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Yuto Kage

Showing results (1-10 of 9) with videos related to

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Chemical Communications (Cambridge, England)|March 8, 2024
One-pot synthesis of azabora[6]helicene by a Schiff base forming reactionYuto Kage, Yuchuan Jiang, Namiki Minakuchi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 28, 2016
Pyrene-Bridged Boron Subphthalocyanine Dimers: Combination of Planar and Bowl-Shaped π-Conjugated Systems for Creating Uniquely Curved π-Conjugated SystemsShota Nakano, Yuto Kage, Hiroyuki Furuta, et al.
Chempluschem|January 22, 2020
Phenylene-Bridged Expanded PorphyrazinesFumiya Iizuka, Yuto Kage, Nagao Kobayashi, et al.
Chempluschem|January 17, 2020
Pyrrolopyrrole Aza-BODIPY Analogues as Near-Infrared Chromophores and Fluorophores: Red-Shift Effects of Substituents on Absorption and Emission SpectraYuto Kage, Hideaki Karasaki, Shigeki Mori, et al.
Organic Letters|January 17, 2020
Subphthalocyanine-Stoppered [2]Rotaxanes: Synthesis and Size/Energy Threshold of SlippageYuto Kage, Soji Shimizu, Gabriele Kociok-Köhn, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 14, 2021
An Electron-Accepting aza-BODIPY-Based Donor-Acceptor-Donor Architecture for Bright NIR EmissionYuto Kage, Seongsoo Kang, Shigeki Mori, et al.
Angewandte Chemie (International Ed. in English)|August 27, 2020
TTF-Annulated Silicon Phthalocyanine Oligomers and Their External-Stimuli-Responsive Orientational OrderingYuta Shiina, Yuto Kage, Ko Furukawa, et al.
Journal of the American Chemical Society|July 18, 2019
Efficient Electrogenerated Chemiluminescence of Pyrrolopyrrole Aza-BODIPYs in the Near-Infrared Region with Tripropylamine: Involving Formation of S<sub>2</sub> and T<sub>2</sub> StatesRyoichi Ishimatsu, Hirosato Shintaku, Yuto Kage, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 17, 2021
Janus Pyrrolopyrrole Aza-dipyrrin: Hydrogen-Bonded Assemblies and Slow Magnetic Relaxation of the Cobalt(II) Complex in the Solid StateToshiharu Ishizaki, Hideaki Karasaki, Yuto Kage, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Chemical Communications (Cambridge, England)|March 8, 2024
One-pot synthesis of azabora[6]helicene by a Schiff base forming reactionYuto Kage, Yuchuan Jiang, Namiki Minakuchi, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|April 28, 2016
Pyrene-Bridged Boron Subphthalocyanine Dimers: Combination of Planar and Bowl-Shaped π-Conjugated Systems for Creating Uniquely Curved π-Conjugated SystemsShota Nakano, Yuto Kage, Hiroyuki Furuta, et al.
Chempluschem|January 22, 2020
Phenylene-Bridged Expanded PorphyrazinesFumiya Iizuka, Yuto Kage, Nagao Kobayashi, et al.
Chempluschem|January 17, 2020
Pyrrolopyrrole Aza-BODIPY Analogues as Near-Infrared Chromophores and Fluorophores: Red-Shift Effects of Substituents on Absorption and Emission SpectraYuto Kage, Hideaki Karasaki, Shigeki Mori, et al.
Organic Letters|January 17, 2020
Subphthalocyanine-Stoppered [2]Rotaxanes: Synthesis and Size/Energy Threshold of SlippageYuto Kage, Soji Shimizu, Gabriele Kociok-Köhn, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 14, 2021
An Electron-Accepting aza-BODIPY-Based Donor-Acceptor-Donor Architecture for Bright NIR EmissionYuto Kage, Seongsoo Kang, Shigeki Mori, et al.
Angewandte Chemie (International Ed. in English)|August 27, 2020
TTF-Annulated Silicon Phthalocyanine Oligomers and Their External-Stimuli-Responsive Orientational OrderingYuta Shiina, Yuto Kage, Ko Furukawa, et al.
Journal of the American Chemical Society|July 18, 2019
Efficient Electrogenerated Chemiluminescence of Pyrrolopyrrole Aza-BODIPYs in the Near-Infrared Region with Tripropylamine: Involving Formation of S<sub>2</sub> and T<sub>2</sub> StatesRyoichi Ishimatsu, Hirosato Shintaku, Yuto Kage, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 17, 2021
Janus Pyrrolopyrrole Aza-dipyrrin: Hydrogen-Bonded Assemblies and Slow Magnetic Relaxation of the Cobalt(II) Complex in the Solid StateToshiharu Ishizaki, Hideaki Karasaki, Yuto Kage, et al.
Pageof 1