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The Anisotropic Responses of a Flexible Metal-Organic Framework Constructed from Asymmetric Flexible Linkers and Heptanuclear Zinc Carboxylate Secondary Building Units.

ABSTRACT: A new porous and flexible metal-organic framework (MOF) has been synthesized from the flexible asymmetric linker N-(4-carboxyphenyl)succinamate (CSA) and heptanuclear zinc oxo-clusters of formula [Zn₇O₂(carboxylate)₁₀DMF₂] involving two coordinated terminal DMF ligands. The structural response of this MOF to the removal or exchange of its guest molecules has been probed using a combination of experimental and computational approaches. The topology of the material, involving double linker connections in the a and b directions and single linker connections along the c axis, is shown to be key in the material's anisotropic response. The a and b directions remain locked during guest removal, whereas the c axis linker undergoes large changes significantly reducing the material's void space. The changes to the c axis linker involve a combination of a hinge motion on the linker's rigid side and conformational rearrangements on its flexible end, which were probed in detail during this process despite the presence of crystallographic disorder along this axis, which prevented accurate characterization by experimental methods alone. Although inactive during guest removal, the flexible ends of the a and b axis linkers are observed to play a prominent role during DMF to DMSO solvent exchange, facilitating the exchange reaction arising in the cluster.

SUBMITTER: Carrington EJ

PROVIDER: S-EPMC6778970 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Metal-organic frameworks constructed from monomeric, dimeric and trimeric phenanthroline citrate zinc building units.

Project description:Adduct of mononuclear and dinuclear citrate zinc complex [Zn(Hcit)(phen)(H2O)][Zn2(Hcit)(phen)2(H2O)3]·13.5H2O (1) and its aggregate [Zn3(Hcit)2(phen)4]n·14nH2O (2) (H4cit = citric acid, phen = 1,10-phenanthroline) were synthesized in weak acidic solutions. The former was obtained from the reaction of zinc nitrate, citric acid and phenanthroline in a molar ratio of 3 : 2 : 3, while a slightly excess of phenanthroline results in the formation of the polymeric product 2 in a molar ratio of 3 : 2 : 4. Transformation of 1 to 2 was finished by the reaction of 1 with an equimolar of phenanthroline in 72% yield. Reverse conversion of 2 to 1 is obtained in 77% yield, showing an equilibrium between 1 and 2. Neutral compound 1 consists of one monomeric anionic unit [Zn(Hcit)(phen)(H2O)]- and one dimeric cationic unit [Zn2(Hcit)(phen)2(H2O)3]+ that connect each other by strong hydrogen bonds [O6?O4w 2.636(2); O7?O3w 2.630(3) Å]. In 2, the citrate ligand links each trinuclear unit [Zn3(Hcit)2(phen)4] to generate an infinite 1D chain that extents into a 3D supramolecular structure by intra- and inter-molecular hydrogen bonds. Moreover, 1 and 2 exhibit strong fluorescence at room temperature.

| S-EPMC3600651 | biostudies-literature

Symmetry-based self-assembled nanotubes constructed using native protein structures: the key role of flexible linkers.

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Printable Zinc-Ion Hybrid Micro-Capacitors for Flexible Self-Powered Integrated Units.

Project description:Wearable self-powered systems integrated with energy conversion and storage devices such as solar-charging power units arouse widespread concerns in scientific and industrial realms. However, their applications are hampered by the restrictions of unbefitting size matching between integrated modules, limited tolerance to the variation of input current, reliability, and safety issues. Herein, flexible solar-charging self-powered units based on printed Zn-ion hybrid micro-capacitor as the energy storage module is developed. Unique 3D micro-/nano-architecture of the biomass kelp-carbon combined with multivalent ion (Zn2+) storage endows the aqueous Zn-ion hybrid capacitor with high specific capacity (196.7 mAh g-1 at 0.1 A g-1). By employing an in-plane asymmetric printing technique, the fabricated quasi-solid-state Zn-ion hybrid micro-capacitors exhibit high rate, long life and energy density up to 8.2 μWh cm-2. After integrating the micro-capacitor with organic solar cells, the derived self-powered system presents outstanding energy conversion/storage efficiency (ηoverall = 17.8%), solar-charging cyclic stability (95% after 100 cycles), wide current tolerance, and good mechanical flexibility. Such portable, wearable, and green integrated units offer new insights into design of advanced self-powered systems toward the goal of developing highly safe, economic, stable, and long-life smart wearable electronics.

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Project description: Not available

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Printable magnesium ion quasi-solid-state asymmetric supercapacitors for flexible solar-charging integrated units.

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Project description:A new Zn-cluster based MOF, [Zn21(BTC)11(?3-OH)3(?4-O)3(H2O)18]·21EtOH (1) (H3BTC?=?1,3,5-benzenetricarboxylic acid), with two different types of cluster nodes has been successfully synthesized from Zn2+ and H3BTC under the solvothermal conditions. Single crystal X-ray diffraction studies reveal that 1 is a 3D trinodal (3,5,6)-c framework which features a large octahedral cage organized by nine Zn3O and nine Zn4O clusters SBUs and twenty-four triangular BTC3- linkers. The Eu3+/Tb3+-incorporated derivative of 1 with 0.251% Eu3+ and 0.269% Tb3+ exhibits tunable luminescence from yellow to white and then to blue-green by changing the excitation wavelength from 308 to 315?nm. Metal ion exchange with Cu2+ affords isomorphous Cu-based MOF with enhanced N2 and CO2 adsorption capacity. In addition, 1 can act as a selective luminescent sensor for Cu2+ and Al3+ ions.

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Dinuclear zinc-catalyzed asymmetric desymmetrization of acyclic 2-substituted-1,3-propanediols: a powerful entry into chiral building blocks.

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