Efficient Synthesis of 1,4-Bis-heteroatom-substituted Tetraselanylbenzenes via 1,4-Dilithiation of Hexaselanylbenzene and Investigation on Their Electronic Properties-Reference-Cited by-同舟云学术

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Efficient Synthesis of 1,4-Bis-heteroatom-substituted Tetraselanylbenzenes via 1,4-Dilithiation of Hexaselanylbenzene and Investigation on Their Electronic Properties

Published:2017-03-16 Issue:9 Volume:12 Page:954-957
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Fujita Masahiro¹,Furukawa Shunsuke¹,Saito Masaichi¹

Affiliation:

1. Department of Chemistry; Graduate School of Science and Engineering; Saitama University; Shimo-okubo, Sakura-ku Saitama 338-8570 Japan

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Reference44 articles.

1. Redox properties of polythiaarene derivatives. A novel class of electron acceptors

2. A persulfurated benzene molecule exhibits outstanding phosphorescence in rigid environments: from computational study to organic nanocrystals and OLED applications

3. Molecular asterisks with a persulfurated benzene core are among the strongest organic phosphorescent emitters in the solid state

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1. Creation of (σ+π)-Mixed Delocalization;Chemistry Letters;2023-08-19

2. σ-Delocalization between Non-bonded Selenium Atoms on Multiply Se-substituted Benzenes;Chemistry Letters;2023-02-05

3. Synthesis and triplet sensitization of bis(arylselanyl)BOPHYs; potential application in triplet–triplet annihilation upconversion;New Journal of Chemistry;2021

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