Faculty Profiles - SHIN Jiyoung

Papers - SHIN Jiyoung

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Use of Ferrocenyl Ni(II) and Zn(II) Porphyrins as Active Organic Electrode Materials for Sodium Secondary Batteries Reviewed

Shaoning Zhang, Jinkwang Hwang, Quan Manh Phung, Kazuhiko Matsumoto, Rika Hagiwara, Ji-Young Shin

Batteries & Supercaps Vol. 7 ( 6 ) page： e202400004-1 - e202400004-6 2024.3

Sufficiently Enriched Dual-Ion Batteries with Ferrocenyl Substituted Nickel(II) Norcorrole Organic Electrodes Reviewed

Shaoning Zhang, Jinkwang Hwang, Quan Manh Phùng, Kazuki Matsumoto, Rika Hagiwara, Ji-Young Shin

Advanced Energy Materials Vol. 13 ( 40 ) page： 2301443 2023.9

Octaphyrin(1.0.1.0.1.0.1.0) as an organic electrode for Li and Na rechargeable batteries Reviewed

Jinkwang Hwang, Kazuhiko Matsumoto, Rika Hagiwara, Si-Yu Liu, Ji-Young Shin

Small Methods Vol. 6 ( 3 ) page： 2101181 2022.3

Dual-Ion NiNc battery: A Sustainable Revolution for Sodium Organic Batteries Reviewed

Jinkwang Hwang, Kazuhiko Matsumoto, Rika Hagiwara, Shusaku Ukai, Hiroshi Shinokubo, Ji-Young Shin

Batteries & Supercaps Vol. 4 ( 10 ) page： 1605 - 1610 2021.8

Exquisite chemistries of meso-pentafluorophenyl and meso- (2,6-dichlorophenyl) dipyrromethanes Invited Reviewed

Ji-Young Shin, An Quang Nguyen

Journal of Porphyrins and Phthalocyanines Vol. 25 ( 10n12 ) page： 885 - 896 2021.10

Dual-ion charge-discharge behaviors of Na-NiNc and NiNc-NiNc batteries Reviewed

Jinkwang Hwang, Rika Hagiwara, Hiroshi Shinokubo, Ji-Young Shin

Materials Advances Vol. 2 page： 2263 - 2266 2021.3

The synthesis and characterization of the octahedral CoIII complex of a pyrrolopyrrolizine derivative formed with dicyanovinylene-bis-(meso-aryl)dipyrrin Reviewed

Ji-Young Shin

RSC Advances Vol. 11 ( 4 ) page： 2015 - 2019 2021.1

Reactions of Antiaromatic Norcorrole Ni(II) Complex with Carbenes Reviewed

Si-Yu Liu, Takaki Fukuoka, Norihito Fukui, Ji-Young Shin, Hiroshi Shinokubo

Organic Letters Vol. 22 ( 11 ) page： 4400 - 4403 2020.5

Meso-1,4-phenylene bridged nickel norcorrole dimer Invited Reviewed

Ji-Young Shin

Journal of Porphyrins and Phthalocyanines Vol. 24 page： 181 - 190 2020.1

Synthesis of pyrrolo[3',2':4,5][1,3]diazepino[2,1,7- cd]pyrrolizine derivatives from dicyanovinylene- bis(meso-aryl)dipyrrin Reviewed

Ji-Young Shin

RSC Advances Vol. 9 ( 68 ) page： 40031 - 40036 2019.12

Exploration of Li-organic batteries using hexaphyrin as an active cathode material Invited Reviewed

Ji-Young Shin, Zhongyue Zhang, Kunio Awaga, Hiroshi Shinokubo

Molecules Vol. 24 ( 13 ) page： 2433 2019.7

Highly-conducting molecular circuits based on antiaromaticity Reviewed

Shintaro Fujii, Santiago Marques-Gonzalez, Ji-Young Shin, Hiroshi Shinokubo, Takuya Masuda, Tomoaki Nishino, Narendra P. Arasu, Hector Vazquez, Manabu Kiguchi

Nature Communications Vol. 8 2017.7

A synthesis of novel expanded porphyrinoids: NiII- induced nitrile cyclization of dicyanovinylene-bis (meso-aryl)dipyrrin Reviewed

Nathan H. Faialaga, Satoru Ito, Hiroshi Shinokubo, Younghoon Kim, Kimoon Kim, Ji-Young Shin

