2236-42-2Relevant articles and documents
Properties modulation of organic semi-conductors based on a donor-spiro-acceptor (D-spiro-A) molecular design: New host materials for efficient sky-blue PhOLEDs
Romain, Maxime,Tondelier, Denis,Jeannin, Olivier,Geffroy, Bernard,Rault-Berthelot, Jo?lle,Poriel, Cyril
, p. 9701 - 9714 (2015)
Four high triplet organic semi-conductors based on the donor-spiro-acceptor design (D-spiro-A) have been synthesized. Their physicochemical and photophysical properties have been studied, compared and discussed in light of the nature of their respective donor/acceptor units. The four compounds have been used as host materials in efficient sky-blue (EQE > 10% at 10 mA cm-2) phosphorescent organic light emitting diodes.
Structure and Reactivity of N-Heterocyclic Alkynyl Hypervalent Iodine Reagents
Le Du, Eliott,Duhail, Thibaut,Wodrich, Matthew D.,Scopelliti, Rosario,Fadaei-Tirani, Farzaneh,Anselmi, Elsa,Magnier, Emmanuel,Waser, Jerome
supporting information, p. 10979 - 10986 (2021/06/08)
Ethynylbenziodoxol(on)e (EBX) cyclic hypervalent iodine reagents have become popular reagents for the alkynylation of radicals and nucleophiles, but only offer limited possibilities for further structure and reactivity fine-tuning. Herein, the synthesis o
Copper-catalyzed selective single arylsulfanylation of aryl diiodides with aryl thiols
Liu, Yunyun,Wang, Hang,Cao, Xiaoji,Fang, Zheng,Wan, Jie-Ping
, p. 2977 - 2982 (2013/11/06)
Selective single arylsulfanylation reactions of aryl diiodides with aryl or hetaryl thiols to give a broad array of iodine-functionalized sulfides were developed. Further elaboration of the iodine-containing products to provide a variety of aryl and hetaryl sulfides through coupling reactions was also demonstrated. Georg Thieme Verlag Stuttgart, New York.
