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3-carboxybenzylophosphonic acid | 142646-13-7

中文名称
——
中文别名
——
英文名称
3-carboxybenzylophosphonic acid
英文别名
3-phosphonomethylbenzoic acid;3-(Phosphonomethyl)benzoic acid
3-carboxybenzylophosphonic acid化学式
CAS
142646-13-7
化学式
C8H9O5P
mdl
——
分子量
216.13
InChiKey
QIDFDDOEXSPDGN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    529.0±60.0 °C(Predicted)
  • 密度:
    1.572±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.4
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    94.8
  • 氢给体数:
    3
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4,4'-联吡啶3-carboxybenzylophosphonic acid 为溶剂, 生成 4,4'-bipyridine (3-carboxybenzylphosphonic acid)2
    参考文献:
    名称:
    超分子的形成网络中的3- carboxybenzylphosphonic酸,其配合物和盐结晶:从配位键,以弱的分子间相互作用†
    摘要:
    3-羧苄基膦酸(H 3 L)(1),三种配合物[Ca(H 2 L)2(H 2 O)3 ] n(2),[Ca(H 2 L)2(H 2 O)2 ] ñ(3)和内[Ca(H 2 L)2(H 2 O)4 ]联吡啶(4)和所述盐的两种多晶型(bipyH 2)(H 2 L)2(5,6),并通过单晶X射线衍射分析确定其结构。化合物2和3是聚合物,而化合物4是单核络合物。在钙离子2,3和4是由monodeprotonated膦酸基团配位(-PO 3 H ^ - )和水分子,羧基残留在质子化形式。在盐的情况下,聚合物链或单体单元通过氢键和离子力连接在一起,以提供三维分层的超分子结构。另外,π⋯π堆积相互作用在化合物4,5和6有助于结构的稳定。
    DOI:
    10.1039/c3ra44614j
  • 作为产物:
    描述:
    参考文献:
    名称:
    超分子的形成网络中的3- carboxybenzylphosphonic酸,其配合物和盐结晶:从配位键,以弱的分子间相互作用†
    摘要:
    3-羧苄基膦酸(H 3 L)(1),三种配合物[Ca(H 2 L)2(H 2 O)3 ] n(2),[Ca(H 2 L)2(H 2 O)2 ] ñ(3)和内[Ca(H 2 L)2(H 2 O)4 ]联吡啶(4)和所述盐的两种多晶型(bipyH 2)(H 2 L)2(5,6),并通过单晶X射线衍射分析确定其结构。化合物2和3是聚合物,而化合物4是单核络合物。在钙离子2,3和4是由monodeprotonated膦酸基团配位(-PO 3 H ^ - )和水分子,羧基残留在质子化形式。在盐的情况下,聚合物链或单体单元通过氢键和离子力连接在一起,以提供三维分层的超分子结构。另外,π⋯π堆积相互作用在化合物4,5和6有助于结构的稳定。
    DOI:
    10.1039/c3ra44614j
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文献信息

  • Fluorescent Properties of Three Carboxyarylphosphonate Polymers with Unusual Polynuclear Zinc(II) Units
    作者:Xiao-Chuan Chai、Hui Li、Fu-Lin Zhou、Qiu-Ping Han、Shao-Fei Song、Yan-Ning Cao
    DOI:10.1002/zaac.201900156
    日期:2019.10.31
    novel [Zn6P4O12] hexanuclear units with “chair“ conformation are tetrahedrally bridged by eight MCP3– to generate a 2D double‐layer, in which the windows are occupied by 2,2′‐bipy molecules. Additionally, 2D correlation analysis of FTIR with thermal perturbation of 3 were discussed. Compounds 1–3 exhibit intense solid state fluorescent emissions. Thermogravimetric analyses suggested the very high stability
    三种新型羧芳基膦酸酯聚合物[Zn 2(PCP)(H 2 PCP)(phen)2 ] · H 2 O} n(1),[Zn(HPCP)(4,4'-bipy)] n(2),并且,[Zn 3(MCP)2(2,2'-联吡啶)] ñ(3)[PCP 3- = p -O 2 C(ç 6 ħ 4)CH 2 PO 3 3-,MCP 3- =米- O 2 C(C 6 H 4)CH 2 PO 3 3–和phen =菲咯啉]的合成并通过单晶X射线衍射进行了表征。化合物1具有由[Zn 4 P 4 O 10 ]四核单元组成的蝴蝶状二聚体,它们通过氢键和π-π堆积相互作用进一步连接到3D超分子框架中。在2中,存在无限的P–O–Zn无机2D(4,4)层,其中HPCP 2–的膦酸酯部分和未识别的4,4'-bipy配体垂直伸出。至于3,新颖的[Zn 6 P 4 O 12具有八个“椅子”构型的六核单元被八个MCP 3–进行四面体桥连以生成2D双层,其中的窗口被2
  • Process for Producing Polyester, Polyester Produced Using Said Process, and Polyester Molded Product
    申请人:Kageyama Katsuhiko
    公开号:US20080249280A1
    公开(公告)日:2008-10-09
    This invention provides a polyester and a polyester molded product, which, while maintaining color tone, transparency, and thermal stability, can realize a high polycondensation rate, are less likely to cause the production of polycondensation catalyst-derived undesired materials, and can simultaneously meet both quality and cost effectiveness requirements, which can exhibit the characteristic features, for example, in the fields of ultrafine fibers, high transparent films for optical use, or ultrahigh transparent molded products. These advantages can be realized by using, in the production of a polyester in the presence of an aluminum compound-containing polyester polycondensation catalyst, an aluminum compound having an absorbance of not more than 0.0132 as measured in the form of an aqueous aluminum compound solution, prepared by dissolving the aluminum compound in pure water to give a concentration of 2.7 g/liter in terms of the amount of aluminum element, under conditions of cell length 1 cm and wavelength 680 nm.
