Check out my first first-author paper in PhD study! 🥳We found an interesting photoactivatable motif! Both of its photophysical and photochemical mechanism behind were studied and we luckily invented an alkyne polymerization to incorporate it into polymers!
Thanks for all the inspiring discussion, patient revision and kind support from my supervisor @BenZhongTANG1 and thanks for the help from all collaborators❤️❤️❤️
I have worked on this project for 4 years and it has finally been online on Nat Commun💍💍💍!!! Check it out if you also love the complicated photophysical pathways in doping RTP systems! We propose a dynamic coupling model that resolve the controversial debate within this field.
Happy to share our findings on room temperature phosphorescence in @J_A_C_S !✨✨✨ Want long-lived AND bright phosphorescence? Try sulfonic acid functionalization!✨✨✨Thanks for the invaluable support from my supervisor @BenZhongTang1 and all collaborators🥰🥰🥰
Bright and Ultralong Organic Phosphorescence via Sulfonic Acid Functionalization for High-Contrast Real-Time Light-Writing Display | Journal of the American Chemical Society @BenZhongTANG1@cuhksz@hkust@HKUniversity https://t.co/02yuNJcFay
Cover: "Ultrafast Excitonic Transitions in Enantiopure and Racemic Squaraine Thin Films" by Robin Bernhardt, Tianyi Wang, Manuela Schiek & Paul H. M. van Loosdrecht et al. @UniCologne@jkulinz@Wiley_Chemistry#chirality#excitons#aggregate
https://t.co/f0AkUQO8Fi
Design of Vinylboron Monomers for the Structural Control of Poly(vinyl alcohol)s via Stereospecific Controlled Radical Polymerization (@J_A_C_S): https://t.co/xONwz5aWey (@ouchi_u).
"Caging-group-free photoactivatable fluorophores with far-red emission" for #MINFLUX, #STED, #PALM superresolution imaging.
New preprint by R. Lincoln, A.N. Butkevich et al.
Check it out at
https://t.co/lSD0Tclo7U
@mpi_mr_hd@mpi_nat#Nanoscopy
New article in Nature Chemistry! R. Lincoln, M.L. Bossi and co-workers present "A general design of caging-group-free photoactivatable fluorophores for live-cell nanoscopy". Open-access download at https://t.co/wH9wefieuJ
Post-processing crystals: Crystals are beautiful but challenging to create. In our new @angew_chem article we report a method for fabricating molecular crystals of specific sizes/aspect ratios by leveraging their photochemical reactivity @NYUADResearch
https://t.co/yNB0oQMt21
Reassessing the Photochemical Upcycling of Polystyrene Using Acridinium Salts (Dario M. Bassani and co-workers) #openaccess#AngewandteVIP 🔓 https://t.co/9NRGwybtoS
Very happy to have contributed to this work from the Hunter group at @Cambridge_Uni on templated-synthesis of recognition-encoded melamine oligomers in @J_A_C_S. https://t.co/1L5N0yP1WV
Observation of Ferroelectricity in Carbapenem Intermediates Enables Reactive Oxygen Species Generation by Ultrasound | Journal of the American Chemical Society #Ferroelectricity#Carbapenem#ROS#Generation#Ultrasound https://t.co/udZMJe6zyB
Cascading chemical reactions: In their @J_A_C_S article, Garcia-Garibay @GaribayLab et al. used a photoreactive Dewar benzene template to align non-reactive molecules. When light is shone on the crystal, the template isomerizes, triggering dimerization:
https://t.co/V61brhcZgi
Giant thermosalience! In their article in @J_A_C_S, Uddin, Gómez-Lor, et al. report a material that undergoes a phase transition with 33% expansion while retaining the single crystal structure and exhibiting an impressive thermosalient effect:
https://t.co/ERQq1bS0xz
Sulfate-binding cages, now available in grams😀! In their article in @J_A_C_S, White et al. report hexa-cationic supramolecular cages that can be prepared up to 14 g from commercial materials in two steps. One of the cages displays strong sulfate binding:
https://t.co/TLHSZLoRIg