Photodissociation of acetylene at 193.3 nm
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- Type
- article
- Published
- 1985-05-21
- Cited by
- 209
- References
- 0
- OpenAlex
- https://openalex.org/W1964077285
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:93461589
Keywords
Citation, Altmetrics, Computer science, Acetylene, Information retrieval
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Cited by
- Photodissociation dynamics of acetylene via the C (1)Pi(u) electronic state.
- Observation of a new 11Δu ← B1Δg transition of C2
- Photodissociation of 1,2-C2H2Br2 at 248 nm: Competition between three-body formation Br+Br+C2H2 and molecular Br2 elimination
- Branching ratios of C2 products in the photodissociation of C2H at 193 nm
- Shock Tube and Modeling Study of Ignition of Acetylene
- Probing chemical dynamics with negative ions.
- Incertitudes photochimiques dans les modèles de l'atmosphère de Titan : Revue et conséquences
- Structure and reactivity of transition metal clusters
- An experimental and theoretical study of the reaction of ethynyl radicals with nitrogen dioxide (HC≡C+NO2)
- The 193 nm photodissociation of CH2=CClF
- Photodissociation of C2H at 193 nm: Branching ratios for the formation of C2 in the X 1Σg+, A 1Πu, and B′ 1Σg+ states
- Relaxation of individual rotational levels of the electronic state of acetylene excited to the 2ν3′ and (ν1′+ν3′+ν6′) vibrational modes
- Thermodynamic properties of linear carbon chain molecules with conjugated triple bonds
- Untangling the chemical evolution of Titan's atmosphere and surface--from homogeneous to heterogeneous chemistry.
- Photodissociation of acetylene: Determination of D00 (HCC–H) by photofragment imaging
- Photodissociation of CH2Br2, 1,1- and 1,2-C2H4Br2 at 248 nm: A simple C–Br bond fission versus a concerted three-body formation
- The Ã-X̃ band system of C2D2: Vibration-rotation constants for the Ã1Au state
- A concerted three-body formation X+Y+C2H4 in the photodissociation of CH2XCH2Y (X,Y=Br,Cl) at 193 nm.
- Two-Photon Spectroscopy of Acetylene - Photodissociation Processes at 9-10 eV Energy Levels
- Photofragment emission yield spectroscopy of acetylene in the D̃ 1Πu, Ẽ 1A, and F̃ 1Σu+ states by vacuum ultraviolet and infrared vacuum ultraviolet double-resonance laser excitations
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