Double partial

The individual terms AE1 12 of the double partial-wave expansion... 

The conformations of the parent calix[6]arenes have been variously described as distorted cone [6 - ], double partial cone and 6 ° winged... 

Containment type (multiple ehoiee single, double, partially double, confinement, N/A) 1 ... 

Extending the macrocycle ring to six-membered ring fives more flexibility to the calix[6]arene molecule compared to three- four- and five-membered calixarenes. For calix[6]arenes eight main (basic) conformations are defined [41] distorted cone, compressed cone, pinched cone, double partial cone, winged, 1,2,3-altemate, 1,3,5-altemate and distorted 1,2,3-altemate. Other conformations are also observed... 

There is only eight crystal structures of calix[7]arenes deposited in CSD. The reason for this is much more difficult synthesis of seven-membered calixarenes and/or difficulties in obtaining monocrystals of this compounds and their complexes/co-crystals. Like for smaller calixarenes discussed above also here the self-inclusion of one of the substituent may occur like in para-t-hvXy -carboxymethoxycalix[7]arene/deuterochloroform clathrate (Fig. 38.25a) [52] or inclusion complexes are obtained. For the later, due to a great degree of flexibility, many conformations of calixarene host molecule is possible but the most observed is a double partial cone, e.g. 1 2 para-t-butyl-calix[7]arene/pyridine inclusion complex where one guest molecule is located in each partial cone cavity (Fig. 38.25b) [53]. In one case the flattened cone conformation was found where the (Fig. 38.25c). In this crystal structure one toluene and one disordered benzene/ toluene molecule are involved in inclusion complex formation with one para-t-butyl-calix[7]arene molecule [54]. 

Figure B2.4.1. Proton NMR spectra of the -dimethyl groups in 3-dimethylamino-7-methyl-l,2,4-benzotriazine, as a fiinction of temperature. Because of partial double-bond character, there is restricted rotation about the bond between the dunethylammo group and the ring. As the temperature is raised, the rate of rotation around the bond increases and the NMR signals of the two methyl groups broaden and coalesce.

The next problem to consider is how chaotic attractors evolve from tire steady state or oscillatory behaviour of chemical systems. There are, effectively, an infinite number of routes to chaos [25]. However, only some of tliese have been examined carefully. In tire simplest models tliey depend on a single control or bifurcation parameter. In more complicated models or in experimental systems, variations along a suitable curve in the control parameter space allow at least a partial observation of tliese well known routes. For chemical systems we describe period doubling, mixed-mode oscillations, intennittency, and tire quasi-periodic route to chaos. 

Figure 2-51. a) The rotational barrier in amides can only be explained by VB representation using two resonance structures, b) RAMSES accounts for the (albeit partial) conjugation between the carbonyl double bond and the lone pair on the nitrogen atom. 

The furanose rings of the deoxyribose units of DNA are conformationally labile. All flexible forms of cyclopentane and related rings are of nearly constant strain and pseudorotations take place by a fast wave-like motion around the ring The flexibility of the furanose rings (M, Levitt, 1978) is presumably responsible for the partial unraveling of the DNA double helix in biological processes. 

Recall that the carbon atom of carbon dioxide bears a partial positive charge because of the electron attracting power of its attached oxygens When hydroxide ion (the Lewis base) bonds to this positively polarized carbon a pair of electrons in the carbon-oxygen double bond leaves carbon to become an unshared pair of oxygen... 

The regioselectivity of elimination is accommodated m the E2 mechanism by noting that a partial double bond develops at the transition state Because alkyl groups... 

A certain species of grasshopper secretes an allenic substance of molecular formula C13H20O3 that acts as an ant repellent The carbon skeleton and location of various substituents in this substance are indicated in the partial structure shown Complete the structure adding double bonds where appropriate... 

To understand the effect of a carbonyl group attached directly to the ring consider Its polarization The electrons m the carbon-oxygen double bond are drawn toward oxy gen and away from carbon leaving the carbon attached to the nng with a partial posi tive charge Using benzaldehyde as an example... 

In resonance terms the shorter carbon-oxygen bond distance in phenol is attrib uted to the partial double bond character that results from conjugation of the unshared electron pair of oxygen with the aromatic ring... 

A few fatty acids with trans double bonds (trans fatty acids) occur naturally but the major source of trans fats comes from partial hydrogenation of vegetable oils m for example the preparation of margarine However the same catalysts that catalyze the... 

The intermediate m hydrogenation formed by reaction of the unsaturated ester with the hydrogenated surface of the metal catalyst not only can proceed to the saturated fatty acid ester but also can dissociate to the original ester having a cis double bond or to its trans stereoisomer Unlike polyunsaturated vegetable oils which tend to reduce serum cholesterol levels the trans fats produced by partial hydrogenation have cholesterol raising effects similar to those of saturated fats... 

Unfilled valences 4 single 2 single 1 double 1 single 1 triple 1 single 2 partial double 3 single... 

In conjugated heterocyclic systems (partial double bond) 135.3(5)... 

Any discussion based on reactivity ratios is kinetic in origin and therefore reflects the mechanism or, more specifically, the transition state of a reaction The transition state for the addition of a vinyl monomer to a growing radical involves the formation of a partial bond between the two species, with a corre sponding reduction of the double-bond character of the vinyl group in the monomer ... 

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