Energy transfer of highly vibrationally excited molecules studied by crossed molecular beam/time-sliced velocity map ion imaging

Energy transfer of highly vibrationally excited molecules has been studied extensively under bulk conditions in the past 40 years. On the other hand, in 1973 Fisk and co-workers reported the first experimental results of collisional energy transfer of highly vibrationally excited KBr using cross-molecular beams. Surprisingly, it is the only crossed molecular beam experiment about the energy transfer of highly vibrationally excited molecules. No other similar crossed molecular beam experiments have been reported in the following four decades. Recently we have studied the energy transfer of highly vibrationally excited molecules using crossed molecular beams/time-of-flight mass spectrometer in combination with time-sliced velocity map ion imaging techniques. Energy transfer probability density functions were accurately obtained and details of energy transfer mechanisms were evidenced from the cross-molecular beam scatterings. This paper reviews our recent work of energy transfer of highly vibrationally excited molecules. The effects of long-lived complex, initial translational energy, initial rotational temperature, vibrational motions, alkylation, attractive potential and electronic state on the energy transfer and supercollisions were discussed, and comparisons to theoretical calculations and experiments conducted under bulk conditions were made.

[1]  H. Dai,et al.  Nanosecond time-resolved FTIR emission spectroscopy: Monitoring the energy distribution of highly vibrationally excited molecules during collisional deactivation , 1998 .

[2]  J. Barker,et al.  Isotope effects in the vibrational deactivation of large molecules , 1992 .

[3]  B. Rabinovitch,et al.  Intermolecular vibrational energy transfer in thermal unimolecular systems , 1977 .

[4]  J. Barker,et al.  Deactivation of highly excited CS2 and SO2 by rare gases , 1998 .

[5]  G. Hartland,et al.  Collisional deactivation of highly vibrationally excited NO2 monitored by time‐resolved Fourier transform infrared emission spectroscopy , 1994 .

[6]  Energy transfer between polyatomic molecules. 3. Energy transfer quantities and probability density functions in self-collisions of benzene, toluene, p-xylene and azulene. , 2006, The journal of physical chemistry. A.

[7]  I. Oref,et al.  Energy transfer between polyatomic molecules II: Energy transfer quantities and probability density functions in benzene, toluene, p-xylene, and azulene collisions. , 2006, The journal of physical chemistry. A.

[8]  Mark C. Wall,et al.  Unraveling the energy dependence in large ΔE (V→RT) energy transfer: Separation of ΔE and probability in the collisional relaxation of highly vibrationally excited pyrazine (Evib=36 000 to 41 000 cm−1) by CO2 , 1999 .

[9]  K. Yoshihara,et al.  Laser flash photolysis of benzene. VIII. Formation of hot benzene from the S2 state and its collisional deactivation , 1983 .

[10]  H. Hippler Direct Observations of Energy Transfer of Vibrationally Highly Excited Triatomic and Large Polyatomic Molecules , 1985 .

[11]  I. Oref,et al.  Collisional energy transfer between Ar and normal and vibrationally and rotationally frozen internally excited benzene-trajectory calculations , 1997 .

[12]  G. Flynn,et al.  Some rotations like it hot: selective energy partitioning in the state resolved dynamics of collisions between CO2 and highly vibrationally excited pyrazine , 1993 .

[13]  C. Parmenter,et al.  Collisional Flow of Vibrational Energy into Surrounding Vibrational Fields within S1 p-Difluorobenzene. Rate Constants for Initial Levels with High Vibrational Excitation , 1995 .

[14]  G. Flynn,et al.  Translational and rotational excitation of the CO2(0000) vibrationless state in the collisional quenching of highly vibrationally excited 2-methylpyrazine: Kinetics and dynamics of large energy transfers , 2000 .

[15]  G. Flynn,et al.  Classical Trajectory Study of Energy Transfer in Pyrazine−CO Collisions† , 2001 .

[16]  J. Barker,et al.  Energy dependence of infrared emission from azulene C–H stretching vibrations , 1988 .

