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Yuya Tanaka

Researcher at Tokyo Institute of Technology

Publications -  65
Citations -  1643

Yuya Tanaka is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Molecular wire & Chemistry. The author has an hindex of 21, co-authored 51 publications receiving 1282 citations. Previous affiliations of Yuya Tanaka include University of Rennes & University of Hong Kong.

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Phosphorescent molecular tweezers based on alkynylplatinum(II) terpyridine system: turning on of NIR emission via heterologous Pt⋯M interactions (M = PtII, PdII, AuIII and AuI)

TL;DR: In this paper, a molecular tweezers-type complex based on a phosphorescent cationic alkynylplatinum(II) terpyridine building block has been synthesized and characterized by NMR, mass spectroscopy, elemental analysis and X-ray diffraction study.
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Multiaddressable molecular rectangles with reversible host-guest interactions: Modulation of pH-controlled guest release and capture

TL;DR: A series of alkynylplatinum(II) terpyridine molecular rectangles has been shown to exhibit reversible capture and release of anticancer therapeutic guests under different pH conditions with instant and drastic color and luminescence responses, indicating their potential in controlled therapeutics delivery on pH modulation.
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Photochromic organometallics with a dithienylethene (DTE) Bridge, [Y-C[triple bond]C-DTE-C[triple bond]C-Y] (Y={MCp*(dppe)}): photoswitchable molecular wire (M=Fe) versus dual photo- and electrochromism (M=Ru).

TL;DR: It was found that, in contrast to the reversible redox behavior of the iron complex 1(Fe), the ruthenium complex 1 (Ru)O undergoes oxidative ring closure to form the dicationic species of the closed isomer 1(Ru)C(2+) and, thus, the r Ruthenium system 1( Ru) shows dual photo- and electrochromism.
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An antiaromatic-walled nanospace

TL;DR: This cage may be considered as a type of NMR shift reagent, moving guest signals well beyond the usual NMR frequency range and opening the way to further probing the effects of an antiaromatic environment on a nanospace.
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A photoswitchable molecular wire with the dithienylethene (DTE) linker, (dppe)(η5-C5Me5)Fe–CC–DTE–CC–Fe(η5-C5Me5)(dppe)

TL;DR: In this article, a redox-active diiron complex with the diethynylated dithienylethene (DTE) linker shows photochromic behavior, which switches on and off the communication performance between the two metal centres.