Xia Yu , Zhenyu Shi , Yanhua Yu , Yuguo Zheng , Qingqing Guo , Xiaoyan Li , Jie Zhao , Weiran Long
{"title":"Syntheses, electrochemical sensors and desulfurization of three octamolybdate-based hybrids decorated by multiple N-donor ligands","authors":"Xia Yu , Zhenyu Shi , Yanhua Yu , Yuguo Zheng , Qingqing Guo , Xiaoyan Li , Jie Zhao , Weiran Long","doi":"10.1016/j.ica.2025.122841","DOIUrl":null,"url":null,"abstract":"<div><div>Three new octamolybdates-based hybrid compounds, [Ag<sub>2</sub>(H<sub>3</sub>X)<sub>2</sub>](Mo<sub>8</sub>O<sub>26</sub>)·2H<sub>2</sub>O (<strong>1</strong>), [Cu<sub>2</sub>(H<sub>2</sub>Y)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>](Mo<sub>8</sub>O<sub>26</sub>)·3H<sub>2</sub>O (<strong>2</strong>) and [Ag<sub>4</sub>(H<sub>2</sub>Y)<sub>4</sub>][Mo<sub>8</sub>O<sub>26</sub>] (<strong>3</strong>) (H<sub>2</sub>X = 2,6-dimethyl-3,5-bis(pyrazol-3-yl)pyridine, H<sub>2</sub>Y = 3-(1H-pyrazol-4-yl)-5-(pyridine-2-yl)-1,2,4-triazole), were obtained using different multiple N-donor ligands under hydrothermal conditions. Their characteristics were identified by single crystal X-ray diffraction analyses, elemental analyses, thermogravimetric analyses (TG) and infrared spectra analyses (IR). The structure of compound <strong>1</strong> is a three-dimensional (3D) supramolecular network composed of 2D layers [Ag<sub>2</sub>(H<sub>3</sub>X)<sub>2</sub>(Mo<sub>8</sub>O<sub>26</sub>)] and crystal water molecules through hydrogen bonds. In compound <strong>2</strong>, (Mo<sub>8</sub>O<sub>26</sub>)<sup>4−</sup> anions function as bidentate bridging ligands to join [Cu<sub>2</sub>(H<sub>2</sub>Y)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>]<sup>4+</sup> units into a 1D chain. Compound <strong>3</strong> is assembled by π‧‧‧π stacking interactions between double chains [Ag<sub>4</sub>(H<sub>2</sub>Y)<sub>4</sub>(Mo<sub>8</sub>O<sub>26</sub>)]<sub>n</sub>. Cyclic voltammetry measurements demonstrate that compounds <strong>1</strong>–<strong>3</strong> can serve as versatile bifunctional electrocatalysts, capable of mediating the reduction of KBrO<sub>3</sub>, NaNO<sub>2</sub>, and H<sub>2</sub>O<sub>2</sub>, as well as facilitating the oxidation of ascorbic acid (AA).They also can serve as amperometric sensors for NO<sub>2</sub><sup>−</sup>. Additionally, their photocatalytic properties were evaluated by the degradation of Methylene blue (MB). Compared with the synthetic precursors of compound <strong>2</strong>, it exhibits better catalytic oxidation desulfurization (ODS) efficiency towards thioanisole (MBT). As a heterogeneous catalyst, compound <strong>2</strong> displays good cyclic stability. After 4 cycles of use, the MBT conversion rate decreases only from an initial 98.7 % to 94 %.</div></div>","PeriodicalId":13599,"journal":{"name":"Inorganica Chimica Acta","volume":"588 ","pages":"Article 122841"},"PeriodicalIF":3.2000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganica Chimica Acta","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002016932500307X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Three new octamolybdates-based hybrid compounds, [Ag2(H3X)2](Mo8O26)·2H2O (1), [Cu2(H2Y)2(H2O)4](Mo8O26)·3H2O (2) and [Ag4(H2Y)4][Mo8O26] (3) (H2X = 2,6-dimethyl-3,5-bis(pyrazol-3-yl)pyridine, H2Y = 3-(1H-pyrazol-4-yl)-5-(pyridine-2-yl)-1,2,4-triazole), were obtained using different multiple N-donor ligands under hydrothermal conditions. Their characteristics were identified by single crystal X-ray diffraction analyses, elemental analyses, thermogravimetric analyses (TG) and infrared spectra analyses (IR). The structure of compound 1 is a three-dimensional (3D) supramolecular network composed of 2D layers [Ag2(H3X)2(Mo8O26)] and crystal water molecules through hydrogen bonds. In compound 2, (Mo8O26)4− anions function as bidentate bridging ligands to join [Cu2(H2Y)2(H2O)4]4+ units into a 1D chain. Compound 3 is assembled by π‧‧‧π stacking interactions between double chains [Ag4(H2Y)4(Mo8O26)]n. Cyclic voltammetry measurements demonstrate that compounds 1–3 can serve as versatile bifunctional electrocatalysts, capable of mediating the reduction of KBrO3, NaNO2, and H2O2, as well as facilitating the oxidation of ascorbic acid (AA).They also can serve as amperometric sensors for NO2−. Additionally, their photocatalytic properties were evaluated by the degradation of Methylene blue (MB). Compared with the synthetic precursors of compound 2, it exhibits better catalytic oxidation desulfurization (ODS) efficiency towards thioanisole (MBT). As a heterogeneous catalyst, compound 2 displays good cyclic stability. After 4 cycles of use, the MBT conversion rate decreases only from an initial 98.7 % to 94 %.
期刊介绍:
Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews.
Topics covered include:
• chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies;
• synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs);
• reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models;
• applications of inorganic compounds, metallodrugs and molecule-based materials.
Papers composed primarily of structural reports will typically not be considered for publication.