Remote Control of Electron Transfer Reaction by Microwave Irradiation: Kinetic Demonstration of Reduction of Bipyridine Derivatives on Surface of Nickel Particle.

Microwave irradiation has great potential to control chemical reactions remotely, particularly reactions that involve electron transfer. In this study, we found that the reduction reaction of bipyridine derivatives on metal nickel particles was accelerated or decelerated by 2.45 GHz microwaves without an alteration of the reaction temperature. The order of the extent of the microwave acceleration of the electron transfer reaction coincided with the negativity of the redox potential of the bipyridine derivatives, i.e., the electron transfer with smaller Δ G was significantly enhanced by microwave irradiation. By applying Marcus' electron transfer theory, we propose two mechanisms of the microwave effect on electron transfer reactions, i.e., vibration of the electrons in Ni particles to make the electron transfer easier and rotation of the water molecules to prevent the reorganization of the hydrated systems after the electron transfer reaction.

[1]  S. Tsubaki,et al.  Acceleration of Water Electrolysis by Accumulation of Microwave Energy at a Pt Disk Electrode , 2017 .

[2]  S. Tsubaki,et al.  Enhancement of anodic current attributed to oxygen evolution on α-Fe2O3 electrode by microwave oscillating electric field , 2016, Scientific Reports.

[3]  Jicheng Zhou,et al.  A new type of power energy for accelerating chemical reactions: the nature of a microwave-driving force for accelerating chemical reactions , 2016, Scientific Reports.

[4]  S. Fujii,et al.  Microwave-enhanced photocatalysis on CdS quantum dots - Evidence of acceleration of photoinduced electron transfer , 2015, Scientific Reports.

[5]  Y. Wada,et al.  Catalytic reactions enhanced under microwave-induced local thermal non-equilibrium in a core-shell, carbon-filled zeolite@zeolite , 2015 .

[6]  A. Stiegman,et al.  Development of Magnetic Nanoparticles as Microwave-Specific Catalysts for the Rapid, Low-Temperature Synthesis of Formalin Solutions , 2013 .

[7]  C. Kappe,et al.  Microwave effects in organic synthesis: myth or reality? , 2013, Angewandte Chemie.

[8]  Y. Wada,et al.  Local Thermal Nonequilibrium on Solid and Liquid Interface Generated in a Microwave Magnetic Field , 2012 .

[9]  S. Suib,et al.  Synergetic Effects of Ultraviolet and Microwave Radiation for Enhanced Activity of TiO2 Nanoparticles in Degrading Organic Dyes Using a Continuous-Flow Reactor , 2012 .

[10]  Y. Wada,et al.  In Situ Observation of Nonequilibrium Local Heating as an Origin of Special Effect of Microwave on Chemistry , 2010 .

[11]  M. Taddei,et al.  Microwave-assisted carbonylation and cyclocarbonylation of aryl iodides under ligand free heterogeneous catalysis. , 2010, The Journal of organic chemistry.

[12]  M. Herrero,et al.  Nonthermal microwave effects revisited: on the importance of internal temperature monitoring and agitation in microwave chemistry. , 2008, The Journal of organic chemistry.

[13]  E. Clennan Viologen embedded zeolites , 2004 .

[14]  S. Horikoshi,et al.  Environmental remediation by an integrated microwave/UV illumination method. V. Thermal and nonthermal effects of microwave radiation on the photocatalyst and on the photodegradation of rhodamine-B under UV/Vis radiation. , 2003, Environmental science & technology.

[15]  P. Gaillard,et al.  MICROWAVE HEATING AS A NEW WAY TO INDUCE LOCALIZED ENHANCEMENTS OF REACTION RATE. NON-ISOTHERMAL AND HETEROGENEOUS KINETICS , 1996 .

[16]  P. Fretwell,et al.  Equilibrium between 2-oxomorpholin-3-yl radicals and viologen radicals. Determination of reduction potentials , 1992 .

[17]  R. G. Wilkins,et al.  Kinetics of reduction of eight viologens by dithionite ion , 1985 .

[18]  K. Honda,et al.  Measurement of the extinction coefficient of the methyl viologen cation radical and the efficiency of its formation by semiconductor photocatalysis , 1982 .

[19]  Rudolph A. Marcus,et al.  On the Theory of Oxidation‐Reduction Reactions Involving Electron Transfer. I , 1956 .