734-59-8Relevant articles and documents
Compound for organic luminescence, and application thereof
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Paragraph 0026; 0030-0031, (2021/03/31)
The invention relates to a compound for organic luminescence, wherein the structure of the compound is shown as a formula (I), R1-R3 are independently selected from hydrogen, a substituted or unsubstituted aryl group, a substituted or unsubstituted heteroaryl group and a substituted or unsubstituted alkyl group respectively, L is selected from substituted or unsubstituted phenyl and substituted orunsubstituted heteroaryl, and Ar1 and Ar2 are respectively and independently selected from substituted or unsubstituted phenyl, naphthyl and anthryl. The compound for organic luminescence can be usedas an electron transport material, and has high stability, high charge transfer capability and high glass transition temperature.
Long-lived emission beyond 1000 nm: control of excited-state dynamics in a dinuclear Tb(iii)-Nd(iii) complex
Fushimi, Koji,Hasegawa, Yasuchika,Kitagawa, Yuichi,Matsuda, Kenji,da Rosa, Pedro Paulo Ferreira
supporting information, p. 8047 - 8050 (2021/08/20)
A long-lived near-infrared Nd(iii) emission is demonstrated using a Tb(iii) donor. The observed emission lifetime of 290 μs at 1057 nm for a Tb(iii)-Nd(iii) dinuclear complex is attributed to the long-lived Tb(iii) donor and the appropriate spacing between the lanthanide ions. This design strategy leads to novel lanthanide photophysics.
Cylindrical micelles by the self-assembly of crystalline-b-coil polyphosphazene-b-P2VP block copolymers. Stabilization of gold nanoparticles
Cortes, Maria De Los Angeles,De La Campa, Raquel,Valenzuela, Maria Luisa,Díaz, Carlos,Carriedo, Gabino A.,Soto, Alejandro Presa
, (2019/05/24)
During the last number of years a variety of crystallization-driven self-assembly (CDSA) processes based on semicrystalline block copolymers have been developed to prepare a number of different nanomorphologies in solution (micelles). We herein present a convenient synthetic methodology combining: (i) The anionic polymerization of 2-vinylpyridine initiated by organolithium functionalized phosphane initiators; (ii) the cationic polymerization of iminophosphoranes initiated by -PR2Cl2; and (iii) a macromolecular nucleophilic substitution step, to prepare the novel block copolymers poly(bistrifluoroethoxy phosphazene)-b-poly(2-vinylpyridine) (PTFEP-b-P2VP), having semicrystalline PTFEP core forming blocks. The self-assembly of these materials in mixtures of THF (tetrahydrofuran) and 2-propanol (selective solvent to P2VP), lead to a variety of cylindrical micelles of different lengths depending on the amount of 2-propanol added. We demonstrated that the crystallization of the PTFEP at the core of the micelles is the main factor controlling the self-assembly processes. The presence of pyridinyl moieties at the corona of the micelles was exploited to stabilize gold nanoparticles (AuNPs).