Switching, electronic structure

In this section, we switch gears slightly to address another contemporary topic, solvation dynamics coupled into the ESPT reaction. One relevant, important issue of current interest is the ESPT coupled excited-state charge transfer (ESCT) reaction. Seminal theoretical approaches applied by Hynes and coworkers revealed the key features, with descriptions of dynamics and electronic structures of non-adiabatic [119, 120] and adiabatic [121-123] proton transfer reactions. The most recent theoretical advancement has incorporated both solvent reorganization and proton tunneling and made the framework similar to electron transfer reaction, [119-126] such that the proton transfer rate kpt can be categorized into two regimes (a) For nonadiabatic limit [120] ... 

An ab initio study using the 6-31G basis set was used to investigate the vibrational and electronic structures of a benzodithiophene and benzodifuran quinone as potential redox switches. The calculated and experimental data were... 

Nitroxides are the most common of the oxygen-centred biradicals to be reported. As a model for spin-crossover molecules, the nitronyl nitroxide (105) was prepared and by oxidation with PbC>2 afforded the triplet biradical (106) which was characterized by ESR (Scheme 15).242 The one-electron oxidation of (105) afforded the singlet cation (107) which was seen to exist in equilibrium with (106) in solution. The authors claim that pH-controlled interconversion between two species of different spin multiplicities in this way may provide die basis for novel magnetic switches or pH sensors. The N.N-dialkylamino nitronyl nitroxides (108) were prepared and afforded die diplet-state biradical cation species by one-electron oxidation with iodine.243 The authors propose that, by the similarity of die electronic structures, diese structures can be regarded as hetero-analogues of trimethylenemethane. A paper confirms die conversion of 3,3-dimethyldioxetane into die corresponding ring-opened 1,2-diol but refutes the... 

Two-terminal devices might seem more natural for the molecular-scale systems than three-terminal ones because of the technological difficulties in manipulating small structures. Furthermore, chemical assembly of molecular devices usually results in a periodic structure. This observation resulted in the idea to have a two-terminal switch, electronically reconfigurable, where a relatively high voltage (e.g. —2V or +2V in [62], which uses a 2-catenane-based molecule) (Fig. (7a)) is applied to close or open the switch, but a relatively low voltage to read (M). 1 V) [60]. These molecular switches [62], a mono-layer of rotaxane molecules, are not field-activated but can be described as small electro-chemical cells, which are characterized by... 

Switching to a basis of orbitals allows us to proceed toward constructing the description of a molecular electronic structure based on the GF approximation under well acceptable restrictions. Indeed, let us assume that the multipliers in eq. (1.181) satisfy the additional condition of strong orthogonality ... 

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