Related Experiment Video
Updated: Dec 28, 2025

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Oxidative instability of boronic acid-installed polycarbonate nanoparticles
Elena Alexandra Garcia1, Diogo Pessoa, Margarita Herrera-Alonso
1Department of Chemical and Biological Engineering, School of Advanced Materials Discovery, Colorado State University, Fort Collins, Colorado 80523, USA. m.herrera-alonso@colostate.edu.
Abstract:
Oxidative stress, caused by the overproduction of reactive oxygen species (ROS), is often observed in degenerative and/or metabolic diseases, tumors, and inflamed tissues. Boronic acids are emerging as a unique class of responsive biomaterials targeting ROS because of their reactivity toward H2O2. Herein, we examine the oxidative reactivity of nanoparticles from a boronic acid-installed polycarbonate. The extent of oxidation under different concentrations of H2O2 was tracked by the change in fluorescence intensity of an encapsulated solvatochromic reporter dye, demonstrating their sensitivity to biologically-relevant concentrations of hydrogen peroxide. Oxidation-triggered particle destabilization, however, was shown to be highly dependent on the concentration of the final oxidized polymer product, and was only achieved if it fell below polymer critical micelle concentration. Our results indicate that these nanocarriers serve as an excellent dual pH/H2O2 responsive vehicle for drug delivery.
More Related Videos
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Radical Reactivity: Steric Effects
Along with electronic...
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Regioselectivity of Electrophilic Additions-Peroxide Effect
Anionic Chain-Growth Polymerization: Overview

