Atom transfer, direct

Zhang J, Grills DC, Huang K-W, Fujita E, Bullock RM. (2005) Carbon-to-metal hydrogen atom transfer Direct observation using time-resolved infrared spectroscopy. /Hot Chem Soc 127 15684-15685. 

The above scheme includes the formation of the oxoiron(IV) porphyrin cation radical via 0-atom transfer from PhIO within an intermediate complex. The double bond approaches from the side and parallel to the porphyrin ring. This geometry is clearly favorable for the cis-olefins. The epoxidation step consists in oxygen atom transfer directly from the oxoiron(IV) to the olefin within an intermediate that has been detected with mCPBA as oxidant [46]. According to... 

In 159 and 163-166 the tertiary amine function is coordinated to the boron atom and transmits the electronic change due to the ester formation to the chromophore. In 160-162 the boron atom is directly connected to the chromophore. After the complexation of the saccharide, the change of the charge transfer, e.g., for 159 [249-251], or the fluorescence bands, e.g., for 160-166 [252-255], can be measured and interpreted. The most selective binding of n-glucose has been achieved with host 164 that forms a 1 1 complex with a macrocyclic structure (Scheme 1). 

The fact that the cyclization is directed toward an acetylenic group and leads to formation of an alkenyl radical is significant. Formation of a saturated iodide could lead to a more complex product mixture because the cyclized product could undergo iodine atom transfer and proceed to add to a second unsaturated center. Vinyl iodides are much less reactive and the reaction product is unreactive. Owing to the potential... 

Methylmalonyl-CoA mutase (MCM) catalyzes a radical-based transformation of methylmalonyl-CoA (MCA) to succinyl-CoA. The cofactor adenosylcobalamin (AdoCbl) serves as a radical reservoir that generates the S -deoxyadenosine radical (dAdo ) via homolysis of the Co—C5 bond [67], The mechanisms by which the enzyme stabilizes the homolysis products and achieve an observed 1012-fold rate acceleration are yet not fully understood. Co—C bond homolysis is directly kineti-cally coupled to the proceeding hydrogen atom transfer step and the products of the bond homolysis step have therefore not been experimentally characterized. 

There is also the rather famous experiment known as 2D INADEQUATE (Incredible Natural Abundance DoublE QUAntum Transfer Experiment) which allows us to correlate carbon-13 with carbon-13. Potentially this experiment is very useful, since it allows us to see directly which carbon atoms are directly bonded. However, you will remember that the natural abundance of carbon-13 is only 1.1%, so a carbon-13/carbon-13 correlation requires us to detect only about 0.01% of the carbon nuclei present. Thus the experiment is very insensitive and requires large amounts of both sample and measuring... 

A hanging mercury drop electrodeposition technique has been used [297] for a carbon filament flameless atomic absorption spectrometric method for the determination of copper in seawater. In this method, copper is transferred to the mercury drop in a simple three-electrode cell (including a counterelectrode) by electrolysis for 30 min at -0.35 V versus the SCE. After electrolysis, the drop is rinsed and transferred directly to a prepositioned water-cooled carbon-filament atomiser, and the mercury is volatilised by heating the filament to 425 °C. Copper is then atomised and determined by atomic absorption. The detection limit is 0.2 pg copper per litre simulated seawater. 

The epoxidation of electron-deficient alkenes, particularly a,P-unsaturated carbonyl compounds, continues to generate much activity in the literature, and this has been the subject of a recent concise review <00CC1215>. Additional current contributions in this area include a novel epoxidation of enones via direct oxygen atom transfer from hypervalent oxido-).3-iodanes (38), a process which proceeds in fair to good yields and with complete retention of... 

All the examples presented under Sect. 4.1 used an iodine atom transfer to generate the desired radicals. Another approach involving abstraction of hydrogen atom is also reported. For instance, ethers and acetals undergo direct intermolecular addition to aldehydes under treatment with Et3B/air... 

There have been numerous kinetic studies of the deuterium isotope effect for proton and hydrogen atom transfer where values for EH — Ev greatly exceed 1.4kcal/mol and the ratio of A factors, AD/AH, are significantly >1.4 values >10 are very common [4]. These observations directly challenge the classical model for proton transfer based upon transition state theory that neglects contributions from k. 

DR. NORTON (Colorado State University) As a novice in this field, something that is starting to worry me about metallic systems is the difficulty of distinguishing between an orthodox proton transfer as opposed to an electron transfer followed by hydrogen atom transfer in the reverse direction. Is this ever a problem in the kinds of more classical systems you have been describing ... 

Perhaps the most interesting of the inner-sphere pathways are those which result in the net transfer of an oxygen atom. The factors governing the viability of this pathway are still speculative. For cobalt-02 adducts, thermochemical considerations suggest that oxygen atom transfer should be accompanied by electron transfer in the reverse direction. Similarly, this pathway should be enhanced for MO2 complexes in which the metal... 

We have attempted to find conditions which will allow us to watch the species build up, to isolate it kinetically, and to observe its reactions directly. That does not imply that the intermediate is unreactive. The remarkable feature of the intermediate in your rhenium system is the apparently facile oxygen atom transfer. 

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