# Dynamic Symmetry in Quantum-Classical Mechanics: Simplicity in Complexity ** Vladimir V. Egorov**^{*}

**Vladimir V. Egorov**

^{*}Russian Academy of Sciences, FSRC “Crystallography and Photonics”, Photochemistry Center, Moscow, Russia

^{*}**Correspondence to:** Vladimir V. Egorov

**Citation:** Egorov VV (2022) Dynamic Symmetry in Quantum-Classical Mechanics: Simplicity in Complexity. Sci Academique 3(1): 1-11

**Received:** 08 February, 2022; **Accepted:** 26 February, 2022; **Publication:** 02 March, 2022

**Abstract**

All kinds of dynamic symmetries in quantum-classical (dozy-chaos) mechanics of elementary electron and/or proton transfers, their physical meaning and applications are discussed.

**Keywords:** Molecular quantum transitions; Singularity; Dozy chaos; Quantum-classical mechanics; Charge transfer; Condensed matter; Direct and reverse processes; Optical band shapes; Egorov resonance

**Introduction to quantum-classical mechanics** As is well known, elementary transfers of electrons and/or protons in the membranes of living cells are integral parts of their functioning (see, e.g., [1,2] and references therein). Therefore, in particular, fundamental theoretical knowledge about the elementary transfers of electrons and/or protons in condensed media is of great interest.

The theory of elementary transfers of electrons and/or protons in condensed media is based on a new physical theory – quantum-classical mechanics [3-6]. As a new theory, quantum-classical mechanics arose as a result of eliminating the singularity that occurs in quantum mechanics in the rates of elementary electron-charge transfers when going beyond the Born-Oppenheimer adiabatic approximation and the Franсk-Condon principle [7,8]. This singularity can be easily demonstrated by the example of a one-dimensional potential box with a movable wall [9,10] (Figure 1). In quantum-classical mechanics, the singularity is eliminated by replacing the infinitesimal imaginary addition *i ϒ* in the energy denominator of the total Green’s function of the system by a finite value

*ϒ>0*[6–8]. The energy

*ϒ*can be considered as the width of the electron-vibrational energy levels in the transient state of the “quantum” transition. However, as shown by a successful comparison of the theory with a large number of experimental data on the shape of the optical bands of polymethine dyes and their aggregates, the energy

*ϒ*is much higher than the energy of the vibrational quantum

*ħω :*[6]. This fact means physically that in the transient state the exchange of motion and energy between the electron (proton) and nuclei is so intense that it leads to chaos both in the motion of the electron and in the motion of nuclei. This chaos is called dozy chaos, and the corresponding new theory is called dozy-chaos mechanics [6]. Dozy chaos leads to the continuity of the energy spectrum in the transient state of the system, which is characteristic of classical mechanics. While the initial and final states of the system can be considered as quantum states in the adiabatic approximation, which differ sharply in their electron-nuclear structure. Therefore, dozy-chaos mechanics can also be called quantum-classical mechanics [6].

*ϒ*>>ħω**Figure 1: **Singularity in the rate of molecular quantum transitions: a potential box with a movable wall (**a**) and the optical absorption band shape dependent on the dozy chaos available to a given quantum transition (**b**); the band shape with the strongly pronounced peak (J-band) corresponds to the least dozy chaos [9]. The wall is fastened to the abscissa axis by a freely movable hinge and can move with a certain friction or without friction against the axis. Such a wall simulates the environmental nuclear reorganization in the molecular “quantum” transitions, where dozy chaos plays the role of friction. In the theory [6], this results in the dozy-chaos dependent optical absorption band being displaced to the red spectral region and narrowed (**b**). The position, the intensity and the width of the optical absorption band are determined by the ratio between the dozy-chaos energy *ϒ* and the reorganization energy *E* (see Section 2). The smaller the value of *ϒ* is, the higher the degree of organization of the molecular “quantum” transition, and the more the intensity and less the width of the optical band (**b**). The position of the wing maximum is determined by the energy *Ε*, whereas the position of the peak is determined by the energy *ϒ* [9]. At high energies *ϒ*, the band shape is close to symmetric and is Gaussian-like. With a decrease in the value of *ϒ*, in the red region of the spectrum, a peak appears against the background of a Gaussian-like band, which, with decreasing *ϒ*, shifts more and more to the red region of the spectrum and becomes more and more pronounced. Thus, with a decrease in the value of the dozy-chaos energy *ϒ*, the band shape transforms from symmetric to asymmetric [4]. (Original citation)—reproduced by permission of The Royal Society of Chemistry.

