{"title":"甲基磺酸镁分子自组装成氢键链和层状网络","authors":"Aishwarya Chauhan, Priyanka Chauhan, Ravi Shankar","doi":"10.1016/j.ica.2025.122890","DOIUrl":null,"url":null,"abstract":"<div><div>The study describes the synthesis and structural features of new hydrogen bonded supramolecular assemblies of the salt [H<sub>2</sub>bix][Mg(SO<sub>3</sub>Me)<sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>] (<strong>1</strong>) and salt cocrystals, [Mg(SO<sub>3</sub>Me)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>][H<sub>2</sub>bpe·2SO<sub>3</sub>Me], denoted as <strong>2</strong>·H<sub>2</sub>bpe·2SO<sub>3</sub>Me (<strong>2a</strong>); <strong>2</strong>·Me<sub>2</sub>bpe·2SO<sub>3</sub>Me (<strong>2b</strong>) and <strong>2</strong>·MV·2SO<sub>3</sub>Me (<strong>2c</strong>) [bix = 1,4-bis(imidazole-1-ylmethyl)benzene, bpe = 1,2-bis(4-pyridyl)ethane, MV = 1,1′-dimethyl 4,4′-bipyridinium]. X-ray crystallographic study reveals that the octahedral complex anion in <strong>1</strong> involves coordinated sulfonate and <em>trans</em>-aqua ligands in intermolecular O-H⋯O hydrogen bonding to afford a layered assembly, while the interaction between the constituent elements in <strong>2a-2c</strong> results in one-dimensional strands. The spatial expanse in these frameworks accommodate the organic cations with distinct conformational features (<em>gauche</em> and <em>trans</em>). The integration of methylviologen in <strong>2c</strong> endows the framework with photochromic property in the solid state, as evident by a visual colour change from white to blue upon illumination with 100-watt Hg lamp. The phenomenon is attributed to the formation of methylviologen radical cation (MV<sup>•+</sup>) and validated by EPR and UV–vis spectroscopy. Treatment of <strong>2c</strong> with one equivalent of hydrazine hydrate under ambient conditions gave [Mg<sub>2</sub>(NH<sub>2</sub>NHCOO)<sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>]·2H<sub>2</sub>O (<strong>3</strong>). The formation of <strong>3</strong> is viewed as resulting from displacement of sulfonate from the precursor complex by <em>in situ</em> formed hydrazido carbonate anion, [N<sub>2</sub>H<sub>3</sub>CO<sub>2</sub>]<sup>−</sup> in the presence of atmospheric CO<sub>2</sub>.</div></div>","PeriodicalId":13599,"journal":{"name":"Inorganica Chimica Acta","volume":"589 ","pages":"Article 122890"},"PeriodicalIF":3.2000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-assembly of molecular magnesium methanesulfonates into hydrogen-bonded strands and layered networks\",\"authors\":\"Aishwarya Chauhan, Priyanka Chauhan, Ravi Shankar\",\"doi\":\"10.1016/j.ica.2025.122890\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The study describes the synthesis and structural features of new hydrogen bonded supramolecular assemblies of the salt [H<sub>2</sub>bix][Mg(SO<sub>3</sub>Me)<sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>] (<strong>1</strong>) and salt cocrystals, [Mg(SO<sub>3</sub>Me)<sub>2</sub>(H<sub>2</sub>O)<sub>4</sub>][H<sub>2</sub>bpe·2SO<sub>3</sub>Me], denoted as <strong>2</strong>·H<sub>2</sub>bpe·2SO<sub>3</sub>Me (<strong>2a</strong>); <strong>2</strong>·Me<sub>2</sub>bpe·2SO<sub>3</sub>Me (<strong>2b</strong>) and <strong>2</strong>·MV·2SO<sub>3</sub>Me (<strong>2c</strong>) [bix = 1,4-bis(imidazole-1-ylmethyl)benzene, bpe = 1,2-bis(4-pyridyl)ethane, MV = 1,1′-dimethyl 4,4′-bipyridinium]. X-ray crystallographic study reveals that the octahedral complex anion in <strong>1</strong> involves coordinated sulfonate and <em>trans</em>-aqua ligands in intermolecular O-H⋯O hydrogen bonding to afford a layered assembly, while the interaction between the constituent elements in <strong>2a-2c</strong> results in one-dimensional strands. The spatial expanse in these frameworks accommodate the organic cations with distinct conformational features (<em>gauche</em> and <em>trans</em>). The integration of methylviologen in <strong>2c</strong> endows the framework with photochromic property in the solid state, as evident by a visual colour change from white to blue upon illumination with 100-watt Hg lamp. The phenomenon is attributed to the formation of methylviologen radical cation (MV<sup>•+</sup>) and validated by EPR and UV–vis spectroscopy. Treatment of <strong>2c</strong> with one equivalent of hydrazine hydrate under ambient conditions gave [Mg<sub>2</sub>(NH<sub>2</sub>NHCOO)<sub>4</sub>(H<sub>2</sub>O)<sub>2</sub>]·2H<sub>2</sub>O (<strong>3</strong>). The formation of <strong>3</strong> is viewed as resulting from displacement of sulfonate from the precursor complex by <em>in situ</em> formed hydrazido carbonate anion, [N<sub>2</sub>H<sub>3</sub>CO<sub>2</sub>]<sup>−</sup> in the presence of atmospheric CO<sub>2</sub>.</div></div>\",\"PeriodicalId\":13599,\"journal\":{\"name\":\"Inorganica Chimica Acta\",\"volume\":\"589 \",\"pages\":\"Article 122890\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-09-04\",\"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/S0020169325003561\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganica Chimica Acta","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0020169325003561","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Self-assembly of molecular magnesium methanesulfonates into hydrogen-bonded strands and layered networks
The study describes the synthesis and structural features of new hydrogen bonded supramolecular assemblies of the salt [H2bix][Mg(SO3Me)4(H2O)2] (1) and salt cocrystals, [Mg(SO3Me)2(H2O)4][H2bpe·2SO3Me], denoted as 2·H2bpe·2SO3Me (2a); 2·Me2bpe·2SO3Me (2b) and 2·MV·2SO3Me (2c) [bix = 1,4-bis(imidazole-1-ylmethyl)benzene, bpe = 1,2-bis(4-pyridyl)ethane, MV = 1,1′-dimethyl 4,4′-bipyridinium]. X-ray crystallographic study reveals that the octahedral complex anion in 1 involves coordinated sulfonate and trans-aqua ligands in intermolecular O-H⋯O hydrogen bonding to afford a layered assembly, while the interaction between the constituent elements in 2a-2c results in one-dimensional strands. The spatial expanse in these frameworks accommodate the organic cations with distinct conformational features (gauche and trans). The integration of methylviologen in 2c endows the framework with photochromic property in the solid state, as evident by a visual colour change from white to blue upon illumination with 100-watt Hg lamp. The phenomenon is attributed to the formation of methylviologen radical cation (MV•+) and validated by EPR and UV–vis spectroscopy. Treatment of 2c with one equivalent of hydrazine hydrate under ambient conditions gave [Mg2(NH2NHCOO)4(H2O)2]·2H2O (3). The formation of 3 is viewed as resulting from displacement of sulfonate from the precursor complex by in situ formed hydrazido carbonate anion, [N2H3CO2]− in the presence of atmospheric CO2.
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.