-Naphtho-fused BODIPYs as near-infrared absorbing dyes, J. Org. Chem., 2016, 81, 1310-1315. DOI: 10.1021/acs.joc.5b02720
  38. Y. Kubo, D. Kakizaki, M. Kogo and Y. Magatani, Water-dispersible boronate nanoparticles as support materials for noble metals in the hydrogenation of levulinic acid to γ-valerolactone, Supramol. Chem., 2016, 28, 91-97. DOI: 10.1080/10610278.2015.1086764
  39. Y. Suda, R. Nishiyabu and Y. Kubo, Multi-thiophene-substituted NIR boron-dibenzopyrromethene dyes: synthesis and their spectral properties, Tetrahedron, 2015, 71, 4174-4182. DOI: 10.1016/j.tet.2015.04.094
  40. Y. Kubo, R. Nishiyabu and T. D. James, Hierarchical supramolecules and organization using boronic acids building blocks, Chem. Commun., 2015, 51, 2005-2020. DOI: 10.1039/C4CC07712A
  41. A. Ozawa, A. Shimizu, R. Nishiyabu and Y. Kubo, Thermo-responsive white-light emission based on tetraphenylethylene- and rhodamine B-containing boronate nanoparticles, Chem. Commun., 2015, 51, 118-121. DOI: 10.1039/C4CC07405J (Highlighted by the ACS Noteworthy Chemistry website)
  42. A. Matsumoto, R. Nishiyabu and Y. Kubo, Synthesis of a borylated boron-dibenzopyrromethene dye enabling the visual detection of H2O2 vapor, RSC Adv., 2014, 4, 37973-37978. DOI: 10.1039/C4RA06061J
  43. R. Nishiyabu, S. Ushikubo, Y. Kamiya and Y. Kubo, A boronate hydrogel film containing organized two-component dyes as a multicolor fluorescent sensor for heavy metal ions in water, J. Mater. Chem. A, 2014, 2, 15846-15852. DOI: 10.1039/C4TA03268C
  44. T. Minami, Y. Liu, A. Akdeniz, P. Koutnik, N. A. Esipenko, R. Nishiyabu, Y. Kubo, and P. Anzenbacher, Jr., Intramolecular indicator displacement assay for anions: supramolecular sensor for glyphosate, J. Am. Chem. Soc., 2014, 136, 11396-11401. DOI: 10.1021/ja504535q
  45. S. Fujiwara, N. Takanashi, R. Nishiyabu and Y. Kubo, Boronate microparticle-supported nano-palladium and nano-gold catalysts for chemoselective hydrogenation of cinnamaldehyde in environmentally preferable solvent, Green. Chem., 2014, 16, 3230-3236. DOI: 10.1039/C4GC00383G
  46. S. Ozawa, R. Nishiyabu, and Y. Kubo, Nanospherical aggregation of isothiouronium-terminated amphiphilic polythiophene: Preparation and vapor-phase detection of volatile organic compounds, J. Nanosci. Nanotech., 2014, 14, 6624-6631. DOI: 10.1166/jnn.2014.9343
  47. Y. Kubo, D. Eguchi, A. Matsumoto, R. Nishiyabu, H. Yakushiji, K. Shigaki and M. Kaneko, Boron-dibenzopyrromethene-based organic dyes for application in dye-sensitized solar cells, J. Mater. Chem. A, 2014, 2, 5204-5211. DOI 10.1039/C3TA15340A
  48. R. Nishiyabu, Y. Sugino, and Y. Kubo, White light emitting boronate microparticles for potential use as reusable bright chemosensors in water, Chem. Commun., 2013, 49, 9869-9871. DOI 10.1039/C3CC45739G
  49. K. Otsuka, T. Kondo, R. Nishiyabu, and Y. Kubo, Solvent-manipulated guest binding and signaling of a fluorescent resorcin[4]arene cavitand with 1,3,2-benzodiazaboryl D-π-A conjugation flaps, J. Org. Chem., 2013, 78, 5782-5787. DOI 10.1021/jo4006238
  50. Y. Liu, T. Minami, R. Nishiyabu, Z. Wang, and P. Anzenbacher, Sensing of carboxylate drugs in urine by a supramolecular sensor array, J. Am. Chem. Soc., 2013, 135, 7705-7712. DOI 10.1021/ja4015748
  51. P. Anzenbacher, Jr., Y. Liu, M. A. Palacios, T. Minami, Z. Wang, and R. Nishiyabu, Leveraging material properties in fluorescence anion sensor arrays: A general approach, Chem. Eur. J., 2013, 19, 8497-8506. DOI 10.1002/chem.201204188
