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Iodine systems

To illustrate how the use of standard potentials may occasionally lead to erroneous conclusions, consider the hexacyanoferrate(II)-hexacyano-ferrate(III) and the iodide-iodine systems. The standard potentials are ... [Pg.364]

There is an absence of cis-to-trans isomerization with conversion or time for the C8 (1,5-cyclooctadiene) polymer. This is shown from 52 to 58% conversion after 1 to 16 hours reaction time in Table II and III. The above review (A0, A2, A3, A5) shows that the cis structure in polymers from 1,5-cyclooctadiene using various chloride catalysts fell below 50% cis even to 20% cis units this means that the second cis double bond from the monomer underwent extensive cis-to-trans isomerization following the ring-opening of the first cis bond. Where cis-2-butene isomerizes to trans structure using other catalyst preparations, there is no evidence of this for cis-2-butene using the iodine system. However, polymer molecular... [Pg.162]

The luminol reaction has also been used for the CL determination of organic substances such as penicillins [32] and tartrate ion [30] in pharmaceutical preparations by their inhibitory effect on the luminol-iodine and luminol-periodate-manganese(II)-TEA system, respectively. As can be seen from Table 1, the results were quite satisfactory. In the indirect determination of penicillins by their inhibitory effect on the luminol-iodine system, the stopped-flow technique improves the accuracy and precision of the analytical information obtained, and also the sample throughput [32], Thus, in only 2-3 s one can obtain the whole CL signal-versus-time profile and calculate the three measured parameters formation and... [Pg.186]

Utilizing Eqs. (34) to (39) in Eq. (33), the potential energy surface for the iodide ion-iodine system as a function of distance x from the electrode and the normalized solvent coordinate qig was determined as given in Fig. 15 as a contour plot. It is observed that far from the electrode surface, the ionic and the atomic states are separated by an energy barrier... [Pg.101]

Li2S204 being the SEI component at the Li anode and the solid discharge product at the carbon cathode. The Li—SOCI2 and Li—SO2 systems have excellent operational characteristics in a temperature range from —40 to 60 °C (SOCI2) or 80 °C (SO2). Typical applications are military, security, transponder, and car electronics. Primary lithium cells have also various medical uses. The lithium—silver—vanadium oxide system finds application in heart defibrillators. The lithium—iodine system with a lithium iodide solid electrolyte is the preferred pacemaker cell. [Pg.18]

P. H. Svensson and L. Kloo, Synthesis, structure and bonding in polyiodide and metal iodide-iodine systems, Chem. Rev., 2003, 103, 1649. [Pg.5]

Indeed, when using ( )/( ) couples, mass transport limitations are evident from the lack of linearity of the photocurrent versus incident power plots (Fig. 17.33) in the presence of a spacer, the photocurrent density produced by the cobalt-mediated cell is very close to the iodide/iodine system at low irradiation intensities (0.018 and... [Pg.558]

The silver(I) fluoride/iodine system was used successfully in the synthesis of the naturally occurring fluorine-containing antibiotic nucleocidin.54... [Pg.243]

The silver(I) fluoride/bromine and silver(I) fluoride/iodine systems can be exploited for generation in situ and electrophilic addition of "bromine monofluoride and iodine monofluoride to cyclohexene, mcthylenecyclohcxane, styrene, indene, and acenaphthylene.55... [Pg.243]

A. H. Zewail The observation of coherent motion in the benzene-iodine system should be related to the l2 motion and hopefully with better time resolution we should be able to resolve it. As for the base-pair experiment, the key motion is that of the N N stretch and N—H asymmetric motions, and our time scale of observation was appropriate for the dynamics to be observed. [Pg.85]

Another popular promoter for glycosylation with thioglycosides is the reagent dimethyl(methylthio)sulfonium triflate (DMTST).60 A comparison between DMTST and NIS/TfOH for the formation of sialoglycoconjugates demonstrated that the iodine system provided superior yields and anomeric selectivity in nearly all cases.61 The yields and stereoselectivity also increased with an increase in solvent polarity, suggesting that enhanced stabilization of the oxacarbenium intermediate, the rate-limiting step in glycosylation, was responsible for the increased... [Pg.17]

It is worth noting that, like SS NMR spectroscopy and likely for the same reasons, little work has been performed on iodine systems in solution. However, preliminary work in our own group has demonstrated that it is possible to use I NMR spectroscopy for kinetic measurements. [Pg.74]

Some redox systems have been developed for certain polymers. The copper/iodine system is well established for polyamide thermal stabilization, and in spite of introducing a heavy metal ion into the polymer, works well in an oxygen-free environment.83 84... [Pg.35]

On the contrary, the pyridinium chlorochromate-iodine system which is a very effective oxidant of silylenol ethers failed with enamines66. [Pg.944]

As in bromine and iodine systems, chlorine atoms bind chloride as in reaction 15. [Pg.79]

