137350-54-0Relevant articles and documents
Polymer Dots with Enhanced Photostability, Quantum Yield, and Two-Photon Cross-Section using Structurally Constrained Deep-Blue Fluorophores
Algar, W. Russ,Burke, Sarah A.,Darwish, Ghinwa H.,Gupta, Rupsa,Hudson, Zachary M.,Kamal, Saeid,Lix, Kelsi,Mayder, Don M.,Nguyen, Giang D.,Tom, Gary,Tonge, Christopher M.,Tran, Michael V.
supporting information, p. 16976 - 16992 (2021/10/25)
Semiconducting polymer dots (Pdots) have emerged as versatile probes for bioanalysis and imaging at the single-particle level. Despite their utility in multiplexed analysis, deep blue Pdots remain rare due to their need for high-energy excitation and sens
Synthesis of Triarylamines via Sequential C-N Bond Formation
Modha, Sachin G.,Popescu, Mihai V.,Greaney, Michael F.
, p. 11933 - 11938 (2017/11/24)
A one-pot domino N-arylation protocol is described using diaryliodonium reagents under copper catalysis. The reaction uses both aryl groups of the diaryliodonium reagent to generate triarylamines starting from simple anilines, representing an atom-economical preparation of an important class of organic material building blocks.
Benzfluorene, emitting layer material using the compound and an organic electroluminescence element
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Paragraph 0190, (2016/11/07)
PROBLEM TO BE SOLVED: To provide a benzofluorene compound exhibiting excellent performance when applied to an organic electroluminescent element, for example. SOLUTION: In the benzofluorene compound, benzene rings condensed to a five-membered ring are each substituted by diphenylamino, and as the whole compound, one cyano group is a substituent of a phenyl group. COPYRIGHT: (C)2013,JPOandINPIT