**Elementary electron transfer, Egorov resonance, and associated symmetries** The simplest version of quantum-classical mechanics is the quantum-classical mechanics of elementary electron transfer in condensed media [6]. One of the remarkable features of this theory is the presence of the so-called Egorov resonance – a resonance between the motion of an electron between a donor and an acceptor and the accompanying motion of reorganization of the environmental nuclei [3-12]:

where Ʈ_{e} is the characteristic time of motion of the electron in the donor-acceptor system, and Ʈ is the characteristic time of motion of the reorganization of nuclear vibrations in the environment. These times are given by the following equations

where *L* is the distance between the donor 1 and the acceptor 2 of an electron ( *L* is equal to the length of the polymethine chain — the main optical chromophore of polymethine dyes) [7-10,12], *J _{1}* is the binding energy of the electron on the donor 1 (electronic energy of the ground state of the dye) [7–10,12],

*m*is the effective mass of the electron, and

The presence of symmetry in the shape of optical bands at high (room) temperatures and large *ϒ* (Figure 1b) is associated with a primitive, Franck–Condon picture of the dynamics of molecular “quantum” transitions. The loss of this symmetry and the appearance of a peak against the background of a wide band wing are related to the effect of self-organization of transition dynamics in dozy-chaos mechanics, which is expressed, in particular, in the “pumping” of dozy chaos from one part of the optical band to another part (from the peak to the wing, see Figure 1b). In a similar context, the series for the shape of the optical bands of a representative polymethine dye, thiapolymethinecyanine, depending on the length of its polymethine chain L, has a quasi-symmetric character with respect to the Egorov resonance (Figure 2), which corresponds to the most organized quantum-classical transition. Note that the Egorov resonance (Er) is a bright nano-phenomenon, since, for example, for the Brooker series (Figure 2), this resonance is near L (Er) = 2 (3 + 2) 0.14 nm = 1.4 nm.

The result for the optical transition-rate constant in quantum-classical mechanics does not change when the sign of the dozy-chaos energy *ϒ* is changed. This symmetry with respect to the change in the sign of *ϒ* is consistent with the physical case that both the virtual acts of transformation of electron movements and energies into nuclear reorganization movements and energies and the reverse acts occur in the transient dozy-chaos state [9,10]. For definiteness, we set *ϒ *> 0 here, there, and everywhere. The Egorov resonance also explains the nature of the well-known narrow and intense J-band of J-aggregates of polymethine dyes [6-8,14-16], which have many different applications (see [16] and references therein).

**The Egorov Resonance and Its “Antisymmetric Twin”**

The five principal parameters of the problem, viz. electron mass *m*, electron-donor binding energy *J _{1} = J*, distance between the donor and the acceptor

*L*, environmental reorganization energy

*E*, and dozy-chaos energy

*γ*, may be combined into three quantities:

