Yutaka Takaguchi

Prof. Yutaka Takaguchi

University of Toyama, Toyama, Japan
orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2005 in Tetrahedron
Verified
Journal Article
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AAAshraful Alam
Ashraful Alam
Yutaka TakaguchiYutaka Takaguchi
Yutaka Takaguchi
HIHideyuki Ito
Hideyuki Ito
TYTakashi Yoshida
Takashi Yoshida
STSadao Tsuboi
Sadao Tsuboi

29 August 2008 in Organic & Biomolecular Chemistry
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Journal Article
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YSYuuki Sako
Yuuki Sako
Yutaka TakaguchiYutaka Takaguchi
Yutaka Takaguchi
A newly designed anthracene derivative having gluconamides at its peripheral branches formed a photo-responsive hydrogel. SEM observation of the xerogel showed a network structure consisting of fibrils. Upon photoirradiation (λ >300 nm) of the hydrogel, regioselective photodimerization of the anthracene moiety occurred to give head-to-tail photodimers and the physical state changed from the gel to the sol.

29 October 2005 in Chemistry Letters
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Journal Article
Closed access
Yutaka TakaguchiYutaka Takaguchi
Yutaka Takaguchi
MTMitsuhiro Tamura
Mitsuhiro Tamura
YSYuuki Sako
Yuuki Sako
YYYasushi Yanagimoto
Yasushi Yanagimoto
STSadao Tsuboi
Sadao Tsuboi
TATakeshi Akasaka
Takeshi Akasaka
Single-walled carbon nanotubes (SWNTs) were well dispersed in both water and organic solvent by the use of fullerodendron as a dispersant. A C60 moiety at the focal point of dendron plays a crucial role in the dispersing process, because dendron having an anthracene unit at the focal point can not disperse SWNTs in THF. The dispersions of SWNTs were characterized by UV–vis–NIR spectroscopy, Raman spectroscopy, SEM, HRTEM, and AFM.

1 July 2003 in Tetrahedron Letters
Verified
Journal Article
Closed access
Yutaka TakaguchiYutaka Takaguchi
Yutaka Takaguchi
YSYuuki Sako
Yuuki Sako
YYYasushi Yanagimoto
Yasushi Yanagimoto
STSadao Tsuboi
Sadao Tsuboi
JMJiro Motoyoshiya
Jiro Motoyoshiya
TATakeshi Akasaka
Takeshi Akasaka

17 June 2014 in Scientific Reports
Verified
Journal Article
Open access
HOHideki Okamoto
Hideki Okamoto
RERitsuko Eguchi
Ritsuko Eguchi
SHShino Hamao
Shino Hamao
HGHidenori Goto
Hidenori Goto
KGKazuma Gotoh
Kazuma Gotoh
YKYoshihiro Kubozono
Yoshihiro Kubozono
A new phenacene-type molecule, [lsqb]8[rsqb]phenacene, which is an extended zigzag chain of coplanar fused benzene rings, has been synthesised for use in an organic field-effect transistor (FET). The molecule consists of a phenacene core of eight benzene rings, which has a lengthy [pgr]-conjugated system. The structure was verified by elemental analysis, solid-state NMR, X-ray diffraction (XRD) pattern, absorption spectrum and photoelectron yield spectroscopy (PYS). This type of molecule is quite interesting, not only as pure chemistry but also for its potential electronics applications. Here we report the physical properties of [lsqb]8[rsqb]phenacene and its FET application. An [lsqb]8[rsqb]phenacene thin-film FET fabricated with an SiO2 gate dielectric showed clear p-channel characteristics. The highest [mgr] achieved in an [lsqb]8[rsqb]phenacene thin-film FET with an SiO2 gate dielectric is 1.74[emsp14]cm2 V-1 s-1, demonstrating excellent FET characteristics; the average [mgr] was evaluated as 1.2(3)[emsp14]cm2 V-1 s-1. The [mgr] value in the [lsqb]8[rsqb]phenacene electric-double-layer FET reached 16.4[emsp14]cm2 V-1 s-1, which is the highest reported in EDL FETs based on phenacene-type molecules; the average [mgr] was evaluated as 8(5)[emsp14]cm2 V-1 s-1. The [mgr] values recorded in this study show that [lsqb]8[rsqb]phenacene is a promising molecule for transistor applications.