Performance information

• Synthesis of a dilithiobutadiene bearing extremely bulky silyl substituents and its reactivity toward functionalized silanes　　　　　　　　　　　　　　　
  Katharina Münster; Shunsuke Kudo; Takuya Kuwabara; Eriko Shimamura; Shunsuke Furukawa; Yusuke Yoshida; Shintaro Ishida; Takeaki Iwamoto; Kazuki Tanifuji; Yasuhiro Ohki; Mao Minoura; Masaichi Saito
  Dalton Transactions, Feb. 2025, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1039/D4DT03537B
  DOI ID：10.1039/D4DT03537B, ORCID：177719608
• Charge Transport through Single-Molecule Junctions with σ-Delocalized Systems
  Shintaro Fujii; Saya Seko; Taichi Tanaka; Yuki Yoshihara; Shunsuke Furukawa; Tomoaki Nishino; Masaichi Saito
  Journal of the American Chemical Society, Volume：146, Number：28, Jul. 2024, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1021/jacs.4c06732
  DOI ID：10.1021/jacs.4c06732, ISSN：1520-5126, ORCID：162867015, SCOPUS ID：85199125072
• Synthesis of O- and N-substituted pentaiodobenzenes bearing σ-symmetric delocalized orbitals using site-selective nucleophilic aromatic substitution reactions
  Takada, Y.; Minoura, M.; Furukawa, S.; Saito, M.
  Chemistry Letters, Volume：53, Number：2, Feb. 2024, [Reviewed], [Corresponding]
  Scientific journal
  DOI：https://doi.org/10.1093/chemle/upad040
  DOI ID：10.1093/chemle/upad040, ISSN：1348-0715, ORCID：165904606, SCOPUS ID：85185764073
• Synthesis of a highly iodinated biphenyl with extension of σ-delocalization
  Takada, Y.; Furukawa, S.; Saito, M.
  Chemistry Letters, Volume：53, Number：3, Feb. 2024, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1093/chemle/upae032
  DOI ID：10.1093/chemle/upae032, ISSN：1348-0715, ORCID：165904604, SCOPUS ID：85187641544
• Creation of (σ+π)-Mixed Delocalization
  Saito, M.; Suzuki, T.; Takahashi, K.; Seko, S.; Furukawa, S.; Fujii, S.
  Chemistry Letters, Volume：52, Number：9, Sep. 2023, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1246/cl.230279
  DOI ID：10.1246/cl.230279, ISSN：1348-0715, ORCID：165904633, SCOPUS ID：85175713898
• σ-Delocalization between Non-bonded Selenium Atoms on Multiply Se-substituted Benzenes
  Saito, M.; Suzuki, T.; Takahashi, K.; Seko, S.; Furukawa, S.; Ishimura, K.