Vol. 46 ( 33 ) page： 10802 - 10808 2017.6

E-Bodipy fluorescent chemosensor for Zn2+ ion

Indranil Roy, Ji-Young Shin, Dinesh Shetty, Jayshree K. Khedkar, Jun Heuk Park, Kimoon Kim

Journal of Photochemistry and Phtobiology A:Chemistry Vol. 331 page： 233 - 239 2016.12

Staked antiaromatic porphyrins Reviewed

Ryo Nozawa, Hiroko Tanaka, Won-Young Cha, Yonseok Hong, Ichiro Hisaki, Soji Shimizu, Ji-Young Shin, Tim Kowalczyk, Stephan Irle, Dongho Kim, hiroshi Shinokubo

Nature Communications 2016.11

Ni(II) tetrahydronocorroles: antiaromatic porphyrinoids with saturated pyrrole units

Ryo Nozawa, Keitaro Yamamoto, Ichiro Hisaki, Ji-Young Shin, Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 52 ( 44 ) page： 7106 - 7109 2016.9

Regioselective Nucleophilic Functionalization of Antiaromatic Nickel(II) Norcorroles

Ryo Nozawa, Keitaro Yamamoto, Ji-Young Shin, Satoru Hiroto, Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 54 ( 29 ) page： 8454 - 8457 2015.6

Macrocyclic dipyrrin dimer bridged by ethylene and dioxyphenylene linkers

Ji-Young Shin, Satoru Hiroto, Hiroshi Shinokubo

Journal of Porphyrins and Phthalocyanines Vol. 19 ( 01n03 ) page： 135 - 139 2015.1

A 3-Pyridyl-5,15-Diazaporphyrin Nickel(II) Complex as a Bidentate Metalloligand for Transition Metals

Ayaka Yamaji, Ji-Young Shin, Yoshihiro Miyake. Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 53 ( 50 ) page： 13924 - 13927 2014.12

Synthesis, reactivity and property of 5,15-dithiaporphyrin copper(II) complex

Naruhiko Wachi, Takeshi Kondo, Satoru Ito, Ji-Young Shin, Hiroshi Shinokubo

Journal of Porphyrins and Phthalocyanines Vol. 18 ( 09 ) page： 675 - 678 2014.9

Ring and Volcano Structures Formed by a Metal Dipyrromethene Complex

Seung Bae Son, Qing Miao, Ji-Young Shin, David Dolphin, Jae Ryang Hahn

Bulletin of the Korean Chemical Society Vol. 35 ( 6 ) page： 1727 - 1731 2014.6

Photodynamics of [26]- and [28]hexaphyrin-bodipy hybrids

Ji-Young Shin, Kilsuk Kim, Jong Min Lim, Takayuki Tanaka, Dongho Kim, Kimoon Kim, Hiroshi Shinokubo, Atsuhiro Osuka

Chemistry-A European Journal Vol. 20 ( 16 ) page： 4574 - 4582 2014.4

An Antiaromatic Electrode- Active Material Enabling High Capacity and Stable Performance of Rechargeable Batteries

Ji-Young Shin, Tetsuya Yamada, Hirofumi Yoshikawa, Kunio Awaga, Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 53 ( 12 ) page： 3096 - 3101 2014.3

Near-IR Absorbing Nickel(II) Porphyrinoids Prepared by Regioselective Insertion of Silylenes into Antiaromatic Nickel(II) Norcorrole

Takaki Fukuoka, Kenya Uchida, Young Mo Sung, Ji-Young Shin, Shintaro Ishida, Jong Min Lim, Satoru Hiroto, Ko Furukawa, Dongho Kim, Takeaki Iwamoto, Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 53 ( 6 ) page： 1506 - 1509 2014.2

Selective Synthesis of a [32]Octaphyrin(1.0.1.0.1.0.1.0) Bis(palladium) Complex by a Metal-Templated Strategy

Hiromitsu Kido, Ji-Young Shin, Hiroshi Shinokubo

Angew. Chem. Int. Ed. Vol. 52 ( 51 ) page： 13727 - 13730 2013.10

Carbolithiation of meso-aryl-substituted 5,15-diazaporphyrin selectively provides 3-alkylated diazachlorins

Ayaka Yamaji, Satoru hiroto, Ji-Young Shin, hiroshi Shinokubo

Chemical Communication Vol. 49 ( 44 ) page： 5064 - 5066 2013.4

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

Tomohiro Ito, Yosuke Hayashi, Soji Shimizu, Ji-Young Shin, Nagao Kobayashi, Hiroshi Shinokubo

Angewandte Chemie International Edition Vol. 51 ( 34 ) page： 8542 - 8545 2012.8

Language：English Publishing type：Research paper (scientific journal)

A ring-contracted sister of porphyrin, norcorrole, has been synthesized efficiently as a stable molecule by a nickel-templated strategy. The norcorrole complex is stable but exhibits a distinct antiaromatic character according to the Hückel rule. Oxidation of the norcorrole complex provides an aromatic oxacorrole complex.