**A Simplified Version of Quantum-Classical Mechanics. Nonradiative Transitions**

The results of quantum-classical mechanics for the optical spectra of polymethine dyes, discussed above, and their J-aggregates [6-8,16] refer, in particular, to cases of sufficiently high self-organization of quantum-classical transitions, which correspond, generally speaking, to weak dozy chaos (*γ ≤ E* or *γ << E*). Cases of low self-organization of quantum-classical transitions, corresponding to strong dozy chaos (*γ ≥ E*), can be interpreted theoretically on the basis of some simplified version of quantum-classical mechanics. The theoretical construction of this simplified version is based on the fact that under strong dozy chaos, the rates of quantum-classical transitions weakly depend on the details of the chaotic dynamics of the transient state [6,10]. These rates depend mainly on the quantum structure of the initial and final states. In other words, the case of strong dozy chaos corresponds to a slight deviation of quantum-classical mechanics from the standard theory based on the Born-Oppenheimer adiabatic approximation and the Franck-Condon principle.In this case, one can avoid considering the dependence of the complete Green’s function of the system on the finite imaginary addition *iγ*, and the Green’s function of elementary electron-charge transfers in condensed media can be approximated by the Gamow exponent depending on the transient energy *ħω _{1}* of the phonon environment (see [6] and references therein).Physically, this circumstance allows us to speak about the nature of the transient state not in terms of dozy chaos, but in terms of a large number of tunnel and over-barrier transitions promoting the “quantum” transition of an elementary charged particle. This theory [18] was developed long before the creation of quantum-classical mechanics, and now it can be considered as its simplified version.On the basis of this simplified version of quantum-classical mechanics, explanations were given for the Brӧnsted laws in proton-transfer reactions [19-21] (see Section 5) and the temperature-dependent electron transfers in Langmuir-Blodgett films (see Refs 20,46 in [6]). From the general result for the rate constant in the simplified version of quantum-classical mechanics [18], in the framework of the Einstein model of nuclear vibrations (ω

_{k}= constant = ω) the simple expression for the rate constant

*K*has been obtained [18]:

(which directly follows from the Brӧnsted relationships (12) and (13)).

**The** **Simplified** **Version** **of** **Quantum-Classical** **Mechanics****: Symmetrization of the Amplitude and Rate Constant of the Transition for the Case of Different Electron-Phonon Interactions on the Donor and Acceptor**

Until now, both in the case of the complete theory for optical processes (Sections 1–3) and in the case of its simplified version for nonradiative processes (Sections 4,5), we have considered the case of the same electron-phonon interaction when a light charged particle, in particular an electron, is localized on the donor or on the acceptor. In other words, it was assumed that the reorganization energy E=E_{1}=E_{2}. For example, “quantum” transitions and the corresponding shapes of optical bands in polymethine dyes are well described by the case of the same value of the electron-phonon interaction on the donor and on the acceptor, because charge alternation occurs in the polymethine chain upon optical excitation [5,10,12]. In this section, we will briefly consider the case of different electron-phonon interactions when an electron is localized on a donor 1 or acceptor 2. This corresponds to different in magnitude the reorganization energy E_{1}≠E_{2}. For example, in the case of nonradiative processes, the change in sign in the heat energy *ħω _{12}* (Equations (9) and (10)) and in the donor-acceptor distance L=|

**L=L**| is associated with the permutation of indices 1 and 2 in the reverse order. The assumption E

_{12}_{1}≠ E

_{2}leads to asymmetry with respect to the permutation of indices 1 and 2 in the expression for the rate constant of transitions and the loss of connection between forward and reverse processes, expressed in Equation (11). To restore this connection, it is necessary to symmetrize the expression for the amplitude and rate constant of electron transfers with respect to different values of the electron-phonon interaction at the donor and at the acceptor, which leads to the case of reorganization energies E

_{1 }≠ E

_{2}. The symmetrization method proposed in [22] consists in the fact that, in addition to the transition amplitude [6,10,12]

(**r **and q are electron and phonon coordinates) which, in view of taking the wave function Ψ_{2} in the Born-Oppenheimer adiabatic approximation Ψ_{2} = Ψ_{2}^{BO} and taking into account the entire dynamics of the transition only in the wave function Ψ_{1}, can be called the amplitude of the transition on the acceptor A_{12}^{a}, we introduce into the theory also the amplitude

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