Graphite reaction with

Montoya et al. [90] found that density function theory (DFT) is even better than the Hartree-Fock method in modeling graphite reactions with gases, as the former can effectively overcome spin contamination. In a follow-up study... 

Other means of forming biaryl derivatives include the use of zinc/silver-graphite reaction with aryl and heteroaryl (including thiophenyl) iodides... 

The reactions with water are summarised in Table 6.3. Since the metals are powerful reducing agents (p. 98) they cannot be prepared in aqueous solution electrolysis of the fused anhydrous halides is usually employed using a graphite anode. 

Eurther heat treatment in excess of 2000°C is referred to as graphitization. Eiber stmcture further densifies as molecular packing and orientation increase. At temperatures of 3000°C or above, the fiber stmcture begins to approach a truly graphitic stmcture with three-dimensional order. Typically, fiber strain to failure decreases as the carbonization temperature exceeds 1500°C because of reaction of impurities with the carbon fiber and the development of an increasingly flaw-sensitive graphitic stmcture (31,34)... 

The reaction with 4-nitrophenol and pentafluorophenol in the presence of KF-18-crown-6 has been investigated. Pentafluorophenoxide anion was found to be a better leaving group [82JFC(20)439]. Alkali metal fluorides on graphite can act as catalysts for nucleophilic substitution of pentafluor-opyridine [90JFC(46)57]. 

Apart from reactions with the electrolyte at the carbon surface, the irreversible specific charge is furthermore strongly affected by the possible co-intercalation of polar solvent molecules between the graphene layers of highly graphitic matrices [139]. This so-called "solvated intercalation reaction" depends (i) on the crystallinity and the morphology of the parent carbonaceous material, which will be discussed in Sec. 

Non-Kolbe electrolysis of alicyclic p-hydroxy carboxylic acids offers interesting applications for the one-carbon ring extension of cyclic ketones (Eq. 35) [242c]. The starting compounds are easily available by Reformatsky reaction with cyclic ketones. Some examples are summarized in Table 13. Dimethylformamide as solvent and graphite as anode material appear to be optimal for this reaction. 

In another study (Ji8), it was found that graphite does not intercalate with neat XeF2 or with solutions of XeFa in acetonitrile. However, reaction with solutions of XeF2 in AHF led to copious xenon evolution, indicating that oxidation does take place, even at room temperature. Broad-line, F- and H-NMR spectra (Ell) showed the presence of both XeF2 and HF in the product, but no definite stoichiometry could be as-... 

Hexafluorides run the gamut of reactions with graphite, from no intercalation except in the presence of a catalyst (WFg), through intercalation with partial reduction (UFg), to intercalation with complete reduction (OsFg). 

The second analytical method uses a combustion system (O Neil et al. 1994) in place of reaction with BrF,. This method was used for the crocodiles because they were represented by very thin caps of enamel. The enamel was powdered and sieved (20 mg), pretreated in NaOCl to oxidize organic material and then precipitated as silver phosphate. Approximately 10-20 mg of silver phosphate were mixed with powdered graphite in quartz tubes, evacuated and sealed. Combustion at 1,200°C was followed by rapid cooling in water which prevents isotopic fractionation between the CO2 produced and the residual solid in the tube. Analyses of separate aliquots from the same sample typically showed precisions of 0.1%o to 0.4%o with 2 to 4 repetitive analyses even though yields are on the order of 25%. 

It should be noted here, that not only the (chemical and morphological) composition of the protective layers at the basal plane surfaces and prismatic surfaces is different, but that these layers also have completely different functions. At the prismatic surfaces, lithium ion transport into/ffom the graphite structure takes place by intercalation/de-intercalation. Here the formed protective layers of electrolyte decomposition products have to act as SEI, i.e., as transport medium for lithium cations. Those protective layers, which have been formed on/at the basal plane surfaces, where no lithium ion transport into/from the graphite structure takes place, have no SEI function. However, these non-SEI layers still protect these anode sites from further reduction reactions with the electrolyte. 

SEM representative images of the surface treated natural graphite SLC-1015 and its untreated precursor SL-20 are shown by Figure 1. The graphite particles with the rounded edges having less active sites tend to limit the reaction on its surfaces and thus improve its cycling performance and safety. 

The successive step in sample preparation is graphitization. Several different reactions can be used. The most well known is probably the iron-catalysed reduction of the collected C02 by reaction with hydrogen [71]... 

The hetero-DA reaction with azadienes, a well known synthetic method for obtaining nitrogen heterocycles, suffers from some difficulties, because of the low reactivity of the diene. For example, azadiene 2 did not react with DMAD under the action of conventional heating [22], Sequential exposure to MW irradiation (30 W) for 10 min on a graphite support (Tmax = 171 °C) led to the adduct 7 with 60% conversion (50% in isolated product) [26, 27]. An equivalent yield was obtained by ultrasonic irradiation of the neat reaction mixture at 50 °C for 50 h [29]. 

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