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Suguru Ito

Researcher at Yokohama National University

Publications -  58
Citations -  778

Suguru Ito is an academic researcher from Yokohama National University. The author has contributed to research in topics: Catalysis & Mechanochromic luminescence. The author has an hindex of 14, co-authored 49 publications receiving 473 citations. Previous affiliations of Suguru Ito include Tokyo Institute of Technology.

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Concentration-dependent circularly polarized luminescence (CPL) of chiral N,N′-dipyrenyldiamines: sign-inverted CPL switching between monomer and excimer regions under retention of the monomer emission for photoluminescence

TL;DR: The reversal of the intensity ratio of monomer and excimer emission between PL and CPL was attributed to a stronger CPL (|gem| = ∼3-4 × 10-3) contribution from the minor excimer component, which should exhibit an efficient chiral environment around the dimeric pyrenes.
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Indolylbenzothiadiazoles with varying substituents on the indole ring: a systematic study on the self-recovering mechanochromic luminescence

TL;DR: In this article, a series of self-recovering mechanochromic fluorophores with different solid-state emission colors and recovery times is described, based on powder X-ray diffraction and DSC analyses of crystalline and amorphous samples.
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Recent Advances in Mechanochromic Luminescence of Organic Crystalline Compounds

TL;DR: A growing number of MCL systems have been proposed as discussed by the authors, which refers to a reversible color change of the solid-state emission induced by mechanical stimulus such as grinding, shearing, and compressing.
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Efficient and versatile mechanochromic luminescence of phenanthroimidazolylbenzothiadiazoles: tricolor switching and directional control over the chromism

TL;DR: In this article, phenanthroimidazolylbenzothiadiazoles are described as a new class of highly emissive solid-state fluorophores that exhibit more versatile MCL properties.
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N-Boc-Indolylbenzothiadiazole Derivatives: Efficient Full-Color Solid-State Fluorescence and Self-Recovering Mechanochromic Luminescence.

TL;DR: It is proposed that the mechanism of the autonomously self-recovering mechanochromic luminescence of 3-methylindolylbenzothiadiazoles is based on a partial amorphization of the crystals upon exposure to the mechanical stimulus, followed by autonomous recovering in the form of recrystallization.