Saturation systems

The formation of the (X-delocalized norbornyl cation via ionization of 2-norbornyl precusors in low-nucleophilicity, superacidic media, as mentioned, can be considered an analog of an intramolecnlar Friedel-Crafts alkylation in a saturated system. Indeed, deprotonation gives nortricyclane,... 

Two air-saturation systems suited for use in water treatment are shown in Figure 15 (31). Such mechanisms faciHtate the release of air that generates much finer bubbles than mechanical air dispersion methods used in mineral flotation practice. 

Fig. 15. Ain-saturator systems used in the practice of water treatment by flotation (31). (a), Injection of air into suction line of recycle pump (b), packed...

Physical and chemical properties of the three most important forms of sodium sulfate are summarized ia Table 3. The solubiUty of sodium sulfate ia water from 0 to 360°C is shown ia Figure 1 (5). The solubiUty of the NaClNa2S04-H2 0-saturated system is also shown. The aqueous solubiUty of sodium sulfate changes rapidly from 0 to 40°C, and addition of NaCl to a saturated solution of Na2S04 dramatically suppresses this solubiUty. These two effects are exploited by all manufacturers of sodium sulfate. 

One-bond couplings ( /ch) in saturated systems do not seem to have been investigated extensively. The value for cyclohexane (an average of couplings to axial and equatorial protons) iSk 123 Hz, and is increased by substitution adjacent to the carbon by an electronegative element, as with the aromatic systems discussed above. 

The method has also been applied to partially saturated systems. For instance, the dipole moments of a series of 1-acylpyrazolines (42) with R = H, Me, Et and Ph have been measured (72CHE445) they range from 3.46 to 4.81 D. When compared with values computed by the fragmentary calculation method, the conclusion was reached that here also the E form predominates. In all these examples the lone pair-lone pair repulsions determine the most stable conformation. 

Nucleophilic attack on ring atoms of large heterocycles is largely confined to saturated systems, saturated parts of partially unsaturated systems, and to carbonyl functions and the like. These reactions are not fundamentally different from those of corresponding acyclic systems, except for transannular reactions. 

The examples that have been presented in this section illustrate the approach that is used to describe structure and reactivity effects within the framework of MO description of structure. In the chapters that follow, both valence bond theory and MO theory will be used in the discussion of structure and reactivity. Qualitative valence bond terminology is normally most straightforward for saturated systems. MO theory provides useful insights into conjugated systems and into effects that depend upon the symmetry of the molecules under discussion. 

Quite a number of mixed sulfur-nitrogen macrocycles have been prepared, but these have largely been by the methods outlined in Chaps. 4 and 5 for the respective heteroatoms. An alternative method, involves the formation of a Schiff base, followed by reduction to the fully saturated system, if desired. An interesting example of the Schiff base formation is found in the reaction formulated in (6.12). Dialdehyde 14 is added to ethylenediamine in a solution containing ferrous ions. Although fully characterized, the yield for the reaction is not recorded. To avoid confusion with the original literature, we note the claim that the dialdehyde [14] was readily prepared in good yield by reaction of the disodium salt of 3-thiapentane-l, 5-diol . The latter must be the dithiol rather than the diol. 

The rotation of an axial CHjI group [cf. (3)] in a polycyclic saturated system is severely hindered by axial substituents on the same face therefore preferred orientations for both an 18- (Figure 12-1) and I9-CH2I (Figure 12-2) in steroids can be written ... 

The following discussion of hydroxamic acids includes saturated systems, e.g., 2, compounds such as 3, derived from aromatic systems, 7V-hydroxyimides such as 7V-hydroxyglutarimide (78), and certain of their derivatives including thiohydroxamic acids. Naturally occurring cyclic hydroxamic acids are discussed to show the range of structural types that has been found, hut macrocyclic polyhydroxamic acids are mentioned very briefly, because several comprehensive reviews of these compounds are already available. The main purpose of this review is to summarize the methods available for the synthesis of cyclic hydroxamic acids, to outline their characteristic reactions, and to present some useful physical data. Their synthesis and some biological properties have previously been reviewed by Coutts. ... 

The classical age of preparative organic chemistry saw the exploration of the extensive field of five-membered heterocyclic aromatic systems. The stability of these systems, in contrast to saturated systems, is not necessarily affected by the accumulation of neighboring heteroatoms. In the series pyrrole, pyrazole, triazole, and tetrazole an increasing stability is observed in the presence of electrophiles and oxidants, and a natural next step was to attempt the synthesis of pentazole (1). However, pentazole has eluded the manifold and continual efforts to synthesize and isolate it. 

When the reaction was followed in an nmr probe, the appearance and disappearance of two intermediates 66 and 67 was observed along with the buildup of product 65. The rate of reaction of 64 at 75° in formic acid, k = 3xl0" sec, is six times faster than the rate of the corresponding saturated system, 2,2-dimethyl-1-pentyl tosylate, k = 5xl0" sec, under identical conditions. If the inductive rate retarding effect of the triple bond is taken into account, then the calculated rate enhancement resulting from triple-bond participation in the solvolysis of 64 is about 3000(81). The... 

In the liver, the bilirubin is removed from albumin and taken up at the sinusoidal surface of the hepato-cytes by a carrier-mediated saturable system. This facilitated transport system has a very large capacity, so that even under pathologic conditions the system does not appear to be rate-limiting in the metabolism of bilirubin. 

The most problematic cases for the Stille reaction involve coupling saturated systems. The tendency for p-elimi nation of alkylpalladium compounds requires special conditions. Zh. v-(dialkylamino)cyclohexylphosphincs have shown considerable success... 

Too small a value of xc means too large a Kc and therefore saturation. System response is subject to imperfect pole-zero cancellation. 

Geminal chlorine or bromine substituents deshield vinylic fluorine significantly, whereas a vicinal chlorine substituent shields the fluorine, much as was the case for the saturated systems. Again similarly, a second vicinal chlorine substituent reverses the trend and shifts the fluorine signal downfield (Scheme 3.45). 

Heibst, E. In Atomic, Molecular, Optical Physics Handbook Drake, G., Ed. AIP Press New Yoik, 1996, p 429 Adams, N. G. In Atomic, Molecular, Optical Physics Handbook Drake, G., Ed. AIP Press New Yoik, 1996, p 441. For three-body systems, a slightly more complex temperature dependence is observed. For saturated systems, more complex treatments are needed —see Gilbert, R. G. Smith, S. C. Theory erf Unimolecular and Recombination Reactions Blackwell Oxford, 1990. 

Delocalisation takes place (cf. 1,3-dienes, p. 13), so that an electron-deficient atom results at C3, as well as at C, as in a simple carbonyl compound. The difference between this transmission via a conjugated system, and the inductive effect in saturated system, is that here the effect suffers much less diminution by its transmission, and the polarity at adjacent carbon atoms alternates. 

Note that (1) in saturated systems proton-proton couplings are seldom observed beyond three bonds, but (2) in aromatic and heterocyclic systems, four- and even five-bond coupling is commonplace. This is because spin coupling is transferred by electrons. Where you have extended conjugation, you can expect to observe coupling over a greater number of bonds. 

Reduced derivatives of all these parent structures (dihydro, tetrahydro, and fully saturated systems) increase greatly the number of possible compounds. Oxo compounds are also possible, and each of the nine parent structures has five different positions where the carbonyl group could be located. 

Several methods based on radical cyclizations have been developed and applied to the synthesis of the fully saturated system. An example (Scheme 11) is provided by the tandem radical cyclization of properly substituted imines 33 obtained from tu-benzeneselenylamines and aldehydes <1995TL5623>. 

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