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    • Soji Shimizu
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Iwasaki LAB
  • ホーム
  • Research
  • Members
    • Soji Shimizu
  • Publications
  • Event
  • More
    • ホーム
    • Research
    • Members
      • Soji Shimizu
    • Publications
    • Event

2020年以降 2019–2010年 2009年–2003年 Reviews Cover Gallery

2019年

Efficient Electrogenerated Chemiluminescence of Pyrrolopyrrole Aza-BODIPYs in the Near-Infrared Region with Tripropylamine: Involving Formation of S2 and T2 States 

Ishimatsu, R.; Shintaku, H.; Kage, Y.; Kamioka, M.; Shimizu, S.; Nakano, K.; Furuta, H.; Imato, T.

J. Am. Chem. Soc. 2019, 141, 11791-11795.

Three-dimensional aromaticity in an antiaromatic cyclophane 

Nozawa, R.; Kim, J.; Oh, J.; Lamping, A.; Wang, Y.; Shimizu, S.; Hisaki, I.; Kowalczyk, T.; Fliegl, H.; Kim, D.; Shinokubo, H.

Nature. Commun. 2019, 10, 3576. 

Bis(1,3-dithiol-2-ylidene)-substituted Subtriazachlorin: A Subphthalocyanine Analogue with Redox Properties

Wang, Y.; Mori, S.; Furuta, H.; Shimizu, S. 

Angew. Chem. Int. Ed. 2019, 58, 10975–10979. 

Pyrrolopyrrole Aza-BODIPY Analogues as Near-Infrared Chromophores and Fluorophores: Red-Shift Effects of Substituents on the Absorption and Emission

Kage, Y.; Karasaki, H.; Mori, S.; Furuta, H.; Shimizu, S. 

ChemPlusChem, 2019, 84, 1648–1652. 

1,3-Dithiole-2-one-Fused Subphthalocyanine and Subporphyrazine: Synthesis and Properties Arising from the 1,3-Dithiole-2-one Units 

Wang, Y.; Uchihara, K.; Mori, S.; Furuta, H.; Shimizu, S. 

Org. Lett. 2019, 21, 3103–3107.

N-Confused Porphyrin-aza-Dipyrrin Chimera: A Versatile Metal Coordination Ligand Using its Unique NH Tautomerism

Fukuda, M.; Mori, S.; Furuta, H.; Shimizu, S. 

Chem. Asian J. 2019, 14, 1697–1702. 

Synthesis and Properties of Redox-Switchable Zinc Complexes of 10,15,20-Triaryl-15-aza-5-oxaporphyrin

Sudoh, K.; Furukawa, K.; Nakano, H.; Shimizu, S.; Matano, Y.

Heteroatom Chemistry, 2018;e21456.

Rational Synthesis of Antiaromatic 5,15-Dioxaporphyrin and Oxidation into β,β-Linked Dimers

Nishiyama, A.; Fukuda, M.; Mori, S.; Furukawa, K.; Fliegl, H.; Furuta, H.; Shimizu, S.

Angew. Chem. Int. Ed. 2018, 57, 9278-9733.

The First Silicon(IV) Corrole Complexes: Synthesis, Structures, Properties, and Formation of a µ-Oxo Dimer

Ueta, K.; Fukuda, M.; Kim, G.; Shimizu, S.; Tanaka, T.; Kim, D.; Osuka, A.

Chem. Eur. J. 2018, 24, 7637-7646.

Blackening aza-BODIPY analogues by simple dimerization: panchromatic absorption of pyrrolopyrrole aza-BODIPY dimer

Kage, Y.; Mori, S.; Ide, M.; Saeki, A.; Furuta, H.; Shimizu, S.

Mater. Chem. Front. 2018, 2, 112-120.

Facile Synthesis of Dimeric aza-BODIPY Analogues from Electron-Deficient Bislactams and Their Intriguing Optical and Electrochemical Properties

Tamada, M.; Iino, T.; Wang, Y.; Ide, M.; Saeki, A.; Furuta, H.; Kobayashi, N.; Shimizu, S.