  52. S. D. Bull, M. G. Davidson, J. M. H. van den Elsen, J. S. Fossey, A. T. A. Jenkins, Y.-B. Jiang, Y. Kubo, F. Marken, K. Sakurai, J. Zhao, and T. D. James, Exploiting the reversible covalent bonding of boronic acids: recognition, sensing, and assembly, Acc. Chem. Res., 2013, 46, 312-326. DOI 10.1021/ar300130w
  53. T. Minami, N. A. Esipenko, B. Zhang, M. E. Kozelkova, L. Isaacs, R. Nishiyabu, Y. Kubo, and P. Anzenbacher, Jr., Supramolecular sensor for cancer-associated nitrosamines, J. Am. Chem. Soc., 2012, 134, 20021-20024. DOI 10.1021/ja3102192
  54. Y. Matsushima, R. Nishiyabu, N. Takanashi, M. Haruta, H. Kimura, and Y. Kubo, Boronate self-assembles with embedded Au nanoparticles; preparation, characterization and their catalytic activities for the reduction of nitroaromatic compounds, J. Mater. Chem., 2012, 22, 24124-24131. DOI 10.1039/C2JM34797K
  55. R. Nishiyabu, H. Kobayashi, and Y. Kubo, Dansyl-containing boronate hydrogel films as fluorescent chemosensor of copper ions in water, RSC Adv., 2012, 2, 6555-6561. DOI 10.1039/C2RA20516E
  56. R. Nishiyabu, S. Teraoka, Y. Matsushima, and Y. Kubo, Fabrication of soft submicrospheres by sequential boronate esterification and their dynamic behavior, ChemPlusChem, 2012, 77, 201-209. DOI 10.1002/cplu.201100008
  57. K. Saito, R. Nishiyabu, M. Iyoda, and Y. Kubo, Gold nanoparticle-templated assembly of oligothiophenes; preparation and film properties, Tetrahedron, 2011, 67, 9685-9689. DOI 10.1016/j.tet.2011.10.032
  58. Y. Kubo, K. Watanabe, R. Nishiyabu, R. Hata, A. Murakami, T. Shoda, and H. Ota, Near-infrared absorbing boron-dibenzopyrromethenes that serve as light-harvesting sensitizers for polymeric solar cells, Org. Lett. 2011, 13, 4574-4577. DOI 10.1021/ol201770g
  59. R. Nishiyabu, Y. Kubo, T. D. James and J. S. Fossey, Boronic acid building blocks: Tools for self assembly, Chem. Commun. (Feature article), 2011, 47, 1124-1150. DOI 10.1039/C0CC02921A (cover picture)
  60. R. Nishiyabu, Y. Kubo, T. D. James and J. S. Fossey, Boronic acid building blocks: Tools for sensing and separation, Chem. Commun. (Feature article), 2011, 47, 1106-1123. DOI 10.1039/C0CC02920C
  61. T. Minami and Y. Kubo, Selective anion-induced helical aggregation of chiral amphiphilic polythiophenes with isothiouronium-appended pendants, Supramol. Chem., 2011, 23, 13-18. DOI 10.1080/10610278.2010.506546
  62. T. Minami, R. Nishiyabu, M. Iyoda and Y. Kubo, Shape-controllable gold nanocrystallization using an amphiphilic polythiophene, Chem. Commun., 2010, 46, 8603-8605. DOI 10.1039/C0CC03179H
  63. Y. Kubo, K. Tsuruzoe, S. Okuyama, R. Nishiyabu and T. Fujihara, Resorcin[4]arene cavitand with 1,3,2-benzodiazaborolyl walls as a fluorescence receptor for ammonium cations, Chem. Commun., 2010, 46, 3604-3606. DOI 10.1016/j.tetlet.2010.01.070
  64. Y. Kubo, Y. Minowa, T. Shoda, and K. Takeshita, Synthesis of a new type of dibenzopyrromethene-boron complex with near-infrared absorption property, Tetrahedron Lett., 2010, 51, 1600-1602. DOI 10.1016/j.tetlet.2010.01.070
  65. T. Minami and Y. Kubo, Fluorescence Sensing of Phytate in Water Using an Isothiouronium-attached Polythiophene, Chem. Asian J., 2010, 5, 605-611. DOI 10.1002/asia.200900444
  66. 久保　由治，分子会合現象を利用した化学センサー系の開発，科学と工業，2010，84，23-31.
