Hideyuki Higashimura

3.6k total citations · 1 hit paper
60 papers, 3.0k citations indexed

About

Hideyuki Higashimura is a scholar working on Organic Chemistry, Inorganic Chemistry and Materials Chemistry. According to data from OpenAlex, Hideyuki Higashimura has authored 60 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Organic Chemistry, 21 papers in Inorganic Chemistry and 13 papers in Materials Chemistry. Recurrent topics in Hideyuki Higashimura's work include Oxidative Organic Chemistry Reactions (10 papers), Conducting polymers and applications (8 papers) and Organic Light-Emitting Diodes Research (8 papers). Hideyuki Higashimura is often cited by papers focused on Oxidative Organic Chemistry Reactions (10 papers), Conducting polymers and applications (8 papers) and Organic Light-Emitting Diodes Research (8 papers). Hideyuki Higashimura collaborates with scholars based in Japan, Germany and United States. Hideyuki Higashimura's co-authors include Shiro Kobayashi, Masaya Matsuoka, Masakazu Saito, Yu Horiuchi, Masatoshi IWATA, Takashi Toyao, Katsunori Mochizuki, Masakazu Anpo, Yoshinao Tamaru and Zen‐ichi Yoshida and has published in prestigious journals such as Journal of the American Chemical Society, Physical review. B, Condensed matter and Progress in Polymer Science.

In The Last Decade

Hideyuki Higashimura

58 papers receiving 3.0k citations

Hit Papers

Visible-Light-Promoted Photocatalytic Hydrogen Production... 2012 2026 2016 2021 2012 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hideyuki Higashimura Japan 25 1.3k 1.1k 1.1k 887 649 60 3.0k
María J. Mancheño Spain 29 1.5k 1.2× 1.3k 1.1× 1.6k 1.4× 519 0.6× 472 0.7× 80 3.4k
Yu‐He Kan China 31 2.0k 1.6× 1.1k 1.0× 1.4k 1.2× 1.1k 1.2× 784 1.2× 164 4.3k
Nasser Safari Iran 32 1.8k 1.4× 1.3k 1.1× 938 0.8× 363 0.4× 338 0.5× 192 3.3k
Ahmet Kılıç Türkiye 32 731 0.6× 569 0.5× 918 0.8× 619 0.7× 301 0.5× 108 2.5k
Wen Weng China 35 1.9k 1.5× 553 0.5× 813 0.7× 586 0.7× 1.1k 1.7× 83 4.1k
Jing‐Wei Xu China 27 867 0.7× 602 0.5× 573 0.5× 343 0.4× 437 0.7× 90 2.3k
M. Hassan Beyzavi United States 28 1.3k 1.1× 1.5k 1.3× 1.5k 1.3× 442 0.5× 188 0.3× 79 3.4k
Pradeep Mathur India 30 707 0.6× 1.6k 1.4× 2.1k 1.9× 766 0.9× 516 0.8× 211 3.7k
Gian Paolo Suranna Italy 33 1.5k 1.2× 357 0.3× 1.1k 0.9× 389 0.4× 1.8k 2.7× 116 3.4k
Andrzej Sobkowiak Poland 23 603 0.5× 521 0.5× 999 0.9× 182 0.2× 354 0.5× 62 2.0k

Countries citing papers authored by Hideyuki Higashimura

Since Specialization
Citations

This map shows the geographic impact of Hideyuki Higashimura's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hideyuki Higashimura with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hideyuki Higashimura more than expected).

Fields of papers citing papers by Hideyuki Higashimura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hideyuki Higashimura. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hideyuki Higashimura. The network helps show where Hideyuki Higashimura may publish in the future.