Tetrahedron Lett. 2017, 58, 3151-3154.

Phenylene-Bridged Expanded Porphyrazines

Iizuka, F.; Kage, Y.; Kobayashi, N.; Furuta, H.; Shimizu, S.

ChemPlusChem, 2017, 82, 1021-1024.

Polymeric Self-Assemblies with Boron-Containing Near-Infrared Dye Dimers for Photoacoustic Imaging Probes

Miki, K.; Enomoto, A.; Inoue, T.; Nabeshima, T.; Saino, S.; Shimizu, S.; Matsuoka, H.; Ohe, K. 

Biomacromolecules, 2017, 18, 249–256.

Supramolecular dimeric structures of pyrazole-containing meso-oxo carbaphlorin analogues

Ishida, M.; Fujimoto, H.; Morimoto, T.; Mori, S.; Toganoh, M.; Shimizu, S.; Furuta, H.

Supramol. Chem. 2017, 29, 8-16.

Stacked antiaromatic porphyrins

Nozawa, R.; Tanaka, H.; Cha, W.-Y.; Hong, Y.; Hisaki, I.; Shimizu, S.; Shin, J.-Y.; Kowalczyk, T.; Irle, S.; Kim, D.; Shinokubo, H.

Nat. Commun. 2016, 7, 13620.

Pyrene-Bridged Boron Subphthalocyanine Dimers: Combination of Planar and Bowl-Shaped π-Conjugated Systems for Creating Uniquely Curved π-Conjugated Systems

Nakano, S.; Kage, Y.; Furuta, H.; Kobayashi, N.; Shimizu, S.

Chem. Eur. J. 2016, 22, 7706-7710.

A novel isoindole-containing polyaromatic hydrocarbon unexpectedly formed during the synthesis of meso-2,6-dichlorophenyl-substituted tribenzosubporphyrin

Shiina, Y.; Karasaki, H.; Mori, S.; Kobayashi, N.; Furuta, H.; Shimizu, S.

J. Porphyrins Phthalocyanine 2016, 20, 1049-1054.

Synthesis of a Tetrabenzotetraaza[8]circulene by a “Fold-In” Oxidative Fusion Reaction

Chen, F.; Hong, Y. S.; Shimizu, S.; Kim, D.; Tanaka, T.; Osuka, A.

Angew. Chem. Int. Ed. 2015, 54, 10639-10642.

Benzo[c,d]indole-containing aza-BODIPY dyes: asymmetrization-induced solid-state emission and aggregation-induced emission enhancement as new properties of a well-known chromophore

Shimizu, S.; Murayama, A.; Haruyama, T.; Iino, T.; Mori, S.; Furuta, H.; Kobayashi, N.

Chem. Eur. J. 2015, 21, 12996-13003.

Ring-fused porphyrins: extension of π-conjugation significantly affects the aromaticity and optical properties of the porphyrin π-systems and Lewis acidity of the central metal ions

Saegusa, Y.; Ishizuka, T.; Komamura, K.; Shimizu, S.; Kotani, H.; Kobayashi, N.; Kojima, T. 

PCCP 2015, 17, 15001-15011.

Cyclophanes Containing Bowl-Shaped Aromatic Chromophores: Three Isomers of anti-[2.2](1,4)Subphthalocyaninophane 

Liu, Q.; Shimizu, S.; Kobayashi, N. 

Angew. Chem. Int. Ed. 2015, 54, 5187-5191.

Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties

Liu, H.; Lu, H.; Zhou, Z.; Shimizu, S.; Li, Z.; Kobayashi, N.; Shen, Z.

Chem. Commun. 2015, 51, 1713-1716.

Rational Molecular Design Towards vis/NIR Absorption and Fluorescence by using Pyrrolopyrrole aza-BODIPY and its Highly Conjugated Structures for Organic Photovoltaics

Shimizu, S.; Iino, T.; Saeki, A.; Seki, S.; Kobayashi, N.

Chem. Eur. J. 2015, 21, 2893–2904.

Sizeable red-shift of absorption and fluorescence of subporphyrazine induced by peripheral push and pull substitution

Liang, X.; Shimizu, S.; Kobayashi, N.

