Related Experiment Video
Updated: Sep 10, 2025

06:23
Preparation of DMMTAV and DMDTAV Using DMAV for Environmental Applications: Synthesis, Purification, and Confirmation
Published on: March 9, 2018
5.6K
Organoarsonate- and Dimethylarsinate-Functionalized Hexamolybdates(V): A Multifaceted Study on Synthesis, Structural
Vinaya Siby1, Arun Pal1, Anupam Sarkar1
1School of Science, Constructor University, Campus Ring 1, 28759 Bremen, Germany.
Inorganic Chemistry
|August 25, 2025
Summary
Eleven novel dimethylarsinate-functionalized arsenomolybdates were synthesized and characterized. Three of these polyanions showed moderate antibacterial activity against tested bacterial strains.
Area of Science:
- Inorganic Chemistry
- Materials Science
- Medicinal Chemistry
Background:
- Arsenomolybdates are a class of inorganic compounds with potential applications in catalysis and medicine.
- Functionalization of these clusters allows for tuning of their properties and exploration of new applications.
Purpose of the Study:
- To synthesize and characterize novel dimethylarsinate-functionalized arsenomolybdates(V).
- To investigate the structural, solution-phase, and gas-phase properties of these compounds.
- To evaluate the antibacterial activity of the synthesized polyanions.
Main Methods:
- One-pot aqueous synthesis method.
- Single-crystal X-ray diffraction, thermogravimetric analysis, elemental analysis for solid-state characterization.
- Multinuclear NMR spectroscopy for solution-phase stability.
- Electrospray ionization mass spectrometry and tandem mass spectrometry for gas-phase behavior.
- Antibacterial screening against Escherichia coli, Bacillus subtilis, Listeria monocytogenes, Salmonella enterica, and Vibrio parahaemolyticus.
Main Results:
- Synthesis and structural characterization of 11 novel dimethylarsinate-functionalized arsenomolybdates(V) with a reduced hexanuclear {MoV6O24} core.
- Diverse organoarsonate, arsenate, or arsenite groups were successfully incorporated, including carboxylated, fluorinated, brominated, and azido derivatives.
- Three of the synthesized polyanions demonstrated moderate antibacterial activity against selected bacterial strains.
- First-time synthesis of 3,5-bis(carboxy)phenylarsonic acid reported.
Conclusions:
- Novel functionalized arsenomolybdates can be efficiently synthesized using a straightforward aqueous method.
- The structural diversity and tunable functionalization of these polyanions are confirmed.
- The moderate antibacterial activity suggests potential for further development in antimicrobial applications.
Related Concept Videos
Diazonium Group Substitution: –OH and –H
2.9K
Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.
2.9K
Structural Isomerism
19.7K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
19.7K
Properties of Organometallic Compounds
1.1K
Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
1.1K

