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1.
Yang Xie Lan-lan Cao Qiang Zhang Jun Chen Gen-bai Chu Yu-jie Zhao Xiao-bin Shan Fu-yi Liu Liu-si Sheng 《化学物理学报(中文版)》2012,25(4):379-388
Vacuum ultraviolet photon-induced ionization and dissociation of isoleucine are investi-gated with synchrotron radiation photoionization mass spectroscopy and theoretical cal-culations. The main fragment ions at m/z=86, 75, 74, 69, 57, 46, 45, 44, 41, 30, 28, and 18 from isoleucine are observed in the mass spectrum at the photon energy of 13 eV. From the photoionization e±ciency curves, appearance energies for the principal fragment ions C5H12N+ (m/z=86)、C2H5NO4+ (m/z=75)、C5H9+ (m/z=69)、C4H9+(m/z=57), and CH4N+(m/z=30) are determined to be 8.84±0.07, 9.25±0.06, 10.20±0.12, 9.25±0.10, and 11.05±0.07 eV, respectively, and possible formation pathways are established in detail by the calculations at the B3LYP/6-31++G(d, p) levels. These proposed channels include simple bond cleavage reactions as well as reactions involving intermediates and transition structures. The experimental and computational appearance energies or barriers are in good agreement. 相似文献
2.
Photoionization and Dissociation Study of 2-Methyl-2-propen-1-ol: Experimental and Theoretical Insights
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Ye-peng Yu Zhao-hui Li Xuan Lin Jun Chen Hang Zhang Yan-bo Li Huang-huang Wang Rui-rui Sun Qing-hui Meng Xiao-bin Shan Fu-yi Liu Liu-si Sheng 《化学物理学报(中文版)》2019,32(3):306-312
The photoionization and dissociation of 2-methyl-2-propen-1-ol (MPO) have been investigated by using molecular beam experimental apparatus with tunable vacuum ultravioletsynchrotron radiation in the photon energy region of 8.0-15.5 eV. The photoionization efficiency (PIE) curves for molecule ion and fragment ions: C4H8O+、C4H7O+、C3H5O+、C4H7+、C4H6+、C4H5+、C2H4O+、C2H3O+、C3H6+、C3H5+、C3H3+、CH3O+、CHO+ have been measured, and the ionization energy (IE) and the appearance energies (AEs) of the fragment ions have been obtained. The stable species and the first order saddle points have been calculated on the CCSD(T)/cc-pvTZ//B3LYP/6-31+G(d,p) level. With combination of theoretical and experimental results, the dissociative photoionization pathways of 2-methyl-2-propen-1-ol are proposed. Hydrogen migrations within the molecule are the dominant processes in most of the fragmentation pathways of MPO. 相似文献
3.
VUV Photoionization and Dissociation of Tyramine and Dopamine: the Joint Experimental and Theoretical Studies
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Photon induced dissociation investigations of neutral tyramine and dopamine are carried out with synchrotron vacuum ultraviolet photoionization mass spectrometry and theoretical calculations. At low photon energy, only molecular ions are measured by virtue of near-threshold photoionization. While increasing photon energy to 11.7 eV or more, four distinct fragment ions are obtained for tyramine and dopamine, respectively. Besides, the ioniza-tion energies of tyramine and dopamine are determined to be 7.98±0.05 and 7.67±0.05 eV by measuring the photoionization efficiency curves of corresponding molecular ions. With help of density function theory calculations, the detailed fragmentation pathways are es-tablished as well. These two molecular cations have similar aminoethyl group elimination pathways, C7H8O2+·(m/z=124) and C7H8O+·(m/z=108) are supposed to be generated by the McLafferty rearrangement via γ-hydrogen (γ-H) shift inducing β-fission. And CH2NH2+ is proposed to derive from the direct fission of C7-C8 bond. Besides, the McLafferty rear-rangement and the C7-C8 bond fission are validated to be dominant dissociation pathways for tyramine and dopamine cations. 相似文献
4.
