ChemInform Abstract: Measurement of Relative Product Yields from the Photolysis of Dichlorine Monoxide (Cl2O).

ChemInform ◽  
2010 ◽  
Vol 32 (50) ◽  
pp. no-no
Author(s):  
Geoffrey D. Smith ◽  
Francisco M. G. Tablas ◽  
Luisa T. Molina ◽  
Mario J. Molina
Keyword(s):  
Product Yields ◽  
Relative Product ◽  
Dichlorine Monoxide

Measurement of Relative Product Yields from the Photolysis of Dichlorine Monoxide (Cl2O)

2001 ◽  
Vol 105 (38) ◽  
pp. 8658-8664 ◽  
Author(s):  
Geoffrey D. Smith ◽  
Francisco M. G. Tablas ◽  
Luisa T. Molina ◽  
Mario J. Molina
Keyword(s):  
Product Yields ◽  
Relative Product ◽  
Dichlorine Monoxide

Relative product yields in the one-photon and vibrationally mediated photolysis of isocyanic acid (HNCO)

2001 ◽  
Vol 114 (24) ◽  
pp. 10835-10844 ◽  
Author(s):  
H. Laine Berghout ◽  
Shizuka Hsieh ◽  
F. Fleming Crim
Keyword(s):  
Isocyanic Acid ◽  
Product Yields ◽  
Relative Product ◽  
The One

Two-color coherent control with SEP preparation: electronic branching in Na2 photodissociation

1994 ◽  
Vol 72 (3) ◽  
pp. 958-965 ◽  
Author(s):  
Jeffrey Dods ◽  
Paul Brumer ◽  
Moshe Shapiro
Keyword(s):  
Coherent Control ◽  
Four Wave Mixing ◽  
Stimulated Emission ◽  
Wave Mixing ◽  
Superposition State ◽  
Product Yields ◽  
Relative Product ◽  
Laser Frequencies

Extensive control over relative product yields is shown to result from weak laser photodissociation in a two-color coherent control scenario. Photodissociation takes place from a superposition state prepared by stimulated emission pumping. The method allows for control in the presence of laser phase jumps by using four-wave mixing to prepare the required laser frequencies. The near UV photodissociation of Na2, resulting in the Na(3s) + Na(4s) and the Na(3s) + Na(3d) products, is used to illustrate the method.

Mechanism of initiation in the thermal polymerization of styrene. Thermal decomposition of cis-3,6-diphenyl-3,4,5,6-tetrahydropyridazine

1969 ◽  
Vol 47 (21) ◽  
pp. 4041-4048 ◽  
Author(s):  
Karl R. Kopecky ◽  
Syamalarao Evani
Keyword(s):  
Thermal Decomposition ◽  
Thermal Polymerization ◽  
Radical Intermediate ◽  
Styrene Polymerization ◽  
Product Yields ◽  
Thermal Initiation ◽  
Temperature Range ◽  
Relative Product

Thermal decomposition of cis-3,6-diphenyl-3,4,5,6-tetrahydropyridazine, 1, (k = 5.6 × 10−4s−1 at 79.5°) results in the formation of about 60% styrene, 27% cis- and 13% trans-1,2-diphenylcyclobutane. The relative product yields vary little over the temperature range 64–133°. This indicates that 1 decomposes exclusively to the 1,4-diphenyl-1,4-butadiyl diradical, 2, and nitrogen. The diradical, 2, cannot be trapped by styrene and 1 is not an initiator of styrene polymerization. Therefore, 2 is not the radical intermediate responsible for the thermal initiation of styrene polymerization.

Fission product yields at intermediate energy

1998 ◽  
Author(s):  
V. A. Rubchenya ◽  
J. Äystö ◽  
P. Dendooven ◽  
S. Hankonen ◽  
A. Jokinen ◽  
...  
Keyword(s):  
Fission Product ◽  
Intermediate Energy ◽  
Product Yields ◽  
Fission Product Yields

Amino acid derived CuII compounds as catalysts for asymmetric oxidative coupling of 2-naphthol

2015 ◽  
Vol 44 (4) ◽  
pp. 1612-1626 ◽  
Author(s):  
Pedro Adão ◽  
Sónia Barroso ◽  
M. Fernanda N. N. Carvalho ◽  
Carlos M. Teixeira ◽  
Maxim L. Kuznetsov ◽  
...  
Keyword(s):  
Amino Acid ◽  
Oxidative Coupling ◽  
Product Yields ◽  
Aqueous Conditions

Several chiral amino acid-derived CuII complexes were prepared and used as catalysts in the aerobic oxidative coupling of 2-naphthol. Moderate homocoupling product yields and enantiomeric excesses were obtained under mild, aqueous conditions.

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