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potassium tris(pentafluoroethyl)trifluorophosphate | 123215-04-3

中文名称
——
中文别名
——
英文名称
potassium tris(pentafluoroethyl)trifluorophosphate
英文别名
Potassium trifluorotris(perfluoroethyl)phosphate
potassium tris(pentafluoroethyl)trifluorophosphate化学式
CAS
123215-04-3
化学式
C6F18P*K
mdl
——
分子量
484.109
InChiKey
CFXJFAHQUPOMMH-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    26.0
  • 可旋转键数:
    3.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为反应物:
    描述:
    potassium tris(pentafluoroethyl)trifluorophosphate 反应 95.0h, 生成 bis(acetonitrile)silver(I) tris(perfluoroethyl)trifluorophosphate
    参考文献:
    名称:
    液态三(全氟乙基)三氟磷酸银盐用作丙烯/丙烷分离的新介质†
    摘要:
    已从以下步骤开始合成了一系列具有各种配体(乙腈ACN,氯乙腈Cl-ACN,丙烯腈丙烯酰基CN,吡啶py,乙二胺en和丙烯C 3 H 6)的三(全氟乙基)三氟磷酸银(Ag [FAP])配合物。 Ag [NO 3 ]和K [FAP]使用三种不同的途径。理化性质以及晶体结构([Ag(ACN)2/4 ] [FAP],[Ag(py)2确定了[[FAP]),并研究了此类银盐在丙烯/丙烷分离过程中的适用性。当与气态丙烯在30°C下接触时,所研究的银络合物要么表现出低熔点,要么形成液态络合物。由于它们的高银含量和显着的丙烯容量,这使它们成为用于液膜和吸收液的分离材料很有希望。测定了丙烯和丙烷的单一(iGSC)和混合(NMR)气体溶解度以及扩散系数(PFG-NMR),以预测根据溶液的理论上银盐的溶解度,膜选择性,容量和传输性质的理论选择性扩散模型。配体的数量和类型对化学络合的影响很大,
    DOI:
    10.1039/c6cp05653a
  • 作为产物:
    描述:
    tris(pentafluoroethyl)difluorophosphorane 在 potassium fluoride 作用下, 以 乙醚 为溶剂, 反应 1.0h, 以100%的产率得到potassium tris(pentafluoroethyl)trifluorophosphate
    参考文献:
    名称:
    Pavlenko, N. V.; Yagupol'skii, L. M., Journal of general chemistry of the USSR, 1989, vol. 59, # 3.1, p. 469 - 473
    摘要:
    DOI:
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文献信息

  • Convenient synthesis of aliphatic (CF3)2N-compounds
    作者:Christoph Breitenstein、Nikolai Ignat’ev、Walter Frank
    DOI:10.1016/j.jfluchem.2017.11.007
    日期:2018.6
    Convenient syntheses of organic compounds bearing the (CF3)2N group by means of nucleophilic substitution reactions with the [N(CF3)2]− anion were developed. The syntheses and properties of previously unknown N,N-bis(trifluoromethyl)glycine (CF3)2NCH2C(O)OH and its derivatives are described.
    开发了通过与[N(CF 3)2 ] -阴离子的亲核取代反应方便地合成带有(CF 3)2 N基团的有机化合物的方法。描述了以前未知的N,N-双(三氟甲基)甘氨酸(CF 3)2 NCH 2 C(O)OH及其衍生物的合成和性质。
  • FLUORINATING REAGENTS WITH (PERFLUORALKYL) FLUOROPHOSPHATE ANION
    申请人:Ignatyev Nikolai (Mykola)
    公开号:US20130023661A1
    公开(公告)日:2013-01-24
    The present invention relates to the use of compounds of the formula (I) as fluorinating reagents, to a process for the fluorination of organic compounds by reaction thereof with compounds of the formula (I), and to compounds of the formula (I).
