scholarly journals The energetics of electron and proton transfer to CO2 in aqueous solution

2021 ◽  
Author(s):  
Xiaohui Yang ◽  
Angel Cuesta ◽  
Jun Cheng
Keyword(s):  
Aqueous Solution ◽  
Reaction Mechanism ◽  
Proton Transfer ◽  
Energy Conversion ◽  
Chemical Energy ◽  
Electrocatalytic Reduction

The electrocatalytic reduction of CO2 is considered an effective method to reduce CO2 emissions and achieve electrical/chemical energy conversion. It is crucial to determine the reaction mechanism so that the...

scholarly journals Reaction Mechanism for Direct Proton Transfer from Carbonic Acid to a Strong Base in Aqueous Solution I: Acid and Base Coordinate and Charge Dynamics

2016 ◽  
Vol 120 (9) ◽  
pp. 2271-2280 ◽  
Author(s):  
Snehasis Daschakraborty ◽  
Philip M. Kiefer ◽  
Yifat Miller ◽  
Yair Motro ◽  
Dina Pines ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Reaction Mechanism ◽  
Proton Transfer ◽  
Carbonic Acid ◽  
Strong Base ◽  
Charge Dynamics ◽  
Acid And Base

scholarly journals Reaction Mechanism for Direct Proton Transfer from Carbonic Acid to a Strong Base in Aqueous Solution II: Solvent Coordinate-Dependent Reaction Path

2016 ◽  
Vol 120 (9) ◽  
pp. 2281-2290 ◽  
Author(s):  
Snehasis Daschakraborty ◽  
Philip M. Kiefer ◽  
Yifat Miller ◽  
Yair Motro ◽  
Dina Pines ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Reaction Mechanism ◽  
Proton Transfer ◽  
Carbonic Acid ◽  
Reaction Path ◽  
Strong Base

Ionic dimerisation of trifluoropropenenitrile and its addition reactions with methyl trifluoropropenoate

1980 ◽  
Vol 45 (2) ◽  
pp. 406-414 ◽  
Author(s):  
Jiří Svoboda ◽  
Oldřich Paleta ◽  
Václav Dědek
Keyword(s):  
Reaction Mechanism ◽  
Proton Transfer ◽  
Substituent Effect ◽  
Solvent Molecule ◽  
Addition Product ◽  
Potassium Fluoride ◽  
Relative Reactivity ◽  
Addition Reactions ◽  
Tertiary Amines ◽  
Optimum Conditions

Dimerisation of trifluoropropenenitrile (I) in the presence of potassium fluoride and tertiary amines afforded a mixture of stereoisomeric perfluoro-4-methyl-pentenedinitriles (II), higher-boiling compounds, and 2,3,3,3-tetrafluoropropanenitrile (III) which arises by proton transfer from the solvent molecule. Under optimum conditions, product II was obtained in about 50% yield. Reaction of the nitrile I with methyl trifluoropropenoate (IV) gave, besides the dimers II and V, the product of addition of the nitrile I to the propenoate, IV, i.e. methyl 4-cyanoperfluoro-2-pentenoate (VI), and the addition product of the propenoate IV to the nitrile I, i.e. methyl 4-cyanoperfluoro-2-methyl-3-butenoate (VII). The relative reactivity if I and IV is discussed. The ratio of stereoisomers in II, V, VI and VII indicates that the magnitude of the steric substituent effect, operating in the reaction mechanism, decreases in the order -CFCF3.(COOCH3) > -CFCF3(CN) > -COOCH3 > -CN.

Photoassisted chemical energy conversion into electricity using a sulfite‑iron photocatalytic fuel cell

2021 ◽  
Vol 881 ◽  
pp. 114940
Author(s):  
Izabela Campos Sena ◽  
Davi de Oliveira Sales ◽  
Tatiana Santos Andrade ◽  
Mariandry Rodriguez ◽  
Adilson Cândido da Silva ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Energy Conversion ◽  
Chemical Energy ◽  
Photocatalytic Fuel Cell

Enhanced solar-to-chemical energy conversion of graphitic carbon nitride by two-dimensional cocatalysts

EnergyChem ◽  
2021 ◽  
Vol 3 (2) ◽  
pp. 100051
Author(s):  
Chuanbiao Bie ◽  
Bei Cheng ◽  
Jiajie Fan ◽  
Wingkei Ho ◽  
Jiaguo Yu
Keyword(s):  
Energy Conversion ◽  
Carbon Nitride ◽  
Graphitic Carbon ◽  
Chemical Energy ◽  
Graphitic Carbon Nitride ◽  
Two Dimensional

scholarly journals Base-enhanced catalytic water oxidation by a carboxylate–bipyridine Ru(II) complex

2015 ◽  
Vol 112 (16) ◽  
pp. 4935-4940 ◽  
Author(s):  
Na Song ◽  
Javier J. Concepcion ◽  
Robert A. Binstead ◽  
Jennifer A. Rudd ◽  
Aaron K. Vannucci ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Proton Transfer ◽  
Water Oxidation ◽  
Proton Acceptor ◽  
Half Time ◽  
X Ray ◽  
X Ray Crystallography ◽  
Buffer Base ◽  
Electron Proton Transfer ◽  
C Nmr

In aqueous solution above pH 2.4 with 4% (vol/vol) CH3CN, the complex [RuII(bda)(isoq)2] (bda is 2,2′-bipyridine-6,6′-dicarboxylate; isoq is isoquinoline) exists as the open-arm chelate, [RuII(CO2-bpy-CO2−)(isoq)2(NCCH3)], as shown by 1H and 13C-NMR, X-ray crystallography, and pH titrations. Rates of water oxidation with the open-arm chelate are remarkably enhanced by added proton acceptor bases, as measured by cyclic voltammetry (CV). In 1.0 M PO43–, the calculated half-time for water oxidation is ∼7 μs. The key to the rate accelerations with added bases is direct involvement of the buffer base in either atom–proton transfer (APT) or concerted electron–proton transfer (EPT) pathways.

Reaction Mechanism of Perovskite KNbO3 in Aqueous Solution

2003 ◽  
Vol 248 ◽  
pp. 27-30
Author(s):  
Kenji Toda ◽  
Saori Tokuoka ◽  
Naotaka Ohtake ◽  
Kazuyoshi Uematsu ◽  
Mineo Sato
Keyword(s):  
Aqueous Solution ◽  
Reaction Mechanism
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