[17]  I. Oref,et al.  Energy transfer between azulene and krypton: comparison between experiment and computation. , 2006, The Journal of chemical physics.

[18]  K. Luther,et al.  Collisional energy transfer probabilities of highly excited molecules from kinetically controlled selective ionization (KCSI). I. The KCSI technique: Experimental approach for the determination of P(E′,E) in the quasicontinuous energy range. , 2000 .

[19]  C. Steel,et al.  Collisional activation of quadricyclane by azulene: An example of very strong collisions , 1988 .

[20]  G. Hartland,et al.  Collisional energy transfer of highly vibrationally excited NO2: The role of intramolecular vibronic coupling and the transition dipole coupling mechanism , 1997 .

[21]  D. Schwarzer,et al.  Multiplex detection of collisional energy transfer using KCSFI. , 2005, Physical chemistry chemical physics : PCCP.

[22]  J. Barker,et al.  Energy‐dependent collisional deactivation of vibrationally excited azulene , 1988 .

[23]  C. Ni,et al.  Alkylation effects on the energy transfer of highly vibrationally excited naphthalene. , 2011, Chemistry, an Asian journal.

[24]  I. Oref,et al.  Energy transfer between polyatomic molecules. 1. Gateway modes, energy transfer quantities and energy transfer probability density functions in benzene-benzene and Ar-benzene collisions. , 2005, Journal of Physical Chemistry B.

[25]  A. Suits,et al.  Pyrazine: Supercollisions or simple reactions? , 1995 .

[26]  Competition between Photochemistry and Energy Transfer in Ultraviolet-Excited Diazabenzenes. 3. Photofragmentation and Collisional Quenching in Mixtures of 2-Methylpyrazine and Carbon Dioxide † , 2000 .

[27]  G. Hartland,et al.  Intramolecular electronic coupling enhanced collisional deactivation of highly vibrationally excited molecules , 1995 .

[28]  Juan Du,et al.  Energy-dependent dynamics of large-DeltaE collisions: highly vibrationally excited azulene (E=20 390 and 38 580 cm(-1)) with CO2. , 2008, The Journal of chemical physics.

[29]  Kieran F. Lim,et al.  TEMPORAL DEPENDENCE OF COLLISIONAL ENERGY TRANSFER BY QUASICLASSICAL TRAJECTORY CALCULATIONS OF THE TOLUENE-ARGON SYSTEM , 1995 .

[30]  G. Flynn,et al.  Connecting quantum state resolved scattering data directly to chemical kinetics: Energy transfer distribution functions for the collisional relaxation of highly vibrationally excited molecules from state resolved probes of the bath , 1997 .

[31]  H. C. Tapalian,et al.  Competition between photochemistry and energy transfer in ultraviolet-excited diazabenzenes. II. Identifying the dominant energy donor for “supercollisions” , 2000 .

[32]  D. Coker,et al.  Trajectory study of supercollision relaxation in highly vibrationally excited pyrazine and CO2. , 2005, The journal of physical chemistry. A.

[33]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[34]  Han,et al.  Collision relaxation cross section of highly vibrationally excited molecules , 2000, Physical Review Letters.

[35]  Michael S. Elioff,et al.  State-Resolved Studies of Collisional Quenching of Highly Vibrationally Excited Pyrazine by Water: The Case of the Missing V → RT Supercollision Channel , 1998 .

[36]  C. Ni,et al.  Energy transfer of highly vibrationally excited biphenyl. , 2010, The Journal of chemical physics.

[37]  C. Ni,et al.  Energy transfer of highly vibrationally excited naphthalene: collisions with CHF3, CF4, and Kr. , 2011, The Journal of chemical physics.

[38]  J. Barker,et al.  Energy‐dependent energy transfer: Deactivation of azulene (S0, Evib) by 17 collider gases , 1983 .

[39]  Jeunghee Park,et al.  Methylation effects in state-resolved quenching of highly vibrationally excited azabenzenes (Evib∼38 500 cm−1). II. Collisions with carbon dioxide , 2001 .