    本发明涉及将式(I)化合物用作氟化试剂,以及通过将有机化合物与式(I)化合物反应来进行有机化合物的氟化的方法,以及式(I)化合物。
  • 감광성 조성물
    申请人:SANYO CHEMICAL INDUSTRIES, LTD. 산요가세이고교 가부시키가이샤(519980687107)
    公开号:KR101486692B1
    公开(公告)日:2015-01-29
    본 발명은 조사한 광을 감쇠 또는 차폐시키는 착색제 등의 물질이 고농도로 존재하는 경우나 두꺼운 막두께인 경우에도 적은 에너지량으로 경화 가능한 감광성 조성물을 제공하는 것을 목적으로 하는 것으로, 본 발명의 감광성 조성물은 하기 (1) ∼ (4) 를 함유하는 감광성 조성물로서, 라디칼 개시제 (A), 산 발생제 (B) 및 염기 발생제 (C) 중의 적어도 1 개가 활성 광선의 조사에 의해 활성종 (H) 를 발생시키고, 그 활성종 (H) 가 라디칼 개시제 (A), 산 발생제 (B) 또는 염기 발생제 (C) 와 반응하여 새로운 활성종 (I) 를 생성하여 그 새로운 활성종 (I) 에 의한 중합성 물질 (D) 의 중합 반응이 진행되고, 그 활성종 (H) 또는 (I) 가 산 또는 염기인 것을 특징으로 한다 ; (1) 라디칼 개시제 (A) (2) 산 발생제 (B) 또는 염기 발생제 (C) (3) 중합성 물질 (D) (4) 착색제 (E), 금속 산화물 분말 (F) 또는 금속 분말 (G).
    本发明旨在提供一种能够在高浓度存在着吸收光或屏蔽光的染色剂等物质或厚膜厚度的情况下,以较少的能量量进行固化的感光性组合物,该感光性组合物包括以下(1)至(4):包含自由基引发剂(A)、酸发生剂(B)和碱发生剂(C)中至少一个,其通过活性光线的照射产生活性种(H),该活性种(H)与自由基引发剂(A)、酸发生剂(B)或碱发生剂(C)反应生成新的活性种(I),并且通过新的活性种(I)进行聚合物(D)的聚合反应进行,其特征在于活性种(H)或(I)为酸或碱;(1)自由基引发剂(A)(2)酸发生剂(B)或碱发生剂(C)(3)聚合物(D)(4)染色剂(E)、金属氧化物粉末(F)或金属粉末(G)。
  • SULFONIUM SALT, PHOTOACID GENERATOR, CURABLE COMPOSITION, AND RESIST COMPOSITION
    申请人:SAN-APRO LTD.
    公开号:US20210147352A1
    公开(公告)日:2021-05-20
    The sulfonium salt has high photosensitivity to i-rays and high compatibility with cationically polymerizable compounds such as epoxy compounds, and is excellent storage stability in formulations containing such compounds. The sulfonium salt is represented by general formula (1). In formula (1), R represents an alkyl group or an aryl group; substituents, R1 to R5, each independently represent an alkyl group, a hydroxy group, an alkoxy group, an aryl group, an aryloxy group, a hydroxy(poly)alkyleneoxy group, or a halogen atom; R6 to R9 each independently represent an alkyl group, an aryl group, or a hydrogen atom; m 1 to m 5 each represent the number of occurrences of each of R1 to R5, m 1 and m 4 represent an integer of 0 to 3, m 2 and m 5 represent an integer of 0 to 4, m 3 represents an integer of 0 to 5, and X − represents a monovalent polyatomic anion.
    砜盐对紫外线具有很高的光敏性,与环氧化合物等阳离子聚合物化合物具有很高的相容性,并且在含有这些化合物的配方中具有优异的储存稳定性。砜盐的通用式表示为(1)。在式(1)中,R代表烷基或芳基;取代基R1至R5分别独立地代表烷基、羟基、烷氧基、芳基、芳氧基、羟基(聚)烷氧基或卤素原子;R6至R9分别独立地代表烷基、芳基或氢原子;m1至m5分别代表R1至R5的出现次数,m1和m4表示0到3的整数,m2和m5表示0到4的整数,m3表示0到5的整数,X−表示一价多原子阴离子。
  • Process for the synthesis of amide bonds with the aid of novel catalysts
    申请人:Merck Patent GmbH
    公开号:US10544186B2
    公开(公告)日:2020-01-28
    The invention relates to a process for the production of amide bonds, in particular peptide bonds, with the aid of novel amide linking reagents containing an anion of the formula (I), to the novel reagents, and to the preparation thereof.