  Chemistry Letters, Volume：52, Number：2, First page：97, Last page：99, Feb. 2023, [Reviewed]
  The Chemical Society of Japan, English, Scientific journal
  DOI：https://doi.org/10.1246/cl.220489
  DOI ID：10.1246/cl.220489, ISSN：1348-0715, ORCID：165904609, SCOPUS ID：85151278172
• Frontispiz: Aktivierung eines biomimetischen [FeFe]‐Hydrogenase‐Komplexes für die H2‐Produktion mit sichtbarem Licht　　　　　　　　　　　　　　　
  Philipp Buday; Chizuru Kasahara; Elisabeth Hofmeister; Daniel Kowalczyk; Micheal K. Farh; Saskia Riediger; Martin Schulz; Maria Wächtler; Shunsuke Furukawa; Masaichi Saito; Dirk Ziegenbalg; Stefanie Gräfe; Peter Bäuerle; Stephan Kupfer; Benjamin Dietzek‐Ivanšić; Wolfgang Weigand
  Angewandte Chemie, May 2022, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1002/ange.202282061
  DOI ID：10.1002/ange.202282061, ORCID：112373522
• Aktivierung eines biomimetischen [FeFe]‐Hydrogenase‐Komplexes für die H2‐Produktion mit sichtbarem Licht**　　　　　　　　　　　　　　　
  Philipp Buday; Chizuru Kasahara; Elisabeth Hofmeister; Daniel Kowalczyk; Micheal K. Farh; Saskia Riediger; Martin Schulz; Maria Wächtler; Shunsuke Furukawa; Masaichi Saito; Dirk Ziegenbalg; Stefanie Gräfe; Peter Bäuerle; Stephan Kupfer; Benjamin Dietzek‐Ivanšić; Wolfgang Weigand
  Angewandte Chemie, May 2022
  Scientific journal
  DOI：https://doi.org/10.1002/ange.202202079
  DOI ID：10.1002/ange.202202079, ORCID：110558821
• Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light**
  Buday, P.; Kasahara, C.; Hofmeister, E.; Kowalczyk, D.; Farh, M.K.; Riediger, S.; Schulz, M.; W{\"a}chtler, M.; Furukawa, S.; Saito, M.; Ziegenbalg, D.; Gr{\"a}fe, S.; B{\"a}uerle, P.; Kupfer, S.; Dietzek-Ivan?i?, B.; Weig; , W.
  Angewandte Chemie - International Edition, Volume：61, Number：20, 2022, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1002/anie.202202079
  DOI ID：10.1002/anie.202202079, ISSN：1521-3773, ORCID：165904620, SCOPUS ID：85126843459
• Ferroelectric columnar assemblies from the bowl-to-bowl inversion of aromatic cores
  Shunsuke Furukawa; Jianyun Wu; Masaya Koyama; Keisuke Hayashi; Norihisa Hoshino; Takashi Takeda; Yasutaka Suzuki; Jun Kawamata; Masaichi Saito; Tomoyuki Akutagawa
  Nature Communications, Volume：12, Number：1, Dec. 2021, [Reviewed], [Lead, Corresponding]
  Organic ferroelectrics, in which the constituent molecules retain remanent polarization, represent an important topic in condensed-matter science, and their attractive properties, which include lightness, flexibility, and non-toxicity, are of potential use in state-of-the-art ferroelectric devices. However, the mechanisms for the generation of ferroelectricity in such organic compounds remain limited to a few representative concepts, which has hitherto severely hampered progress in this area. Here, we demonstrate that a bowl-to-bowl inversion of a relatively small organic molecule with a bowl-shaped π-aromatic core generates ferroelectric dipole relaxation. The present results thus reveal an unprecedented concept to produce ferroelectricity in small organic molecules, which can be expected to strongly impact materials science.
  Springer Science and Business Media LLC, Scientific journal
  DOI：https://doi.org/10.1038/s41467-021-21019-4
  DOI ID：10.1038/s41467-021-21019-4, eISSN：2041-1723, ORCID：88040012
• Transition-Metal Capping to Suppress Back-Donation to Enhance Donor Ability
  Saito, M.; Hamada, J.; Furukawa, S.; Hada, M.; Dost{\'a}l, L.; R??i?ka, A.
