Identical conditions, chemical

Figure 12 Both panels depict one-pulse MAS SSNMR spectra, acquired spinning at a speed of 12 kHz and at a magnetic field of 9.4 T. On the left, pure Ti02 samples are examined as prepared, and after heating at 400 and 500 °C. On the right, Ti02-V20s samples were examined under identical conditions. Chemical shifts were referenced to titanium isopropoxide (see Table 1 and main text). Reprinted with permission from Ref. [73], Copyright 2015 American Chemicai Society.

Prior to conducting the DOE (design of experiments) described in Table 3, it was established that no reaction took place in the absence of a catalyst and that the reactions were conducted in the region where chemical kinetics controlled the reaction rate. The results indicated that operating the reactor at 1000 rpm was sufficient to minimize the external mass-transfer limitations. Pore diffusion limitations were expected to be minimal as the median catalyst particle size is <25 pm. Further, experiments conducted under identical conditions to ensure repeatability and reproducibility in the two reactors yielded results that were within 5%. 

The precipitates were collected in sintered glass crucibles, washed with alcohol, and dried in vacuum. The weight of silver chloride was 0.3488 g. Authentic samples of TBTC1 (M T Chemicals), when gravimetrically analyzed under identical conditions, gave an assay of 95%. Thus the conversion from TBTA to TBTC1 is 94% in sample 4-4. 

Antibacterial sulfonamides contain two N-atoms, the sulfonamido (N1) and the para primary amino (N4). The sulfonamido group, in contrast to a carboxamido group, is chemically and metabolically stable. In other words, hydrolytic cleavage of sulfonamides to produce a sulfonic acid and an amine has never been observed. We, therefore, focus our discussion on the primary amino group, acetylation of which is one of the major metabolic pathways for some sulfonamides. Hydrolysis of the N4-acety luted metabolites back to the parent sulfonamide can occur in the liver, kidney, and intestinal tract. The reaction is strongly influenced by the structure of the parent amine e.g., N4-acetylsulfisoxazole (4.121) was deacetylated by intestinal bacteria whereas /V4-acctyIsulI anilamide (4.122) under identical conditions was not [78][79],... 

The chondrite-normalized REE patterns for basement-hosted uranium oxides are similar, except for a small variation of LREE abundances, indicating identical physico-chemical deposition conditions (T, pH, fluid composition) for the Eastern part of the Athabasca Basin basement. The previous REE distinction made between Ingress and Egress deposits (Fayek Kyser 1997) is not confirmed by the present study, because both types have similar REE abundance and fractionations, indicating the similarity of the sources and the processes for both deposit types. Thus, these results suggest... 

Whereas Cgg and C g are easy to reduce, their oxidation occius at comparatively high anodic potentials [1, 2]. Theoretical investigations predict the first oxidation potential ofCgg to be comparable to that of naphthalene [3]. Anodic electrochemistry with fuUerenes has been carried out with Cgg films [4] as well as in solution [5-7]. Cyclic voltammetry of Cgg in a 0.1 M solution of Bu4NPFg in trichloroethylene (TCE) at room temperatare exhibits a chemically reversible, one-electron oxidation wave at -tl.26 V vs Fc/Fc (Figiue 8.1) [7]. Under identical conditions, a one-electron, chemically reversible oxidation is also observed for Cyg. The oxidation of Cyg occurs 60 mV more negative than that of Cgg at -tl.20 V vs Fc/Fc. The energy difference between the first oxidation and the first reduction potential is a measiue of the... 

Differential thermal analysis (DTA) involves heating (or cooling) a test sample and an inert reference sample under identical conditions and recording any temperature difference which develops between them. Any physical or chemical change occurring to the test sample which involves the evolution of heat will cause its temperature to rise temporarily above that of the reference sample, thus giving rise to an exothermic peak on a DTA plot. Conversely, a process which is accompanied by the absorption of heat will cause the temperature of the test sample to lag behind that of the reference material, leading to an endothermic peak. 

Tetrahydrothiophene (88) has properties typical of aliphatic thioethers (e.g. diethyl sulfide) and is readily oxidized, both chemically and metabolically, to the sulfoxide (89) and sulfone (90). Incubation of (88) (5 p,mol) with rat-liver monooxygenases in the presence of appropriate cofactors results in the conversion of about 10% of the starting material to the sulfoxide in 30 minutes, whereas the sulfone is formed only in trace amounts (80UP10900). Incubation of the synthetic sulfoxide (89) under identical conditions affords the sulfone (90) in very... 

C-Aminoindoles autoxidize extremely rapidly. Consequently, comparatively few chemical reactions have been examined. The 2-amino derivative exists in the 3H-indole tautomeric form (473) and is protonated and alkylated on the annular nitrogen atom (72HC(25-2)179). The 1-methyl derivative (474) exits predominantly as such and not as the alternative 2-imino-3//-indole tautomer and is protonated at the 3-position to give a cation having the same electronic structure as that of the protonated (473). Acylation of (473) yields l-acetyl-2-acetylaminoindole, via the initial acylation of the annular nitrogen atom. Confirmation of this route has been established by the observation that 2-acetylaminoindole, obtained by hydrolysis of the diacetylated compound, is acetylated under identical conditions... 

One must be aware of the possible occurrence of certain problems in isotope dilution analysis. One of these is incomplete isotopic exchange, in which the active and inactive atoms do not mix. This lack of exchange can be due to differing physical and chemical states of tracer and inactive materials. Steps must be taken to ensure complete exchange. One must also be sure that the labeled position in any compound is relatively inert. If the atom in question is very labile, one can get a reduction in specific activity without any dilution having taken place. To compare specific activities, all samples must be counted under identical conditions with proper corrections for self-absorption in samples of varying mass. 

A quantity of each of three chemical fertilizers was applied to three groups of five corn plants each, with all plants growing under identical conditions of temperature, rainfall, soil, seed, etc. From the following measures of corn growth (height after one month), determine whether there is any reason for one fertilizer to be better than another... 

Sakamoto et al. also demonstrated an absolute oxetane synthesis in the solid-state photolysis of Y-( ,(3-unsaturatcd carbonyl)benzoylformamides 43. [28] The X-ray analysis of Y-isopropyl substituted imide 43a revealed that the crystal system was monoclinic and the space group P2. Crystals of 43a were powdered and photolyzed at 0°C. The imide undergoes the [2+2] cycloaddition to afford the bicyclic oxetane 44a, which is a mixture of diastereomers, namely, syn- and anh-isomers at the C-7 position. In this reaction optically active. syn-oxctanc 44a with 37% ee (84% chemical yield) and racemic anti-44a were obtained. The solid-state photoreaction proceeded even at -78°C, and optically active syn-44n which showed ee value as high as >95% ee, (conv 100%, chemical yield 89%) was formed in a higher diastereomeric ratio (syn/anti = 6.5). Under identical conditions A-bcnzyl substituted 43b was irradiated in the solid state. 

Kabasakalian and coworkers 87) have achieved the cathodic reduction of steroidal ketones in ethanol-20% H20 with 0.2 M (C4H9)4NC1 as the supporting electrolyte. The reactions proceeded with very high chemical yield and were rather stereoselective. Electrolysis of androstane-17 3-ol-3-one (64) at —2.6 V(SCE) gave the 3p-equatorial alcohol 65 quantitatively. Under identical conditions the exocyclie carbonyl of 66 was also reduced and the corresponding alcohol was obtained in 92% yield. But, the reaction was less stereoselective and the ratio of the 2O0-/2Oa epimers was 74/26. 

---