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Two novel porous materials, namely, Zn4O(TPB)4/3(BDC) and chiral Zn4O(TPB)4/3(chir-BDC), have been synthesised by copolymerisation of the newly developed triarylborane linker 4,4′4′′-boranetriyltris(3,5-dimethylbenzoic acid) (H3TPB) with the linear 1,4-benzenedicarboxylic acid (H2BDC) and chir-H2BDC, respectively. The compounds adopt ith-d topology and are microporous. The BET surface area of Zn4O(TPB)4/3(BDC) determined from the nitrogen adsorption isotherm measured at 77 K is 2874 m2 g−1 and both frameworks are accessible to organic dye molecules, the largest being Rhodamine B. Thus, the two compounds are the first examples of non-interpenetrated, highly accessible metal–organic frameworks comprising a triarylborane linker. The framework shows an enhanced isosteric heat of CO2 adsorption in comparison to the isoreticular DUT-6 compound.

Graphical abstract: Copolymerisation at work: the first example of a highly porous MOF comprising a triarylborane-based linker

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