  67. 南　豪，西藪　隆平，久保　由治，化学刺激応答型π共役ポリマーのトポロジー制御とその応用，未来材料，2010，10，10-16.
  68. S. Horie and Y. Kubo, Fluorescence-based Indicator Displacement Assay for Phosphosugar Detection Using Zinc(II) Dipicolylamine-appended Phenylboronic Acid, Chem. Lett., 2009, 38, 616-617.DOI 10.1246/cl.2009.616
  69. K. Kataoka, S. Okuyama, T. Minami, T. D. James, and Y. Kubo, Amine-triggered molecular capsules using dynamic boronate esterification, Chem. Commun., 2009, 1682-1684. DOI 10.1039/b900102f
  70. Y. Kubo, W. Yoshizumi, and T. Minami, Development of Chemical Stimuli-responsive Organogel Using Boronate Ester-substituted Cyclotricatechylene, Chem. Lett., 2008, 37, 1238-1239.DOI:10.1246/cl.2008.1238.
  71. A. Nonaka, S. Horie, T. D. James, and Y. Kubo, A pyrophosphate-induced reorganization of reporter-receptor assembly via boronate esterification; new strategy of a turn-on fluorescent detection of multi-phosphates in aqueous solution, Org. Biomol. Chem., 2008, 6, 3621-3625. DOI 10.1039/b808027e
  72. T. Minami, K. Kaneko, T. Nagasaki, and Y. Kubo, Isothiouronium-based amphiphilic gold nanoparticles with a colorimetric response to hydrophobic anions in water: a new strategy for fluoride ion detection in the presence of a phenylboronic acid, Tetrahedron Lett., 2008, 49, 432-436. DOI 10.1016/j.tetlet.2007.11.120
  73. K. Kataoka, T. D. James, and Y. Kubo, Ion Pair-Driven Heterodimeric Capsule based on Boronate Esterification: Construction and the Dynamic Behavior, J. Am. Chem. Soc., 2007, 129, 15126-15127.DOI: 10.1021/ja076792f
  74. Y. Ishii, Y. Soeda, and Y. Kubo, Chirality induction on cation-driven assembly using a crowned metalloporphyrin, Chem. Commun., 2007, 2953-2955. DOI: 10.1039/b703670a
  75. Y. Ishii, T. Yoshizawa, and Y. Kubo, Dibenzo-diaza-30-crown-10-appended bis(zinc porphyrin) tweezers: synthesis and crown-assisted chiroptical behavior, Org. Biomol. Chem., 2007, 5, 1210-1217. DOI 10.1039/b701317e
  76. Y. Ishii, Y. Onda, and Y. Kubo, 2,2'-Biphenyldiol-bridged bis(free base porphyrin): synthesis and chiroptical probing of asymmetric amino alcohols, Tetrahedron Lett., 2006, 47, 8221-8225. DOI 10.1016/j.tetlet.2006.09.106
  77. Y. Kubo, T. Ishida, T. Minami, and T. D. James, Highly Selective Fluoride Ion Detection Based on a Fluorescent Alizarin-o-Aminomethylphenylboronic Acid Ensemble in Aqueous MeOH Solution, Chem. Lett., 2006, 35, 996-997. DOI 10.1246/cl.2006.996
  78. Y. Kubo and Y. Ishii, Molecular manipulation based on allosteric crown-appended units and related systems, J. Nanosci. Nanotech., 2006, 6, 1489-1509.
