首页> 外文学位 >Part~I. Diphosphate complexes of polyoxotungstates and polyoxomolybdates. Part~II. Structures of potassium(3) (arsenic(2) (arsenate) molybdenum(12) oxygen(36)) . 4 water, potassium(10) (hydrogen(2) tungsten(12) oxygen(42)) . 7.5 water, and cesium(6) (molybdenum(7) oxygen(24)) . 7 water.
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Part~I. Diphosphate complexes of polyoxotungstates and polyoxomolybdates. Part~II. Structures of potassium(3) (arsenic(2) (arsenate) molybdenum(12) oxygen(36)) . 4 water, potassium(10) (hydrogen(2) tungsten(12) oxygen(42)) . 7.5 water, and cesium(6) (molybdenum(7) oxygen(24)) . 7 water.

机译:第一部分聚氧钨酸盐和聚氧钼酸盐的二磷酸盐复合物。第二部分钾(3)(砷(2)(砷酸)钼(12)氧(36))的结构。 4水,钾(10)(氢(2)钨(12)氧(42))。 7.5水和铯(6)(钼(7)氧(24))。 7水。

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摘要

In Part I, four new structural types of heteropolyanions are presented. They are diphosphate complexes of polyoxotungstates and polyoxomolybdates. The hetero groups are diphosphate (O{dollar}sb3{dollar}POPO{dollar}sb3sp{lcub}4-{rcub}{dollar}) and its hydrolytically stable analogs methylenediphosphonate (O{dollar}sb3{dollar}PCH{dollar}sb2{dollar}PO{dollar}sb3sp{lcub}4-{rcub}{dollar}) and (dimethylamino) methylenediphosphonate (O{dollar}sb3{dollar}PCHN(CH{dollar}sb3)sb2{dollar}PO{dollar}sb3sp{lcub}4-{rcub}{dollar}), respectively.; The first structural type has the formula {dollar}rmlbrack(Osb3PXPOsb3)sb4Wsb{lcub}12{rcub}Osb{lcub}36{rcub}rbracksp{lcub}16-{rcub} (X = CHsb2, O){dollar}. The two anions ((O{dollar}sb3{dollar}POPO{dollar}sb3)sb4{dollar}W{dollar}sb{lcub}12{rcub}{dollar}O{dollar}sb{lcub}36{rcub}rbracksp{lcub}16-{rcub}{dollar} (I) and ((O{dollar}sb3{dollar}PCH{dollar}sb2{dollar}PO{dollar}sb3)sb4{dollar}W{dollar}sb{lcub}12{rcub}{dollar}O{dollar}sb{lcub}36{rcub}sp{lcub}16-{rcub}{dollar} (II) are isostructural and are formed in aqueous solution. The open cyclic structure of I and II is an unusual new polyoxometalate conformation with external heterogroups.; The second structural type, ((O{dollar}sb3{dollar}PCH{dollar}sb2{dollar}PO{dollar}sb3{dollar})Mo{dollar}sb6{dollar}O{dollar}sb{lcub}18{rcub}{dollar}(H{dollar}sb2{dollar}O){dollar}sb4rbracksp{lcub}4-{rcub}{dollar} (III), is also formed in aqueous solution. It consists of a six-membered ring of MoO{dollar}sb6{dollar} octahedra, which alternate in sharing edges and corners. Based on spectroscopic evidence the pyrophosphate analog (IV) almost certainly has the same structure. The molybdenum analogs of I and II, ((O{dollar}sb3{dollar}PCH{dollar}sb2{dollar}PO{dollar}sb3)sb4{dollar}Mo{dollar}sb{lcub}12{rcub}{dollar}O{dollar}sb{lcub}36{rcub}rbracksp{lcub}16-{rcub}{dollar} (V) and ((O{dollar}sb3{dollar},POPO{dollar}sb3)sb4{dollar}Mo{dollar}sb{lcub}12{rcub}{dollar}O{dollar}sb{lcub}36{rcub}rbracksp{lcub}16-{rcub}{dollar} (VI) are proposed. Anions IV and VI are possible intermediates in the molybdate-catalyzed hydrolysis of pyrophosphate. The third structural type, ( ((O{dollar}sb3{dollar}PCHN(CH{dollar}sb3) sb2{dollar}PO{dollar}sb3{dollar})W{dollar}sb2{dollar}O{dollar}sb6rbracksp4-)infty{dollar}, is formed in aqueous solution and represents a novel linear polymeric heteropolyanion of tungsten. It consists of negatively-charged chains with {dollar}rmlbrack (Osb3PCHN(CHsb3)sb2POsb3)Wsb2Osb6rbracksp{lcub}4-{rcub}{dollar} (VII) as the repeat unit.; The fourth structural type, ((O{dollar}sb3{dollar}POPO{dollar}sb3{dollar})Mo{dollar}sb{lcub}18{rcub}{dollar}O{dollar}sb{lcub}54{rcub}rbracksp{lcub}4-{rcub}{dollar} (VIII), is formed in a mixed aqueous-organic solvent. It is based on fusion of two B-type PMo{dollar}sb9{dollar}O{dollar}sb{lcub}34{rcub}{dollar} - moieties. Consequently the enclosed pyrophosphate anion is constrained to have a linear P-O-P bond (177.7{dollar}spcircpm 1.3{dollar}) and an eclipsed conformation. The green one-electron reduced species ((O{dollar}sb3{dollar}POPO{dollar}sb3{dollar})Mo{dollar}sb{lcub}18{rcub}{dollar}O{dollar}sb{lcub}54{rcub}rbracksp{lcub}5-{rcub}{dollar} (VIII{dollar}spprime{dollar}) and the blue two-electron reduced species ((O{dollar}sb3{dollar}POPO{dollar}sb3{dollar})Mo{dollar}sb{lcub}18{rcub}{dollar}o{dollar}sb{lcub}54{rcub}rbracksp{lcub}6-{rcub}{dollar} (VIII{dollar}sp{lcub}primeprime{rcub}{dollar}) show single {dollar}sp{lcub}31{rcub}{dollar}p NMR resonances. The ESR spectrum of afrozen solution (77 K) of VIII{dollar}spprime{dollar} is a barely resolved axial pattern.; In Part II the crystal structures of K{dollar}sb3{dollar} (As{dollar}sb2{dollar}(AsO{dollar}sb4{dollar})Mo{dollar}sb{lcub}12{rcub}{dollar}O{dollar}sb{lcub}36{rcub}{dollar}), K{dollar}sb{lcub}10{rcub}{dollar} (H{dollar}sb2{dollar}W{dollar}sb{lcub}12{rcub}{dollar}O
机译:在第一部分中,提出了四种新的杂多阴离子结构类型。它们是聚氧钨酸盐和聚氧钼酸盐的二磷酸盐复合物。杂基是二磷酸(O {dollar} sb3 {dollar} POPO {dollar} sb3sp {lcub} 4- {rcub} {dollar})及其水解稳定的类似物亚甲基二膦酸酯(O {dollar} sb3 {dollar} PCH {dollar} sb2 {dollar} PO {dollar} sb3sp {lcub} 4- {rcub} {dollar})和(二甲氨基)亚甲基二膦酸酯(O {dollar} sb3 {dollar} PCHN(CH {dollar} sb3)sb2 {dollar} PO {dollar } sb3sp {lcub} 4- {rcub} {dollar})。第一种结构类型具有公式{dollar} rmlbrack(Osb3PXPOsb3)sb4Wsb {lcub} 12 {rcub} Osb {lcub} 36 {rcub} rbracksp {lcub} 16- {rcub}(X = CHsb2,O){dollar}。