Soji Shimizu

发表

Core-modified phthalocyanines and subphthalocyanines: A synthetic strategy towards core-modification and novel properties arising from the inner ring-expansion

H. Furuta, Soji Shimizu, 2015 .

Effects of carbon-metal-carbon linkages on the optical, photophysical, and electrochemical properties of phosphametallacycle-linked coplanar porphyrin dimers.

Kazuaki Matsumoto, Y. Matano, H. Imahori, 2012, Journal of the American Chemical Society.

Nonlinear optical properties and excited-state dynamics of highly symmetric expanded porphyrins.

Dongho Kim, J. Sessler, Masaaki Suzuki, 2006, Journal of the American Chemical Society.

Phenylene-Bridged Expanded Porphyrazines.

H. Furuta, N. Kobayashi, Soji Shimizu, 2017, ChemPlusChem.

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

Dongho Kim, A. Osuka, Kento Ueta, 2018, Chemistry.

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

H. Furuta, N. Kobayashi, Soji Shimizu, 2016, Chemistry.

Structurally-modified subphthalocyanines: molecular design towards realization of expected properties from the electronic structure and structural features of subphthalocyanine.

N. Kobayashi, Soji Shimizu, 2014, Chemical communications.

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.

H. Furuta, Shigeki Mori, N. Kobayashi, 2015, Chemistry.

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

N. Kobayashi, Soji Shimizu, Hua Zhu, 2011, Chemical communications.

Dearomatization-induced transannular cyclization: synthesis of electron-accepting thiophene-S,S-dioxide-fused biphenylene.

S. Yamaguchi, N. Kobayashi, Soji Shimizu, 2014, Journal of the American Chemical Society.

Facile synthesis of dimeric aza-BODIPY analogues from electron-deficient bislactams and their intriguing optical and electrochemical properties

A. Saeki, H. Furuta, N. Kobayashi, 2017 .

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

H. Furuta, Shigeki Mori, Soji Shimizu, 2019, Angewandte Chemie.

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

H. Furuta, Shigeki Mori, Soji Shimizu, 2019, Angewandte Chemie.

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

A. Saeki, H. Furuta, Shigeki Mori, 2018 .

Recent Advances in Subporphyrins and Triphyrin Analogues: Contracted Porphyrins Comprising Three Pyrrole Rings.

Soji Shimizu, 2017, Chemical reviews.

Structurally‐Modified Subphthalocyanines: Molecular Design Towards Realization of Expected Properties from the Electronic Structure and Structural Features of Subphthalocyanine

N. Kobayashi, Soji Shimizu, 2014 .

Subazaphenalenephthalocyanine: a subphthalocyanine analogue bearing a six-membered ring unit.

N. Kobayashi, Soji Shimizu, Hua Zhu, 2010, Angewandte Chemie.

para-Benzihemiporphyrazine and Its Expanded [3+3]-type Analogue

N. Kobayashi, Soji Shimizu, Yuta Sato, 2012 .

Synthesis and properties of β,β-sp3-hybridized subphthalocyanine analogues.

N. Kobayashi, Soji Shimizu, T. Otaki, 2012, Chemical communications.

Core-modified phthalocyanine analogues with a seven-membered ring unit in place of a five-membered ring unit

N. Kobayashi, Soji Shimizu, Hua Zhu, 2012 .

Chiral 1,2-subnaphthalocyanines.

T. Nyokong, N. Kobayashi, Soji Shimizu, 2011, Journal of the American Chemical Society.

A core-expanded subphthalocyanine analogue with a significantly distorted conjugated surface and unprecedented properties.

N. Kobayashi, Soji Shimizu, S. Nakano, 2014, Angewandte Chemie.

Azaphenalene phthalocyanines: phthalocyanine analogues with six-membered-ring units instead of five-membered-ring units.

N. Kobayashi, Soji Shimizu, Hua Zhu, 2010, Chemistry.

Tetrathiafulvalene-annulated subphthalocyanines.

N. Kobayashi, Soji Shimizu, Y. Yamazaki, 2013, Chemistry.

Gold(II) phthalocyanine revisited: synthesis and spectroscopic properties of gold(III) phthalocyanine and an unprecedented ring-contracted phthalocyanine analogue.

C. Walsby, N. Kobayashi, D. Leznoff, 2012, Chemistry.

Pyrene-fused subphthalocyanine.