5.
Qiao Ma Ming-qiang Huang Xian-yun Liu Yan-bo Gai Xiao-xiao Lin Cheng-qiang Yang Liu-si Sheng Xiao-bin Shan Wei-jun Zhang 《化学物理学报(中文版)》2017,30(1):43-49
Theoretical calculations have been carried out to investigate the possible dissociation channels of isoprene. We focus on the major fragment ions of C5H7+,C5H5+,C4H5+,C3H6+,C3H5+,C3H4+,C3H3+ and C2H3+, which were observed experimentally from the isoprene dissociative photoionization. The energy calculations were performed with the CBS-QB3 model. All the geometries and energies of the fragments, intermediates and transition states involved in the dissociations channels were determined. Finally, the mechanisms of the dissociation pathways were discussed on the comparison of theoretical and experimental results. 相似文献
6.
Jun Chen Maoqi Cao Bin Wei Mengmeng Ding Xiaobin Shan Fuyi Liu Liusi Sheng 《Journal of mass spectrometry : JMS》2016,51(2):169-181
In this work, photoionization and dissociation of cyclohexene have been studied by means of coupling a reflectron time‐of‐flight mass spectrometer with the tunable vacuum ultraviolet (VUV) synchrotron radiation. The adiabatic ionization energy of cyclohexene as well as the appearance energies of its fragment ions C6H9+, C6H7+, C5H7+, C5H5+, C4H6+, C4H5+, C3H5+ and C3H3+ were derived from the onset of the photoionization efficiency (PIE) curves. The optimized structures for the transition states and intermediates on the ground state potential energy surfaces related to photodissociation of cyclohexene were characterized at the ωB97X‐D/6‐31+g(d,p) level. The coupled cluster method, CCSD(T)/cc‐pVTZ, was employed to calculate the corresponding energies with the zero‐point energy corrections by the ωB97X‐D/6‐31+g(d,p) approach. Combining experimental and theoretical results, possible formation pathways of the fragment ions were proposed and discussed in detail. The retro‐Cope rearrangement was found to play a crucial role in the formation of C4H6+, C4H5+ and C3H5+. Intramolecular hydrogen migrations were observed as dominant processes in most of the fragmentation pathways of cyclohexene. The present research provides a clear picture of the photoionization and dissociation processes of cyclohexene in the 8‐ to 15.5‐eV photon energy region. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
7.
Ming Wang Jun Chen Wei-fei Fei Zhao-hui Li Ye-peng Yu Xuan Lin Xiao-bin Shan Fu-yi Liu Liu-si Sheng 《化学物理学报(中文版)》2017,30(4):379-388
The photoionization and photodissociation of 1,4-dioxane have been investigated with a reflectron time-of-flight photoionization mass spectrometry and a tunable vacuum ultraviolet synchrotron radiation in the energy region of 8.0-15.5 eV. Parent ion and fragment ions at m/z 88, 87, 58, 57, 45, 44, 43, 41, 31, 30, 29, 28 and 15 are detected under supersonic conditions. The ionization energy of DX as well as the appearance energies of its fragment ions C4H7O2+, C3H6O+, C3H5O+, C2H5O+, C2H4O+, C2H3O+, C3H5+, CH3O+, C2H6+, C2H5+/CHO+, C2H4+ and CH3+ was determined from their photoionization efficiency curves. The optimized structures for the neutrals, cations, transition states and intermediates related to photodissociation of DX are characterized at the B3LYP/6-31+G(d,p) level and their energies are obtained by G3B3 method. Possible dissociative channels of the DX are proposed based on comparison of experimental AE values and theoretical predicted ones. Intramolecular hydrogen migrations are found to be the dominant processes in most of the fragmentation pathways of 1,4-dioxane. 相似文献
8.