[40]  M. Matzen,et al.  A classical trajectory study of inelastic collisions between highly vibrationally excited KBr and Ar , 1977 .

[41]  J. Troe,et al.  Collisional deactivation of vibrationally highly excited polyatomic molecules. II. Direct observations for excited toluene , 1983 .

[42]  Jeunghee Park,et al.  Methylation effects on the collisional quenching of vibrationally excited benzene derivatives by unexcited parent molecules , 2000 .

[43]  C. Ni,et al.  Supercollisions and energy transfer of highly vibrationally excited molecules. , 2005, The Journal of chemical physics.

[44]  G. Flynn,et al.  Competition between photochemistry and energy transfer in ultraviolet-excited diazabenzenes. I. Photofragmentation studies of pyrazine at 248 nm and 266 nm , 2000 .

[45]  J. Barker,et al.  Vibrational relaxation of highly excited toluene , 1991 .

[46]  J. Troe,et al.  Collisional deactivation of vibrationally highly excited polyatomic molecules. IV. Temperature dependence of 〈ΔE〉. , 1984 .

[47]  G. Hartland,et al.  Observation of large vibration‐to‐vibration energy transfer collisions (ΔE≳3500 cm−1) in quenching of highly excited NO2 by CO2 and N2O , 1994 .

[48]  E. Korobkova,et al.  State-resolved collisional quenching of vibrationally excited pyrazine (E(vib) = 37,900 cm(-1)) by D35Cl(v = 0). , 2005, The Journal of chemical physics.

[49]  K. Luther,et al.  Collisional energy transfer probabilities of highly excited molecules from KCSI. III. Azulene: P(E′,E) and moments of energy transfer for energies up to 40 000 cm−1 via self-calibrating experiments , 2003 .

[50]  C. Ni,et al.  Energy transfer of highly vibrationally excited phenanthrene and diphenylacetylene. , 2011, Physical chemistry chemical physics : PCCP.

[51]  J. Troe,et al.  Direct observation of collisional deactivation of highly excited toluene , 1981 .

[52]  Svante Arrhenius,et al.  Discussion on “the radiation theory of chemical action” , 1922 .

[53]  C. Ni,et al.  Energy transfer of highly vibrationally excited naphthalene. II. Vibrational energy dependence and isotope and mass effects. , 2008, The Journal of chemical physics.

[54]  C. Ni,et al.  Time-sliced ion imaging study of I2 and I2+ photolysis at 532 nm. , 2005, Physical chemistry chemical physics : PCCP.

[55]  Mark C. Wall,et al.  “Supercollision” energy dependence: State-resolved energy transfer in collisions between highly vibrationally excited pyrazine (Evib=37 900 cm−1 and 40 900 cm−1) and CO2 , 1998 .

[56]  B. Stewart,et al.  State-resolved collisional relaxation of highly vibrationally excited pyridine by CO2: Influence of a permanent dipole moment , 1998 .

[57]  J. Barker,et al.  Collisional deactivation of highly vibrationally excited pyrazine , 1996 .

[58]  J. Erinjeri,et al.  Population distributions in the vibrational deactivation of benzene and benzene-d6. First and second moments derived from two-color infrared fluorescence measurements , 1993 .

[59]  Michael S. Elioff,et al.  Vibrational Energy Gain in the ν2 Bending Mode of Water via Collisions with Hot Pyrazine (Evib = 37900 cm-1): Insights into the Dynamics of Energy Flow† , 2000 .

[60]  K. Tang,et al.  The collisional flow of vibrational energy into surrounding vibrational fields within S1 benzene , 1983 .

[61]  M. Chou,et al.  Inelastic scattering of vibrationally excited KBr by small polar molecules , 1973 .

[62]  D. Havey,et al.  Full state-resolved energy gain profiles of CO2 (J = 2-80) from collisions of highly vibrationally excited molecules. 1. Relaxation of pyrazine (E = 37900 cm(-1)). , 2010, Journal of Physical Chemistry A.

[63]  R. Gilbert,et al.  Supercollision events in weak collisional energy transfer of highly excited species , 1991 .

