Amines complexation, solvent effect

Most reactions involve reactants and products that are dispersed in a solvent. If the amount of solvent is changed, either by diluting or concentrating the solution, the concentrations of ah reactants and products either decrease or increase. The effect of these changes in concentration is not as intuitively obvious as when the concentration of a single reactant or product is changed. As an example, let s consider how dilution affects the equilibrium position for the formation of the aqueous silver-amine complex (reaction 6.28). The equilibrium constant for this reaction is... 

A new assumption to be discussed in this section is that the fourth-order kinetics in SatAr by amines in aprotic solvents is due to the formation of the substrate-catalyst molecular complex. Since 1982, Forlani and coworkers149 have advocated a model in which the third order in amine is an effect of the substrate-nucleophile interaction on a rapidly established equilibrium preceding the substitution process, as is shown in Scheme 15 for the reaction of 4-fluoro-2,4-dinitrobenzene (FDNB) with aniline (An), where K measures the equilibrium constant for ... 

We have examined the proton transfer reaction AH-B A -H+B in liquid methyl chloride, where the AH-B complex corresponds to phenol-amine. The intermolecular and the complex-solvent potentials have a Lennard-Jones and a Coulomb component as described in detail in the original papers. There have been other quantum studies of this system. Azzouz and Borgis performed two calculations one based on centroid theory and another on the Landau-Zener theory. The two methods gave similar results. Hammes-Schiffer and Tully used a mixed quantum-classical method and predicted a rate that is one order of magnitude larger and a kinetic isotope effect that is one order of magnitude smaller than the Azzouz-Borgis results. 

Solvent effects and adduct formation of [VO(acac)2l and other [VO(j8-diketonato)2] complexes have been studied by several methods361,366,52 -532 and in coordinating solvents [VO(acac)2] is known to add a sixth ligand according to equation (36). Older reports include a spectrophotometric and calorimetric study of [VO(acac)2] and [VO(tfacac)2] adducts.521 With [VO(acac)2] in nitrobenzene, the enthalpy change for reaction (36) ranges from 44.3 kJ mol-1 for n-decylamine to 24.3 kJ mol-1 for methanol. Equilibrium constants K were between 1000 and —0.6. [VO(acac)2] is not a sensitive indicator of relative base strength.521 For [VO(acac)2], A0 decreases by —3 G (and go increases by —0.0004) as amine adducts are formed.522... 

Macroscopic solvent effects can be described by the dielectric constant of a medium, whereas the effects of polarization, induced dipoles, and specific solvation are examples of microscopic solvent effects. Carbenium ions are very strong electrophiles that interact reversibly with several components of the reaction mixture in addition to undergoing initiation, propagation, transfer, and termination. These interactions may be relatively weak as in dispersive interactions, which last less than it takes for a bond vibration (<10 14 sec), and are thus considered to involve "sticky collisions. Stronger interactions lead to long-lived intermediates and/or complex formation, often with a change of hybridization. For example, onium ions are formed with -donors. Even stable trityl ions react very rapidly with amines to form ammonium ions [41], and with water, alcohol, ethers, and esters to form oxonium ions. Onium ion formation is reversible, with the equilibrium constant depending on the nucleophile, cation, solvent, and temperature (cf., Section IV.C.3). 

Another example of intramolecular CT complex formation is provided by trans-4-dimethvlamino-4 -(1-oxobutvl)stilbene Solvent effects on the spectrum give a value of 22D for the excited state dipole moment. The effect of electric field on the fluorescence of 4-(9-anthry1)-N.N.-2.3,5,G-hexamethy1-aniline shows this compound forms an excited state whose dipole moment does not change with solvent . Chiral discrimination in exciplex formation between 1-dipyrenylamine and chiral amines is very weak . In the probe molecule PRODAN (6-propionyl)-2-(dimethylamino)—naphthalene the initially formed excited state converts to a lower CT state as directly evidenced by time-resolved spectra in n-butanol. Rate constants for intramolecular electron transfer have been measured in both singlet and triplet states of covalently porphyrin-amide-quinone molecules . Intramolecular excimer formation occurs during the lifetime of the excited state of bis-(naphthalene)hydrazides which are used as photochemical deactivators of metals in polyethylene . ... 

Structure of the complex was fiirther confirmed by X-ray crystal structure analysis. We have also observed an interesting solvent effect on this reaction. Whereas the borate complex prepared fi om R-a-methylbenzylamine and S-bi-2-naphthol is insoluble in CH3CN, the complex obtained using the same amine and R-bi-2-naphthol is insoluble in THF. This interesting solubility difference has been exploited in resolving ( )-bi-2-naphthol to obtain the enantiomers in >99% ee as shown in Scheme 6. The chiral amine can be recovered in 90% yield after the resolution. 

A recent interesting application of solvent effects has been the use of optically-active solvents in the determination of the optical purity and the absolute configuration of solutes. Work so far has centred on resonances and organic solutes, covering various alcohols, amines, sulphoxides, a-hydroxy- and a-amino-acids, and epoxides (the solvent here being an optically active nematic phase ). There are also reports on disymmetric nickel(II) complexes, and the use of resonances. ... 

---