Herein, we report on a new Cu-based MOF material, Cu(2)(dhtp), structurally homologous to the honeycomb-like M(2)(dhtp) series. This has been crystallized under solvothermal conditions using copper nitrate and 2,5-dihydroxyterephthalic acid as an organic linker, being the nature of the co-solvent in the synthesis media an important variable over the final physical properties of the material. The presence of isopropanol as a co-solvent leads to the formation of a pure crystalline phase with textural properties comparable to M(2)(dhtp) homologues. The interesting results in CO(2) adsorption properties of this new material, especially its isosteric heat of adsorption, make it a suitable MOF to be further evaluated under real conditions of industrial CO(2) capture.

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Poly(styrenesulfonic acid)-functionalized materials based on poly(styrenesulfonic acid sodium salt) incorporated via aqueous atom transfer radical polymerization (ATRP) initiated from the surface of large-pore mesoporous SBA-15 silica support have been synthesized. The inorganic-organic nature of these hybrid materials makes them particularly desirable for acid-catalyzed reactions that require extended and hydrophobic surface areas with a narrow pore diameter distribution in the mesoporous range. Acidic hybrid materials were prepared by grafting the ATRP-initiator (3-(chlorodimethylsilyl)propyl bromoisobutyrate) on the silica surface, subsequent polymerization of the styrenesulfonic acid sodium salt monomer, and final sodium ion exchange by acid activation. Conventional and ultra-large-pore SBA-15 silica supports with nominal (BJH) pore diameter ranging from 8 to 32 nm were used for the incorporation of different polymer loadings at different polymerization times. The silylation of ATRP-initiator-functionalized SBA-15 supports has allowed a better control of the ATRP within the mesoporous structure. The use of ultra-large-pore SBA-15 supports provides a remarkable increase of the porosity which allowed us to properly allocate the polymer. The hybrid poly(styrenesulfonic acid)-modified materials showed good catalytic activities in the esterification of oleic acid with n-butanol, particularly in terms of intrinsic activity per acid site.

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