Stacking-induced different performance of mechanochromic luminescence and room-temperature phosphorescence based on two analogous AIEgens synthesized by a green photo-oxidation reaction

2021 ◽  
Author(s):  
Yue Yu ◽  
Jianai Chen ◽  
Sijie Tan ◽  
Changjiang Zhou ◽  
Weijun Li ◽  
...  
Keyword(s):  
Oxidation Reaction ◽  
Room Temperature ◽  
Room Temperature Phosphorescence ◽  
Aggregation State ◽  
Photo Oxidation ◽  
Mechanochromic Luminescence

We reported two similar AIEgens obtained by photo-oxidation reaction. They exhibited different luminescence behaviors in aggregation state due to the different stacking manners, especially the distance and overlapping areas between the molecules.

CuWO4 as a photocatalyst for room temperature aerobic benzylamine oxidation

2018 ◽  
Vol 54 (9) ◽  
pp. 1101-1104 ◽  
Author(s):  
Aaron D. Proctor ◽  
Shobhana Panuganti ◽  
Bart M. Bartlett
Keyword(s):  
Oxidative Coupling ◽  
Oxidation Reaction ◽  
Room Temperature ◽  
Photo Oxidation

We report the first example of a controlled photo-oxidation reaction on CuWO4, the aerobic oxidative coupling of benzylamine.

scholarly journals Conformationally-flexible and moderately electron-donating units-installed D–A–D triad enabling multicolor-changing mechanochromic luminescence, TADF and room-temperature phosphorescence

2018 ◽  
Vol 54 (50) ◽  
pp. 6847-6850 ◽  
Author(s):  
Youhei Takeda ◽  
Takahito Kaihara ◽  
Masato Okazaki ◽  
Heather Higginbotham ◽  
Przemyslaw Data ◽  
...  
Keyword(s):  
Room Temperature ◽  
Room Temperature Phosphorescence ◽  
Mechanochromic Luminescence

A novel multi-color-changing MCL compound has been developed that also shows TADF and RTP.

scholarly journals Revealing Internal Heavy Chalcogen Atom Effect on the Photophysics of Dibenzo[a,j]phenazine-Cored Donor–Acceptor–Donor Triad

2021 ◽  
Author(s):  
Shimpei Goto ◽  
Yuya Nitta ◽  
Nicolas Decarli ◽  
Leonardo Evaristo de Sousa ◽  
Patrycja Stachelek ◽  
...  
Keyword(s):  
Room Temperature ◽  
Photophysical Properties ◽  
Heavy Atom ◽  
Delayed Fluorescence ◽  
Room Temperature Phosphorescence ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
Donor Acceptor ◽  
Mechanochromic Luminescence ◽  
Atom Effect

<div><div><div><p>A new twisted donor–acceptor–donor (D–A–D) multi-photofunctional organic molecule comprising of phenoselenazine as the electron-donors (Ds) and dibenzo[a,j]phenazine (DBPHZ) as the electron-acceptor (A) has been developed. The developed selenium-incorporated D–A–D compound is featured with multi-color polymorphism, distinct mechanochromic luminescence, chemically-stimulated luminochromism, thermally-activated delayed fluorescence, and room- temperature phosphorescence. The internal heavy atom effect on the photophysical properties of the D–A–D system has been investigated through the comparison with the physicochemical properties of a previously developed sulfur analogue and a tellurium analogue.</p></div></div></div>

scholarly journals Revealing Internal Heavy Chalcogen Atom Effect on the Photophysics of Dibenzo[a,j]phenazine-Cored Donor–Acceptor–Donor Triad

2021 ◽  
Author(s):  
Shimpei Goto ◽  
Yuya Nitta ◽  
Nicolas Decarli ◽  
Leonardo Evaristo de Sousa ◽  
Patrycja Stachelek ◽  
...  
Keyword(s):  
Room Temperature ◽  
Photophysical Properties ◽  
Heavy Atom ◽  
Delayed Fluorescence ◽  
Room Temperature Phosphorescence ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
Donor Acceptor ◽  
Mechanochromic Luminescence ◽  
Atom Effect

<div><div><div><p>A new twisted donor–acceptor–donor (D–A–D) multi-photofunctional organic molecule comprising of phenoselenazine as the electron-donors (Ds) and dibenzo[a,j]phenazine (DBPHZ) as the electron-acceptor (A) has been developed. The developed selenium-incorporated D–A–D compound is featured with multi-color polymorphism, distinct mechanochromic luminescence, chemically-stimulated luminochromism, thermally-activated delayed fluorescence, and room- temperature phosphorescence. The internal heavy atom effect on the photophysical properties of the D–A–D system has been investigated through the comparison with the physicochemical properties of a previously developed sulfur analogue and a tellurium analogue.</p></div></div></div>

DNA Inspirited Rational Construction of Nonconventional Luminophores with Efficient and Color-Tunable Afterglow