  Organometallics, Volume：39, Number：23, Dec. 2020, [Reviewed]
  American Chemical Society ({ACS}), Scientific journal
  DOI：https://doi.org/10.1021/acs.organomet.0c00534
  DOI ID：10.1021/acs.organomet.0c00534, ISSN：1520-6041, ORCID：165904613, SCOPUS ID：85094603012
• Hybrid Molecular Junctions Using Au–S and Au−π Bindings　　　　　　　　　　　　　　　
  Shintaro Fujii; Madoka Iwane; Shunsuke Furukawa; Tomofumi Tada; Tomoaki Nishino; Masaichi Saito; Manabu Kiguchi
  The Journal of Physical Chemistry C, Volume：124, Number：17, First page：9261, Last page：9268, Apr. 2020, [Reviewed]
  American Chemical Society ({ACS}), Scientific journal
  DOI：https://doi.org/10.1021/acs.jpcc.9b11725
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85085063009&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85085063009&origin=inward
  DOI ID：10.1021/acs.jpcc.9b11725, ISSN：1932-7447, eISSN：1932-7455, ORCID：72294607, SCOPUS ID：85085063009
• Stereoselective thermal isomerization of triphosphasumanenes, utilized for stereocontrolled synthesis　　　　　　　　　　　　　　　
  Yuki Suda; Shunsuke Furukawa; Masaichi Saito
  Chemistry Letters, Volume：49, Number：4, First page：419, Last page：422, Apr. 2020, [Reviewed], [Corresponding]
  Chemical Society of Japan, English, Scientific journal
  DOI：https://doi.org/10.1246/cl.200032
  DOI ID：10.1246/cl.200032, ISSN：1348-0715, SCOPUS ID：85083728766
• Synthesis and properties of perfluoroalkylated TIPS-pentacenes
  Agou, T.; Suzuki, S.; Kanno, Y.; Hosoya, T.; Fukumoto, H.; Mizuhata, Y.; Tokitoh, N.; Suda, Y.; Furukawa, S.; Saito, M.; Kubota, T.
  Tetrahedron, Volume：75, Number：47, First page：130678, Last page：130678, Nov. 2019, [Reviewed]
  Elsevier {BV}, Scientific journal
  DOI：https://doi.org/10.1016/j.tet.2019.130678
  DOI ID：10.1016/j.tet.2019.130678, ISSN：1464-5416, ORCID：165904615, SCOPUS ID：85073541463
• Inverted Sandwich Rh Complex Bearing a Plumbole Ligand and Its Catalytic Activity　　　　　　　　　　　　　　　
  Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Ryota Owada; Shunsuke Furukawa; Radhika Narayanan; Minori Abe; Masahiko Hada; Ken Tanaka; Yoshihiko Yamamoto
  Organometallics, Volume：38, Number：16, First page：3099, Last page：3103, Aug. 2019, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1021/acs.organomet.9b00339
  DOI ID：10.1021/acs.organomet.9b00339, ISSN：0276-7333, eISSN：1520-6041, ORCID：59307625, Web of Science ID：WOS:000483435900001
• Anionic stannaferrocene and its unique electronic state
  Saito, M.; Matsunaga, N.; Hamada, J.; Furukawa, S.; Tada, T.; Herber, R.H.
  Chemistry Letters, Volume：48, Number：2, First page：163, Last page：165, Jan. 2019, [Reviewed], ［International magazine］
  English, Scientific journal
  DOI：https://doi.org/10.1246/cl.180880
  DOI ID：10.1246/cl.180880, ISSN：1348-0715, ORCID：165904608, SCOPUS ID：85060582064
• Double aromaticity arising from σ- and π-rings
  Shunsuke Furukawa; Masahiro Fujita; Yoshihiko Kanatomi; Mao Minoura; Miho Hatanaka; Keiji Morokuma; Kazuya Ishimura; Masaichi Saito
  Communications Chemistry, Volume：1, Number：1, Sep. 2018, [Reviewed], [Lead]
  Springer Science and Business Media LLC, Scientific journal
  DOI：https://doi.org/10.1038/s42004-018-0057-4
  DOI ID：10.1038/s42004-018-0057-4, ISSN：2399-3669, eISSN：2399-3669, ORCID：88480870
• Heterobimetallic triple-decker complexes derived from a dianionic aromatic stannole ligand　　　　　　　　　　　　　　　
  Masaichi Saito; Naoki Matsunaga; Jumpei Hamada; Shunsuke Furukawa; Mao Minoura; Susann Wegner; Juri Barthel; Christoph Janiak
  Dalton Transactions, Volume：47, Number：27, First page：8892, Last page：8896, May 2018, [Reviewed]
  Royal Society of Chemistry ({RSC}), Scientific journal
  DOI：https://doi.org/10.1039/C8DT01455H
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049339612&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85049339612&origin=inward
  DOI ID：10.1039/C8DT01455H, ISSN：1477-9226, eISSN：1477-9234, ORCID：44839236, PubMed ID：29774331, SCOPUS ID：85049339612
• Disodium Benzodipyrrole Sulfonate as Neutral Hole-Transporting Materials for Perovskite Solar Cells　　　　　　　　　　　　　　　
  Rui Shang; Zhongmin Zhou; Hiroki Nishioka; Henry Halim; Shunsuke Furukawa; Izuru Takei; Naoya Ninomiya; Eiichi Nakamura
  Journal of the American Chemical Society, Volume：140, Number：15, First page：5018, Last page：5022, Apr. 2018, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1021/jacs.8b01783
  DOI ID：10.1021/jacs.8b01783, ISSN：0002-7863, eISSN：1520-5126, ORCID：43357982, Web of Science ID：WOS:000430642000015
• Synthesis and properties of spiro-type heterasumanenes containing group 14 elements as bridging atoms†
  Furukawa, S.; Hayashi, K.; Yamagishi, K.; Saito, M.