Co-authorship network of co-authors of Hideyuki Higashimura

This figure shows the co-authorship network connecting the top 25 collaborators of Hideyuki Higashimura. A scholar is included among the top collaborators of Hideyuki Higashimura based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hideyuki Higashimura. Hideyuki Higashimura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Raut, Vivek S., et al.. (2023). Enzyme-inspired catalysts with high activity and selectivity for oxidative polymerization of 2-phenylphenol. Catalysis Science & Technology. 13(17). 4968–4977.
3.
Toyao, Takashi, Masakazu Saito, Satoru Dohshi, et al.. (2016). Construction of Pt complex within Zr-based MOF and its application for hydrogen production under visible-light irradiation. Research on Chemical Intermediates. 42(11). 7679–7688. 35 indexed citations
4.
Quernheim, Martin, Hai‐Wei Liang, Qi Su, et al.. (2014). Cobalt Phenanthroline–Indole Macrocycles as Highly Active Electrocatalysts for Oxygen Reduction. Chemistry - A European Journal. 20(44). 14178–14183. 22 indexed citations
5.
Toyao, Takashi, Masakazu Saito, Satoru Dohshi, et al.. (2014). Development of a Ru complex-incorporated MOF photocatalyst for hydrogen production under visible-light irradiation. Chemical Communications. 50(51). 6779–6779. 144 indexed citations
6.
Kajiwara, T., Masakazu Higuchi, Akihiro Yuasa, Hideyuki Higashimura, & Susumu Kitagawa. (2013). One-dimensional alignment of strong Lewis acid sites in a porous coordination polymer. Chemical Communications. 49(89). 10459–10459. 39 indexed citations
7.
Tanaka, Daiki, Joji Ohshita, Yousuke Ooyama, et al.. (2013). Synthesis, Optical Properties, and Crystal Structures of Dithienostannoles. Organometallics. 32(15). 4136–4141. 25 indexed citations
8.
Ohshita, Joji, Daiki Tanaka, Yousuke Ooyama, et al.. (2012). Synthesis of dithienosilole-based highly photoluminescent donor–acceptor type compounds. Dalton Transactions. 42(10). 3646–3646. 15 indexed citations
9.
Ohshita, Joji, et al.. (2011). Synthesis and optical properties of a bis(diphenylphosphino)dithienosilole‐digold(I) complex. Heteroatom Chemistry. 22(3-4). 514–517. 5 indexed citations
10.
Habaue, Shigeki, et al.. (2007). Novel vanadium catalyst system with tartaric acid salts for highly selective asymmetric oxidative coupling polymerization. Polymer. 48(22). 6565–6570. 6 indexed citations
11.
Habaue, Shigeki, et al.. (2007). Asymmetric oxidative coupling polymerization of dihydroxynaphthalene derivatives with cobalt-salen complexes. Polymer Bulletin. 59(3). 303–310. 6 indexed citations
12.
Higashimura, Hideyuki, et al.. (2006). Synthesis of Poly (binaphthol)s by Highly Selective Asymmetric Oxidative Coupling Polymerization. KOBUNSHI RONBUNSHU. 63(5). 297–305. 2 indexed citations
13.
Higashimura, Hideyuki. (2005). Radical-Controlled Oxidative Polymerization of Phenols. Journal of Synthetic Organic Chemistry Japan. 63(10). 970–981. 3 indexed citations
14.
Fujisawa, Kiyoshi, Tetsuya Ono, Yoko Ishikawa, et al.. (2004). Copper(II) complexes with a novel tris(3,5-diisopropyl-1-pyrazolyl)methane ligand, [Cu(X2){HC(3,5-iPr2pz)3}] (X Cl and NO3). Inorganic Chemistry Communications. 7(3). 330–332. 20 indexed citations
15.
Kobayashi, Shiro & Hideyuki Higashimura. (2003). Oxidative polymerization of phenols revisited. Progress in Polymer Science. 28(6). 1015–1048. 258 indexed citations
16.
17.
Kobayashi, Shiro, Hiroshi Uyama, Hiroyuki Tonami, et al.. (2001). Regio- and chemo-selective polymerization of phenols catalyzed by oxidoreductase enzyme and its model complexes. Macromolecular Symposia. 175(1). 1–10. 14 indexed citations
18.
Higashimura, Hideyuki, Kiyoshi Fujisawa, Yoshihiko Moro‐oka, et al.. (2000). New crystalline polymers: poly(2,5-dialkyl-1,4-phenylene oxide)s. Macromolecular Rapid Communications. 21(16). 1121–1124. 24 indexed citations
19.
Iida, Takuya, Yukio Hasegawa, Hideyuki Higashimura, & M. Aihara. (1993). Density bistability in an interacting electron-hole system in coherently excited semiconductors. Physical review. B, Condensed matter. 47(15). 9328–9337. 16 indexed citations
20.
Tabushi, Iwao, Y. KURODA, Masahiko Yamada, Hideyuki Higashimura, & Ronald Breslow. (1985). ChemInform Abstract: A‐(MODIFIED B6)‐B‐(Ω‐AMINO(ETHYLAMINO))‐β‐CYCLODEXTRIN AS AN ARTIFICIAL B6 ENZYME FOR CHIRAL AMINOTRANSFER REACTION. Chemischer Informationsdienst. 16(52). 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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