2020 ◽  
Author(s):  
Yunzhong Wang ◽  
Saixing Tang ◽  
Yating Wen ◽  
Shuyuan Zheng ◽  
Bing Yang ◽  
...  
Keyword(s):  
Rational Design ◽  
Room Temperature ◽  
Double Helix ◽  
Mechanical Grinding ◽  
Room Temperature Phosphorescence ◽  
Color Tunable ◽  
Potential Applications ◽  
Rational Construction ◽  
Double Helix Structure ◽  
Made In

<div>Persistent room-temperature phosphorescence (p-RTP) from pure organics is attractive </div><div>due to its fundamental importance and potential applications in molecular imaging, </div><div>sensing, encryption, anticounterfeiting, etc.1-4 Recently, efforts have been also made in </div><div>obtaining color-tunable p-RTP in aromatic phosphors5 and nonconjugated polymers6,7. </div><div>The origin of color-tunable p-RTP and the rational design of such luminogens, </div><div>particularly those with explicit structure and molecular packing, remain challenging. </div><div>Noteworthily, nonconventional luminophores without significant conjugations generally </div><div>possess excitation-dependent photoluminescence (PL) because of the coexistence of </div><div>diverse clustered chromophores6,8, which strongly implicates the possibility to achieve </div><div>color-tunable p-RTP from their molecular crystals assisted by effective intermolecular </div><div>interactions. Here, inspirited by the highly stable double-helix structure and multiple </div><div>hydrogen bonds in DNA, we reported a series of nonconventional luminophores based on </div><div>hydantoin (HA), which demonstrate excitation-dependent PL and color-tunable p-RTP </div><div>from sky-blue to yellowish-green, accompanying unprecedentedly high PL and p-RTP </div><div>efficiencies of up to 87.5% and 21.8%, respectively. Meanwhile, the p-RTP emissions are </div><div>resistant to vigorous mechanical grinding, with lifetimes of up to 1.74 s. Such robust, </div><div>color-tunable and highly efficient p-RTP render the luminophores promising for varying </div><div>applications. These findings provide mechanism insights into the origin of color-tunable </div><div>p-RTP, and surely advance the exploitation of efficient nonconventional luminophores.</div>

Clustering-Triggered Efficient Room Temperature Phosphorescence from Nonconventional Luminophores

2019 ◽  
Author(s):  
Shuyuan Zheng ◽  
Taiping Hu ◽  
Xin Bin ◽  
Yunzhong Wang ◽  
Yuanping Yi ◽  
...  
Keyword(s):  
Room Temperature ◽  
High Efficiency ◽  
Spin Orbit Coupling ◽  
Design Rationale ◽  
Emission Mechanism ◽  
Room Temperature Phosphorescence ◽  
Electronic Interactions ◽  
Energy Gaps ◽  
Theoretical Results

Pure organic room temperature phosphorescence (RTP) and luminescence from nonconventional luminophores have gained increasing attention. However, it remains challenging to achieve efficient RTP from unorthodox luminophores, on account of the unsophisticated understanding of the emission mechanism. Here we propose a strategy to realize efficient RTP in nonconventional luminophores through incorporation of lone pairs together with clustering and effective electronic interactions. The former promotes spin-orbit coupling and boost the consequent intersystem crossing, whereas the latter narrows energy gaps and stabilizes the triplets, thus synergistically affording remarkable RTP. Experimental and theoretical results of urea and its derivatives verify the design rationale. Remarkably, RTP from thiourea solids with unprecedentedly high efficiency of up to 24.5% is obtained. Further control experiments testify the crucial role of through-space delocalization on the emission. These results would spur the future fabrication of nonconventional phosphors, and moreover should advance understanding of the underlying emission mechanism.<br>

Reversible two-channel mechanochromic luminescence for a pyridinium-based white-light emitter with room-temperature fluorescence–phosphorescence dual emission

2019 ◽  
Vol 21 (27) ◽  
pp. 14728-14733 ◽  
Author(s):  
Xiao Ma ◽  
Jipeng Li ◽  
Chensheng Lin ◽  
Guoliang Chai ◽  
Yangbin Xie ◽  
...  
Keyword(s):  
White Light ◽  
Room Temperature ◽  
Mechanical Grinding ◽  
Dual Emission ◽  
Light Emitter ◽  
Mechanical Pressing ◽  
Mechanochromic Luminescence ◽  
White Light Emitter

For a pyridinium-based emitter with fluorescence–phosphorescence dual emission, mechanical grinding induces phosphorescence disappearance and mechanical pressing induces extraordinary phosphorescence enhancement.

scholarly journals Tipping the Balance with the Aid of Stoichiometry: Room Temperature Phosphorescence versus Fluorescence in Organic Cocrystals

2015 ◽  
Vol 15 (4) ◽  
pp. 2039-2045 ◽  
Author(s):  
Simone d’Agostino ◽  
Fabrizia Grepioni ◽  
Dario Braga ◽  
Barbara Ventura
Keyword(s):  
Room Temperature ◽  
Room Temperature Phosphorescence
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