Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds and their preparation method and applications for catalyzing the degradation of chemical warfare agent simulants

Patent metadata

Field	Value
Publication number	US-11358133-B2
Application number	US-201816476012-A
Country	US
Kind code	B2
Filing date	May 16, 2018
Priority date	May 16, 2018
Publication date	Jun 14, 2022
Grant date	Jun 14, 2022

Abstract

Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, and their preparation method and applications in catalyzing the degradation of chemical warfare agent simulants. In the synthesis, Na2MoO4, p-hydroxybenzonic acid (PHBA), alanine (Ala), KCl, transition metal cations and As2O3 as raw materials and water are used as solvent. At room temperature, 2-chloroethyl ethyl sulfide (CEES) and the prepared polyoxometalate hybrid compounds were mixed together in anhydrous ethanol and stirred, and H2O2 was subsequently added into the reaction system. The catalytic reaction for the degradation of CEES was finished within 5 min under stirring. In the catalytic hydrolysis of diethyl cyanophosphonate (DECP), the catalyst, DECP, DMF and H2O were put together and mixed fully. The prepared polyoxometalate hybrid compounds have the advantages of high conversion, high selectivity and easy recyclability in catalyzing the degradation of two types of chemical warfare agent simulant.

First claim

The invention claimed is:

1. Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, wherein the compounds are composed of carboxylic acid modified polyoxomolybdate [AsMo 6 O 21 (Ala)(PHBA) 2 ] 5− covalently linked by metal cations selected from (Co 2+ , Ni 2+ , Zn 2+ , or Mn 2+ ) to form 1-dimensional (1D) chain structures; a chemical formula is K 2 H[(H 2 O) 4 M][AsMo 6 O 21 (Ala)(PHBA) 2 ]·nH 2 O; wherein M=Co 2+ , Ni 2+ , Zn 2+ , Mn 2+ ; Ala=alanine, PHBA=p-hydroxybenzonic acid; n=6.5, 9, 7.5, 7.5, a value of n corresponds to M=Co 2+ , Ni 2+ , Zn 2+ , Mn 2+ , respectively;
crystals of the metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds belong to triclinic crystal system and P-1 space group;
when M=Co 2+ , cell parameters of compound 1 are a=12.0872(8) Å, b=12.5682(8) Å, c=17.2255(13) Å, α=76.700(4)°, β=74.058(4)°, γ=76.399(4)°;
when M=Ni 2+ , cell parameters of compound 2 are a=11.9612(4) Å, b=12.5318(3) Å, c=17.1943(4) Å, α=76.4990(10) °, β=74.053(2)°, γ=76.535(2)°;
when M=Zn 2+ , cell parameters of compound 3 are a=12.1425(2) Å, b=12.5739(2)Å, c=17.2226(3)Å, α=76.4430(10) °, β=74.0620(10)°, γ=76.2250(10)°;
when M=Mn 2+ , cell parameters of compound 4 are a=12.2865(7) Å, b=12.6065(7) Å, c=17.2145(11) Å, α=76.319(3) °, β=73.933(3)°, γ=76.064(3)°;
compounds 1-4 are isostructural, and an asymmetric unit of compounds 1-4 contains one crystallographically independent [AsMo 6 O 21 ] 3− anion, one Co 2+ , Ni 2+ , Zn 2+ or Mn 2+ cation, two K + cations, two p-hydroxybenzoic acids and one protonated alanine molecule; firstly, the [AsMo 6 O 21 (Ala)(PHBA) 2 ] 5− units are joined together by Co 2+ via Co—O—Mo bond, Ni 2+ via Ni—O—Mo bond, Zn 2+ via Zn—O—Mo bond and Mn 2+ via Mn—O—Mo bond, respectively, to form a 1D linear chain; then strong hydrogen bonds between 1D chains produce a 2-dimensional (2D) supramolecular layer; finally, these 2D layers are linked together to generate a 3-dimensional (3D) supramolecular framework via the hydrogen bonds.

2. A preparation method of the metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds according to claim 1 is as follows:
firstly, Na 2 MoO 4 , PHBA, Ala, KCl and As 2 O 3 were dissolved in water, and a pH value of a mixture was adjusted to 3.5-4.5 with 4 M HCl; then an excessive amount of CoCl 2 was added to the reaction mixture; a mole ratio of these materials Na 2 MoO 4 , PHBA, Ala, KCl, As 2 O 3 and CoCl 2 are 6:2:1:2-3:1:1-3; finally, the mixture was heated and stirred in water bath for 1-5 hours at 75-100° C.; a filtrate was kept undisturbed after it cooled under ambient conditions until crystals produced; the crystals are the metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, which were then washed and dried.

3. The preparation method according to claim 2 , wherein CoCl 2 is replaced by NiCl 2 , ZnCl 2 , or MnCl 2 .

4. The preparation method according to claim 2 , wherein CoCl 2 is replaced by Co(NO 3 ) 2 or CoSO 4 .

5. An application of the metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds according to claim 1 in catalyzing the degradation of 2-chloroethyl ethyl sulfide (CEES), wherein the operation is as follows:
CEES and the metal ion-directed carboxylic acid modified polyoxometalates were mixed together in anhydrous ethanol; then, H 2 O 2 was subsequently added in this reaction system under stirring; the catalytic degradation was finished after 5 minutes; mole ratio of CEES, the metal ion-directed carboxylic acid modified polyoxometalates and oxidant is 200:3:200-300; the catalytic degradation route is as follow:

6. An application of the metal ion-directed carboxylic acid modified polyoxometalate hybrid compounds according to claim 1 in catalyzing the degradation of diethyl cyanophosphonate (DECP), wherein the operation is as follows:
DECP, N N-dimethylformamide (DMF) and H 2 O were mixed together under stirring, and then the metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds were subsequently added into the catalytic mixture; the catalytic degradation was completed after 10 minutes; a mole ratio of DECP and catalyst is 1000:1; the catalytic degradation route is as follow:

Assignees

• Univ Dalian Tech

Inventors

• An Haiyan
• Hou Yujiao

Classifications

• B01J2231/70

  Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues · CPC title

• B01J2531/72

  Manganese · CPC title

• B01J2531/26

  Zinc · CPC title

• B01J31/34

  of chromium, molybdenum or tungsten · CPC title

• B01J23/18

  Arsenic, antimony or bismuth · CPC title