Iodine atoms

The most widely used reactions are those of electrophilic substitution, and under controlled conditions a maximum of three substituting groups, e.g. -NO2 (in the 1,3,5 positions) can be introduced by a nitric acid/sul-phuric acid mixture. Hot cone, sulphuric acid gives sulphonalion whilst halogens and a Lewis acid catalyst allow, e.g., chlorination or brom-ination. Other methods are required for introducing fluorine and iodine atoms. Benzene undergoes the Friedel-Crafts reaction. ... 

Although the transition to difhision control is satisfactorily described in such an approach, even for these apparently simple elementary reactions the situation in reality appears to be more complex due to the participation of weakly bonding or repulsive electronic states which may become increasingly coupled as the bath gas density increases. These processes manifest tliemselves in iodine atom and bromine atom recombination in some bath gases at high densities where marked deviations from TronnaF behaviour are observed [3, 4]. In particular, it is found that the transition from Lto is significantly broader than... 

The analysis of recent measurements of the density dependence of has shown, however, that considering only the variation of solvent structure in the vicinity of the atom pair as a fiinction of density is entirely sufficient to understand tire observed changes in with pressure and also with size of the solvent molecules [38]. Assuming that iodine atoms colliding with a solvent molecule of the first solvation shell under an angle a less than (the value of is solvent dependent and has to be found by simulations) are reflected back onto each other in the solvent cage, is given by... 

Resonant processes of some importance include resonant electronic to electronic energy transfer (E-E), such as the pumping process of the iodine atom laser... 

This technique with very high frequency resolution was used to study the population of different hyperfme structure levels of the iodine atom produced by the IR-laser-flash photolysis of organic iodides tluough multiphoton excitation ... 

Consequently, the reaction yield F in figure B2.5.15 is shown as a fiinction of the fluence, F. At the end of a laser-pulse sequence with a typical fluence F 3 J cm, practically 100% of the CF I is photolysed. As described in section B2.5.4.3. the product-level distribution of the iodine atoms fonned in this type of reaction can be detemiined... 

Figure B2.5.15. Iodine atom fonnation in the IR laser ehemistry of CF I (exeitation at 1074.65 em probe on the F = 4 —> F = 3 hyperfme stnieture transition, see figure B2.5.12.) (a) The absorbanee as a fiinetion of time (effeetive absorption eross seetion frill eiirve, left ordinate) shows elear steps at eaeh maximum of the mode loeked CO2 laser pulse sequenee (intensity, broken eurve, right ordinate), (b) The Ifaetion Fp of dissoeiating moleeules as a frinetion of fluenee F.

As an example, we mention the detection of iodine atoms in their P3/2 ground state with a 3 + 2 multiphoton ionization process at a laser wavelength of 474.3 run. Excited iodine atoms ( Pi/2) can also be detected selectively as the resonance condition is reached at a different laser wavelength of 477.7 run. As an example, figure B2.5.17 hows REMPI iodine atom detection after IR laser photolysis of CF I. This pump-probe experiment involves two, delayed, laser pulses, with a 200 ns IR photolysis pulse and a 10 ns probe pulse, which detects iodine atoms at different times during and after the photolysis pulse. This experiment illustrates a frindamental problem of product detection by multiphoton ionization with its high intensity, the short-wavelength probe laser radiation alone can photolyse the... 

Figure B2.5.17. (a) Time-dependent intensity / and redueed fluenee F/Fq for a single-mode CO2 laser pulse used in the IR laser photolysis of CF I. Fq is the total fluenee of the laser pulse, (b) VIS-REMPI iodine atom signals obtained with CO2 laser pulses of different fluenee (after [113]).

He Y, Pochert J, Quack M, Ranz R and Seyfang G 1995 Dynamics of unimolecular reactions induced by monochromatic infrared radiation experiment and theory for C F XI—> C F X + I probed with hyperfine-, Doppler- and uncertainty limited time resolution of iodine atom infrared absorption J. Chem. Soc. Faraday Discuss. 102 275-300... 

Iodine is a dark-coloured solid which has a glittering crystalline appearance. It is easily sublimed to form a bluish vapour in vacuo. but in air, the vapour is brownish-violet. Since it has a small vapour pressure at ordinary temperatures, iodine slowly sublimes if left in an open vessel for the same reason, iodine is best weighed in a stoppered bottle containing some potassium iodide solution, in which the iodine dissolves to form potassium tri-iodide. The vapour of iodine is composed of I2 molecules up to about 1000 K above this temperature, dissociation into iodine atoms becomes appreciable. 

