Electron transport, comparative

Electron transport Comparing the energetics of the oxidation of NADH from NADH... 

Figure 1. The channels which can be available for proton release in different cells. These may be activated by ligands attached to receptors or signals generated by the electron transport system. The electron transport across the membrane can also be accompanied by proton movement, depending on the orientation of electron transport, but th is movement would be I imited because of the slow rate of electron transport compared to the rapid rate which can be elicited through channels. Any possible relation of oxidase control to the H+-ATPase or the H -K+-ATPase has not been tested by inhibitors such as bafilomycin or omeprazole, respectively (Swallow et al., 1990).

This is a crucial point because (as we will see) proton transport is coupled with ATP synthesis. Oxidation of one FADHg in the electron transport chain results in synthesis of approximately two molecules of ATP, compared with the approximately three ATPs produced by the oxidation of one NADH. Other enzymes can also supply electrons to UQ, including mitochondrial 5w-glyc-erophosphate dehydrogenase, an inner membrane-bound shuttle enzyme, and the fatty acyl-CoA dehydrogenases, three soluble matrix enzymes involved in fatty acid oxidation (Figure 21.7 also see Chapter 24). The path of electrons from succinate to UQ is shown in Figure 21.8. 

The huge literature on the electronic conductivity of dry conducting polymer samples will not be considered here because it has limited relevance to their electrochemistry. On the other hand, in situ methods, in which the polymer is immersed in an electrolyte solution under potential control, provide valuable insights into electron transport during electrochemical processes. It should be noted that in situ and dry conductivities of conducting polymers are not directly comparable, since concentration polarization can reduce the conductivity of electrolyte-wetted films considerably.139 Thus in situ conductivities reported for polypyrrole,140,141 poly thiophene,37 and poly aniline37 are orders of magnitude lower than dry conductivities.15... 

A term that is nearly synonymous with complex numbers or functions is their phase. The rising preoccupation with the wave function phase in the last few decades is beyond doubt, to the extent that the importance of phases has of late become comparable to that of the moduli. (We use Dirac s terminology [7], which writes a wave function by a set of coefficients, the amplitudes, each expressible in terms of its absolute value, its modulus, and its phase. ) There is a related growth of literature on interference effects, associated with Aharonov-Bohm and Berry phases [8-14]. In parallel, one has witnessed in recent years a trend to construct selectively and to manipulate wave functions. The necessary techniques to achieve these are also anchored in the phases of the wave function components. This trend is manifest in such diverse areas as coherent or squeezed states [15,16], electron transport in mesoscopic systems [17], sculpting of Rydberg-atom wavepackets [18,19], repeated and nondemolition quantum measurements [20], wavepacket collapse [21], and quantum computations [22,23]. Experimentally, the determination of phases frequently utilizes measurement of Ramsey fringes [24] or similar methods [25],... 

It is important that mitochondrial oxygen radical production depends on the type of mitochondria. Recently, Michelakis et al. [78] demonstrated that hypoxia and the proximal inhibitors of electron transport chain (rotenone and antimycin) decreased mitochondrial oxygen radical production by pulmonary arteries and enhanced it in renal arteries. This difference is probably explained by a lower expression of the proximal components of electron transport chain and a greater expression of mitochondrial MnSOD in pulmonary arteries compared to renal arteries. 

Electrochemical communication between electrode-bound enzyme and an electrode was confirmed by such electrochemical characterizations as differential pulse voltammetxy. As shown in Fig. 11, reversible electron transfer of molecularly interfaced FDH was confirmed by differential pulse voltammetry. The electrochemical characteristics of the polypyrrole interfaced FDH electrode were compared with those of the FDH electrode. The important difference between the electrochemical activities of these two electrodes is as follows by the employment of a conductive PP interface, the redox potential of FDH shifted slightly as compared to the redox potential of PQQ, which prosthetic group of FDH and the electrode shuttling between the prosthetic group of FDH and the electrode through the PP interface. In addition, the anodic and cathodic peak shapes and peak currents of PP/FDH/Pt electrode were identical, which suggests reversibility of the electron transport process. 

Inspired by good electron transport properties and high PL of PBD and, particularly, a claim by Heeger and co workers [68] of exceptional performance of PBD MEH-PPV mixtures (EL of up to 50% of the PL yield), Bryce and coworkers [697] reported the first poly(PBD) homopolymer (604) and its aza-derivative (605). The device ITO/PEDOT/MEH-PPV 604/A1 showed cT>i" of 0.26%, compared to 0.01% obtained with MEH-PPV alone in an identically prepared device. 

Compared to Alq3, the EAs of these compounds are slightly higher (3.3 eV), which in part explains their superior electron transport properties. 

Another large band-gap electron transport host is 3-phenyl-4-(l -naphthyl)-5-phenyl-1,2,4-triazole (TAZ), which has a HOMO (-6.6 eV) and LUMO (-2.6 eV). Using TAZ1 (109) as the host, a maximum EQE (ext) of 15.5% and a luminous power efficiency of 40 lm/W can be achieved in a phosphorescent OLED the value of phosphorescent decay lifetime of 7% Ir(ppy)3 in the TAZ (t-650 ns) is longer than that in CBP (t-380 ns) and the phosphorescence efficiency is approximately proportional to the excited state lifetime [174]. 

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