Solution reaction design: electroaccepting and electrodonating powers of ions in solution
1 State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, People's Republic of China
2 State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China
Citation and License
Nanoscale Research Letters 2012, 7:6 doi:10.1186/1556-276X-7-6Published: 5 January 2012
By considering a first-order variation in electroaccepting and electrodonating powers, ω±, induced by a change from gas to aqueous solution phase, the solvent effect on ω± for charged ions is examined. The expression of electroaccepting and electrodonating powers in the solution phase, ω±s, is obtained through establishing the quantitative relationship between the change of the ω± due to the solvation and the hydration free energy. It is shown that cations are poorer electron acceptors and anions are poorer electron donors in solution compared to those in gas phase. We have proven that the scaled aqueous electroaccepting power, ω+s, of cations can act as a good descriptor of the reduction reaction, which is expected to be applied in the design of solution reactions.