    本发明提供了一种聚酯和聚酯成型产品,可以在保持色调、透明度和热稳定性的同时,实现高聚酯化速率,不太可能引起聚酯化催化剂来源的不良材料的生产,并且可以同时满足质量和成本效益的要求,这些优点可以在超细纤维、用于光学的高透明薄膜或超高透明成型产品等领域展现出特征性能。通过在含有铝化合物聚酯聚合催化剂的聚酯生产中使用具有吸光度不超过0.0132的铝化合物,可以实现这些优点。该吸光度是在细胞长度为1厘米,波长为680纳米的条件下,将铝化合物溶解在纯水中以给定铝元素量浓度为2.7克/升形成的水溶性铝化合物溶液中测量得出的。
  • POLYESTER, PROCESS FOR PRODUCTION OF POLYESTER, AND POLYESTER MOLDED ARTICLE
    申请人:Toyo Boseki Kabushiki Kaisha
    公开号:EP1932867A1
    公开(公告)日:2008-06-18
    Disclosed is a polyester produced from an aluminum compound and a phosphorus compound in the presence of a polycondensation catalyst. The polyester contains a polyester-insoluble, aluminum-containing insoluble particle in an amount of 1000 ppm or less as quantified by the method disclosed in the description, and contains an acid terminal group at a ratio of 10 to 50 eq/ton. The polyester can provide a highly transparent molded article produced through drawing (e.g., a film or hollow molded article) and is useful in the fields of highly transparent optical films, ultra-highly transparent molded articles or the like.
    本发明公开了一种在缩聚催化剂存在下由铝化合物和磷化合物制得的聚酯。该聚酯含有聚酯不溶物、含铝不溶物颗粒,按描述中公开的方法定量,其含量为 1000 ppm 或更少,并含有酸性末端基团,其比例为 10 至 50 eq/吨。该聚酯可提供通过拉丝生产的高透明模塑品(如薄膜或中空模塑品),在高透明光学薄膜、超高透明模塑品等领域非常有用。
  • Garuti; Ferranti; Ronerti, Pharmazie, 1992, vol. 47, # 4, p. 295 - 297
    作者:Garuti、Ferranti、Ronerti、Katz、Budriesi、Chiarini
    DOI:——
    日期:——
  • Four divalent transition metal carboxyarylphosphonate compounds: Hydrothermal synthesis, structural chemistry and generalized 2D FTIR correlation spectroscopy studies
    作者:Ran Lei、Xiaochuan Chai、Hongxin Mei、Hanhui Zhang、Yiping Chen、Yanqiong Sun
    DOI:10.1016/j.jssc.2010.04.037
    日期:2010.7
    Four divalent transition metal carboxyarylphosphonates, [Ni(4,4'-bipy)H2L1(HL1)(2)(H2O)(2)]center dot 2H(2)O 1, [Ni-2(4,4'-bipy)(L-2)(OH)(H2O)(2)]. 3H(2)O 2, Mn(phen)(2)(H2L1)(2) 3 and Mn(phen)(HL2) 4 (H3L1=p-H2O3PCH2-C6H4-COOH, H3L2=m-H2O3PCH2-C6H4-COOH, 4,4'-bipy=4,4'-bipyridine, phen=1,10-phenanthroline) were synthesized under hydrothermal conditions. 1 features 1D linear chains built from Ni(II) ions bridging 4,4'-bipy. In 2, neighboring Ni-4 cluster units are connected by pairs of H3L2 ligands to form 1D double-crankshaft chains, which are interconnected by pairs of 4,4'-bipy into 2D sheets. 3 exhibits 2D supramolecular layers via the R-2(2)(8) ringed hydrogen bonding units. 4 has 1D ladderlike chains, in which the 4-membered rings are cross-linked by the organic moieties of the H3L2 ligands. Additionally, 2D FTIR correlation analysis is applied with thermal and magnetic perturbation to clarify the structural changes of functional groups from H3L1 and H3L2 ligands in the compounds more efficiently. (C) 2010 Elsevier Inc. All rights reserved.
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