  Materials Chemistry Frontiers, Volume：2, Number：5, Feb. 2018, [Reviewed], [Lead, Corresponding]
  Royal Society of Chemistry ({RSC}), Scientific journal
  DOI：https://doi.org/10.1039/C7QM00590C
  DOI ID：10.1039/C7QM00590C, ISSN：2052-1537, ORCID：165904625, SCOPUS ID：85054124124
• Anisotropic Crystals Based on a Main-Group Coordination Polymer with Alignment of Rigid π Skeletons　　　　　　　　　　　　　　　
  Masaichi Saito; Tomoki Akiba; Shunsuke Furukawa; Mao Minoura; Masahiko Hada; Hiroshi Y. Yoshikawa
  Organometallics, Volume：36, Number：14, First page：2487, Last page：2490, Jul. 2017, [Reviewed]
  American Chemical Society ({ACS}), Scientific journal
  DOI：https://doi.org/10.1021/acs.organomet.7b00217
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85025679539&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85025679539&origin=inward
  DOI ID：10.1021/acs.organomet.7b00217, ISSN：0276-7333, eISSN：1520-6041, ORCID：34611345, SCOPUS ID：85025679539
• Formation of dibenzopentalene-linking polymers under the two-zone CVD and wet conditions
  Saito, M.; Suda, Y.; Furukawa, S.; Nakae, T.; Kojima, T.; Sakaguchi, H.
  Chemistry Letters, Volume：46, Number：8, May 2017, [Reviewed]
  The Chemical Society of Japan, Scientific journal
  DOI：https://doi.org/10.1246/cl.170396
  DOI ID：10.1246/cl.170396, ISSN：1348-0715, ORCID：165904617, SCOPUS ID：85026625804
• Triphosphasumanene Trisulfide: High Out-of-Plane Anisotropy and Janus-Type π-Surfaces　　　　　　　　　　　　　　　
  Shunsuke Furukawa; Yuki Suda; Junji Kobayashi; Takayuki Kawashima; Tomofumi Tada; Shintaro Fujii; Manabu Kiguchi; Masaichi Saito
  Journal of the American Chemical Society, Volume：139, Number：16, First page：5787, Last page：5792, Apr. 2017, [Reviewed], [Lead, Corresponding]
  American Chemical Society ({ACS}), Scientific journal
  DOI：https://doi.org/10.1021/jacs.6b12119
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018319574&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85018319574&origin=inward
  DOI ID：10.1021/jacs.6b12119, ISSN：0002-7863, eISSN：1520-5126, ORCID：33184063, PubMed ID：28387119, SCOPUS ID：85018319574
• Cover Picture: Efficient Synthesis of 1,4-Bis-heteroatom-substituted Tetraselanylbenzenes via 1,4-Dilithiation of Hexaselanylbenzene and Investigation on Their Electronic Properties (Chem. Asian J. 9/2017)　　　　　　　　　　　　　　　
  Masahiro Fujita; Shunsuke Furukawa; Masaichi Saito
  Chemistry - An Asian Journal, Volume：12, Number：9, First page：947, Last page：947, Apr. 2017, [Reviewed]
  Wiley-Blackwell, Scientific journal
  DOI：https://doi.org/10.1002/asia.201700309
  DOI ID：10.1002/asia.201700309, ORCID：33184139
• Efficient Synthesis of 1,4-Bis-heteroatom-substituted Tetraselanylbenzenes via 1,4-Dilithiation of Hexaselanylbenzene and Investigation on Their Electronic Properties
  Fujita, M.; Furukawa, S.; Saito, M.
