{"title":"Synthesis and Structure of the Mn(II) Complexes with Tripyrazolylborate Ligands: Mn[HB(pz)3]2 and Mn[HB(3,5‐Me2‐pz)3]2","authors":"Y. Xing, K. Aoki, F. Bai","doi":"10.1081/SIM-120039263","DOIUrl":null,"url":null,"abstract":"Abstract Mn(II) complexes Mn[HB(pz)3]2 (1) (pz = pyrazole) and Mn[HB(3,5‐Me2‐pz)3]2 (2) have been obtained by the reaction of Mn(OOCCH3)2 with NaHB(pz)3 and NaHB(3,5‐Me2‐pz)3 in MeOH, respectively. The two complexes (1) and (2) were characterized by IR, elemental analyses, and x‐ray diffraction. Complex (1) crystallizes in the space group C2/c, a = 18.971(3) Å, b = 13.700(3) Å, c = 19.056(3) Å, β = 111.378(10), V = 4612.0(13) Å3, Z = 2. Complex (2) crystallizes in the space group R‐3, a = 10.9832(18) Å, b = 10.983(2) Å, c = 24.785(3) Å, γ = 120°, V = 2589.3(7) Å3, Z = 3. X‐ray structure analysis has shown that the complexes (1) and (2) all are monomeric neutral complexes, and possess similar coordination modes around the metal Mn centers. In addition, some related bonding distances, angles, and structural properties are discussed.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"150 1","pages":"1149 - 1163"},"PeriodicalIF":0.0000,"publicationDate":"2004-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/SIM-120039263","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
Abstract Mn(II) complexes Mn[HB(pz)3]2 (1) (pz = pyrazole) and Mn[HB(3,5‐Me2‐pz)3]2 (2) have been obtained by the reaction of Mn(OOCCH3)2 with NaHB(pz)3 and NaHB(3,5‐Me2‐pz)3 in MeOH, respectively. The two complexes (1) and (2) were characterized by IR, elemental analyses, and x‐ray diffraction. Complex (1) crystallizes in the space group C2/c, a = 18.971(3) Å, b = 13.700(3) Å, c = 19.056(3) Å, β = 111.378(10), V = 4612.0(13) Å3, Z = 2. Complex (2) crystallizes in the space group R‐3, a = 10.9832(18) Å, b = 10.983(2) Å, c = 24.785(3) Å, γ = 120°, V = 2589.3(7) Å3, Z = 3. X‐ray structure analysis has shown that the complexes (1) and (2) all are monomeric neutral complexes, and possess similar coordination modes around the metal Mn centers. In addition, some related bonding distances, angles, and structural properties are discussed.