It turns out that the CSP approximation dominates the full wavefunction, and is therefore almost exact till t 80 fs. This timescale is already very useful The first Rs 20 fs are sufficient to determine the photoadsorption lineshape and, as turns out, the first 80 fs are sufficient to determine the Resonance Raman spectrum of the system. Simple CSP is almost exact for these properties. As Fig. 3 shows, for later times the accuracy of the CSP decays quickly for t 500 fs in this system, the contribution of the CSP approximation to the full Cl wavefunction is almost negligible. In addition, this wavefunction is dominated not by a few specific terms of the Cl expansion, but by a whole host of configurations. The decay of the CSP approximation was found to be due to hard collisions between the iodine atoms and the surrounding wall of argons. Already the first hard collision brings a major deterioration of the CSP approximation, but also the role of the second collision can be clearly identified. As was mentioned, for t < 80 fs, the CSP... 

The iodine atom in iodobenzene (unlike that in the corresponding aliphatic compounds) is very resistant to the action of alkalis, potassium cyanide, silver nitrite, etc. This firm attachment of the iodine atom to the benzene ring is typical of aromatic halides generally, although in suitably substituted nitio-compounds, such as chloro-2,4-dinitrobenzene, the halogen atom does possess an increased reactivity (p. 262). 

Simple fragmentation of the molecular ion of iodobenzene gives a fragment ion, CjH,. The difference in measured masses between the molecular and fragment ions gives the mass of the ejected neutral iodine atom. 

The importance of ozone in the stratosphere has been stressed in Section 9.3.8. The fact that ozone can be decomposed by the halogen monoxides CIO, BrO and 10 means that their presence in the stratosphere contributes to the depletion of the ozone layer. For example, iodine, in the form of methyl iodide, is released into the atmosphere by marine algae and is readily photolysed, by radiation from the sun, to produce iodine atoms which can react with ozone to produce 10 ... 

However, because of the avoided crossing of the potential energy curves the wave functions of Vq and Fi are mixed, very strongly at r = 6.93 A and less strongly on either side. Consequently, when the wave packet reaches the high r limit of the vibrational level there is a chance that the wave function will take on sufficient of the character of Na + 1 that neutral sodium (or iodine) atoms may be detected. 

Unlike the situation regarding the crossing between the Vq and Fj potentials for Nal (see Figure 9.41), that for NaBr results in very efficient and rapid dissociation to give Na + Br when it is excited to Fj. Flow would you expect the fluorescence intensity from the neutral bromine atoms to vary with time compared with that for iodine atoms from Nal in Figure 9.42 ... 

Physical Properties. The absorption of x-rays by iodine has been studied and the iodine crystal stmcture deterrnined (12,13). Iodine crystallizes in the orthorhombic system and has a unit cell of eight atoms arranged as a symmetrical bipyramid. The cell constants at 18°C (14) are given in Table 1, along with other physical properties. Prom the interatomic distances of many iodine compounds, the calculated effective radius of the covalently bound iodine atom is 184 pm (15). 

Chemical Properties. The electron configuration of the iodine atom is [Kr]4d ° and its ground state is. Principal oxidation states... 

Iodine reacts with hydrocarbons to form iodine compounds, but compared to the other halogens, the equiUbria are unfavorable because the displacement step with the iodine atom is endothermic, requiring 4066.3 J (971.9 cal) for methane and 799.9 J (191.2 cal) for toluene. Hydrogen iodide can be used to reduce an alkah iodide to hydrocarbon plus molecular iodine. 

The steric bulk of the three iodine atoms in the 2,4,6-triiodoben2ene system and the amide nature of the 1,3,5-substituents yield rotational isomers of the 5-A/-acyl-substituted 2,4,6-triiodoisophthalamides. Rotational motion in the bonds connecting the side chains and the aromatic ring is restricted. These compounds also exhibit stereoisomerism when chiral carbon atoms are present on side chains. (R,5)-3-Amino-l,2-propanediol is incorporated in the synthesis of iohexol (11) and ioversol (12) and an (3)-2-hydroxypropanoyl group is used in the synthesis of iopamidol (10). Consequendy, the resulting products contain a mixture of stereoisomers, ie, meso-isomers, or an optical isomer. 

Cyclizations involving iodine-atom transfers have been developed. Among the most effective examples are reactions involving the cyclization of 6-iodohexene derivatives. The 6-hexenyl radical generated by iodine-atom abstraction rapidly cyclizes to a cyclo-pentylmethyl radical. The chain is propagated by iodine-atom transfer. 

No satisfactory explanation has been advanced for the reductive removal of one iodine atom. The di-iodination procedure does not appear to be useful with 3jS-hydroxy-A -steroids, but 3-keto-A systems do not interfere. 

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