DOI： 10.1002/anie.201204395

Synthesis of a class of 5-((5-(pyrrol-2-yl-methylene)-pyrrol-2-yl)methylene)- furan-2-ones and the formation of a furanone dipyrrin imino ether Reviewed

Ji-Young Shin, David Dolphin

New Journal of Chemistry Vol. 35 ( 11 ) page： 2483 - 2487 2011.11

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

A class of a-furanyl dipyrrins 2 were prepared by refluxing THF solutions of DDQ adducts 1 with the appropriate alcohols in the presence of AlCl3 and further subsequent reaction of the cyano-group results in the formation of an imino ether upon MeOH addition.

DOI： 10.1039/C1NJ20415G

Structural Studies of the Self-Assemblies Created with Dipyrrins Reviewed

Ji-Young Shin, Brian O. Patrick, Seung Bae Son, Jae Ryang Hahn, David Dolphin

Bulletin of the Korean Chemical Society Vol. 31 ( 4 ) page： 1004 - 1012 2010.4

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

Three-dimensional superstructures of unique self-assemblies generated by exploring the conformational flexibility of various dipyrromethenes through creation of hydrogen-bonds with metal-halide anions are reported and the conformational diversity is thoroughly described in the solid and in solution by X-ray diffraction anal. and variable temperature NMR spectroscopy. The tetrahedral or octahedral structures of their precursors, various metal-dipyrromethene complexes, are also reported, based on the crystallographic data. STM images of the self-assemblies observed on graphite surfaces present interesting arrangements and appear as tubular bunches.

DOI： 10.5012/bkcs.2010.31.4.1004

BODIPY-hexaphyrin hybrids Reviewed

Ji-Young Shin, Takayuki Tanaka, Atsuhiro Osuka, Qing Miao, David Dolphin

Chemistry-A European Journal Vol. 15 ( 47 ) page： 12955 - 12959 2009.12

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

BODIPY-appended [28]- and [26]hexaphyrins (see figure) were prepared and the efficient intramolecular excitation energy transfer from the BODIPY part to the hexaphyrin part was revealed in both hybrids. Importantly this is the first example of the intramolecular energy transfer with a Möbius aromatic [28]hexaphyrin as an energy acceptor.

DOI： 10.1002/chem.200902407

Linear fully-conjugated meso-aryl pentaphyrin Reviewed

Ji-Young Shin, Steven S. Hepperle, David Dolphin

Tetrahedron Letters Vol. 50 ( 49 ) page： 6909 - 6912 2009.12

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

A meso-2,6-dichlorophenyl pentapyrrin was prepared using a modified method for dipyrrane synthesis followed by simple DDQ oxidation. The fully conjugated structures formed via redox inter-conversions were studied using crystallographic as well as observed and calculated spectral data.

DOI： 10.1016/j.tetlet.2009.09.145

Observation of coexistence of 1D and 2D nanostructures in cobalt dipyrromethene trimer complexes adsorved on a graphite surface Reviewed

Sung Bae Son, Su Jin Kee, Jae Ryang Hahn, Li Ma, Ji-Young Shin, David Dolphin

Applied Surface Science Vol. 259 ( 4 ) page： 1176 - 1179 2009.11

Facile synthesis of dicyanovinyl-di(meso-aryl)dipyrromethenes via a dipyrromethene-DDQ adduct Reviewed

Ji-Young Shin, Brian O. Patrick, David Dolphin

Organic and Biomolecular Chemistry Vol. 7 ( 10 ) page： 2032 - 2035 2009.5

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

The dicyano-substituted vinyl dipyrromethene 4 and com- pound 5 are near-planar and were prepared from a simple meso-aryl dipyrromethane via the DDQ adduct 3; the unique structures of 3, 4 and 5 were confirmed by X-ray diffraction analysis.

