Abstract
Structure and bonding for a series of oxo-bridged and sulphur bridged alkali-metal centers (M-X-M: Li, Na and K; X=O, S) are studied for various M-X-M angles. The structures for these charge-transfer systems are compared with H-X-H. These charge- transfer systems show bonding and structures that are distinctively different from the covalent H-X-H molecules. The singlet-triplet gap for all of these molecules are positive suggesting the stabilization of the spin-paired configuration instead of the paramagnetic state. The variation in the exchange-coupling constant (J) with the change in M-X-M angle suggest that the singlet- triplet gap for these systems can be reduced through stabilization of geometries with M-X-M angles differing from the ground state geometries. Strategies are proposed for reducing the singlet-triplet gaps in these systems by confining them inside fullerenes.