Y.-H. Xing , J.-Q. Xu , H.-R. Sun , D.-M. Li , Y. Xing , Y.-H. Lin , H.-Q. Jia
{"title":"A new dinuclear molybdenum(V)-sulfur complex containing citrate ligand: Synthesis and characterization of K2.5Na2NH4[Mo2O2S2(cit)2].5H2O","authors":"Y.-H. Xing , J.-Q. Xu , H.-R. Sun , D.-M. Li , Y. Xing , Y.-H. Lin , H.-Q. Jia","doi":"10.1016/S0992-4361(99)80014-9","DOIUrl":null,"url":null,"abstract":"<div><p>The complex, K<sub>2.5</sub>Na<sub>2</sub>NH<sub>4</sub>[Mo<sub>2</sub>O<sub>2</sub>S<sub>2</sub>(cit)<sub>2</sub>]·5H<sub>2</sub>O (1), was obtained by crystallization from a solution of (NH<sub>4</sub>)<sub>2</sub>MoS<sub>4</sub>, potassium citrate (K<sub>3</sub>cit) and hydroxyl sodium in methanol and water under an atmosphere of pure nitrogen at ambient temperature. The crystals are triclinic, space group P1¯, a = 7.376 (3)Å, b = 14.620 (2) Å, c = 14.661 (1) Å, α = 71.10 (1)°, β = 81.77 (1)°, γ = 78.27(2)°, R = 0.0584 for 2545 observed (I > 2σ (I)) reflections. Single crystal structure analysis reveals that citrate ligand coordinated to molybdenum atom through two carboxylato oxygens and one deprotonated hydroxyl oxygen together with two bridging sulfur atoms and a terminal oxygen atom completes distorted coordination octahedron around each molybdenum atom. Principal dimensions are Mo = O<sub>1</sub>, 1.707 Å (av); Mo-S<sub>b</sub>, 2.341 Å (av); Mo-O<sub>(hydroxyl)</sub>, 2.021 Å (av); Mo-O<sub>(α-carboxyl)</sub>, 2.1290 Å (av) and Mo-O<sub>(β-carboxyl)</sub>, 2.268(av) Å. IR spectrum is in agreement with the structure.</p></div>","PeriodicalId":100507,"journal":{"name":"European Journal of Solid State and Inorganic Chemistry","volume":"35 10","pages":"Pages 745-756"},"PeriodicalIF":0.0000,"publicationDate":"1998-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0992-4361(99)80014-9","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Solid State and Inorganic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0992436199800149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9
Abstract
The complex, K2.5Na2NH4[Mo2O2S2(cit)2]·5H2O (1), was obtained by crystallization from a solution of (NH4)2MoS4, potassium citrate (K3cit) and hydroxyl sodium in methanol and water under an atmosphere of pure nitrogen at ambient temperature. The crystals are triclinic, space group P1¯, a = 7.376 (3)Å, b = 14.620 (2) Å, c = 14.661 (1) Å, α = 71.10 (1)°, β = 81.77 (1)°, γ = 78.27(2)°, R = 0.0584 for 2545 observed (I > 2σ (I)) reflections. Single crystal structure analysis reveals that citrate ligand coordinated to molybdenum atom through two carboxylato oxygens and one deprotonated hydroxyl oxygen together with two bridging sulfur atoms and a terminal oxygen atom completes distorted coordination octahedron around each molybdenum atom. Principal dimensions are Mo = O1, 1.707 Å (av); Mo-Sb, 2.341 Å (av); Mo-O(hydroxyl), 2.021 Å (av); Mo-O(α-carboxyl), 2.1290 Å (av) and Mo-O(β-carboxyl), 2.268(av) Å. IR spectrum is in agreement with the structure.