N. Kobayashi, Soji Shimizu, S. Nakano, 2011, Chemical communications.

meso-aryl expanded porphyrins: synthesis, structures, and coordination chemistry

A. Osuka, Soji Shimizu, 2004 .

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

Hua Lu, N. Kobayashi, Zhen Shen, 2015, Chemical communications.

Rectangular-shaped expanded phthalocyanines with two central metal atoms.

M. Uchiyama, A. Muranaka, N. Kobayashi, 2012, Journal of the American Chemical Society.

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

H. Furuta, Shigeki Mori, N. Kobayashi, 2016 .

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

N. Kobayashi, Soji Shimizu, Shoma Hirokawa, 2014 .

Control of chromophore symmetry by positional isomerism of peripheral substituents.

N. Kobayashi, Soji Shimizu, Yukio Haseba, 2014, Chemistry.

Metalation chemistry of meso-aryl-substituted expanded porphyrins

A. Osuka, Soji Shimizu, 2006 .

Comparative photophysics of [26]- and [28]hexaphyrins(1.1.1.1.1.1): large two-photon absorption cross section of aromatic [26]hexaphyrins(1.1.1.1.1.1).

Dae Won Cho, Dongho Kim, Masaaki Suzuki, 2005, Journal of the American Chemical Society.

Three-dimensional aromaticity in an antiaromatic cyclophane

Dongho Kim, H. Shinokubo, Heike Fliegl, 2019, Nature Communications.

Periphery-Fused Chiral A2B-Type Subporphyrin

N. Kobayashi, Soji Shimizu, Shoma Hirokawa, 2021, Molecules.

TTF‐Annulated Silicon Phthalocyanine Oligomers and Their External‐Stimuli‐Responsive Orientational Ordering

Heng Wang, H. Yoshikawa, H. Furuta, 2020, Angewandte Chemie.

TTF-Annulated Silicon Phthalocyanine Oligomers and Their External-Stimuli-Responsive Orientational Ordering.

Heng Wang, H. Yoshikawa, H. Furuta, 2020, Angewandte Chemie.

Effect of peripheral fused ring substitution on the optical spectroscopy and electronic structure of metal phthalocyanine complexes

T. Nyokong, Wadzanai Chidawanyika, N. Kobayashi, 2009 .

Expanded dipyrrins with electron-withdrawing substituents: broad range of absorption in the visible region

N. Kobayashi, Soji Shimizu, Xu Liang, 2014 .

Core-modified rubyrins containing dithienylethene moieties.

R. Herges, N. Kobayashi, Zhen Shen, 2014, Angewandte Chemie.

Rational molecular design towards Vis/NIR absorption and fluorescence by using pyrrolopyrrole aza-BODIPY and its highly conjugated structures for organic photovoltaics.

A. Saeki, N. Kobayashi, S. Seki, 2015, Chemistry.

Synthesis of a Tetrabenzotetraaza[8]circulene by a "Fold-In" Oxidative Fusion Reaction.

Dongho Kim, A. Osuka, Takayuki Tanaka, 2015, Angewandte Chemie.

Group 12 metal complexes of [26]hexaphyrin(1.1.1.1.1.1).

A. Osuka, Shigeki Mori, Soji Shimizu, 2007, Inorganic chemistry.

Biscopper complexes of meso-aryl-substituted hexaphyrin: gable structures and varying antiferromagnetic coupling.

T. Yokoyama, A. Osuka, K. Furukawa, 2004, Journal of the American Chemical Society.

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

T. Ishizuka, Hiroaki Kotani, Takahiko Kojima, 2015, Physical chemistry chemical physics : PCCP.

Dicopper and disilver complexes of octaphyrin(1.1.1.1.1.1.1.1): reversible hydrolytic cleavage of the pyrrolic ring to a keto-imine.

A. Osuka, Y. Tanaka, Soji Shimizu, 2005, Angewandte Chemie.

Oxidative nitration reaction of antiaromatic 5,15-dioxaporphyrin

H. Furuta, Shigeki Mori, Soji Shimizu, 2020 .

Gram-scale synthesis of nickel(II) norcorrole: the smallest antiaromatic porphyrinoid.

Tomohiro Ito, H. Shinokubo, N. Kobayashi, 2012, Angewandte Chemie.

aza-BODIPY synthesis towards vis/NIR functional chromophores based on a Schiff base forming reaction protocol using lactams and heteroaromatic amines.

