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Updated: Feb 3, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Mitomycin C radical cation studied by pulse radiolysis
1Ludwig Boltzmann Institute for Radiation Chemistry and Radiation Biology, Institute of Theoretical Chemistry and Molecular Structure Biology, Althanstr, 14, A-1090 Vienna, Austria.
The study investigated the mitomycin C radical cation (MMC.+) using pulse radiolysis. This MMC radical cation may also play a role in radiotherapy, alongside the known radical anion.
Area of Science:
- Chemical Kinetics
- Radiation Chemistry
- Biochemistry
Background:
- Mitomycin C (MMC) is a crucial chemotherapy agent.
- The radical anion (MMC.-) is known to be involved in radiotherapy.
- The role of other MMC redox species remains less understood.
Purpose of the Study:
- To investigate the formation and characteristics of the mitomycin C radical cation (MMC.+) in aqueous solution.
- To determine the spectroscopic and kinetic properties of MMC.+.
- To assess the potential role of MMC.+ in radiotherapy.
Main Methods:
- Pulse radiolysis technique was employed.
- Sulfate radical anions (SO4.-) were used as the one-electron oxidizing agent.
- Spectroscopic analysis (absorption maxima and molar extinction coefficients) and kinetic studies (rate constants) were performed.
Main Results:
- The radical cation of mitomycin C (MMC.+) was successfully formed and characterized.
- Key spectroscopic data include absorption maxima at 295, 400, and 500 nm with specific molar extinction coefficients.
- Rate constants for MMC.+ formation (k = 1.2 x 10^10 dm3 mol-1 s-1) and decay (2k = 4.6 x 10^8 dm-3 mol-1 s-1) were determined.
Conclusions:
- The formation and properties of the mitomycin C radical cation (MMC.+) were elucidated.
- Findings suggest that MMC.+ could potentially contribute to radiotherapy efficacy in specific oxidative environments.
- This expands the understanding of mitomycin C's redox chemistry in biological contexts.
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