To create a lightly cross-linked network, an ultraviolet (UV) photoinitiator can be incorporated. Here, we present the first use of perfluorophenylazide chemistry to control precisely a polyacrylate network for application as a PSA.

When an aryl azide is exposed to UV light (250 to 350 nm), it forms a nitrene group that can initiate addition reactions with double bonds, insertion into C–H and N–H sites, or subsequent ring expansion to react with a nucleophile (e.g., primary amines).

The UV Cleavable Biotin-Azide allows the tagging of alkyne modified substrates via copper-catalyzed click chemistry, and subsequent release under mild photolysis conditions (365 nm) and results in a significant decrease of background signal due to non-specifically bound proteins.

The azide functionality can be activated thermally or by UV light under formation of highly reactive nitrenes, which are capable of insertion and addition reactions (see Scheme 3).

When an aryl azide is exposed to UV-light, it forms a nitrene group that can initiate addition reactions with double bonds, insertion into C-H and N-H sites, or subsequent ring expansion to react as a nucleophile with primary amines (Figure 2).

To create a lightly cross-linked network, an ultraviolet (UV) photoinitiator can be incorporated. Here, we present the first use of per fluorophenylazide chemistry to control precisely a polyacrylate network for application as a PSA.

The photochemistry of para- and ortho-biphenylyl azides and 1-naphthyl azide was studied by ultrafast spectroscopy. In every case, the singlet azide second excited states were observed by transient absorption spectroscopy and were found to have lifetimes of hundreds of femtoseconds.

In this study, the epidemiology of sodium azide exposures between 1920 and 2020 was investigated. For the determination the azide concentration in biological samples, a simple, precise and...

This DBCO-Azide method requires to activate the biomolecule #1 with DBCO reagent, and the biomolecule #2 with azide, then to mixing the two activated biomolecules to form a conjugate. Features • Biocompatibility – no cytotoxic Copper catalyst required – Nice of in-vivo applications.

UV Cleavable Biotin-PEG2-Azide is a biotin linker. The azide group can react with either alkyne moiety in Cu(I)-catalyzed Click Chemistry reaction or DBCO moiety in copper-free Click Chemistry reaction to form a stable triazole linkage.