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Probing Ultrafast Dissociation Dynamics of Chloroiodomethane in the B Band by Time-Resolved Mass Spectrometry 被引量:1

Probing Ultrafast Dissociation Dynamics of Chloroiodomethane in the B Band by Time-Resolved Mass Spectrometry
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摘要 Ultrafast dissociation dynamics of chloroiodomethane (CH2ICl) in the B band is studied by femtosecond time- resolved time-of-flight (TOF) mass spectrometry. Time-resolved TOF mass signal of parent ion (CH2ICl+) and main daughter ion (CH2Cl+) are obtained. The curve for the transient signal of CH2ICl+ is simple and can be well fitted by an exponential decay convoluted with a Gaussian function. The decay constant determined to be less than 35 fs reflects the lifetime of the B band. Significant substituent effects on photodissociation dynamics of CH2IC1 compared with CH3I are discussed. The dissociation time from the parent ion CH2IC1+ to the daughter ion CH2Cl+ is determined in the experiment. The optimized geometry of the ionic state of CH2ICl and the ionization energy are calculated for further analysis of the measurements. In addition, compared with the parent ion, a new decay component with time constant of -596 fs is observed for CH2Cl+, and reasonable mechanisms are proposed for the explanation. Ultrafast dissociation dynamics of chloroiodomethane (CH2ICl) in the B band is studied by femtosecond time- resolved time-of-flight (TOF) mass spectrometry. Time-resolved TOF mass signal of parent ion (CH2ICl+) and main daughter ion (CH2Cl+) are obtained. The curve for the transient signal of CH2ICl+ is simple and can be well fitted by an exponential decay convoluted with a Gaussian function. The decay constant determined to be less than 35 fs reflects the lifetime of the B band. Significant substituent effects on photodissociation dynamics of CH2IC1 compared with CH3I are discussed. The dissociation time from the parent ion CH2IC1+ to the daughter ion CH2Cl+ is determined in the experiment. The optimized geometry of the ionic state of CH2ICl and the ionization energy are calculated for further analysis of the measurements. In addition, compared with the parent ion, a new decay component with time constant of -596 fs is observed for CH2Cl+, and reasonable mechanisms are proposed for the explanation.
出处 《Chinese Physics Letters》 SCIE CAS CSCD 2017年第3期21-24,共4页 中国物理快报(英文版)
基金 Supported by the National Natural Science Foundation of China under Grant Nos 11304157,21303255 and 11475229 the‘Six Talent Peaks’Project in Jiangsu Province under Grant No 2015-JNHB-011 the College Students Practice Innovative Training Program of Nuist under Grant No 201610300042
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