Minoru Yamaji

Research Field

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Citations (478)

Hydrogen atom abstraction and electron transfer of triplet 2,3-dihalo-1,4-naphthoquinones studied by the cidep technique and laser flash photolysis

Research on Chemical Intermediates (1998)

Iwao Amada Minoru Yamaji Masami Sase Haruo Shizuka Takuji Shimokage

Flash photolysis

Hydrogen atom abstraction

Semiquinone

Hydrogen atom

10.1163/156856798x00212

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Citations (10)

IDENTIFICATION AND SEPARATION OF THE TWO OVERLAPPING SINGLET 1(π, π^*) ABSORPTION BANDS OF 1, 4-TETRACENEQUINONE

Spectroscopy Letters (2001)

Takaò Itoh Minoru Yamaji Haruo Shizuka

Absorption and fluorescence spectra of 1, 4-tetracenequinone (1, 4-TQ) have been measured in solution and the two overlapping 1(π, π*) absorption bands with comparable intensities were separated. Based on the spectroscopic data, the energy levels of the low-lying 1(π, π*) excited states of 6, 15-hexacenequinone were discussed in relation to those of 1, 4-TQ.

10.1081/sl-100002285

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Citations (3)

Spectral Properties and Charge-transfer Complexes of the Cyclophanes Having the Pyrene Moiety

Chemistry Letters (2007)

Akihiko Tsuge Yukihiro Ikeura Tetsuji Moriguchi Minoru Yamaji

Abstract Novel cyclophanes having the pyrene moiety have been synthesized. The fluorescence and phosphorescence properties have been examined in terms of their structure. It has been found out that their charge-transfer complexes reflect the transannular π–π interaction based on the structure.

Moiety

Cyclophane

Spectral Properties

10.1246/cl.2007.1016

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Citations (6)

Fabrication and characterization of thin-film field-effect transistors with alkyl-phenyl[n]phenacenes (n = 4–6)

Journal of Materials Chemistry C (2022)

Yanting Zhang Ritsuko Eguchi Hideki Okamoto Kenta Goto Fumito Tani

3-Decyl-10-phenyl[5]phenacene (PhC10-PIC) molecule shows good FET characteristics in case of using ZrO 2 gate dielectric, owing to strong fastener effect and large π-overlap.

Characterization

10.1039/d2tc03383f

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Electronic and Steric Effects of Cyclic Amino Substituents of Luciferin Analogues on a Firefly Luciferin–Luciferase Reaction

Chemistry Letters (2017)

Michio Kakiuchi Soichiro Ito Masahiro Kiyama Fumiya Goto Takuto Matsuhashi

Bioluminescent and spectroscopic properties of luciferin analogues with cyclic amino substituents (1-pyrrolidinyl, piperidino, 1-azepanyl, and morpholino groups) at the 6′ position were investigated by comparing with those of 6′-dimethylaminoluciferin, to provide information on spatial and molecular environmental properties of the active site in Photinus pyralis luciferase.

Luciferin

10.1246/cl.170361

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Citations (13)

CCDC 294909: Experimental Crystal Structure Determination

The Cambridge Structural Database (2006)

Hajime Maeda K. Nishimura Kosuke Mizuno Minoru Yamaji Juro Oshima

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

10.5517/cc9ww67

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CCDC 1539207: Experimental Crystal Structure Determination

The Cambridge Structural Database (2018)

Minoru Yamaji Hideki Okamoto Kenta Goto Shin‐ichiro Kato Fumito Tani

10.5517/ccdc.csd.cc1nnnvt

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CCDC 1881151: Experimental Crystal Structure Determination

The Cambridge Structural Database (2019)

Minoru Yamaji Kazuhiro Tomonari Keisuke Ikuma Kenta Goto Fumito Tani