The selectivity control toward aldehyde in the aromatic alcohol oxidation remains a grand challenge using molecular oxygen under mild conditions. In this work, we designed and synthesized Pt/PCN-224(M) composites by integration of Pt nanocrystals and porphyrinic metal-organic frameworks (MOFs), PCN-224(M). The composites exhibit excellent catalytic performance in the photo-oxidation of aromatic alcohols by 1 atm O at ambient temperature, based on a synergetic photothermal effect and singlet oxygen production. Additionally, in opposition to the function of the Schottky junction, injection of hot electrons from plasmonic Pt into PCN-224(M) would lower the electron density of the Pt surface, which thus is tailorable for the optimized catalytic performance via the competition between the Schottky junction and the plasmonic effect by altering the light intensity. To the best of our knowledge, this is not only an unprecedented report on singlet oxygen-engaged selective oxidation of aromatic alcohols to aldehydes but also the first report on photothermal effect of MOFs.

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Two stable, non-interpenetrated MOFs, PCN-521 and PCN-523, were synthesized by a symmetry-guided strategy. Augmentation of the 4-connected nodes in the fluorite structure with a rigid tetrahedral ligand and substitution of the 8-connected nodes by the Zr/Hf clusters yielded MOFs with large octahedral interstitial cavities. They are the first examples of Zr/Hf MOFs with tetrahedral linkers. PCN-521 has the largest BET surface area (3411 m(2) g(-1)), pore size (20.5×20.5×37.4 Å) and void volume (78.5%) of MOFs formed from tetrahedral ligands. This work not only demonstrates a successful implementation of rational design of MOFs with desired topology, but also provides a systematic way of constructing non-interpenetrated MOFs with high porosity.

For the remediation of oil spills and organic solvent leakage into water, it is desirable to develop not only advanced sorbents with a high adsorption capability but also labor-and time-saving apparatuses that can work continuously without human intervention. In this work, we synthesized a novel and highly stable porous coordination polymer (PCP, also called metal-organic framework), University of Science and Technology of China-6 (USTC-6), with a corrugated -CF 3 surface that features high hydrophobicity. The uniform growth of USTC-6 throughout a graphene oxide (GO)-modified sponge was achieved and yielded a macroscopic USTC-6@GO@sponge sorbent, which repels water and exhibits a superior adsorption capacity for diverse oils and organic solvents. Remarkably, the sorbent can be further assembled with tubes and a self-priming pump to build a model apparatus that affords consecutive and efficient oil recovery from water. The easy and fast recovery of oils/organic solvents from water based on such an apparatus indicates that it has great potential for future water purification and treatment.

The hydrogenation efficiency of nitro compounds was found to be greatly boosted by coupling with dehydrogenation of ammonia borane. The Pd@MIL-101 with tiny Pd NPs is exceptionally efficient and recyclable in the tandem reactions and diverse nitro compounds can be selectively reduced to the corresponding amines in 1.5-5 min with quantitative yields.