𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The photolysis of NH3 in the presence of substituted acetylenes: A possible source of oligomers and HCN on Jupiter

✍ Scribed by James P. Ferris; Richard R. Jacobson; Jean Claude Guillemin


Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
503 KB
Volume
95
Category
Article
ISSN
0019-1035

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Ketone photolysis in the presence of oxy
✍ S. A. Carr; M. T. Baeza-Romero; M. A. Blitz; B. J. S. Price; P. W. Seakins 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 307 KB

## Abstract Previous studies have shown a significant OH yield from the reaction of RCO radicals (generated from the photolysis of corresponding ketone) with oxygen below total pressures of 200 Torr. The potential of these reactions as a source of OH radicals for flash photolytic kinetic studies is

00/03549 Influence of air-staging on the
📂 Article 📅 2000 🏛 Elsevier Science ⚖ 217 KB

08 Steam raising (boiler operation/design) compatible with the EU, Turow decided to, replace and upgrade six units (l-6) from 200 to 230 MW units and remove one unit 7. Units 8, 9 and 10 were equipped with dry sorbent desulfurization technology. Units 1 and 2 were replaced with new clean coal, circu

Micellar effects on a ligand substitutio
✍ Rafael Jiménez; Elena Bueno; Israel Cano; Elizabeth Corbacho; M. Eugenia Fernánd 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 96 KB 👁 2 views

## Abstract The kinetics of substitution of H~2~O by Ru(NH~3~)~5~pz^2+^ (pz = pyrazine) in Fe(CN)~5~H~2~O^3−^ have been studied in micellar aqueous solutions of sodium dodecylsulfate (SDS). Experimental results are discussed by using an approach based on the transition‐state theory. This approach i

Friedländer synthesis of poly-substitute
✍ Esmat Tavakolinejad Kermani; Hojatollah Khabazzadeh; Tayebeh Jazinizadeh 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 105 KB

## Abstract A rapid and an efficient method for the preparation of a variety of substituted quinolines has been developed through the reactions of __o__‐aminoarylketones with carbonyl compounds containing a reactive α‐methylene moiety in the presence of molten [Et~3~NH][HSO~4~] under solvent‐free c