两种阴离子((O {dollar} sb3 {dollar} POPO {dollar} sb3)sb4 {dollar} W {dollar} sb {lcub} 12 {rcub} {dollar} O {dollar} sb {lcub} 36 {rcub} rbracksp {lcub} 16- {rcub} {dollar}(I)和((O {dollar} sb3 {dollar} PCH {dollar} sb2 {dollar} PO {dollar} sb3)sb4 {dollar} W {dollar} sb { lcub} 12 {rcub} {dollar} O {dollar} sb {lcub} 36 {rcub} sp {lcub} 16- {rcub} {dollar}(II)是同构结构,在水溶液中形成。 I和II是具有外部杂基的不寻常的新多金属氧酸盐构象。;第二种结构类型,((O {dollar} sb3 {dollar} PCH {dollar} sb2 {dollar} PO {dollar} sb3 {dollar})Mo {dollar sb6 {dollar} O {dollar} sb {lcub} 18 {rcub} {dollar}(H {dollar} sb2 {dollar} O){dollar} sb4rbracksp {lcub} 4- {rcub} {dollar}(III)是它由MoO {dollar} sb6 {dollar}八面体的六元环组成,它们在边和角处共享,基于光谱证据,焦磷酸盐类似物(IV)几乎具有相同的结构。 I和II的钼类似物((O {dollar} sb3 {dollar} PCH {dollar} sb2 {dollar} PO {dollar} sb3)sb4 {dollar} Mo {dollar} sb {lcub} 12 {rcub} {dollar} O {dollar} sb {lcub } 36 {rcub} rbracksp {lcub} 16- {rcub} {dollar}(V)和((O {dollar} sb3 {dollar},POPO {dollar} sb3)sb4 {dollar} Mo {dollar} sb {lcub}提出了12 {rcub} {dollar} o {dollar} sb {lcub} 36 {rcub} rbracksp {lcub} 16- {rcub} {dollar}(VI)。阴离子IV和VI是钼酸盐催化焦磷酸水解的可能中间体。第三种结构类型,(((O {dollar} sb3 {dollar} PCHN(CH {dollar} sb3)sb2 {dollar} PO {dollar} sb3 {dollar})W {dollar} sb2 {dollar} O {dollar} sb6rbracksp4 -)infty {dollar},是在水溶液中形成的,代表一种新型的线性钨聚合物杂多阴离子,它由带有{dollar} rmlbrack(Osb3PCHN(CHsb3)sb2POsb3)Wsb2Osb6rbracksp {lcub} 4- {rcub}的带负电荷的链组成{美元}(VII)作为重复单元。第四种结构类型,((O {dollar} sb3 {dollar} POPO {dollar} sb3 {dollar})Mo {dollar} sb {lcub} 18 {rcub} {dollar } O {dollar} sb {lcub} 54 {rcub} rbracksp {lcub} 4- {rcub} {dollar}(VIII)在混合的水性有机溶剂中形成,它基于两种B型PMo的融合{dollar} sb9 {dollar} O {dollar} sb {lcub} 34 {rcub} {dollar}-部分,因此封闭的焦磷酸盐阴离子被约束为具有线性POP键(177.7 {dollar} spcircpm 1.3 {dollar}),并且绿色的单电子还原物种((O {dollar} sb3 {dollar} POPO {dollar} sb3 {dollar})Mo {dollar} sb {lcub} 18 {rc ub} {dollar} O {dollar} sb {lcub} 54 {rcub} rbracksp {lcub} 5- {rcub} {dollar}(VIII {dollar} spprime {dollar})和蓝色的两电子还原物种((O {dollar} sb3 {dollar} POPO {dollar} sb3 {dollar})Mo {dollar} sb {lcub} 18 {rcub} {dollar} o {dollar} sb {lcub} 54 {rcub} rbracksp {lcub} 6- { rcub} {dollar}(VIII {dollar} sp {lcub} primeprime {rcub} {dollar})显示单个{dollar} sp {lcub} 31 {rcub} {dollar} p NMR共振。 VIII {dollar} spprime {dollar}的冻结溶液(77 K)的ESR谱图几乎未解析。在第二部分中,K {dollar} sb3 {dollar}(As {dollar} sb2 {dollar}(AsO {dollar} sb4 {dollar})Mo {dollar} sb {lcub} 12 {rcub} {dollar} O的晶体结构{dollar} sb {lcub} 36 {rcub} {dollar}),K {dollar} sb {lcub} 10 {rcub} {dollar}(H {dollar} sb2 {dollar} W {dollar} sb {lcub} 12 { rcub} {dollar} O

著录项

  • 作者

    Kortz, Ulrich.;

  • 作者单位

    Georgetown University.;

  • 授予单位 Georgetown University.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 1995
  • 页码 465 p.
  • 总页数 465
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 无机化学;
  • 关键词

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