Soji Shimizu, 2019, Chemical communications.

Tungsten(VI) Complex of N-Fused Porphyrin Absorbing Near-Infrared Light beyond 1000 nm.

H. Furuta, Shigeki Mori, Masatoshi Ishida, 2020, Chemistry, an Asian journal.

Subphthalocyanine-Stoppered [2]Rotaxanes: Synthesis and Size/Energy Threshold of Slippage.

G. Kociok‐Köhn, H. Furuta, G. Pantoș, 2020, Organic letters.

Stacked antiaromatic porphyrins

S. Irle, Dongho Kim, H. Shinokubo, 2016, Nature Communications.

Pyrrolopyrrole aza-BODIPY analogues: a facile synthesis and intense fluorescence.

Y. Araki, N. Kobayashi, Soji Shimizu, 2013, Chemical communications.

meso-Aryl substituted rubyrin and its higher homologues: structural characterization and chemical properties.

J. Sessler, A. Osuka, H. Shinokubo, 2008, Chemistry.

Regioselective nucleophilic substitution reaction of meso-hexakis(pentafluorophenyl) substituted [26]hexaphyrin

Masaaki Suzuki, A. Osuka, Soji Shimizu, 2003 .

Copper 1,19‐Diaza‐21,24‐dicarbacorrole: A Corrole Analogue with an N−N Linkage Stabilizes a Ground‐State Singlet Organocopper Species

H. Furuta, Shigeki Mori, Masatoshi Ishida, 2020, Angewandte Chemie.

Copper 1,19-Diaza-21,24-Dicarbacorrole: A Corrole Analog with an N-N Linkage Stabilizes Ground-State Singlet Organocopper.

H. Furuta, Shigeki Mori, Masatoshi Ishida, 2020, Angewandte Chemie.

meso-Trifluoromethyl-substituted expanded porphyrins.

N. Aratani, A. Osuka, Soji Shimizu, 2006, Chemistry.

Group 10 metal complexes of meso-aryl-substituted [26]hexaphyrins with a metal-carbon bond.

A. Osuka, Shigeki Mori, Soji Shimizu, 2005, Inorganic chemistry.

[40]nonaphyrin(1.1.1.1.1.1.1.1.1) and its heterometallic complexes with palladium-carbon bonds.

A. Osuka, Soji Shimizu, Y. Kamimura, 2007, Chemistry.

Internally 1,4-phenylene-bridged meso aryl-substituted expanded porphyrins: the decaphyrin and octaphyrin cases.

A. Osuka, Soji Shimizu, Shohei Saito, 2005, Angewandte Chemie.

N-fused pentaphyrins and their rhodium complexes: oxidation-induced rhodium rearrangement.

A. Osuka, H. Furuta, Shigeki Mori, 2005, Chemistry.

Phthalocyanine and Related Analogues

Soji Shimizu, 2021 .

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

Heike Fliegl, H. Furuta, Shigeki Mori, 2018, Angewandte Chemie.

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

Heike Fliegl, H. Furuta, Shigeki Mori, 2018, Angewandte Chemie.

Nickel and palladium complexes of seco-tribenzoporphyrazines derived from one-pot condensation of 1,3-diiminoisoindoline

N. Kobayashi, T. Fukuda, Soji Shimizu, 2013 .

Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes

N. Kobayashi, Soji Shimizu, Akito Miura, 2013 .

Recent Advances in the Chemistry of Phthalocyanines as Functional Chromophores

N. Kobayashi, Soji Shimizu, 2015 .

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

N. Kobayashi, Soji Shimizu, Xu Liang, 2014, Chemical communications.

Metalation chemistry of meso-aryl-substituted expanded porphyrins

A. Osuka, Soji Shimizu, 2006 .

Thermal splitting of Bis-Cu(II) octaphyrin(1.1.1.1.1.1.1.1) into two Cu(II) porphyrins.

S. Fujita, N. Aratani, A. Osuka, 2004, Journal of the American Chemical Society.

Synthesis and spectroscopic properties of fused-ring-expanded aza-boradiazaindacenes.

Hua Lu, N. Kobayashi, Zhen Shen, 2011, Chemistry, an Asian journal.

Conformational changes of meso-aryl substituted expanded porphyrins upon protonation: effects on photophysical properties and aromaticity.

Jong Min Lim, Dongho Kim, A. Osuka, 2009, The journal of physical chemistry. B.