Chem. Commun. 2014, 50, 13781–13784.

Unexpected formation of a triphyrin in the reaction of dibromodipyrromethene and N,N-dimethylaminoethanol

Shimizu, S.; Hirokawa, S.; Kobayashi, N.

J. Porphyrins Phthalocyanines 2014, 18, 727-734.

Dearomatization-Induced Transannular Cyclization: Synthesis of Electron-Accepting Thiophene-S,S-Dioxide-Fused Biphenylene

Fukazawa, A.; Oshima, H.; Shimizu, S.; Kobayashi, N.; Yamaguchi, S.

J. Am. Chem. Soc. 2014, 136, 8738-8745.

Core-Modified Rubyrins Containing Dithienylethene Moieties

Zhou, S.; Chang, Y.; Shimizu, S.; Mack, J.; Schütt, C.; Herges, R.; Shen, Z.; Kobayashi, N.

Angew. Chem. Int. Ed. 2014, 53, 6563-6567.

A Core-Expanded Subphthalocyanine Analogue with a Significantly Distorted Conjugated Surface and Unprecedented Properties

Shimizu, S.; Nakano, S.; Kojima, A.; Kobayashi, N.

Angew. Chem. Int. Ed. 2014, 53, 2408-2412.

Control of Chromophore Symmetry by Positional Isomerism of Peripheral Substituents

Shimizu, S.; Haseba, Y.; Yamazaki, M.; Kumazawa, G.; Kobayashi, N.

Chem. Eur. J. 2014, 20, 4822-4828.

Expanded Dipyrrins with Electron-Withdrawing Substituents: Broad Range of Absorption in the Visible Region

Liang, X.; Shimizu, S.; Kobayashi, N.

Tetrahedon Lett. 2014, 55, 256–258.

A μ-Oxo Hetero Dimer of Silicon Phthalocyanine and Naphthalocyanine

Oniwa, k.; Shimizu, S.; Shiina, Y.; Fukuda, T.; Kobayashi, N.

Chem. Commun. 2013, 49, 8341–8343.

Tetrathiafulvalene-Annulated Subphthalocyanines

Shimizu, S.; Yamazaki, Y.; Kobayashi, N.

Chem. Eur. J. 2013, 19, 7324–7327.

Nickel and Palladium Complexes of Seco-tribenzoporphyrazines Derived From One-pot Condensation of 1,3-Diiminoisoindoline

Sugita, I.; Shimizu, S.; Fukuda, T.; Kobayashi, N.

Tetrahedron Lett. 2013, 54, 1599–1601.

Pyrrolopyrrole Aza-BODIPY analogues: a facile synthesis and intense fluorescence

Shimizu, S.; Iino, T.; Araki, Y.; Kobayashi, N.

Chem. Commun. 2013, 49, 1621-1623.

Highly Deformed Phthalocyanine as a Suitable Scaffold for Pristine Fullerenes

Shimizu, S.; Miura, A.; Kobayashi, N.

CrystEngComm 2013, 15, 3759–3762.

Gold(II) Phthalocyanine Revisited: Synthesis and Spectroscopic Properties of Gold(III) Phthalocyanine and an Unprecedented Ring-Contracted Phthalocyanine Analogue

Wong, E. W. Y.; Miura, A.; Wright, M. D.; He, Q.; Walsby, C. J.; Shimizu, S.; Kobayashi, N.; Leznoff, D. B.

Chem. Eur. J. 2012, 18, 12404-12410.

Gram-Scale Synthesis of Nickel(II) Norcorrole: The Smallest Antiaromatic Porphyrinoid

Ito, T.; Hayashi, Y.; Shimizu, S.; Shin, J.-Y.; Kobayashi, N.; Shinokubo, H.

Angew. Chem. Int. Ed. 2012, 51, 8542-8545.

para-Benzihemiporphyrazine and its expanded [3+3]-type analogue

Shimizu, S.; Sato, Y.; Kobayashi, N.

Chem. Lett. 2012, 41, 702-704.

