Probing Coherent Vibrations of Organic Phosphonate Radical Cations with Femtosecond Time-Resolved Mass Spectrometry

Molecules

Derrick Ampadu Boateng¹  Mi’KaylaD. Word¹  KatharineMoore Tibbetts¹ 

[1] Department of Chemistry, Virginia Commonwealth University, Richmond, VA 23284, USA;

关键词: femtosecond spectroscopy;    pump–probe;    mass spectrometry;    wave packet dynamics;    organic phosphonates;   

DOI  :  10.3390/molecules24030509

来源: DOAJ

【 摘 要 】

Organic phosphates and phosphonates are present in a number of cellular components that can be damaged by exposure to ionizing radiation. This work reports femtosecond time-resolved mass spectrometry (FTRMS) studies of three organic phosphonate radical cations that model the DNA sugar-phosphate backbone: dimethyl methylphosphonate (DMMP), diethyl methylphosphonate (DEMP), and diisopropyl methylphosphonate (DIMP). Upon ionization, each molecular radical cation exhibits unique oscillatory dynamics in its ion yields resulting from coherent vibrational excitation. DMMP has particularly well-resolved 45 fs ( $732\pm 28$ cm ${}^{-1}$ ) oscillations with a weak feature at 610⁻650 cm ${}^{-1}$ , while DIMP exhibits bimodal oscillations with a period of ∼55 fs and two frequency features at $554\pm 28$ and 670⁻720 cm ${}^{-1}$ . In contrast, the oscillations in DEMP decay too rapidly for effective resolution. The low- and high-frequency oscillations in DMMP and DIMP are assigned to coherent excitation of the symmetric O⁻P⁻O bend and P⁻C stretch, respectively. The observation of the same ionization-induced coherently excited vibrations in related molecules suggests a possible common excitation pathway in ionized organophosphorus compounds of biological relevance, while the distinct oscillatory dynamics in each molecule points to the potential use of FTRMS to distinguish among fragment ions produced by related molecules.

【 授权许可】

Unknown