While reduction reactions are ubiquitous in chemistry, it is very challenging to further reduce electron-rich compounds, especially the anionic ones. In this work, the reduction of 1,3-butadienyl dianion, the anionic conjugated olefin, has been realized by divalent rare-earth metal compounds (SmI2), resulting in the formation of novel 2-butene tetraanion bridged disamarium(III) complexes. Density functional theory (DFT) analyses reveal two features: (i) the single electron transfer (SET) from 41 atomic orbitals (AOs) of each Sm center to the antibonding pi*-orbitals of 1,3-butadienyl dianion is feasible and the new HOMO formed by the bonding interaction between Sm Sd orbitals (AOs) and the pi*-orbitals of 1,3-butadienyl dianion can accept favorably 2e(-) from 4f AOs of Sm(II); (ii) the 2-butene tetraanionic ligand serves as a unique 10e(- )donating system, in which 4e(-) act as two sigma-donation bonding interactions while the rest 6e(-) as three pi-donation bonding interactions. The disamarium(III) complexes represent a unique class of the bridged bis-alkylidene rare-earth organometallic complexes. The ligand-based reductive reactivity of 2-butene tetraanion bridged disamarium(III) complexes demonstrates that 2-butene tetraanionic ligand serves as a 3e(-) reductant toward cyclooctatetraene (COT) to provide doubly COT-supported disamarabutadiene complexes. The reaction of the disamarium(III) complexes with Cp*Li produces the doubly Cp*-coordinated Sm(III) complexes via salt metathesis. In addition, the reaction with Mo(CO)(6) affords the oxycydopentadienyl dinuclear complex via CO insertion.