Synthesis and Properties of  β,β-sp3-Hybridized Subphthalocyanine Analogues

Shimizu, S.; Otaki, T.; Yamazaki, Y.; Kobayashi, N.

Chem. Commun. 2012, 48, 4100–4102.

Synthesis of 5,10,15-Triazaporphyrins–Effect of Benzo-annulation on the Electronic Structures

Shimizu, S.; Ito, Y.; Oniwa, K.; Hirokawa, S.; Miura, Y.; Matsushita, O.; Kobayashi, N.

Chem. Commun. 2012, 48, 3851–3853.

Rectangular-Shaped Expanded Phthalocyanines with Two Central Metal Atoms

Matsushita, O.; Derkacheva, V. M.; Muranaka, A.; Shimizu, S.; Uchiyama, M.; Luk’yanets, E. A.; Kobayashi, N.

J. Am. Chem. Soc. 2012, 134, 3411–3418.

Effects of Carbon–Metal–Carbon Linkage on the Optical, Photophysical, and Electrochemical Properties of Phosphametallacycle-Linked Coplanar Porphyrin Dimers

Matano, Y.; Matsumoto, K.; Hayashi, H.; Nakao, Y.; Kumpulainen, T.; Chukharev, V.; Tkachenko, N. V.; Lemmetyinen, H.; Shimizu, S.; Kobayashi, N.; Sakamaki, D.; Ito, A.; Tanaka, K.; Imahori, H.

J. Am. Chem. Soc. 2012, 134, 1825–1839.

Core-Modified Phthalocyanine Analogues with a Seven-membered Unit in place of a Five-membered Ring Unit

Shimizu, S.; Uemura, K.; Zhu, H.; Kobayashi, N.

Tetrahedron Lett. 2012, 53, 579–581.

Solvent- and Temperature-Dependent Conformational Changes between Hückel Antiaromatic and Möbius Aromatic Species in meso-Trifluoromethyl-Substituted [28]Hexaphyrins

Yoon, M.-C.; Kim, P.; Yoo, H.; Shimizu, S.; Koide, T.; Tokuji, S.; Saito, S.; Osuka, A.; Kim, D.

J. Phys. Chem. B. 2011, 115, 14928–14937.

Chiral 1,2-Subnaphthalocyanines

Shimizu, S.; Miura, A.; Khene, S.; Nyokong, T.; Kobayashi, N.

J. Am. Chem. Soc. 2011, 133, 17322–17328.

Azepiphthalocyanine—an unprecedented large twist of a π-conjugation system upon core-modification with a seven-membered ring unit

Shimizu,S.; Zhu, H.; Kobayashi, N.

Chem. Commun. 2011, 47, 3072–3074.

Synthesis and Spectroscopic Properties of Fused-Ring-Expanded Aza-Boradiazaindacenes

Lu, H.; Shimizu, S.; Mack, J.; You, X.; Shen, Z.; Kobayashi, N.

Chem. Asian. J. 2011, 6, 1026–1037.

Pyrene-fused subphthalocyanine

Shimizu, S.; Nakano, S.; Hosoya, T.; Kobayashi, N.

Chem. Commun. 2011, 47, 316-318.

Subazaphenalenephthalocyanine: A Subphthalocyanine Analogue Bearing a Six-Membered Ring Unit

Zhu, H.; Shimizu, S.; Kobayashi, N.

Angew. Chem. Int. Ed. 2010, 49, 8000-8003.

Azaphenalene Phthalocyanines: Phthalocyanine Analogues with Six-Membered Ring Units Instead of Five-Membered Ring Units

Shimizu, S.; Zhu, H.; Kobayashi, N.

Chem. Eur. J. 2010, 16, 11151–11159. 

meso-Trifluoromethyl-Substituted Subporphyrin from Ring-Splitting Reaction of meso-Trifluoromethyl-Substituted [32]Heptaphyrin(1.1.1.1.1.1.1)

Sakamoto, R.; Saito, S.; Shimizu, S.; Inokuma, Y.; Aratani, N.; Osuka, A.

Chem. Lett. 2010, 39, 439–441.

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