Charge transfer complex, formation

The first quantitative model, which appeared in 1971, also accounted for possible charge-transfer complex formation (45). Deviation from the terminal model for bulk polymerization was shown to be due to antepenultimate effects (46). Mote recent work with numerical computation and C-nmr spectroscopy data on SAN sequence distributions indicates that the penultimate model is the most appropriate for bulk SAN copolymerization (47,48). A kinetic model for azeotropic SAN copolymerization in toluene has been developed that successfully predicts conversion, rate, and average molecular weight for conversions up to 50% (49). 

The ethylenediamine derivative [31] possesses higher promoting activities than other diamines. This phenomenon may be ascribed to the copromoting effect of the two amino groups on the decomposition of persulfate through a CCT (contact charge transfer complex) formation. So we proposed the initiation mechanism via CCT as the intimate ion pair and deprotonation via CTS (cyclic transition state) as follows ... 

In the last two decades a number of phenomena found many years ago in azo coupling and other substitution reactions have been elucidated with regard to their structural and mechanistic basis. These include charge-transfer complex formation, radical pairs as transient intermediates, and changes in product ratios due to mixing effects — a phenomenon which was not understandable at all only a few years ago (see Secs. 12.8 and 12.9). 

The proton is not the only entity that can dissociate from a substrate or bond to it. We can enumerate other interactions, such as metal-ligand complexation, ion-pair formation, charge-transfer complex formation, etc. For the sake of brevity, we treat all of these as... 

The ability of compounds with double bonds to act both as electron donors and as electron acceptors in charge transfer complex formation is well known (81,82). Hammond (83) has studied the correlations of association constants and of the energy of the charge transfer absorption of 2-substituted-l,4-benzoquinones complexed with hexamethylbenzene with the Hammett equation. Charton (84) has studied the correlation with eq. (2) of association constants of 1-substituted propenes with Ag. ... 

More recently, Kim et al. synthesized dendritic [n] pseudorotaxane based on the stable charge-transfer complex formation inside cucurbit[8]uril (CB[8j) (Fig. 17) [59]. Reaction of triply branched molecule 47 containing an electron deficient bipyridinium unit on each branch, and three equiv of CB[8] forms branched [4] pseudorotaxane 48 which has been characterized by NMR and ESI mass spectrometry. Addition of three equivalents of electron-rich dihydrox-ynaphthalene 49 produces branched [4]rotaxane 50, which is stabilized by charge-transfer interactions between the bipyridinium unit and dihydroxy-naphthalene inside CB[8]. No dethreading of CB[8] is observed in solution. Reaction of [4] pseudorotaxane 48 with three equiv of triply branched molecule 51 having an electron donor unit on one arm and CB[6] threaded on a diaminobutane unit on each of two remaining arms produced dendritic [ 10] pseudorotaxane 52 which may be considered to be a second generation dendritic pseudorotaxane. 

Fig. 17. Dendritic [4]pseudorotaxanes and [10]pseudorotaxanes based on the stable charge-transfer complex formation in CB[8] cavity...

SAQ 4.6 The thermodynamic quantities of charge-transfer complex formation for the reaction... 

There is no evidence for ground state charge-transfer complex formation between stilbenes and neutral amines. Amine cations and dications are powerful electron acceptors and can form ground state complexes in which t-1 serves as the electron donor. Complex formation between t-1 and the organic dication methyl viologen is responsible for quenching of the fluorescence of surfactant stilbenes in organized assemblies (112). 

Recently, a novel series of amorphous molecular materials based on carbazole and methine dyes has been synthesized [89], These molecular materials exhibit a very interesting charge-transfer complex formation and large PR responses. 

Oxidation potentials measure the energy required to remove an electron from a molecule. To check whether in a partial electron transfer in charge transfer complex formation, a similar correlation would hold, the equilibrium constant... 

P.K. Shukla et al., Reactions of guanine with methyl chloride and methyl bromide 06-methylation versus charge transfer complex formation. Int. J. Quantum Chem. 107, 1270-1283(2007)... 

The binding by the charge transfer complex formation is observed in polymerizations of p-nitrophenylphenylalanine NCA and some p-nitrophenyl derivatives of a-amino acid NCA by the nucleophile-containing polymer catalysts (103). Results are shown in Table 9. 

The effect of the hydrogen bond formation is much greater than that of the charge transfer complex formation in this polymerization reaction. 

Electron donation-acceptance reactions, which are considered to be Lewis acid-base interactions, also include the formation of coordination compounds, complex formation through hydrogen bonding, charge transfer complex formation, and so on. It should be apparent that the Lewis theory of acids and bases encompasses a great deal of both inorganic and organic chemistry. 

---