  79. Y. Kubo, S. Uchida, Y. Kemmochi, and T. Okubo, Isothiouronium-modified gold nanoparticles capable of colorimetric sensing of oxoanions in aqueous MeOH solution, Tetrahedron Lett., 2005, 46, 4369-4372. DOI 10.1016/j.tetlet.2005.04.074
  80. Y. Kubo, T. Ishida, A. Kobayashi, and T. D. James, Fluorescent alizarin-phenylboronic acid ensembles: design of self-organized molecular sensors for metal ions and anions, J. Mater. Chem., 2005, 15, 2889-2895. DOI: 10.1039/b501243k
  81. Y. Kubo, A. Kobayashi, T. Ishida, Y. Misawa and T. D. James, Detection of anions using a fluorescent alizarin-phenylboronic acid ensemble, Chem. Commun., 2005, 2846-2848. DOI: 10.1039/b503588k
  82. Y. Misawa, Y. Kubo, S. Tokita, H. Ohkuma, and H. Nakahara, An Isothiouronium-derived Organized Monolayer at the Air-Water Interface: Design of Film-based Anion Sensor Systems for H2PO4-, Chem. Lett., 2004, 33, 1118-1119. DOI 10.1246/cl.2004.1118
  83. Y. Kubo, Y. Ishii, T. Yoshizawa, and S. Tokita, Effective cation-assisted chirality induction using a dibenzo-diaza-30-crown-10 with bis(zinc(II) porphyrin) units, Chem. Commun., 2004, 1394-1395. DOI: 10.1039/b403684k
  84. Y. Kubo, M. Kato, Y. Misawa, and S. Tokita, A fluorescence-active 1,3-bis(isothiouronium)-derived naphthalene exhibiting versatile binding modes toward oxoanions in aqueous MeCN solution: new methodology for sensing oxoanions, Tetrahedron Lett., 2004, 45, 3769-3773. DOI 10.1016/j.tetlet.2004.03.076
  85. Y. Misawa, Y. Kubo, S. Tokita, H. Ohkuma, and H. Nakahara, Characterization of Organized Molecular Layers Including Amphiphilic Isothiouronium Derivatives, Trans. Mater. Res. Soc. Jpn., 2004, 29, 3155-3158.
  86. T. Tozawa, T. Tachikawa, S. Tokita, and Y. Kubo, Chirality-induction of a Dibenzo-30-crown-10 Congener Promoted by an Ion-pair Coordinated Self-assembly, New J. Chem., 2003, 27, 221-223.
  87. Y. Kubo, S. Ishihara, M. Tsukahara, and S.Tokita, Isothiouronium-derived Simple Fluorescent Chemosensors of Anions, J. Chem. Soc., Perkin Trans. 2, 2002, 1455-1460.
  88. Y. Kubo, S. Obara, and S. Tokita, Metal Ionically-Controlled Optical Signaling Based on a Chromoionophore-derived Calix[4]crown, Supramol. Chem., 2002, 14, 2-3, 171-177.
  89. T. Tozawa, S. Tokita, and Y. Kubo, An Allosteric Crown Ether-induced Activity Control for the Cleavage of a Phosphodiester Bond, Tetrahedron Lett., 2002, 43, 3455-3457.
  90. K. Kumamoto, Y. Misawa, S. Tokita, Y. Kubo, and H. Kotsuki, High-pressure-promoted Condensation of Isothiocyanates with Aminopyridines: Efficient Synthesis of Pyridine-thiourea Conjugates as Building Blocks for Hydrogen-bonding Receptors, Tetrahedron Lett., 2002, 43, 1035-1038.
  91. Y. Kubo, Chromogenic Receptors as Potentially Hyper-structured Molecules, Hyper-structured Molecules Ⅲ: Chemistry, Physics and Applecations, Gordon and Brech Sci. Pub., 2002, 136-149.
  92. Y. Kubo, T. Ohno, J.Yamanaka, S. Tokita, T. Iida, and Y. Ishimaru, Chirality-transfer Control Using a Heterotopic Zinc(II) Porphyrin Dimer, J. Am. Chem. Soc., 2001, 123, 12700-12701.