DOI： 10.1039/b904446a

Oxidized forms of triyrrane: alpha-tripyrrinone, beta-tripyrrinone and C2 symmetric hexapyrrole Reviewed

Ji-Young Shin, Steven S. Hepperle, Brian O. Patrick, David Dolphin

Chemical Communication Vol. 2009 ( 17 ) page： 2323 - 2325 2009.5

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

Alpha- and beta-tripyrrinone isomers and a C2 symmetric hexapyrrole were isolated from the oxidation of meso-perfluorophenyl tripyrrane withDDQ under aerobic conditions, and the structure of the alpha-triyrrinone was determined by X-ray crystallographic analysis.

DOI： 10.1039/b901171b

Self-assembly of oligomeric linear dipyrromethene metal complexes Reviewed

Qing Miao, Ji-Young Shin, Brian O. Patrick, David Dolphin

Chemical Communication page： 2541 - 2543 2009.5

facile synthesis of unsubstituted beta,beta'-linked diformyldipyrromethanes Reviewed

Zhan Zhang, Ji-Young Shin, David Dolphin

Journal of Organic Chemistry Vol. 73 ( 23 ) page： 9515 - 9517 2008.12

Language：English Publishing type：Research paper (scientific journal)

Unsubstituted beta,beta'-linked diformyldipyrromethanes are promising precursors for the synthesis of novel poly dipyrromethene ligands and N-confused porphyrins. A strategy has been developed to selectively synthesize unsubstituted beta,beta'-linked diformyldipyrromethanes in moderate yields starting from 2-formylpyrrole.

DOI： 10.1021/jo802114h

Metal Complexes of dipyrromethenes linked by rigid spacer arms Reviewed

Li Ma, Ji-Young Shin, Brian O. Patrick, David Dolphin

Crystal Engineering Communication Vol. 10 ( 11 ) page： 1531 - 1533 2008.11

Language：English Publishing type：Research paper (scientific journal)

Metal complexes using ligands where two terminal dipyrromethenes are connected by rigid spacers, having different dihedral angles, show unique macrocyclic structures which contain large cavities in their centers and produce crystals with tunnels of varying structures depending upon their crystal packing motifs.

DOI： 10.1039/b814586e

Self-assembly via intermolecular hydrogen-bonding between o-/m-/p-NH2 and BF2 groups on dipyrromethenes Reviewed

Ji-Young Shin, Brian O. Patrick, David Dolphin

Tetrahedron Letters Vol. 49 ( 38 ) page： 5515 - 5518 2008.9

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

Boron difluoride dipyrromethenes bearing configurationally different amine groups on a meso-phenyl ring were prepared and crystallized. The ortho- and para-amino groups allow the phenyl group to inductively release greater electron density into the dipyrromethenes resulting in relatively strong inter- molecular hydrogen-bonding with the terminal BF2 groups, whereas the meta-analog formed weaker hydrogen-bonds. The intensities of the 1H NMR peaks in concentrated solutions all increased with F-decoupling.

DOI： 10.1016/j.tetlet.2008.07.045

Conformational flexibility of dipyrromethenes: supramolecular assemblies with hydroquinones Reviewed

Ji-Young Shin, Brian O. Patrick, David Dolphin

Crystal Engineering Communication Vol. 10 ( 8 ) page： 1539 - 1541 2008.8

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

The structure of a self-assembled system containing a protonated dipyrromethene with deprotonated/reduced dichlorodicyanoquinone (DDQ) was determined by X-ray diffraction analysis. The assembly exhibits a highly hydrogen-bonded structure, with an unusual asymmetric conformation for the dipyrromethene.

DOI： 10.1039/b800367j

Structure, formation and catalytic studies of a meso palladioporphyrin intermediate in a heck coupling Reviewed

Michael M. Jang, Ji-Young Shin, Brian O. Patrick, David Dolphin

Dalton Transaction page： 2598 - 2062 2008.5

Language：English Publishing type：Research paper (scientific journal)

A meso-palladioporphyrin intermediate was isolated from a Heck reaction between an iodoporphyrin and a non-activated olefin using a Pd(PPh3)2Cl2/Et3N system; its structure was characterized by NMR, MS and X-ray crystallography. Studies on its formation indicate that the Pd(II) catalyst was reduced in situ by Et3N with the assistance of water. The catalytic activity of the intermediate was confirmed by stoichiometric and catalytic reactions using a more reactive olefin, ethyl acrylate.