G. Vall-llosera M. Coreno P. Erman M.A. Huels K. Jakubowska A. Kivimki E. Rachlew M. Stankiewicz 《International journal of mass spectrometry》2008,275(1-3):55-63
Photoionisation mass spectrometry was used to obtain the fragmentation pathways of pyridine, pyridazine, pyrimidine, pyrazine and s-triazine molecules upon absorption of 23.0, 15.7 and 13.8 eV synchrotron photons. The ionic fragments observed vary from molecule to molecule, however C2H2+, HCN+and HCNH+ are common to all five molecules at the three photon energies. Furthermore, the presence of C2H2N2+, C3H3N+ and C4H4+ in the spectra of some of the molecules suggests dissociation pathways via loss of HCN moieties. The respective parent cations, m/q=79, 80 and 81 have a greater yield at low photon energies when compared to the most intense fragment peak in each spectra. We recorded two of the fragment cation yields, as well as the parent photoion yield curves of pyridine, pyridazine, and pyrimidine in the 8–30 eV range. The formation of abundant cation fragments show a strong propensity of the molecules for dissociation after the absorption of VUV photons higher than 14 eV. The differences in relative fragment yields from molecule to molecule, and when changing the excitation energy, suggest significant bond rearrangements and nuclear motion during the dissociation time. Thus, bond cleavage is dependent on the photon energy deposited in the molecule and on intramolecular reactivity. With the aid of photoion yield curves and energy estimations we have assigned major peaks in the spectra and discussed their fragmentation pathways. 相似文献
9.
Yu-jie Zhao You-sheng Zhan Li Li Xin Li Xiang-yu Lian Pei Huang Liu-si Sheng Jun Chen 《化学物理学报(中文版)》2017,30(3):303-311
The photoionization and dissociation photoionization of toluene have been studied using quantum chemistry methods.The geometries and frequencies of the reactants,transition states and products have been performed at B3LYP/6-311++G (d,p) level,and single-point energy calculations for all the stationary points were carried out at DFT calculations of the optimized structures with the G3B3 level.The ionization energies of toluene and the appearance energies for major fragment ions,C7H7+,C6H5+,C5H6+,C5H5+,are determined to be 8.90,11.15 or 11.03,12.72,13.69,16.28 eV,respectively,which are all in good agreement with published experimental data.With the help of available published experimental data and theoretical results,four dissociative photoionization channels have been proposed:C7H7++H,C6H5++CH3,C5H6++C2H2,C5H5++C2H2+H.Transition structures and intermediates for those isomerization processes are determined in this work.Especially,the structures of C5H6+ and C5H5+ produced by dissociative photoionization of toluene have been defined as chain structure in this work with theoretical calculations. 相似文献
10.
Xianyun Liu Weijun Zhang Zhenya Wang Mingqiang Huang Xibin Yang Ling Tao Yue Sun Yuntao Xu Xiaobin Shan Fuyi Liu Liusi Sheng 《Journal of mass spectrometry : JMS》2009,44(3):404-409
Vacuum ultraviolet (VUV) dissociative photoionization of isoprene in the energy region 8.5–18 eV was investigated with photoionization mass spectroscopy (PIMS) using synchrotron radiation (SR). The ionization energy (IE) of isoprene as well as the appearance energies (AEs) of its fragment ions C5H7+, C5H5+, C4H5+, C3H6+, C3H5+, C3H4+, C3H3+ and C2H3+ were determined with photoionization efficiency (PIE) curves. The dissociation energies of some possible dissociation channels to produce those fragment ions were also determined experimentally. The total energies of C5H8 and its main fragments were calculated using the Gaussian 03 program and the Gaussian‐2 method. The IE of C5H8, the AEs for its fragment ions, and the dissociation energies to produce them were predicted using the high‐accuracy energy model. According to our results, the experimental dissociation energies were in reasonable agreement with the calculated values of the proposed photodissociation channels of C5H8. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
11.
