scholarly journals 2P252 Proton-coupled electron transfer and hydrogen-bond distance of TyrZ - D1-His190 in Photosystem II(18B. Photobiology:Photosynthesis,Poster)

2014 ◽  
Vol 54 (supplement1-2) ◽  
pp. S236
Author(s):  
Miwa Sugiura ◽  
Shogo Ogami ◽  
Fabrice Rappaport ◽  
Alain Boussac
2007 ◽  
Vol 111 (43) ◽  
pp. 12599-12604 ◽  
Author(s):  
David L. Jenson ◽  
Amaris Evans ◽  
Bridgette A. Barry

2013 ◽  
Vol 91 (2) ◽  
pp. 155-168
Author(s):  
Waled Tantawy ◽  
Ahmed Hashem ◽  
Nabil Yousif ◽  
Eman Flefel

The thermochemistry of the hydrogen atom transfer reactions from the H2O–BX2 radical system (X = H, CH3, NH2, OH, F) to carbon dioxide, formic acid, and (or) formaldehyde, which produce hydroxyformyl, dihydroxymethyl, and hydroxymethyl radicals, respectively, were investigated theoretically at ROMP2/6–311+G(3DF,2P)//UB3LYP/6–31G(D) and UG3(MP2)-RAD levels of theory. Surprisingly, in the cases of a strong Lewis acid (X = H, CH3, F), the spin transfer process from the water–boryl radical to the carbonyl compounds was barrier-free and associated with a dramatic reduction in the B–H bond dissociation energy (BDE) relative to that of isolated water–borane complexes. Examining the coordinates of these reactions revealed that the entire hydrogen atom transfer process is governed by the proton-coupled electron transfer (PCET) mechanism. Hence, the elucidated mechanism has been applied in the cases of weak Lewis acids (X = NH2, OH), and the variation in the accompanied activation energy was attributed to the stereoelectronic effect interplaying in CO2 and HCOOH compared with HCHO. We ascribed the overall mechanism as a SA-induced five-center cyclic PCET, in which the proton transfers across the so-called complexation-induced hydrogen bond (CIHB) channel, while the SOMOB–LUMOC=O′ interaction is responsible for the electron migration process. Owing to previous reports that interrelate the hydrogen-bonding and the rate of proton-coupled electron-transfer reactions, we postulated that “the rate of the PCET reaction is expected to be promoted by the covalency of the hydrogen bond, and any factor that enhances this covalency could be considered an activator of the PCET process.” This postulate could be considered a good rationale for the lack of a barrier associated with the hydrogen atom transfer from the water-boryl radical system to the carbonyl compounds. Light has been shed on the water–boryl radical reagent from the thermodynamic perspective.


2006 ◽  
Vol 87 (1) ◽  
pp. 21-24 ◽  
Author(s):  
James M. Mayer ◽  
Ian J. Rhile ◽  
Frank B. Larsen ◽  
Elizabeth A. Mader ◽  
Todd F. Markle ◽  
...  

1966 ◽  
Vol 88 (1) ◽  
pp. 184-185 ◽  
Author(s):  
Thomas C. Farrar ◽  
W. Ryan ◽  
Alan Davison ◽  
J. W. Faller

2015 ◽  
Vol 119 (24) ◽  
pp. 7366-7377 ◽  
Author(s):  
Muhamed Amin ◽  
Leslie Vogt ◽  
Witold Szejgis ◽  
Serguei Vassiliev ◽  
Gary W. Brudvig ◽  
...  

2019 ◽  
Vol 23 (11n12) ◽  
pp. 1336-1345
Author(s):  
S. Jimena Mora ◽  
Daniel A. Heredia ◽  
Emmanuel Odella ◽  
Uma Vrudhula ◽  
Devens Gust ◽  
...  

Benzimidazole phenol-porphyrin dyads have been synthesized to study proton-coupled electron transfer (PCET) reactions induced by photoexcitation. High-potential porphyrins have been chosen to model P680, the photoactive chlorophyll cluster of photosynthetic photosystem II (PSII). They have either two or three pentafluorophenyl groups at the meso positions to impart the high redox potential. The benzimidazole phenol (BIP) moiety models the Tyr[Formula: see text]-His190 pair of PSII, which is a redox mediator that shuttles electrons from the water oxidation catalyst to P680[Formula: see text]. The dyads consisting of a porphyrin and an unsubstituted BIP are designed to study one-electron one-proton transfer (E1PT) processes upon excitation of the porphyrin. When the BIP moiety is substituted with proton-accepting groups such as imines, one-electron two-proton transfer (E2PT) processes are expected to take place upon oxidation of the phenol by the excited state of the porphyrin. The bis-pentafluorophenyl porphyrins linked to BIPs provide platforms for introducing a variety of electron-accepting moieties and/or anchoring groups to attach semiconductor nanoparticles to the macrocycle. The triads thus formed will serve to study the PCET process involving the BIPs when the oxidation of the phenol is achieved by the photochemically produced radical cation of the porphyrin.


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