Related Experiment Video
Updated: May 24, 2025

Surface Functionalization of Metal-Organic Frameworks for Improved Moisture Resistance
Published on: September 5, 2018
Inorganic Borate Functionalized {Ni} Polyoxometalates: From Cluster to Cage Cluster
Yu Wang1, Jun-Jun Sun2, Hai-Lou Li3
1MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.
Abstract:
In aqueous solution systems, an all-inorganic Ni6-added polyoxometalate (Ni6AP) [Ni6(μ3-OH)3(H2O)12(B-α-SiW9O34)]1- ({NiSiW}, here, {Ni} = Ni6(μ3-OH)3(H2O)12) has been made via a hydrothermal method. By introducing inorganic boron sources, a B3O3(OH)6 ({B}) cluster was precisely anchored onto {Ni} to form a [B3O3(OH)6Ni6(μ3-OH)2(H2O)8(B-α-SiW9O34)]3- ({BNi6(OH)2(H2O)8SiW}) through replacing four terminal water molecules and condensing with one hydroxyl of the {Ni} cluster. Subsequently, the addition of further boron sources facilitated the in situ growth of B-O clusters on the basis of {BNi6(OH)2(H2O)8SiW}, which resulted in the successful synthesis of {[B7O8O2/3(OH)6Ni6(μ3-OH)2(H2O)8(B-α-SiW9O34)]3}7- ({BNi6(OH)2(H2O)8SiW}3 or {B}@{Ni6(OH)2(H2O)8SiW}3). It is the first all-inorganic cage cluster constructed by NiAPs and B-O clusters, which successfully realizes the inorganic borate functionalized POMs from a single cluster to a cage cluster. The central {B7O8O2/3(OH)6}3 ({B}) cluster exhibits an uncommon cavity configuration. Meanwhile, we have conducted a discussion of the possible formation mechanism of B-O functionalized NiAPs. Furthermore, these three compounds efficiently accelerate the oxidative transformation of sulfides, and the number of B atoms in compounds relatively affects the selectivity of the products.
More Related Videos
08:56Synthesis of a Borylated Ibuprofen Derivative Through Suzuki Cross-Coupling and Alkene Boracarboxylation Reactions
Published on: November 30, 2022
04:51Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
Published on: June 23, 2023
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Cationic Chain-Growth Polymerization: Mechanism
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3