  Chemistry - An Asian Journal, Volume：12, Number：9, First page：954, Last page：957, Mar. 2017, [Reviewed]
  Wiley-Blackwell, Scientific journal
  DOI：https://doi.org/10.1002/asia.201700164
  DOI ID：10.1002/asia.201700164, ISSN：1861-471X, ORCID：165904605, SCOPUS ID：85015308443
• Synthesis and reactivity of a ruthenocene-type complex bearing an aromatic π-ligand with the heaviest group 14 element　　　　　　　　　　　　　　　
  Marisa Nakada; Takuya Kuwabara; Shunsuke Furukawa; Masahiko Hada; Mao Minoura; Masaichi Saito
  Chem. Sci., Volume：8, Number：4, First page：3092, Last page：3097, Feb. 2017, [Reviewed]
  Royal Society of Chemistry ({RSC}), Scientific journal
  DOI：https://doi.org/10.1039/c6sc04843a
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85016458912&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85016458912&origin=inward
  DOI ID：10.1039/c6sc04843a, ISSN：2041-6520, eISSN：2041-6539, ORCID：33184138, SCOPUS ID：85016458912
• Benzodipyrrole-based Donor–Acceptor-type Boron Complexes as Tunable Near-infrared-Absorbing Materials　　　　　　　　　　　　　　　
  Nakamura, T.; Furukawa, S.; Nakamura, E.
  Chemistry - An Asian Journal, Volume：11, Number：14, Jul. 2016, [Reviewed], [Corresponding]
  Scientific journal
  DOI：https://doi.org/10.1002/asia.201600673
  DOI ID：10.1002/asia.201600673, ISSN：1861-471X, ORCID：165904616, PubMed ID：27311060, SCOPUS ID：84978032326
• The Chemistry of Heterasumanenes　　　　　　　　　　　　　　　
  Saito, Masaichi; Furukawa, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
  Chemical Record, Volume：16, Number：1, First page：64, Last page：72, Oct. 2015, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1002/tcr.201500211
  DOI ID：10.1002/tcr.201500211, ISSN：1527-8999, eISSN：1528-0691, ORCID：28346160, Web of Science ID：WOS:000371261600006
• Hexaaryl-benzodipyrroles: Properties and application as amorphous carrier-transporting materials　　　　　　　　　　　　　　　
  Tsuji, H.; Yokoi, Y.; Furukawa, S.; Nakamura, E.