Perfluorinated meso-aryl-substituted expanded porphyrins.

A. Osuka, H. Furuta, Soji Shimizu, 2003, Angewandte Chemie.

Axial ligand exchange reactions of meso-aryl subporphyrins-axially fluoro-substituted subporphyrin and a mu-oxo dimer and trimer of subporphyrins.

A. Matsuda, N. Kobayashi, Soji Shimizu, 2009, Inorganic chemistry.

Synthesis and properties of redox-switchable zinc complexes of 10,15,20-triaryl-15-aza-5-oxaporphyrin

H. Nakano, Y. Matano, K. Furukawa, 2018, Heteroatom Chemistry.

meso-Aryl-substituted [26]hexaphyrin(1.1.0.1.1.0) and [38]nonaphyrin(1.1.0.1.1.0.1.1.0) from oxidative coupling of a tripyrrane.

A. Osuka, Soji Shimizu, R. Taniguchi, 2005, Angewandte Chemie.

Solvent- and temperature-dependent conformational changes between Hückel antiaromatic and Möbius aromatic species in meso-trifluoromethyl substituted [28]hexaphyrins.

Dongho Kim, A. Osuka, Hyejin Yoo, 2011, The journal of physical chemistry. B.

An Electron-Accepting aza-BODIPY-Based Donor-Acceptor-Donor Architecture for Bright NIR Emission.

C. Adachi, Dongho Kim, H. Furuta, 2021, Chemistry.

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

H. Furuta, Shigeki Mori, Masatoshi Ishida, 2017 .

Ring size selective synthesis of meso-aryl expanded porphyrins

Masaaki Suzuki, A. Osuka, H. Furuta, 2003 .

Near-infrared absorbing pyrrolopyrrole aza-BODIPY-based donor–acceptor polymers with reasonable photoresponse

C. Adachi, Takuma Yasuda, A. Saeki, 2020 .

Rational design of pyrrolopyrrole-aza-BODIPY-based acceptor-donor-acceptor triads for organic photovoltaics application.

Takuma Yasuda, H. Furuta, Soji Shimizu, 2020, Chemical communications.

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

T. Imato, H. Furuta, K. Nakano, 2019, Journal of the American Chemical Society.

Post-Modification of Pyrrolopyrrole Aza-BODIPY toward High Near-Infrared Fluorescence Brightness.

C. Adachi, Yitong Wang, H. Nakanotani, 2023, Organic letters.

Panchromatic small-molecule organic solar cells based on a pyrrolopyrrole aza-BODIPY with a small energy loss

Takuma Yasuda, H. Furuta, Soji Shimizu, 2022, Dyes and Pigments.

Synthesis of N,N-difluoroboryl complexes of 3,3′-diarylazadiisoindolylmethenes

N. Kobayashi, Soji Shimizu, E. Lukyanets, 2008 .

Synthesis of 5,10,15-triazaporphyrins--effect of benzo-annulation on the electronic structures.

Yuki Ito, K. Oniwa, N. Kobayashi, 2012, Chemical communications.

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

H. Furuta, Shigeki Mori, Soji Shimizu, 2019, Chemistry, an Asian journal.

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

H. Furuta, Shigeki Mori, Soji Shimizu, 2019, ChemPlusChem.

Janus Pyrrolopyrrole aza-Dipyrrin: Hydrogen-Bonded Assemblies and Slow Magnetic Relaxation of the Cobalt(II) Complex in the Solid State.

Yitong Wang, H. Furuta, Shigeki Mori, 2021, Chemistry.

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

H. Matsuoka, K. Ohe, T. Nabeshima, 2017, Biomacromolecules.

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

H. Furuta, Shigeki Mori, Soji Shimizu, 2019, Organic letters.

Spontaneous Assembly and Three-Dimensional Stacking of Antiaromatic 5,15-Dioxaporphyrin on HOPG.

K. Yoshizawa, H. Furuta, Shigeki Mori, 2022, Angewandte Chemie.

Cyclophanes containing bowl-shaped aromatic chromophores: three isomers of anti-[2.2](1,4)subphthalocyaninophane.

N. Kobayashi, Soji Shimizu, Quan Liu, 2015, Angewandte Chemie.

Meso-trifluoromethyl-substituted subporphyrin from ring-splitting reaction of meso-trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1)

N. Aratani, Y. Inokuma, Soji Shimizu, 2010 .