Two mesoporous ordered carbon materials (MOCs) have been synthesized from silica templates by using sucrose as the carbon precursor. The textural characterization using Ar, N-2, and CO2 adsorption combined with neutron diffraction showed that the two samples exhibit a significant microporous volume close to 0.5 cm(3)/g and an ordered network of mesopores. For both MCM48 and SBA15 templated carbons, adsorption first proceeds with the filling of micropores and then by the filling of mesopores with an adsorption energy close to the enthalpy of vaporization of bulk hydrogen. The hydrogen isosteric heat of adsorption in the micropores (6-8 kJ/mol) is significantly larger than that on the graphite surface (similar to 4 kJ/mol) but still too small for a reasonable use of these MOCs as hydrogen adsorbents for storage at room temperature. The neutron scattering study showed that the structure at 10 K of the adsorbed deuterium phase is poorly organized; it exhibits short and medium range orders of about 13 angstrom in micropores and about 20 angstrom in mesopores, respectively. The average distance between adsorbed molecules decreases with coverage by about 10%. In the mesopores, the diffracted line is consistent with a pseudohexagonal packing.