Gemma Vall‐llosera Michael A. Huels Prof. Dr. Marcello Coreno Dr. Antti Kivimäki Dr. Katarzyna Jakubowska Marek Stankiewicz Prof. Dr. Elisabeth Rachlew Prof. Dr. 《Chemphyschem》2008,9(7):1020-1029
We have measured the synchrotron‐induced photofragmentation of isolated 2‐deoxy‐D ‐ribose molecules (C5H10O4) at four photon energies, namely, 23.0, 15.7, 14.6, and 13.8 eV. At all photon energies above the molecule′s ionization threshold we observe the formation of a large variety of molecular cation fragments, including CH3+, OH+, H3O+, C2H3+, C2H4+, CHxO+ (x=1,2,3), C2HxO+ (x=1–5), C3HxO+ (x=3–5), C2H4O2+, C3HxO2+ (x=1,2,4–6), C4H5O2+, C4HxO3+ (x=6,7), C5H7O3+, and C5H8O3+. The formation of these fragments shows a strong propensity of the DNA sugar to dissociate upon absorption of vacuum ultraviolet photons. The yields of particular fragments at various excitation photon energies in the range between 10 and 28 eV are also measured and their appearance thresholds determined. At all photon energies, the most intense relative yield is recorded for the m/q=57 fragment (C3H5O+), whereas a general intensity decrease is observed for all other fragments— relative to the m/q=57 fragment—with decreasing excitation energy. Thus, bond cleavage depends on the photon energy deposited in the molecule. All fragments up to m/q=75 are observed at all photon energies above their respective threshold values. Most notably, several fragmentation products, for example, CH3+, H3O+, C2H4+, CH3O+, and C2H5O+, involve significant bond rearrangements and nuclear motion during the dissociation time. Multibond fragmentation of the sugar moiety in the sugar–phosphate backbone of DNA results in complex strand lesions and, most likely, in subsequent reactions of the neutral or charged fragments with the surrounding DNA molecules. 相似文献
12.
Huanhuan Wang Mingqiang Huang Hao Chen Xiaobin Shan Zhenya Wang Fuyi Liu Liusi Sheng 《Journal of mass spectrometry : JMS》2023,58(8):e4967
This study employed a vacuum ultraviolet synchrotron radiation source and reflectron time-of-flight mass spectrometry (TOF-MS) to investigate the photoionization and dissociation of styrene. By analyzing the photoionization mass spectrum and efficiency curve alongside G3B3 theoretical calculations, we determined the ionization energy of the molecular ion, appearance energy of fragment ions, and relevant dissociation pathways. The major ion peaks observed in the photoionization mass spectra of styrene correspond to C8H8+, C8H7+ and C6H6+. The ionization energy of styrene is measured as 8.46 ± 0.03 eV, whereas the appearance energies of C8H7+ and C6H6+ are found to be 12.42 ± 0.03 and 12.22 ± 0.03 eV, respectively, in agreement with theoretical values. The main channel for the photodissociation of styrene molecular ions is the formation of benzene ions, whereas the dissociation channel that loses hydrogen atoms is the secondary channel. Based on the experimental results and empirical formulas, the required dissociation energies (Ed) of C8H7+, C8H6+ and C6H6+ are calculated to be (3.96 ± 0.06), (4.00 ± 0.06) and (3.76 ± 0.06) eV, respectively. Combined with related thermochemical parameters, the standard enthalpies of formations of C8H8+, C8H7+, C8H6+ and C6H6+ are determined to be 964.2, 1346.3, 1350.2 and 1327.0 kJ/mol, respectively. Based on the theoretical study, the kinetic factors controlling the styrene dissociation reaction process are determined by using the Rice–Ramsperger–Kassel–Marcus (RRKM) theory. This provides a reference for further research on the atmospheric photooxidation reaction mechanism of styrene in atmospheric and interstellar environments. 相似文献
13.
