Stability increased

A rigidized molecule obtained when the two a-carbons of the trimethine chain are linked by a dimethylene bridge cannot be planar. According to the resonance concept, its stability increases as a bathochromic effect of 41 nm is observed (122). The of the bistyryl dye obtained by the substitution of the -proton in the chain of a styryl dye by a dialkylamino group is nearly the same as for the parent styryl dye (123). 

Therrhal stability increases with increasing molecular weight. 

Carbocations are stabilized by alkyl substituents attached directly to the positively charged carbon Alkyl groups are electron releasing sub stituents Stability increases in the order... 

Type B thermocouples (Table 11.56) offer distinct advantages of improved stability, increased mechanical strength, and higher possible operating temperatures. They have the unique advantage that the reference junction potential is almost immaterial, as long as it is between 0°C and 40°C. Type B is virtually useless below 50°C because it exhibits a double-value ambiguity from 0°C to 42°C. 

Heteroeyeles structurally based on the phenalene ring system form an interesting elass, frequently possessing distinetive eolours. With nitrogen as the central atom we have the unstable 9b-azaphenalene (24), whieh has only fairly reeently been prepared and is still comparatively little studied (76JCS(Pl)34l). The cyclazine nomenclature is commonly applied to this and related compounds thus, (24) is (3.3.3)cyclazine. With further aza substitution, in positions alternant to the central atom, their stability increases the heptaazaphenalene (25) is (thermally) a very inert compound, derivatives of which, e.g. the triamine, have been known since the early days of organic chemistry (see Chapter 2.20). 

Strong nucleophiles such as Grignard reagents. In general, ortho esters are difficult to prepare directly from acids and are therefore more often prepared from the nitrile. Simple ortho esters derived from normal alcohols are the least stable in terms of acid stability and stability toward Grignard reagents, but as the ortho ester becomes more constrained its stability increases. 

Thermal stability increases with increasing atomic weight, as expected. Nitrates have been widely used as molten salt baths and heat transfer media, e.g. the 1 1 mixture LiNOs. KNOs melts at 125 C and the ternary mixture of 40% NaN02, 7% NaNOs and 53% KNO3 can be used from its mp 142 up to about 600 C. 

This last reaction is typical of many in which F3CIO can act as a Lewis base by fluoride ion donation to acceptors such as MF5 (M = P, As, Sb, Bi, V, Nb, Ta, Pt, U), M0F4O, Sip4, BF3, etc. These products are all white, stable, crystalline solids (except the canary yellow PtFe ) and contain the [F2CIO] cation (see Fig. 17.26h) which is isostructural with the isoelectronic F2SO. Chlorine trifluoride oxide can also act as a Lewis acid (fluoride ion acceptor) and is therefore to be considered as amphoteric (p. 225). For example KF, RbF and CsF yield M [F4C10] as white solids whose stabilities increase with increasing size of M+. Vibration spectroscopy establishes the C4 structure of the anion (Fig. 17.29g). 

Their thermal stability increases with molecular weight. Thus the Cs and Rb octafluoro complexes only decompose above 400°C, whereas the Na complex decomposes below 100°C. NaF can therefore conveniently be used to separate XeFg from XeF2 nd XeF4, with which it does not react, the purified XeFe being regenerated on heating. 

Recently a definitive study of several isoxazol-5-ones using infrared and ultraviolet spectroscopy (Table I) has shown that the balance between the various tautomers is a delicate one and that all three of the structural types can predominate depending upon the nature of the substituents and the conditions of the experiment. However, the hydroxy form is only found when it is stabilized by chelation (i.e., a carbonyl substituent in the 4-position). The other compounds exist in the CH form in nonpolar media increasing polarity of the solvent stabilizes increasing amounts of the more polar NH forms. 

A study of the relative stability of tra 5-2-azidothiazole 32b with respect to the corresponding cis conformer 32a showed that 32b is destabilized in the gas phase but appears to be the more stable conformer in solution (Scheme 23). The stability increases with increasing polarity of the solvent [98JA4723]. 

Table 3.1-5 Melting points and heats of fusion for isomeric [BMIM][PFg] and [PMIM][PFs] ionic liquids, showing melting point and crystal stability increasing with the degree of branching in the alkyl substituent.

Thiepin, as a seven-membered conjugated system with sulfur as heteroatom, is a member of the 8 7t-electron heteroannulenes which are antiaroinatic according to Hiickel s rule. In contrast to oxepin, thiepin is not stable at room temperature and no valence isomerism with an arene sulfide has been observed. Stable thiepins are obtained only when two bulky substituents, e.g. /ert-butyl, are introduced into positions 2 and 7. In benzothiepins the annellation effect of the aromatic rings contributes decisively to the stability of these compounds stability increases with an increasing number of fused benzene rings. 

Generally not shock sens deton on heating peroxy formic and acetic acids can explode at —20° stability increases as mw increases... 

There is no cross a conjugation in normal isomers (n = 0), while any branching gives rise to at least one cross conjugation (n 0). For example, the cross conjugation number n is 0 for n-pentane, 2 for 2-methylbutane, and 12 for neopentane. The stability increases with n (Scheme 25). 

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