Cyanonaphthalene and cyanonaphthyl radicals: Vibrational structures via computed negative ion photoelectron spectra and thermochemistry of 1- and 2-cyanonaphthalene.

A double harmonic oscillator model is applied to compute the negative ion photoelectron spectra (NIPES) of the 1- and 2-cyanonaphthalene (CNN) radical anions. The computed Franck-Condon factors utilize optimized structures and harmonic vibrational frequencies obtained using density functional theory with the B3LYP 6-311++G (2d,2p) basis set while considering the mode-mixing Duschinsky effects. To test the accuracy of our model, the NIPES of α and β naphthyl radical anions were computed, and a strong agreement between the slow electron velocity-map ion imaging spectra and the predicted spectra was found.

Cyanocyclopentadiene-Annulated Polycyclic Aromatic Radical Anions: Predicted Negative Ion Photoelectron Spectra and Singlet-Triplet Energies of Cyanoindene and Cyanofluorene Radical Anions.

Isomer-specific negative ion photoelectron spectra (NIPES) of cyanoindene (CHCN) and cyanofluorene (CHN), acquired through the computation of Franck-Condon (FC) factors that utilize harmonic vibrational frequencies and normal mode vectors derived from density functional theory (DFT) at the B3LYP/aug-cc-pVQZ and 6-311++G(2d,2p) basis sets, are reported. The adiabatic electron affinity (EA) values of the ground singlet (S) and the lowest lying triplet (T) states are used to predict site-specific S-T energies (Δ). The vibrational spectra of the S and T states are typified by ring distortion and ring C-C stretching vibrational progressions.

Predicted Negative Ion Photoelectron Spectra of 1-, 2-, and 9-Cyanoanthracene Radical Anions and Computed Thermochemical Values of the Three Cyanoanthracene Isomers.

In this work, the negative ion photoelectron spectra of 1-, 2-, and 9-cyanoanthracene (anthracenecarbonitrile, ACN) radical anions, obtained via the calculation of Franck-Condon (FC) factors based on a harmonic oscillator model, are reported. The FC calculations utilize harmonic vibrational frequencies and normal mode vectors derived from density functional theory using the B3LYP/6-311++G (2d,2p) basis set. The removal of an electron from the doublet anion allows for the computation of the negative ion photoelectron spectra that represents the neutral ground singlet state (S) and the lowest triplet state (T) in each of the three ACN molecules.

From Benzonitrile to Dicyanobenzenes: The Effect of an Additional CN Group on the Thermochemistry and Negative Ion Photoelectron Spectra of Dicyanobenzene Radical Anions.

The negative ion photoelectron spectra of 1,2-dicyanobenzene (-DCNB), 1,3-dicyanobenzene (-DCNB), and 1,4-dicyanobenzene (-DCNB) radical anions (DCNB·), acquired through the computation of Frack-Condon (FC) factors, are presented. The FC calculations utilize harmonic frequencies and normal mode vectors derived from density functional theory at the B3LYP/aug-cc-pVQZ basis set. All the totally symmetric vibrational modes are treated with Duschinsky rotations to yield neutral DCNBs in their singlet (S) and lowest triplet (T) states, following an electron removal from the doublet anionic ground state.

Negative Ion Photoelectron Spectra of Deprotonated Benzonitrile Isomers via Computation of Franck-Condon Factors.

Negative ion photoelectron spectra of (-), (-), and (-) deprotonated benzonitrile (-, -, -CH(CN)) isomers as well as the associated thermochemical values corresponding to deprotonation at -, -, and -positions in CH(CN) are presented. Quantum mechanical results based on the density functional theory (DFT) utilizing the aug-cc-pVQZ basis set indicate that the -, -, -CH(CN) radicals have electron affinity values (EAs) of 1.901, 1.

Photoelectron spectroscopy and thermochemistry of o-, m-, and p-methylenephenoxide anions.

The anionic products following (H + H+) abstraction from o-, m-, and p-methylphenol (cresol) are investigated using flowing afterglow-selected ion flow tube (FA-SIFT) mass spectrometry and anion photoelectron spectroscopy (PES). The PES of the multiple anion isomers formed in this reaction are reported, including those for the most abundant isomers, o-, m- and p-methylenephenoxide distonic radical anions. The electron affinity (EA) of the ground triplet electronic state of neutral m-methylenephenoxyl diradical was measured to be 2.

Anion photoelectron spectroscopy of deprotonated ortho-, meta-, and para-methylphenol.

The anion photoelectron spectra of ortho-, meta-, and para-methylphenoxide, as well as methyl deprotonated meta-methylphenol, were measured. Using the Slow Electron Velocity Map Imaging technique, the Electron Affinities (EAs) of the o-, m-, and p-methylphenoxyl radicals were measured as follows: 2.1991±0.

Low-temperature branching ratios for the reaction of state-prepared N2(+) with acetonitrile.

In this work, the primary product branching ratio (BR) for the reaction of state-prepared nitrogen cation (N(2)(+)) with acetonitrile (CH(3)CN), a possible minor constituent of Titan's upper atmosphere, is reported. The ion-molecule reaction occurs in the collision region of the supersonic nozzle expansion that is characterized by a rotational temperature of 45 ± 5 K. A BR of 0.

Primary branching ratios for the low-temperature reaction of state-prepared N2+ with CH4, C2H2, and C2H4.

Product branching ratios (BRs) are reported for ion-molecule reactions of state-prepared nitrogen cation (N(2)(+)) with methane (CH(4)), acetylene (C(2)H(2)). and ethylene (C(2)H(4)) at low temperature using a modified ion imaging apparatus. These reactions are performed in a supersonic nozzle expansion characterized by a rotational temperature of 40 ± 5K.

UV photodissociation of ethylamine cation: a combined experimental and theoretical investigation.

Direct current (DC) slice imaging of state-selected ions is combined with high-level ab initio calculations to give insight into reaction pathways, dynamics, and energetics for ethylamine cation photodissociation at 233 nm. These reaction pathways are of interest for understanding the rich chemistry of Titan's ionosphere recently revealed by the Cassini mission. The result for the H-loss product has a bimodal translational energy distribution, indicating two distinct H-loss pathways: these are assigned to triplet CH(3)CH(2)NH(+) product ions and the singlet CH(3)CHNH(2)(+) species.

Photodissociation of heptane isomers and relative ionization efficiencies of butyl and propyl radicals at 157 nm.

We report an ion imaging and time-of-flight mass spectroscopy study of the photodissociation of a variety of heptane isomers using 157 nm dissociation and ionization. Time-of-flight mass spectra show that C(3)H(7) + C(4)H(9) is the dominant detected product channel following one-color 157 nm dissociation/ionization of heptanes. The results further allow determination of the relative ionization efficiencies of 1- and 2-butyl and propyl radicals at 157 nm.