The dissociative photoionization of molecular‐beam cooled CH2CO in a region of ?10–20 eV was investigated with photoionization mass spectrometry using a synchrotron radiation as the light source. Photoionization efficiency curves of CH2CO+ and of observed fragment ions CH2+, CHCO+, HCO+, C2O+, CO+, and C2H2+ were measured to determine their appearance energies. Relative branching ratios as a function of photon energy were determined. Energies for formation of these observed fragment ions and their neutral counterparts upon ionization of CH2CO are computed with the Gaussian‐3 method. Dissociative photoionization channels associated with six observed fragment ions are proposed based on comparison of determined appearance energies and predicted energies. The principal dissociative processes are direct breaking of C=C and C‐H bonds to form CH2+ + CO and CHCO+ + H, respectively; at greater energies, dissociation involving H migration takes place. 相似文献
14.
Agata Biaoska Zbigniew Ciunik 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):o182-o185
Comparison of the structures of strychninium N‐phthaloyl‐β‐alaninate N‐phthaloyl‐β‐alanine, C21H23N2O2+·C11H8NO4−·C11H9NO4, and brucinium N‐phthaloyl‐β‐alaninate 5.67‐hydrate, C23H27N2O4+·C11H8NO4−·5.67H2O, reveals that, unlike strychninium cations, brucinium cations display a tendency to produce stacking interactions with cocrystallizing guests. 相似文献
15.
Magorzata Katarzyna Cabaj Roman Gajda Anna Hoser Anna Makal Paulina Maria Dominiak 《Acta Crystallographica. Section C, Structural Chemistry》2019,75(8):1036-1044
Crystals of hypoxanthinium (6‐oxo‐1H,7H‐purin‐9‐ium) nitrate hydrates were investigated by means of X‐ray diffraction at different temperatures. The data for hypoxanthinium nitrate monohydrate (C5H5N4O+·NO3?·H2O, Hx1 ) were collected at 20, 105 and 285 K. The room‐temperature phase was reported previously [Schmalle et al. (1990). Acta Cryst. C 46 , 340–342] and the low‐temperature phase has not been investigated yet. The structure underwent a phase transition, which resulted in a change of space group from Pmnb to P21/n at lower temperature and subsequently in nonmerohedral twinning. The structure of hypoxanthinium dinitrate trihydrate (H3O+·C5H5N4O+·2NO3?·2H2O, Hx2 ) was determined at 20 and 100 K, and also has not been reported previously. The Hx2 structure consists of two types of layers: the `hypoxanthinium nitrate monohydrate' layers (HX) observed in Hx1 and layers of Zundel complex H3O+·H2O interacting with nitrate anions (OX). The crystal can be considered as a solid solution of two salts, i.e. hypoxanthinium nitrate monohydrate, C5H5N4O+·NO3?·H2O, and oxonium nitrate monohydrate, H3O+(H2O)·NO3?. 相似文献
16.
Matteo Lanza W. Joe Acton Simone Jürschik Philipp Sulzer Kostiantyn Breiev Alfons Jordan Eugen Hartungen Gernot Hanel Lukas Märk Chris A. Mayhew Tilmann D. Märk 《Journal of mass spectrometry : JMS》2013,48(9):1015-1018
The isomers 4‐methylethcathinone and N‐ethylbuphedrone are substitutes for the recently banned drug mephedrone. We find that with conventional proton transfer reaction mass spectrometry (PTR‐MS), it is not possible to distinguish between these two isomers, because essentially for both substances, only the protonated molecules are observed at a mass‐to‐charge ratio of 192 (C12H18NO+). However, when utilising an advanced PTR‐MS instrument that allows us to switch the reagent ions (selective reagent ionisation) from H3O+ (which is commonly used in PTR‐MS) to NO+, O2+ and Kr+, characteristic product (fragment) ions are detected: C4H10N+ (72 Da) for 4‐methylethcathinone and C5H12N+ (86 Da) for N‐ethylbuphedrone; thus, selective reagent ionisation MS proves to be a powerful tool for fast detection and identification of these compounds. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
17.