    该发明涉及一种利用含有公式(I)阴离子的新型酰胺连接试剂生产酰胺键的方法,特别是肽键的方法,涉及新型试剂及其制备方法。
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同类化合物

氯(双五氟乙基)膦 5-萘-2-基-1,3-噁唑 1-氯-2-[2-氯乙基(甲基)磷基]乙烷 1-丁基-1-甲基吡咯烷鎓三(五氟乙基)三氟磷酸盐 1,1,1,3,3,3-六氟-2-(2,2,2-三氟-1-羟基-1-(三氟甲基)乙基磷酰基)-2-丙醇 bis(pentafluoroethyl)phosphinyl amide 1-butylpyridinium bis(pentafluoroethyl)phosphinate N,N-butylmethylpyrrolidinium bis(pentafluoroethyl)-phosphinate bis(pentafluoroethyl)phosphinate anion triethylmethylammonium bis(pentafluoroethyl)-phosphinate bis(dimethylamino)chlorocarbenium bis(pentafluorethyl)phosphinate 1-methyl-1-propargylpyrrolidinium bis(pentafluoro-ethyl)phosphinate N,N-dimethylpyrrolidinium bis(pentafluoroethyl)-phosphinate 1-butyl-3-methylimidazolium bis(pentafluoroethyl)phosphinate propargyl bis(pentafluoroethyl)phosphinate 1,3-dimethylimidazolium bis(pentafluoroethyl)phosphinate 1-propargyl-3-methylimidazolium bis(pentafluoroethyl)-phosphinate 1-ethyl-3-methylimidazolium bis(nonafluorobutyl)-phosphinate tetrabutylammonium tris(pentafluoroethyl)trifluorophosphate bis-(2,2-dichloro-1-hydroxy-ethyl)-phosphinic acid 2,2,3,3,4,4,5,5-octafluoropentyl bis(pentafluoroethyl) phosphinate 2-methyl-1,1,3,3-tetramethylisouronium bis(pentafluoroethyl)phosphinate ethyl bis(nonafluorobutyl)phosphinate fluorobis(pentafluoroethyl)phosphane tetraethylammonium bis(nonafluorobutyl)tetrafluorophosphate tetraethylammonium tris(pentafluoroethyl)trifluorophosphate tris(pentafluoroethyl)phosphane ethyl bis(pentafluoroethyl)phosphinate N,N,N',N'-tetramethyl-N''-ethylguanidinium bis(pentafluoroethyl)phosphinate 3-bromopropyl bis(pentafluoroethyl)phosphinate Tetramethylammonium tris(pentafluorophosphate Bis-(2-chlor-ethyl)-thiophosphinsaeure-ethylester ethyl bis(pentafluoroethyl)phosphinite Bis-heptafluorpropyl-fluorphosphin trimethylsilyl bis(pentafluoroethyl)phosphinite tris(undecafluoroisopentyl)phosphine oxide 1-(Bis-undecafluoropentyl-phosphinoyl)-1,1,2,2,3,3,4,4,5,5,5-undecafluoro-pentane Bis-(2-chlor-ethyl)-chlorphosphin 1,1,1,3,3,3,1',1',1',3',3',3'-dodecafluoro-2,2'-phosphanediyl-bis-propan-2-ol Bis-<2-chlor-aethyl>-chlormethyl-phosphinoxid Tri(β-chlorethyl)phosphinoxid cis-[(C2F5)2P(methyl)]4Pt Perfluorhexylphosphinsaeure bis-(2,2,2-trichloro-1-hydroxy-ethyl)-phosphinic acid ethyl ester bis(pentafluoroethyl)phosphinyl bromide (S)-4-benzyl-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4,5-dihydrooxazole (S)-2-(2-(bis(pentafluoroethyl)phosphino)phenyl)-4-phenyl-4,5-dihydrooxazole tetra(n-butyl)phosphonium tris(pentafluoroethyl)trifluorophosphate silver bis(heptafluoropropyl)phosphinate Tris(2,2,3,3,4,4,5,5-octafluoropentyl)phosphine