Near-UV photodissociation dynamics of CH2I2

被引:18
作者
Toulson, Benjamin W. [1 ]
Alaniz, Jonathan P. [1 ]
Hill, J. Grant [2 ]
Murray, Craig [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
关键词
ABSORPTION CROSS-SECTIONS; AUXILIARY BASIS-SETS; PHOTOFRAGMENT SPECTRA; CHEMISTRY; IODINE; GAS; DISSOCIATION; SPECTROSCOPY; PHOTOLYSIS; DEPENDENCE;
D O I
10.1039/c6cp01063f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The near-UV photodissociation dynamics of CH2I2 has been investigated using a combination of velocity-map (slice) ion imaging and ab initio calculations characterizing the excited states. Ground state I(P-2(3/2)) and spin-orbit excited I*(P-2(1/2)) atoms were probed using 2 + 1 resonance-enhanced multiphoton ionization (REMPI) or with single-photon VUV ionization. Two-color ion images were recorded at pump wavelengths of 355 nm, 266 nm and 248 nm, and one-color ion images at the REMPI wavelengths of similar to 304 nm and similar to 280 nm. Analysis of the ion images shows that, regardless of iodine spin-orbit state, similar to 20% of the available energy is partitioned into translation E-T at all excitation wavelengths indicating that the CH2I co-fragment is formed highly internally excited. The translational energy distributions comprise a slow, "statistical" component that peaks near zero and faster components that peak away from zero. The slow component makes an increasingly large contribution to the distribution as the excitation wavelength is decreased. The C-I bond dissociation energy of D-0 = 2.155 +/- 0.008 eV is obtained from the trend in the E-T release of the faster components with increasing excitation energy. The I and I* ion images are anisotropic, indicating prompt dissociation, and are characterized by beta parameters that become increasingly positive with increasing E-T. The decrease in beta at lower translational energies can be attributed to deviation from axial recoil. MRCI calculations including spin-orbit coupling have been performed to identify the overlapping features in the absorption spectrum and characterize one-dimensional cuts through the electronically excited potential energy surfaces. The excited states are of significantly mixed singlet and triplet character. At longer wavelengths, excitation directly accesses repulsive states primarily of B-1 symmetry, consistent with the observed <beta >, while shorter wavelengths accesses bound states, also of B-1 symmetry that are crossed by repulsive states.
引用
收藏
页码:11091 / 11103
页数:13
相关论文
共 50 条
  • [41] The near ultraviolet photodissociation dynamics of 2-and 3-substituted thiophenols: Geometric vs. electronic structure effects
    Marchetti, Barbara
    Karsili, Tolga N. V.
    Cipriani, Maicol
    Hansen, Christopher S.
    Ashfold, Michael N. R.
    JOURNAL OF CHEMICAL PHYSICS, 2017, 147 (01)
  • [42] Electronic state spectroscopy of diiodomethane (CH2I2): Experimental and computational studies in the 30 000-95 000 cm-1 region
    Mandal, Anuvab
    Singh, Param Jeet
    Shastri, Aparna
    Jagatap, B. N.
    JOURNAL OF CHEMICAL PHYSICS, 2014, 140 (19)
  • [43] Fate of transient isomer of CH2I2: Mechanism and origin of ionic photoproducts formation unveiled by time-resolved x-ray liquidography
    Park, Sungjun
    Choi, Jungkweon
    Ki, Hosung
    Kim, Kyung Hwan
    Oang, Key Young
    Roh, Heegwang
    Kim, Joonghan
    Nozawa, Shunsuke
    Sato, Tokushi
    Adachi, Shin-ichi
    Kim, Jeongho
    Ihee, Hyotcherl
    JOURNAL OF CHEMICAL PHYSICS, 2019, 150 (22)
  • [44] Photodissociation dynamics of C3H5I in the near-ultraviolet region
    Sumida, Masataka
    Hanada, Takuya
    Yamasaki, Katsuyoshi
    Kohguchi, Hiroshi
    JOURNAL OF CHEMICAL PHYSICS, 2014, 141 (10)
  • [45] Photodissociation dynamics of the A 2Σ+ state of SH and SD radicals
    Rose, R. A.
    Orr-Ewing, A. J.
    Yang, C.-H.
    Vidma, K.
    Groenenboom, G. C.
    Parker, D. H.
    JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (03)
  • [46] Infrared photodissociation of cold CH3+-He2 complexes
    Toepfer, Matthias
    Schmid, Philipp C.
    Kohguchi, Hiroshi
    Yamada, Koichi M. T.
    Schlemmer, Stephan
    Asvany, Oskar
    MOLECULAR PHYSICS, 2019, 117 (9-12) : 1481 - 1485
  • [47] Energy dependence of photodissociation dynamics of trimethylamine over the S2 and S1 excited states
    Onitsuka, Yuuki
    Kadowaki, Yuki
    Tamakubo, Atsuya
    Yamasaki, Katsuyoshi
    Kohguchi, Hiroshi
    CHEMICAL PHYSICS LETTERS, 2019, 716 : 28 - 34
  • [48] Exploring wavepacket dynamics behind strong-field momentum-dependent photodissociation in CH2BrI+
    Gonzalez-Vazquez, Jesus
    Gonzalez, Leticia
    Nichols, Sarah R.
    Weinacht, Thomas C.
    Rozgonyi, Tamas
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (42) : 14203 - 14216
  • [49] Communication: First observation of ground state I(2P3/2) atoms from the CH3I photodissociation in the B-band
    Gonzalez, M. G.
    Rodriguez, J. D.
    Rubio-Lago, L.
    Banares, L.
    JOURNAL OF CHEMICAL PHYSICS, 2011, 135 (02)
  • [50] MALDI mass spectrometry for probing the anti- staphylococcal capability of TiO2 nanoparticles via near-UV and laser irradiation
    Gopal, Judy
    Narayana, Jayaram Lakshmaiah
    Hasan, Nazim
    Wu, Hui-Fen
    NEW JOURNAL OF CHEMISTRY, 2015, 39 (06) : 4909 - 4918