Citation: Yang E, Zhou Li-Xin, Zhang Yong-Fan. Theoretical Study on the Interaction between β-D-ribose(RI) and Bivalent and Monovalent Cations[J]. Acta Physico-Chimica Sinica, ;2002, 18(03): 253-259. doi: 10.3866/PKU.WHXB20020313
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The interactions of βDribose(RI) with metal cations in groups Ia(Li+、Na+、K+、Rb+、Cs+)、Ib(Cu+、Ag+、Au+)、Ⅱa (Mg2+、Ca2+ 、Sr2+ 、Ba2+) and Ⅱb (Zn2+ 、Cd2+ 、Hg2+ ) were studied at the HartreeFock and MP2 levels employing all electron(AE) and pseudopotential treatments. Relativistic effective core potentials (RECP) were used for all the ions, with the exception of Li+. AE and RECP treatments were tested for the Na+、K+、Cu+、Mg2+、Ca2+ and Zn2+ complexes; od agreement between the results of AE and RECP suggests that pseudopotentials can be used with confidence also for heavy metal cations. However, in order to ensure the precision of computation,EDEF and EBSSE must be taken into account. The deformation of βDribose caused by bivalent ions are more serious than those caused by monovalent ions. Stabilization energies(ΔE) and interaction Gibbs energies(ΔG) of complexes with bivalent ions are smaller than those with monovalent ions. Therefore, the interaction between bivalent ions and βDribose is stronger than that between monovalent ions and βDribose. And in the same group the stability of complexes decreases with increasing atomic number of the metal ions(except the Au+RI complex), because ΔE and ΔG added with increasing atomic number of the metal ions.
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