  Heterocycles, Volume：90, Number：1, 2015, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.3987/COM-14-S(K)16
  DOI ID：10.3987/COM-14-S(K)16, ISSN：1881-0942, ORCID：165904621, SCOPUS ID：84923306345, Web of Science ID：WOS:000349505800025
• Synthesis of pi-Extended Dibenzophospholes by Intramolecular Radical Cyclization and Their Properties　　　　　　　　　　　　　　　
  Furukawa, Shunsuke; Haga, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
  Organic Letters, Volume：16, Number：12, First page：3228, Last page：3231, 2014, [Reviewed], [Lead]
  Scientific journal
  DOI：https://doi.org/10.1021/ol501189u
  DOI ID：10.1021/ol501189u, ISSN：1523-7060, eISSN：1523-7052, ORCID：28346164, Web of Science ID：WOS:000337869800015
• Synthesis of Triphosphatruxene via Sextuple Aromatic Nucleophilic Substitution and Simple Isolation of Stereoisomers　　　　　　　　　　　　　　　
  Kojima, Tatsuo; Furukawa, Shunsuke; Tsuji, Hayato; Nakamura, Eiichi
  Chemistry Letters, Volume：43, Number：5, First page：676, Last page：677, 2014, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1246/cl.131195
  DOI ID：10.1246/cl.131195, ISSN：0366-7022, CiNii Articles ID：130004868120, ORCID：28346165, Web of Science ID：WOS:000335619600036
• Near-infrared absorbing heterocyclic quinoid donors for organic solar cell devices　　　　　　　　　　　　　　　
  Ay, E.; Furukawa, S.; Nakamura, E.
  Organic Chemistry Frontiers, Volume：1, Number：8, 2014, [Reviewed], [Corresponding]
  Scientific journal
  DOI：https://doi.org/10.1039/c4qo00182f
  DOI ID：10.1039/c4qo00182f, ISSN：2052-4129, ORCID：165904632, SCOPUS ID：84939554026, Web of Science ID：WOS:000364429800016
• Formation of a polycrystalline film of donor material on PEDOT:PSS buffer induced by crystal nucleation　　　　　　　　　　　　　　　
  Harano, K.; Okada, S.; Furukawa, S.; Tanaka, H.; Nakamura, E.
  Journal of Polymer Science, Part B: Polymer Physics, Volume：52, Number：12, 2014, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1002/polb.23493
  DOI ID：10.1002/polb.23493, ISSN：1099-0488, ORCID：165904601, SCOPUS ID：84900481023, Web of Science ID：WOS:000335977500005
• Tripyridyltruxenes: Thermally stable cathode buffer materials for organic thin-film Solar Cells　　　　　　　　　　　　　　　
  Tsuji, H.; Ota, Y.; Furukawa, S.; Mitsui, C.; Sato, Y.; Nakamura, E.
  Asian Journal of Organic Chemistry, Volume：1, Number：1, 2012, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1002/ajoc.201200021
  DOI ID：10.1002/ajoc.201200021, ISSN：2193-5807, ORCID：165904602, SCOPUS ID：84896544221, Web of Science ID：WOS:000325943800005
• The first observation of electroluminescence from di(2-naphthyl)disilene, an Si=Si double bond-containing pi-conjugated compound　　　　　　　　　　　　　　　
  Tamao, Kohei; Kobayashi, Megumi; Matsuo, Tsukasa; Furukawa, Shunsuke; Tsuji, Hayato
  Chemical Communications, Volume：48, Number：7, First page：1030, Last page：1032, 2012, [Reviewed]
  Scientific journal
  DOI：https://doi.org/10.1039/c1cc16067b
  Scopus：https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84855376343&origin=inward
  Scopus Citedby：https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84855376343&origin=inward
  DOI ID：10.1039/c1cc16067b, ISSN：1359-7345, eISSN：1364-548X, ORCID：28346166, SCOPUS ID：84855376343, Web of Science ID：WOS:000299649900027
• Design, Synthesis, and Characterization of Functionalized Silepins: High Quantum Yield Blue Emitters　　　　　　　　　　　　　　　
  Mercier, Lauren G.; Furukawa, Shunsuke; Piers, Warren E.; Wakamiya, Atsushi; Yamaguchi, Shigehiro; Parvez, Masood; Harrington, Ross W.; Clegg, William