DOI： 10.1039/b801163j

Facile synthesis of large meso-pentafluorophenyl-substituted expanded porphyrin Reviewed

Yashuo Tanaka, Ji-Young Shin, Atsuhiro Osuka

European Journal of Organic Chemistry page： 1341 - 1349 2008.3

Language：English Publishing type：Research paper (scientific journal)

Acid-catalyzed condensation of meso-pentafluorophenyl di- pyrromethane and pentafluorobenzaldehyde at 0 degrees gave a series of expanded porphyrins with even number of pyrrolic subunits up to octadecaphyrin(1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1) in improved yields, particularly for larger expanded porphyrins. The solid-state structure of decaphyrin(1.1.1.1.1.1.1.1.1.1) was revealed by X-ray diffraction analysis to be a crescent-like conformation. The Soret-like absorption bands are increasingly redshifted as the size of the ring increases, but such a trend becomes nearly saturated for hexadecaphyrins (1.1.1.1.1.1.1.1.1.1.1.1.1.1.1.1) which exhibit bands in the near-infrared region at 939 and 953 nm, respectively.

DOI： 10.1002/ejoc.200701132

Möbius aromaticity in N-fused [24]pentaphyrin upon Rh(I) metalation Reviewed

Jong Kang Park, Zin Seok Yoon, Min-Chul Yoon, Kil Suk Kim, Shegeki Mori, Ji-Young Shin, Atsuhiro Osuka, Dongho Kim

Journal of the American Chemical Society Vol. 130 ( 6 ) page： 1824 - 1825 2008.2

Language：English Publishing type：Research paper (scientific journal)

NFP5s are interesting platfroms to realize Huckel aromaticity, Huckel antiaromaticity, and Moebius aromaticity depending on the number of pai-electrons, meso-substituent, and metalation. Rh-[24]NFP5 has been comfirmed as a Moebius aromatic molecule by the crystal structure, 1H NMR spectrum, NICS calculation, and TPA cross-section values. This molecule is the smallest Moebius aromatic system with distinct diatropic ring current.

DOI： 10.1021/ic7004216

Group 12 metal complexes of [26]hexaphyrin(1,1,1,1,1,1) Reviewed

Shigeki Mori, Soji Shimizu, Ji-Young Shin, Atsuhiro Osuka

Inorganic Chemistry Vol. 46 ( 11 ) page： 4374 - 4376 2007.5

New Zn complexes derivatives for red OLEDs host materials Reviewed

Ae-Ran Hyun, Soo-Kang Kim, In-Nam Kang, Jong-Wook Pack, Ji-Young Shin, OK-Keun Son

Molecular Crystal and Liquid Crystal Vol. 463 page： 33 - 39 2007.2

Language：English Publishing type：Research paper (scientific journal)

New two metal complexes, di-(Phenyl dipyrrylmethene)zinc (Zn(PPM)2) and di-(Pentafluorophenyl dipyrrylmethene)zinc (Zn(PFPPM)2) as a host material instead of Alq3 were synthesized. To evaluate electroluminescent properties, multi- layered organic light-emitting devices were fabricated by using 4-(dicyanomethy- lene)-2-tert-buthyl-6-(1,1,7,7-tetramethyljulolidyl-9-enyl)-4H-pyran (DCJTB) as a dopant and Alq3 as an electron transporting layer. Alq3 and Zn(PPM)2 host EL devices exhibited DCJTB emission peak at around 617 nm due to energy transfer from Alq3 and Zn(PPM)2 to DCJTB. However Zn(PFPPM)2 host device shows no DCJTB emission peak because Zn(PFPPM)2 device emit EL light of 563 and 700 nm. The Zn(PPM)2 device showed same luminance efficiency as Alq3 device, but showed better power efficiency of 1.2 times than Alq3 device.

DOI： 10.1080/15421400601021471

N-fused Pentaphyrins and Their Rhodium Complexes: Oxidation-Induced Rhodium Rearrangement Reviewed

Shigeki Mori, Ji-Young Shin, Soji Shimizu, Fumiaki Ishikawa, Hiroyuki Furuta, Atsuhiro Osuka

Chemistry-A European Journal Vol. 11 ( 8 ) page： 2417 - 2425 2005.4

Language：English Publishing type：Research paper (scientific journal)

meso-Aryl-substituted pentaphyrins were isolated in the modified Rothemund-Lindsey porphyrin synthesis and a [22]NFP5 and [24]NFP5, which were reversibly interconvertible by means of two electron reduction with NaBH4 or two-electron oxidation with DDQ. Judging from 1H NMR data, [22]NFP5 is aromatic and possesses a diatropic ring current, while [24]NFP5 exhibits partial antiaromatic character. Metalation of [22]NFP5 with rhodium(I) salt led to isolation of rhodium complexes, whose structures were unambiguously characterized by X-ray diffraction analyses and were assigned as conjugated 24- and 22-pai electronic systems, respectively. Upon the treatment with DDQ, those are interconvertible with an unprecedented rearrangement of the rhodium atom.

