The substitution effects on the geometry and the electronic structure of the ferrocene are systematically and comparatively studied using the density functional theory. It is found that -NH(2) and -OH substituents exert different influence on the geometry from -CH(3), -SiH(3), -PH(2), and -SH substituents. The topological analysis shows that all the C-C bonds in a-g are typical opened-shell interactions while the Fe-C bonds are typical closed-shell interactions. NBO analysis indicates that the cooperated interaction of d --> pi* and feedback pi --> d + 4s enhances the Fe-ligand interaction. The energy partitioning analysis demonstrates that the substituents with the second row elements lead to stronger iron-ligand interactions than those with the third row elements. The molecular electrostatic potential predicts that the electrophiles are expected to attack preferably the N, O, P, or S atoms in Fer-NH(2), Fer-OH, Fer-PH(2), and Fer-SH, and attack the ring C atoms in Fer-SiH(3) and Fer-CH(3). In turn, the nucleophiles are supposed to interact predominantly by attacking the hydrogen atoms. The simulated theoretical excitation spectra show that the maximum absorption peaks are red-shifted when the substituents going from second row elements to the third row elements.

No abstract

No abstract

Red block crystals of the title compound are prepared by slow evaporation of an aqueous solution containing Co(OAc)2, K8[γ‐SiW10O36], NaHCO3, and KCl (10 °C, 14 d; 47% yield).

Na2 [{Y(H2O) 7}4Sb2W22O76] ·14H2O is synthesized from an aqueous HNO3 solution of Y2O3 and Na9[SbW9O33], (pH 2.2 adjusted with 4 M HCl, 95 °C, 2 h, 50% yield).