[64]  K. Luther,et al.  Collisional energy transfer of highly vibrationally excited toluene and pyrazine: Transition probabilities and relaxation pathways from KCSI experiments and trajectory calculations. , 2001 .

[65]  J. Barker,et al.  Collisional deactivation of highly vibrationally excited benzene pumped at 248 nm , 1990 .

[66]  J. Troe,et al.  Direct study of energy transfer of vibrationally highly excited CS2 molecules , 1985 .

[67]  C. Ni,et al.  Energy transfer of highly vibrationally excited naphthalene. III. Rotational effects. , 2008, The Journal of chemical physics.

[68]  R. Weisman,et al.  Vibrational relaxation of T1 pyrazine: Results from the refined competitive radiationless decay method , 1998 .

[69]  J. Barker,et al.  Vibrationally excited populations from IR-multiphoton absorption. III: Energy transfer between 1,1,2-trifluoroethane and argon , 1986 .

[70]  C. Ni,et al.  Energy transfer of highly vibrationally excited naphthalene. I. Translational collision energy dependence. , 2007, The Journal of chemical physics.

[71]  J. Barker,et al.  Memory effects during collisional energy transfer from highly excited CS2 , 1996 .

[72]  D. Havey,et al.  Effects of alkylation on deviations from Lennard-Jones collision rates for highly excited aromatic molecules: collisions of methylated pyridines with HOD. , 2009, The journal of physical chemistry. A.

[73]  J. Barker,et al.  Time dependent thermal lensing measurements of V–T energy transfer from highly excited NO2 , 1990 .

[74]  I. Oref,et al.  Differential cross-sections and energy transfer quantities in azulene/argon collisions , 2008 .

[75]  C. Ni,et al.  Energy transfer of highly vibrationally excited 2-methylnaphthalene: Methylation effects. , 2008, The Journal of chemical physics.

[76]  C. Ni,et al.  Experimental and computational investigation of energy transfer between azulene and krypton , 2006 .

[77]  K. Luther,et al.  Collisional energy transfer probabilities of highly excited molecules from kinetically controlled selective ionization (KCSI). II. The collisional relaxation of toluene: P(E′,E) and moments of energy transfer for energies up to 50 000 cm−1 , 2000 .

[78]  J. Barker,et al.  Excitation of CO2 by energy transfer from highly vibrationally excited benzene derivatives , 1991 .

[79]  K. Luther,et al.  Multiphoton Ionization Studies of Energy Transfer in Highly Excited Ground State Molecules , 1988 .

[80]  C. Ni,et al.  Generation and characterization of highly vibrationally excited molecular beam. , 2006, The Journal of chemical physics.

[81]  D. Clary,et al.  Mechanisms for supercollisions , 1995 .

[82]  G. Flynn,et al.  The collisional deactivation of highly vibrationally excited pyrazine by a bath of carbon dioxide: Excitation of the infrared inactive (1000),(0200), and (0220) bath vibrational modes , 1998 .

[83]  J. Troe,et al.  Ultraviolet spectra of vibrationally highly excited CS2 molecules , 1984 .

[84]  J. D. Lambert Vibrational and Rotational Relaxation in Gases , 1978 .

[85]  J. Troe,et al.  Measurement of internal energies by hot ultraviolet absorption spectroscopy: spectra of excited azulene molecules , 1985 .

[86]  A. Lemoff,et al.  Observation of an energy threshold for large ΔE collisional relaxation of highly vibrationally excited pyrazine (Evib=31 000–41 000 cm−1) by CO2 , 1999 .

[87]  M. Chou,et al.  Inelastic scattering of vibrationally excited KBr by small nonpolar and essentially nonpolar partners , 1973 .

[88]  C. Ni,et al.  Energy transfer of highly vibrationally excited azulene. III. Collisions between azulene and argon. , 2006, The Journal of chemical physics.

[89]  F. Crim,et al.  Single collision studies of vibrational energy transfer mechanisms , 1977 .

[90]  T. Ichimura,et al.  Collisional deactivation of highly vibrationally excited hexafluorobenzene molecules , 1987 .

