Internal energy content of n-butylbenzene, bromobenzene, iodobenzene and aniline molecular ions generated by two-photon ionization at 266 nm. A photodissociation study

نویسندگان

  • Yoon
  • Hwang
  • Choe
  • Kim
چکیده

A technique to investigate photodissociation kinetics on a nanosecond time scale has been devised for molecular ions generated by multiphoton ionization (MPI) using mass-analyzed ion kinetic energy spectrometry. The branching ratio or rate constant has been determined for the photodissociation of the n-butylbenzene, bromobenzene, iodobenzene, and aniline molecular ions generated by MPI at 266 nm. The ion internal energies have been estimated by comparing the measured kinetic data with the previous energy dependence data. The analysis has shown that only those molecular ions generated by two-photon ionization contribute to the photodissociation signals. Around half of the available energy has been found to remain as molecular ion internal energy in the two-photon ionization process. Copyright 1999 John Wiley & Sons, Ltd.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Mass Spectrometric Observations on Reactions of Excited Ions

Reactions have been observed between excited ions of carbon disulfide and carbon disulfide, water, iodine and ethylene. The ions CS3\ C,S,+, C2S3\ H2OS+, CSI+, SI+, C2H : iS+ and C2H4S+ are formed in these reactions. An additional contribution to the C2S2+ ion results from reaction of CS+ with CS2 • The reaction of I2+ with CS2 leads to the ion CS2I+. Reactions of excited molecular ions have al...

متن کامل

Time-resolved photodissociation study of singly protonated peptides with a histidine residue generated by matrix-assisted laser desorption ionization: dissociation rate constant and internal temperature.

Product ion yields in post-source decay and time-resolved photodissociation at 193 and 266 nm were measured for some peptide ions with a histidine residue ([HF(6) + H](+), [F(6)H + H](+), and [F(3)HF(3) + H](+)) formed by matrix-assisted laser desorption ionization (MALDI). Compared with similar data for peptide ions without any basic residue reported previously, significant reduction in dissoc...

متن کامل

Evidence for concerted ring opening and C-Br bond breaking in UV-excited bromocyclopropane.

Photodissociation of gaseous bromocyclopropane via its A-band continuum has been studied at excitation wavelengths ranging from 230 nm to 267 nm. Velocity-map images of ground-state bromine atoms (Br), spin-orbit excited bromine atoms (Br(∗)), and C3H5 hydrocarbon radicals reveal the kinetic energies of these various photofragments. Both Br and Br(∗) atoms are predominantly generated via repuls...

متن کامل

Dissociative multiphoton ionization of NO2 studied by time-resolved imaging.

We have studied dissociative multiphoton ionization of NO2 by time-resolved velocity map imaging in a two-color pump-probe experiment using the 400 and 266 nm harmonics of a regeneratively amplified titanium-sapphire laser. We observe that most of the ion signal appears as NO+ with approximately 0.28 eV peak kinetic energy. Approximately 600 fs period oscillations indicative of wave packet moti...

متن کامل

Characterization of nitrogen-containing radical products from the photodissociation of trimethylamine using photoionization detection

The outcome of neutral and photoionized N~CH3!2 primary products of trimethylamine photodissociation at 193 nm is determined by combining photoionization detection with supporting G3 theoretical calculations. N~CH3!2 primary products with very little internal energy show an experimentally observed ionization onset of 9.160.2 eV, but do not appear at the parent ion (m/e544). Instead, the parent ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Rapid communications in mass spectrometry : RCM

دوره 13 14  شماره 

صفحات  -

تاریخ انتشار 1999