✦ LIBER ✦

The kinetics of the reactions of 2,6-di-t-butyl-4-methylphenol and 2,4,6-trimethylphenol with nitrogen dioxide in solution

✍ Scribed by Robert G. Coombes; Andrew W. Diggle; Stewart P. Kempsell

Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 208 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)84442-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

15N-labelling studies of the reaction of

15N-labelling studies of the reaction of 2,6-di-t-butyl-4-methyl-4-nitrocyclohexa-2,5-dienone with nitrogen dioxide; A revised mechanism

✍ Michael P. Hartshorn; Richard G. Jensen; A.Grant Waller; Graeme J. Wright 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 241 KB

16 h gives the 4,5,6-trinitro ketone (2), labelled (15N02) at C6 but not at C4, and recovered 4-nitrodienone (1) in which extensive loss of 15N02 has occurred. The mechanistic implications of these and related results are discussed. Reaction Of 2,6-di-t-butyl-4-methylphenol (3) with excess nitrogen

The kinetics of disproportionation of th

The kinetics of disproportionation of the 2,6-di-t-butyl-4-methyl phenoxy radical

✍ R. Stebbins; F. Sicilio 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 467 KB

Reaction of 2,6-di-t-butyl-4-propionylph

Reaction of 2,6-di-t-butyl-4-propionylphenoxy radical with ethyl ferulate.

✍ G. Brunow; T. Ilus 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 90 KB

Synthesis of new functionalized mono- an

Synthesis of new functionalized mono- and bisphosphinates with 2,6-di-tert-butyl-4-methylphenol fragments

✍ Andrey A. Prishchenko; Mikhail V. Livantsov; Olga P. Novikova; Ludmila I. Livant 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 111 KB 👁 1 views

## Abstract Convenient procedures for the synthesis of functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol (ionol) fragments, starting from the available 3,5‐di‐tert‐butyl‐4‐benzaldehyde and its derivatives, are proposed, and some properties of the new phosphorus‐substitu

Photo-oxidation of 2,4,6-trimethylphenol

Photo-oxidation of 2,4,6-trimethylphenol in aqueous laboratory solutions and natural waters: kinetics of reaction with singlet oxygen

✍ Paul G. Tratnyek; Jürg Hoigné 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 757 KB

The role of dopant geometry in the photo

The role of dopant geometry in the photoinduced formation of radical pairs in crystals of 2,6-di-tert-butyl-4-methylphenol and 2,6-di-tert-butylphenol

✍ Georgii G. Lazarev; Vladimir L. Kuskov; Francisco Lara; Federico García; Anton R 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 550 KB

Radical pairs are formed by photolysis of single crystals of 2,6-di-tert-butyl-4-methylphenol (ionol) (1) or 2,6-di-tert-butylphenol (2 ), doped by several different molecules, and investigated by the EPR method. A possible two-hydrogen-atom transfer is discussed as the photochemical act.