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Glowing dyes

The chemiluminescent magic unfolds within the outer plastic tube of the glow stick, housing a solution of oxalate ester and an electron-rich dye, along with a glass vial filled with hydrogen peroxide. The signature snap signifies the breaking of the glass vial, releasing hydrogen peroxide. The ensuing chemical reaction involves several steps, ultimately producing light.
Though the precise structure of the high-energy intermediate formed in the reaction remains somewhat mysterious, it's known to be a good electron acceptor, facilitating the exchange of electrons between the dye and carbon dioxide. The dye, now a positively charged radical cation, gains excess energy, leading to the emission of light when it returns to its ground state.
The origin of glow stick chemistry traces back to a janitor's closet in New Jersey in 1962, where Edwin A. Chandross discovered the foundational reaction while working at Bell Laboratories. Despite initial skepticism, the chemistry of glow sticks captured attention, leading to further innovations by American Cyanamid chemists who refined the chemistry using less reactive oxalate esters and experimented with various dyes.
Beyond their novelty appeal, glow sticks serve crucial purposes, with the US military investing in their development. Cyalume Technologies, a company rooted in American Cyanamid, provides glow sticks for military training exercises and field operations, highlighting their practical applications in emergencies. Chemical innovations have enhanced safety, extended glow stick lifetimes, and broadened their operating temperatures, ensuring reliable performance in diverse conditions.
From the darkroom experiments of a curious chemist to military applications and the novelty market, the glow stick has illuminated our lives for nearly 60 years, showcasing the enduring impact of clever chemistry on practical and entertaining aspects of our world.

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  glow-dye
Glow sticks illuminate through the chemical reaction between oxalate esters and hydrogen peroxide, resulting in the creation of a high-energy intermediate, potentially identified as 1,2-dioxetanedione. This intermediate engages with dye, prompting the dye to transition to an excited state (denoted by *), ultimately emitting light as it returns to its relaxed state.