Kyushu University Academic Staff Educational and Research Activities Database
List of Reports
Soji Shimizu Last modified date:2024.04.01

Associate Professor / Department of Applied Chemistry / Faculty of Engineering


Reports
1. Soji Shimizu, 5,15-Diheteroporphyrins synthesized from α,α'-dihalodipyrrin as a key building block, HETEROCYCLES, 10.3987/rev-20-927, 2020.04.
2. Soji Shimizu, Aza-BODIPY synthesis towards vis/NIR functional chromophores based on a Schiff base forming reaction protocol using lactams and heteroaromatic amines, Chemical Communications, 10.1039/c9cc03365c, 2019.01, Aza-BODIPY is a class of heteroatom-containing BODIPY analogues targeting near infrared (NIR) chromophores and fluorophores. As a synthetic strategy towards aza-BODIPY structures, we have, recently, developed a Schiff base forming reaction using readily available lactams and heteroaromatic amines. Absorption and fluorescence of a series of compounds cover the whole range of the ultraviolet (UV)/visible (vis)/NIR regions. In addition, some compounds exhibit solid state emission, aggregation-induced emission enhancement, tunable fluorescence in the vis/NIR regions and non-linear optical properties. Furthermore, simple dimerization of aza-BODIPY chromophores caused unusual panchromatic absorption, whereas in combination with an N-confused porphyrin skeleton, multi-state NH tautomerism was achieved. In this Feature Article, wide applicability of this Schiff base forming reaction and optical and electrochemical properties of aza-BODIPY analogues thus synthesized are summarized including recent applications, such as bioimaging, photothermal cancer therapy and organic photovoltaics..
3. Soji Shimizu, Recent Advances in Subporphyrins and Triphyrin Analogues: Contracted Porphyrins Comprising Three Pyrrole Rings, Chemical Reviews, 2016.10.
4. Soji Shimizu, Hiroyuki Furuta, Core-modified phthalocyanines and subphthalocyanines: a synthetic strategy towards core-modification and novel properties arising from the inner ring-expansion, 2016.03.
5. Soji Shimizu, Nagao Kobayashi, Structurally-modified subphthalocyanines: molecular design towards realization of expected properties from the electronic structure and structural features of subphthalocyanine, 2014.04.