Akiyoshi Hishikawa Atsushi Iwamae Kennosuke Hoshina Mitsuhiko Kono Kaoru Yamanouchi 《Research on Chemical Intermediates》1998,24(7):765-784
The Coulomb explosion process of N2O in an intense laser-field (∼5 PW/cm2) has been investigated by the high-resolution time-of-flight (TOF) spectroscopy. Six two-body explosion pathways involving
the NO+, NO2+, N2
+ molecular ions have been securely identified from the momentum-scaled TOF spectra of the fragment ions. Assuming a linear
geometry, three-body explosion pathways were investigated by sequential and concerted explosion models. When the concerted model is adopted, the observed momentum distributions of six atomic ion channels; N+, N2+, N3+, O+, O2+ and O3+, were well fitted using the Gaussian momentum distribution with the optimized bond elongation factor of 2.2(3). From the
yields of individual Coulomb explosion pathways determined by the fit, the abundance of the parent ions, N2Oz+ (z=2–8), prior to the two- body and three-body explosion processes was found to have a smooth distribution with a maximum
at z∼3. 相似文献
18.
In continuation of our studies in the new area of multiple photon laser dissociation of ions, we report evidence for the sequential two photon dissociation of cyanobenzene radical cation, C6H5CN+, to produce predominantly C6H+4 and HCN. The complete excitation function for this process, as well as for a single photon process occurring at higher energies, are compared to the photoelectron spectrum of cyanobenzene to elucidate the nature of the transitions involved. An exact kinetic expression is derived and used to obtain information about the absorption spectra of C6H5CN+ in its ground vibronic state and with internal energy between 2.0 and 2.8 eV. Finally, data from our earlier study of benzene radical cation is reanalyzed and discussed. 相似文献
19.
Daisuke Hashizume Masataka Iegaki Masanori Yasui Fujiko Iwasaki Jiben Meng Zhong Wen Teruo Matsuura 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(9):1067-1072
Five two‐component molecular crystals, benzimidazolium 3‐nitrobenzoate, C7H7N2+·C7H4NO4?, (I), benzimidazolium 4‐nitrobenzoate, C7H7N2+·C7H4NO4?, (II), 1H‐benzotriazole–3‐nitrobenzoic acid (1/1), C6H5N3·C7H5NO4, (III), imidazolium 3‐nitrobenzoate, C3H5N2+·C7H4NO4?, (IV), and imidazolium 4‐nitrobenzoate, C3H5N2+·C7H4NO4?, (V), were prepared with the aim of making chiral crystals. Only (I) crystallizes in a chiral space group. The molecules of (I) and (II) are linked by hydrogen bonds to form 21 spiral chains. In (III), (IV) and (V), macrocyclic structures are formed from two acid and two base components, by an alternate arrangement of the acid and base moieties. 相似文献
20.
Graham Smith Urs D. Wermuth Jonathan M. White 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(8):o575-o581
The crystal structures of quinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate trihydrate, C9H8N+·C7H5O6S−·3H2O, (I), 8‐hydroxyquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate monohydrate, C9H8NO+·C7H5O6S−·H2O, (II), 8‐aminoquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate dihydrate, C9H9N2+·C7H5O6S−·2H2O, (III), and 2‐carboxyquinolinium 3‐carboxy‐4‐hydroxybenzenesulfonate quinolinium‐2‐carboxylate, C10H8NO2+·C7H5O6S−·C10H7NO2, (IV), four proton‐transfer compounds of 5‐sulfosalicylic acid with bicyclic heteroaromatic Lewis bases, reveal in each the presence of variously hydrogen‐bonded polymers. In only one of these compounds, viz. (II), is the protonated quinolinium group involved in a direct primary N+—H⋯O(sulfonate) hydrogen‐bonding interaction, while in the other hydrates, viz. (I) and (III), the water molecules participate in the primary intermediate interaction. The quinaldic acid (quinoline‐2‐carboxylic acid) adduct, (IV), exhibits cation–cation and anion–adduct hydrogen bonding but no direct formal heteromolecular interaction other than a number of weak cation–anion and cation–adduct π–π stacking associations. In all other compounds, secondary interactions give rise to network polymer structures. 相似文献