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Theoretical studies on the influence of metallic cations on ring opening of propylene oxide catalyzed by metal-salen complexes
Authors:Lei Chen  Hui-Qing Yang  Cheng-Yu Jin  Zhao-Xu Chen
Institution:1. Institute of Theoretical and Computational Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China

Contribution: Conceptualization, Supervision, Writing - original draft, Writing - review & editing;2. Institute of Theoretical and Computational Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China

Contribution: ?Investigation, Writing - review & editing;3. Institute of Theoretical and Computational Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China

Abstract:We studied the ring opening of propylene oxide (PO) by salen-M coordinated OH? group M = Al(III), Sc(III), Cr(III), Mn(III), Fe(III), Co(II), Co(III), Ni(II), Cu(II), Zn(II), Ru(III) and Rh(III)]. The results show that the ring-opening energy barriers for M(II) complexes are much lower than those with M(III) complexes in the gas phase, and the barriers correlate linearly with the negative charges on the OH? group and the Fukui function condensed on the OH? group. The nucleophilicity ordering in the gas phase can be rationalized by the ratio of formal positive charges/radius of M cations. Solvent effect greatly increases the barriers of M(II) complexes but slightly changes the results of M(III) ones, making the barriers similar. Analysis indicates that the reaction heats are linearly proportional to the reverse reaction barriers. The relationships established here can be used to estimate the ring-opening barriers and to screen epoxide ring-opening catalysts.
Keywords:density functional calculations  metal-salen complexes  propylene oxide hydration  ring opening  structure-activity correlation
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