𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The Recoil tritium labelling reaction as a function of tritium energy and molecular size

✍ Scribed by D. S. Urch; M. J. Welch; A. J. Johnston


Publisher
John Wiley and Sons
Year
1967
Tongue
French
Weight
322 KB
Volume
3
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Hydrocarbons can easily be labelled by recoil tritium atoms. Near the end of the recoil track, after the triton has been neutralised and whilst it still retains some excess translational energy, a tritium atom can replace hydrogen atoms in C-H bonds with high collision Cficiency. Results of studies on this reaction in hydrocarbons (ethylene, ethane, propylene, butane, n-pen fane and trans-butene-2) are analysed using the Estrup-Wolfgang method. It is found that the reactivity integral ( I ) for the labelling reaction increases with the size of the molecule labelled and that it is usually larger for an alkene than for the corresponding alkane. Furthermore, it is shown that the labelling reaction commences at relatively higher tritium atom energies as the size of the molecule is increased. The implications of these results for the formation of tracer amounts of tritium labelled hydrocarbons are discussed.


πŸ“œ SIMILAR VOLUMES


Tritium labelling of ribonuclease by the
✍ M. Noyer; A. G. Schnek; J. LΓ©onis; M. Winand πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 French βš– 386 KB

## Abstract When lyophilized samples of bovine pancreatic ribonuclease are exposed to tritium gas, the exchange process can be markedly improved by applying high frequency electric discharges. Labelling has been carried out for 5, 15 or 30 minutes periods. Labile radioactivity, was then removed by

Super high specific activity tritium lab
✍ Leyi Gong; Howard Parnes πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 French βš– 406 KB πŸ‘ 2 views

We describe herein the synthesis of polybromodiphenylacetic acid (&), a fragment common to the tritiation substrates (a) and (JJ) of the sodium channel blocker, PD-85639 (1) and the angiotensin II inhibitor EXP-655 (2) respectively. Preparation of (a) and (11) followed by reductive debromonation wit

The labelling with tritium of 2-(dimethy
✍ W. Hespe; W. Th. Nauta πŸ“‚ Article πŸ“… 1966 πŸ› John Wiley and Sons 🌐 French βš– 235 KB

Orphenadrine hydrochloride and a related ether were labelled with tritium in the 2-(dimethylamino)-ethyl moiety, by reduction of the corresponding amides with tritiated lithium aluminium hydride (yields 72 and 51 %, resp., specijic radioactivity .57,8 ni Clg in both cases). Hydrolysis of one of the