  Organometallics, Volume：30, Number：6, First page：1719, Last page：1729, 2011, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1021/om2000597
  DOI ID：10.1021/om2000597, ISSN：0276-7333, eISSN：1520-6041, ORCID：28346168, Web of Science ID：WOS:000288470900055
• Application of the sila-Friedel-Crafts reaction to the synthesis of pi-extended silole derivatives and their properties　　　　　　　　　　　　　　　
  Furukawa, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
  Dalton Transactions, Volume：39, Number：39, First page：9329, Last page：9329, 2010, [Reviewed], [Lead]
  Scientific journal
  DOI：https://doi.org/10.1039/c0dt00136h
  DOI ID：10.1039/c0dt00136h, ISSN：1477-9226, eISSN：1477-9234, ORCID：28346169, Web of Science ID：WOS:000282220500024
• Development of a Sila-Friedel-Crafts Reaction and Its Application to the Synthesis of Dibenzosilole Derivatives　　　　　　　　　　　　　　　
  Furukawa, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki
  Journal of the American Chemical Society, Volume：131, Number：40, First page：14192, Last page：+, 2009, [Reviewed], [Lead]
  English, Scientific journal
  DOI：https://doi.org/10.1021/ja906566r
  DOI ID：10.1021/ja906566r, ISSN：0002-7863, ORCID：28346170, Web of Science ID：WOS:000271271500033
• Formation of a stable sulfenic acid by hydrolysis of a thionitrate and a sulfenyl bromide　　　　　　　　　　　　　　　
  Goto, Kei; Shimada, Keiichi; Furukawa, Shunsuke; Miyasaka, Shinji; Takahashi, Yusuke; Kawashima, Takayuki
  Chemistry Letters, Volume：35, Number：8, First page：862, Last page：863, 2006, [Reviewed]
  English, Scientific journal
  DOI：https://doi.org/10.1246/cl.2006.862
  DOI ID：10.1246/cl.2006.862, ISSN：0366-7022, CiNii Articles ID：10018187382, CiNii Books ID：AA00603318, ORCID：28346171, Web of Science ID：WOS:000240713700018

• THE SOCIETY OF SYNTHETIC ORGANIC CHEMISTRY, JAPAN

• 電荷輸送性を有するσ非局在系分子の開発と電子状態の解明　　　　　　　　　　　　　　　
  01 Apr. 2024 - 31 Mar. 2027
  Grant amount(Total)：4680000, Direct funding：3600000, Indirect funding：1080000
  Grant number：24K08378
• Comprehensive structure determination of carbon nanotubes　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research (B), 01 Apr. 2021 - 31 Mar. 2024
  Grant amount(Total)：16510000, Direct funding：12700000, Indirect funding：3810000
  Grant number：21H01758
• σ非局在系開殻分子を鍵とする多次元分子ネットワークの構築　　　　　　　　　　　　　　　
  01 Apr. 2020 - 31 Mar. 2023
  Grant amount(Total)：4290000, Direct funding：3300000, Indirect funding：990000
  Grant number：20K05459
• Creation of Carrier Transporting Molecules utilizing Interactions between sigma-Symmetric Orbitals　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Challenging Research (Exploratory), 29 Jun. 2018 - 31 Mar. 2020
  FURUKAWA Shunsuke, Saitama University
  Grant amount(Total)：6370000, Direct funding：4900000, Indirect funding：1470000
  The purpose of this study is to construct the theory of charge transporting organic molecules utilizing the interaction between σ-symmetric orbitals.
  In this study, new molecular systems of "orthogonal σ-conjugated molecule" and "σ-π mixed conjugated molecule" were synthesized, and the charge transporting ability was evaluated.
  The synthesis of the orthogonal σ-conjugated molecules were very difficult, and the target compounds could not be obtained. Some of the σ-π mixed conjugated molecules could be synthesized by optimizing the reaction conditions, and that these molecular orbitals formed a network structure showing three-dimensional interaction.