DOI： 10.1002/chem.200401042

Protonated Dipyrromethenes and Tetrahalozinc Anions as Synthons in the Solid State Reviewed

Ji-Young Shin, David Dolphin, Brian, O. Patrick

Crystal Growth & Design Vol. 4 ( 4 ) page： 659 - 661 2004.6

Authorship：Lead author Language：English Publishing type：Research paper (scientific journal)

(HL)2ZnBr4 and (HL)2ZnCl4 were prepared by the addition of HBr and Hcl into a acetonitrile solution of Zn(II)L2, and their structures were determined by X-ray diffraction analysis. The X-ray crystallographic data show super structures that have hydrogen bonds between the terahalozinc anions and the protonated dipyrromethene cations.

DOI： 10.1021/cg049979g

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

Masaaki Suzuki, Soji Shimizu, Ji-Young Shin, Atsuhiro Osuka

Tetrahedron Letters Vol. 44 ( 24 ) page： 4597 - 4601 2003.6

Ring size selective synthesis of meso-aryl expanded porphyrins

Ryuichiro Taniguchi, Soji Shimizu, Masaaki Suzuki, Ji-Young Shin, Hiroyuki Furuta, Atsuhiro Osuka

Tetrahedron Letters Vol. 44 ( 12 ) page： 2505 - 2507 2003.3

Perfluorinated meso-Aryl Substituted Expaned Porphyrins Reviewed

Soji Shimizu, Ji-Young Shin, Hiroyuki Furuta, Rami Ismael, Atsuhiro Osuka

Angewandte Chemie International Edition Vol. 42 ( 1 ) page： 78 - 82 2003.1

Language：English Publishing type：Research paper (scientific journal)

DOI： 10.1002/anie.200390058

meso-Aryl Substituted Expanded Porphyrins

Ji-Young Shin, Hiroyuki Furuta, Kenji Yoza, Shinetsu Igarashi, Atsuhiro Osuka

Journal of the American Chemical Society Vol. 123 ( 29 ) page： 7190-7191 2001.7

N-Fused Pentaphyrin Reviewed

Ji-Young Shin, Hiroyuki Furuta, Atsuhiro Osuka

Angewandte Chemie International Edition Vol. 40 ( 3 ) page： 619 - 621 2001.2

Language：English Publishing type：Research paper (scientific journal)

DOI： 10.1002/1521-3773(20010202)40:3<619::AID-ANIE619>3.0.CO;2-X

Orientation Effects on Excited State Dynamics of Zinc Porphyrin-Free Base Porphyrin-Pyromellitimide Triads

Atsuhiro Osuka, Ji-Young Shin, Ryusho Yoneshima, Hideo Shiratori, Takeshi Ohno, Koichi Nozaki, Yoshinobu Nishimura, Iqao Yamazaki, Seiji Taniguchi, Takenori Shimizu, Tadashi Okada

Journal of Porphyrins and Phthalocyanines Vol. 3 ( 8 ) page： 729 - 741 1999.12

An efficient model of cytochrome P-450 monooxygenase reactivity: polymer-supported metalloprotoporphyrin IX (M=Fe, Mn)

Ji-Young Shin, Kyung-A Kim, Hye Gyun Kim, Insook Rhee Pang, Do-Gyun Kim, Ki-Jung Paeng

Bulletin of the Korean Chemical Society Vol. 19 ( 8 ) page： 875 - 878 1998.8

Simultaneous observation of Fe-F and F-Fe-F stretching vibrations of fluoride anion ligated tetraphenylporphyrin iron(III) by resonance raman spectroscopy

Insook Rhee Paeng, Ji-Young Shin, Hakhyun Nam, Do-Gyun Kim, Ki-Jung Paeng

Bulletin of the Korean Chemical Society Vol. 18 ( 7 ) page： 730 - 733 1997.7

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Papers - SHIN Jiyoung