The use of Moriarty s hypervalent iodine system vide supra) has been extended to reaction with silyl enol ethers. In this case a more activated electrophile is required and the reactions are carried out with iodosylbenzene in the pres ice of boron trifluoiide etherate. However, yields are only moderate and the process seems less useful than the corresponding ketone/enol application. [Pg.166]

The classical work of Eley and collaborators described the vinyl ethers-iodine systems as being characterised by the parallel complexation of the monomer by the catalyst and initiation due to the attack of I onto the double bond. It was on this mechanistic basis that Okamura et applied their scheme to calculate propagation rate constants in 1,2-dichloroethane and -hexane. A criticism of that method has already been given in the previous section and the low values of kp obtained in this study prove that the gross approximations implicit in the method, mainly the neglect of the iodine bound to the polymer, introduce large errors in the estimate of the rate constants. [Pg.83]

Direct excitation of electron-transfer states may yield surprising results. This is the case with the bimolecular benzene iodine charge-transfer complex. In solutions this system is the prototypical case of charge transfer as reported by Mulliken [262]. The characteristic 280 nm absorption band of the benzene-iodine system is distinct from any absorption features of neat iodine or benzene. It has been identified as being due to a promotion of the HOMO benzene n electron to a a LUMO orbital on iodine resulting in benzene iodine electron transfer. [Pg.3046]

Nucleophilic Attack at Halogen. This field of activity continues to be dominated by applications of well-known phosphine-positive halogen combinations. Alcohols can be oxidised to the related aldehydes and ketones under mild conditions by the DMSO-Ph3PX2 system, which provides an alternative to the Swern oxidation." The triphenylphosphine-iodine system has been... [Pg.46]

Fig. 9.1 Infrared absorption spectra of dimethylacctamide-iodine system (1) dimethylaceta-mide only (2-6) increasing concentrations of iodine. Peak at 1662 cm is from free di-mcihylacetaniide. that at 1619 cm" is from the DMA L adduct. (From Schmulbach, C. D. Diago, R. S. J. Am. Clu iii. Soc. I960, 82. 4484. Reproduced with permission.]... Fig. 9.1 Infrared absorption spectra of dimethylacctamide-iodine system (1) dimethylaceta-mide only (2-6) increasing concentrations of iodine. Peak at 1662 cm is from free di-mcihylacetaniide. that at 1619 cm" is from the DMA L adduct. (From Schmulbach, C. D. Diago, R. S. J. Am. Clu iii. Soc. I960, 82. 4484. Reproduced with permission.]...
Conjugate reduction. Conjugated dienamides undergo regioselective reduction with the borohydride iodine system in THF at 0° at one of the double bonds, forming y,5-unsaturated amides. [Pg.346]

Many of the bromine and iodine systems listed in the Tables 20 and 21 were studied due to their practical use for metal halide lamps [438]. Particularly important for such lamps are the systems Nal-Scl3, Nal-Snij, and Nal-Dyl3 on account of the radiation emitted by the elements Na, Sc, and Dy. [Pg.175]

Devices based on electrochemical phenomena represent a multimillion-dollar market annually for health care (15). Applications are probably most important in the sphere of population well-being. For example, experience with heart pacemakers shows that the typical use is for those in the 60- to 80-year age bracket who will lead a relatively active and normal life and have a "statistically average" life expectancy with the assistance of a pacemaker. Without this device, the person would be debilitated and have a life expectancy of only 1 to 2 years. The current market for pacemakers is estimated at nearly 300,000 per year worldwide, about half that in the United States (15). With a battery cost on the order of 100 for an implanted pacemaker, the dollar value ranges from 15 to 30 million for the batteries alone (predominantly lithium-iodine systems). The total cost associated with implanting pacemakers is a hundred times greater. [Pg.43]

Acetic add has been produced by the carbonylation of methanol for a very long time, with the earliest industrial development dating back to 1925 (British Celanese. BASF Badische Anilin und Soda Fabrik J, and is based on the use of catalysts containing phosphoric add and copper phosphate. The development of cobait/iodine systems led to... [Pg.52]


See other pages where Iodine systems is mentioned: [Pg.533]    [Pg.535]    [Pg.537]    [Pg.367]    [Pg.404]    [Pg.249]    [Pg.187]    [Pg.185]    [Pg.187]    [Pg.15]    [Pg.290]    [Pg.107]    [Pg.161]    [Pg.886]    [Pg.94]    [Pg.416]    [Pg.112]    [Pg.20]    [Pg.533]    [Pg.535]    [Pg.537]   
See also in sourсe #XX -- [ Pg.315 , Pg.453 ]




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Iodine in biological systems

Iodine initiating system

System carbon tetrachloride-iodine

Tandem Catalytic Systems Involving Hypervalent Iodine and other Co-catalysts

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