  Grant number：18K19067
• Creation of Main Group Compounds Behaving Like Transition-metal Compounds and Their Reactivity　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Challenging Research (Exploratory), Jun. 2017 - Mar. 2019
  Saito Masaichi; Furukawa Shunsuke, Saitama University
  Grant amount(Total)：6500000, Direct funding：5000000, Indirect funding：1500000
  We have focused on the reactivity of a zero-valent main group compounds stabilized by a butadiene as a 4pi electron donor that we have already synthesized and is still the only one example of a zero-valent main group compounds stabilized by a butadiene ligand. We have found a unique ligand exchange reaction in the zero-valent tin compound, which is normally observed in the zero-valent transition-metal compounds. The stability of the zero-valent tin compounds is highly dependent on substituents on the carbon atoms. We have also succeeded in the synthesis of the first example of a zero-valent lead compound stabilized by a butadiene ligand.
  Grant number：17K19113
• Main Group pi-Figuration　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area), Jul. 2014 - Mar. 2019
  Saito Masaichi; Furukawa Shunsuke, Saitama University
  Grant amount(Total)：38090000, Direct funding：29300000, Indirect funding：8790000
  We have accomplished the creation of pi-systems that cannot be accessed by the use of only carbon atoms but can be synthesized by taking advantage of heavy main group atoms, which adopt a wide variety of structures and exhibit a wide variety of reactivities. We have succeeded in the creation of a out-of-plane anisotropic pi-conjugated compound by the introduction of phosphorus functionalities. We have demonstrated a bowl-to-bowl inversion of a pi-conjugated compound bearing long C-main group atom bonds as a new strategy for the creation of organoferroelectric compounds. We have succeeded in the synthesis of a coordination polymer by the use of a vacant orbital of a divalent tin compound and a wide variety of transition-metal complexes that bear unique electronic structures derived from an aromatic dianionic tin compound.
  Grant number：26102006
• Creation of pi-Conjugated System Possessing a Long Exciton Diffusion Length toward Efficient Organic Solar Cells　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Challenging Exploratory Research, 01 Apr. 2016 - 31 Mar. 2018
  FURUKAWA Shunsuke; SAEKI Akinori, Saitama University
  Grant amount(Total)：3770000, Direct funding：2900000, Indirect funding：870000
  During this research, we found two unexpected results. First, we have succeeded in synthesizing new organolead compounds known as plumbylenoid. We revealed the structures and properties of the obtained the species. Second, we have created a new pi-conjugated molecules having front/back two-faced character. We elucidated its electronic character, and demonstrated the surface treatment of metal surfaces by using the obtained compound.
  Grant number：16K13945
• 光感応性大環状へテラスマネンの創製と高効率光電荷移動システムの開発　　　　　　　　　　　　　　　
  01 Apr. 2015 - 31 Mar. 2017
  Grant amount(Total)：6240000, Direct funding：4800000, Indirect funding：1440000
  Grant number：15H00918
• Development of Near-Infrared Absorbing Materials for Effcient Organic Solar Cells　　　　　　　　　　　　　　　
  Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research, Grant-in-Aid for Young Scientists (B), 01 Apr. 2014 - 31 Mar. 2016
  FURUKAWA Shunsuke, Saitama University
  Grant amount(Total)：3640000, Direct funding：2800000, Indirect funding：840000
  The purpose of this research is to develop new class of near-infrared absorbing materials, which are beneficial for efficient organic solar cells. In this study, new quinoid-type materials have been synthesized, and were found to be efficient near-infrared absorbing materials (absorption wavelength: ~890 nm). By applying these materials to donor layers of organic solar cells, a photocurrent conversion at near-infrared region has been achieved.
  As a new class of the longer wavelength absorbing materials, donor-acceptor type boron complexes has been designed and synthesized. These boron complexes showed longer wavelength absorptions up to 1050 nm, which are essential for absorbing the sunlight.
  Grant number：26870144
• 典​型​元​素​を​活​用​し​た​ヘ​テ​ロ​ー​π​共​役​化​合​物​群​の​創​製　　　　　　　　　　　　　　　
  Competitive research funding
• 有機機能性材料、有​機​​デバイス​の​研​究　　　　　　　　　　　　　　　
  Competitive research funding