2016
DOI: 10.1002/ejoc.201690004
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Room‐Temperature Phosphorescence of Crystalline 1,4‐Bis(aroyl)‐2,5‐dibromobenzenes (Eur. J. Org. Chem. 3/2016)

Abstract: The cover picture shows optical and phosphorescent images of 2,5‐dibromo‐1,4‐bis(4‐trifluoromethylphenylcarbonyl)benzene in crystals under ambient conditions with a simplified Jablonski diagram and the molecular structure of 1,4‐bis(aroyl)‐2,5‐dibromobenzene. The room‐temperature phosphorescence is observed only in crystals, but neither in solution nor in a doped polymer film. Thus, a class of the bis(aroyl)benzenes can serve as chromophores that exhibit crystallization‐induced room‐temperature phosphorescence… Show more

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“…However, unlike inorganic and organometallic phosphors, [30][31][32][33][34] the fabrication of efficient pure organic RTP luminogens remains challenging, owing to the spin-forbidden intersystem crossing (ISC) process and the high susceptibility of phosphorescence to molecular motions and external quenchers. [3][4][5][7][8][9][10][11][12][13] Even though great advances have been achieved for the molecular design of pure organic RTP through incorporation of halogens, aromatic carbonyls, and heteroatoms, [7][8][9][10][11][12][13] as well as effective suppression of nonradiative processes by supramolecular interactions, [35,36] micelle stabilization, [37] absorption on solid substrate, [38] crystal-lization, [3,4,7,[15][16][17] embedding into rigid matrices, [5,23,39] chemical bonding to polymer chains, [14] etc., the development of pure organic RTP remains in its infant stage. Furthermore, persistent RTP (p-RTP) with naked eye visible emission after ceasing the excitation is even difficult to achieve, despite it has diverse promising applications in advanced OLEDs, bioimaging, encryption and anticounterfeiting.…”
Section: Introductionmentioning
confidence: 99%
“…However, unlike inorganic and organometallic phosphors, [30][31][32][33][34] the fabrication of efficient pure organic RTP luminogens remains challenging, owing to the spin-forbidden intersystem crossing (ISC) process and the high susceptibility of phosphorescence to molecular motions and external quenchers. [3][4][5][7][8][9][10][11][12][13] Even though great advances have been achieved for the molecular design of pure organic RTP through incorporation of halogens, aromatic carbonyls, and heteroatoms, [7][8][9][10][11][12][13] as well as effective suppression of nonradiative processes by supramolecular interactions, [35,36] micelle stabilization, [37] absorption on solid substrate, [38] crystal-lization, [3,4,7,[15][16][17] embedding into rigid matrices, [5,23,39] chemical bonding to polymer chains, [14] etc., the development of pure organic RTP remains in its infant stage. Furthermore, persistent RTP (p-RTP) with naked eye visible emission after ceasing the excitation is even difficult to achieve, despite it has diverse promising applications in advanced OLEDs, bioimaging, encryption and anticounterfeiting.…”
Section: Introductionmentioning
confidence: 99%