  93. 久保由治、ホストーゲスト相互作用に基づく光機能性分子システム、オレオサイレンス「生体機能関連化学の新展開 (I)」、2001, 6, 617-625.
  94. 久保　由治、物質認識の可視化とキラル識別，化学と教育，2001，49，472-475.
  95. S. Houbrechts, Y. Kubo, T. Tozawa, S. Tokita, T. Wada, and H. Sasabe, Second-order Nonlinear Optical Properties of Functionalized Ionophores: Cation Steered Modulation of the First Hyperpolarizability, Angew. Chem. Int. Ed., 2000, 39, 3859-3862.
  96. S. Houbrechts, T. Wada, H. Sasabe, and Y. Kubo, Control of the First Hyperpolarizability of Functionalized Mesostructures through Cation Binding, Nonlinear Optics, 2000, 25, 309-314.
  97. T. Tozawa, Y. Misawa, S. Tokita, and Y. Kubo, A Regioselectively Bis(thiourea)-substituted Dibenzo-diaza-30-crown-10: A New Strategy for the Developement of Multi-site Receptors,Tetrahedron Lett., 2000, 41, 5219-5223.
  98. Y. Kubo, M. Tsukahara, S. Ishihara, and S.Tokita, A Simple Anion Chemosensor Based on a Naphthalene-thiouronium Dyad, Chem. Commun., 2000, 653-654.
  99. Y. Kubo, S. Obara, and S. Tokita, Effective Signal Control (off-on-off Action) by Metal Ionic Inputs on a New Chromoionophore-based Calix[4]crown, Chem. Commun., 1999, 2399-2400.
  100. Y. Kubo, T. Wada, and H. Sasabe, Indoaniline-derived Calix[4]arenes as A New NLO-chromogenic System, Nonlinear Optics, 1999, 22, 31-34.
  101. Y. Kubo, Y. Murai, J. Yamanaka, S. Tokita, and Y. Ishimaru, A New Biphenyl-20-crown-6-derived Zinc(II) Porphyrin Dimer with a Potentially Heterotropic Allostery, Tetrahedron Lett., 1999, 40, 6019-6023.
  102. Y. Kubo, Binaphthyl-appended Chromogenic Receptors: Synthesis and Application to their Colorimetric Recognition of Amines, SYNLETT (account), 1999, 161.
  103. Y. Kubo, Chromogenic Receptors: Versatility of the Colorimetric Recognizing Behavior, J. Inclusion Phenom. Mol. Recognit. Chem. (Special Issue), 1998, 32, 235.
  104. Y. Kubo, N. Hirota, S. Maeda, and S. Tokita, Naked-eye Detectable Chiral Recogniiton Using a Chromogenic Receptor,   Anal. Sci. (Special Issue), 1998, 14, 183.
  105. 久保　由治、クロモジェニックレセプター：カチオン認識から不斉認識へ、有機合成化学協会誌、1997, 55, 506.
  106. Y. Kubo, T. Takaba, and S. Aramaki, N-Cyano-N'-diethylaminophenyl-1,4-naphthoquinonediimines : New Chromophores for Second-order Nonlinear Optical Materials, Chem. Lett., 1997, 255.
  107. Y. Kubo, S. Maeda, S. Tokita, and M. Kubo, Colorimetric Chiral Recognition by a Molecular Sensor, Nature, 1996, 382, 522.
  108. Y. Kubo, S. Tokita, Y. Kojima, Y. T. Osano, and T. Matsuzaki, A New Family of Indoaniline-Derived Calix[4]arenes: Synthesis and Optical Recognition Properties as a Chromogenic Receptor, J. Org. Chem., 1996, 61, 3758.
  109. Y. Kubo, S.Maruyama, N. Ohhara, M. Nakamura, and S. Tokita, Molecular Recognition of Butylamines by a Binaphthyl-derived Chromogenic Calix[4]crown,  J. Chem. Soc., Chem. Commun., 1995, 1727.
  110. Y. Kubo, S. Aramaki, Y. Okamoto, and T. Murayama, Novel Naphthoquinone Methide Dyes for Second-order Nonlinear Optical Materials, J. Chem. Soc., Chem. Commun., 1995, 969.

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