[91]  A. Linhananta,et al.  Quasiclassical trajectory calculations of collisional energy transfer in propane systems: Multiple direct-encounter hard-sphere model , 2002 .

[92]  Jeunghee Park,et al.  Collisional quenching of vibrationally excited methyl-substituted pyrazine and pyridine series by CO2 , 2001 .

[93]  K. Yoshihara,et al.  ArF laser flash photolysis of hexafluorobenzene vapor: Formation of hot molecules and their collisional relaxation , 1985 .

[94]  J. Barker,et al.  Energy transfer rates for vibrationally excited gas-phase azulene in the electronic ground state , 1981 .

[95]  Jeunghee Park,et al.  The steric hindrance of methyl groups in collisional quenching of highly vibrationally excited methyl-substituted pyrazines by He, Ar, and Kr , 2001 .

[96]  J. Barker,et al.  Vibrationally excited populations from IR‐multiphoton absorption. I. Absorbed energy and reaction yield measurements , 1985 .

[97]  A. Linhananta,et al.  Quasiclassical trajectory calculations of collisional energy transfer in propane systems , 2000 .

[98]  H. C. Tapalian,et al.  Translational and rotational excitation of the CO2(0000) vibrationless state in the collisional quenching of highly vibrationally excited perfluorobenzene: Evidence for impulsive collisions accompanied by large energy transfers , 1997 .

[99]  I. Oref,et al.  Trajectory calculations of relative center of mass velocities in collisions between Ar and toluene , 1996 .

[100]  A. Mebel,et al.  Photodissociation of azulene at 193 nm: ab initio and RRKM study. , 2005, The journal of physical chemistry. A.

[101]  Michael S. Elioff,et al.  State-resolved collisional quenching of highly vibrationally excited pyridine by water: The role of strong electrostatic attraction in V→RT energy transfer , 1999 .

[102]  J. Troe,et al.  Unimolecular processes in vibrationally highly excited cycloheptatrienes. II. Steady‐state photoisomerization , 1979 .

[103]  C. Steel,et al.  Collisional activation of cyclobutene by hexafluorobenzene: A chemical probe for highly energetic collisions in reactive systems , 1989 .

[104]  Collisional Energy Transfer between Hot Pyrazine and Cold CO: A Classical Trajectory Study † , 2004 .

[105]  Faraday Discuss , 1985 .

[106]  A. Mebel,et al.  Acetylene Elimination in Photodissociation of Neutral Azulene and Its Cation: An Ab Initio and RRKM Study , 2006 .

[107]  R. Weisman,et al.  Efficient collisional vibrational relaxation of triplet state molecules: Pyrazine deuteration and methylation effects , 1999 .

[108]  J. Troe,et al.  Collisional deactivation of vibrationally highly excited polyatomic molecules. III. Direct observations for substituted cycloheptatrienes , 1983 .

[109]  C. Ni,et al.  Energy transfer of highly vibrationally excited azulene. II. Photodissociation of azulene-Kr van der Waals clusters at 248 and 266 nm. , 2006, The Journal of chemical physics.

[110]  J. Barker,et al.  Temperature effects in the collisional deactivation of highly vibrationally excited pyrazine by unexcited pyrazine , 1996 .

[111]  J. Barker,et al.  Vibrationally excited populations from IR‐multiphoton absorption. II. Infrared fluorescence measurements , 1985 .

[112]  J. Troe,et al.  Unimolecular processes in vibrationally highly excited cycloheptatrienes. III. Direct k (E) measurements after laser excitation , 1983 .

[113]  J. Troe,et al.  Direct observation of excited-state dynamics by hot UV absorption spectroscopy after IR multiphoton excitation , 1985 .

[114]  J. Troe,et al.  Collisional energy transfer of vibrationally highly excited molecules. V. UV absorption study of azulene , 1985 .

[115]  J. Troe,et al.  Falloff curves of the recombination reaction O + SO + M .fwdarw. SO2 + M in a variety of bath gases , 1985 .