perfluorododecanoic chloride | 108497-50-3

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 酰卤
• 英文名称: perfluorododecanoic chloride
• 英文别名: 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-Tricosafluorododecanoyl chloride；2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-tricosafluorododecanoyl chloride
• CAS: 108497-50-3
• 化学式: C₁₂ClF₂₃O
• 分子量: 632.548
• InChiKey: VXOGRRZNIDNITI-UHFFFAOYSA-N

物化性质

• 沸点：
  209.9±35.0 °C(Predicted)
• 密度：
  1.752±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  8.6
• 重原子数：
  37
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  24

反应信息

• 作为反应物：
  描述：

  perfluorododecanoic chloride 在 吡啶 、 氨 作用下， 以 苯 为溶剂， 反应 12.0h， 生成 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-Tricosafluorododecanamide
  参考文献：
  名称：

  N-Alkyl Perfluoroalkanamides as Low Molecular-Mass Organogelators

  摘要：

  A new class of low molecular-mass organogelators (LMOGs), N-alkyl perfluoroalkanamides, F(CF2)(n)CONH(CH2)(m)H, is described. The molecules are designed to exploit the incompatibilities of their three molecular parts, and the results demonstrate that this strategy can be used to tune molecular aggregation and gel stability. The gelating properties of these LMOGs have been examined in a wide variety of organic liquids (including alkanes, alcohols, toluene, n-perfluorooctane, CCl4, and DMSO) as a function of the N-alkyl and perfluoroalkyl chain lengths by X-ray diffraction, polarizing optical microscopy, infrared spectroscopy, differential scanning calorimetry, and small-angle neutron scattering (SANS). The gels are thermally reversible and require generally very low concentrations (<2 wt %) of LMOG. Several of the gels are stable for very long periods at room temperature. The incompatibility of the fluorocarbon and hydrocarbon segments causes the LMOGs to aggregate, probably into lamellae within the fibrils that constitute the basic unit of the gel networks. The SANS studies show that the cross-sections of fibers in the gel networks of LMOGs with shorter perfluoroalkyl chains are much larger than those with longer ones. Comparisons with the gelating properties of some analogous esters (F(CF2)(n)CO2(CH2)(m)H) and diblock perfluoroalkylalkanes (F(CF2)(n)(CH2)(m)H) indicate that additional ordering within the aggregate units is enforced by the intermolecular H bonding among amide groups that is evidenced by IR spectroscopy. Analyses of these results and structure/solvent correlations are provided.

  DOI：

  10.1021/ja0362407
• 作为产物：
  描述：

  全氟十二酸 在 氯化亚砜 作用下， 生成 perfluorododecanoic chloride
  参考文献：
  名称：

  [EN] PORPHYRIN DERIVATIVES AND USES THEREOF
  [FR] DÉRIVÉS DE PORPHYRINE ET LEURS UTILISATIONS

  摘要：

  The present invention relates generally to porphyrin derivatives and their use in detecting poly- and perfluoroalkyl substances (PFAS). In particular, the present invention is directed to porphyrin derivatives having at least one receptor arm comprising an anion binding group substituted with a poly- or perfluorinated aliphatic group and their use as sensors for the detection of PFAS.

  公开号：

  WO2022178593A1

文献信息

• Synthesis, Reaction, and Recycle of Fluorous Palladium Catalysts for an Asymmetric Allylic Alkylation without Using Fluorous Solvents
  作者：Takashi Mino、Yutaka Sato、Akio Saito、Youichi Tanaka、Hiroaki Saotome、Masami Sakamoto、Tsutomu Fujita

  DOI：10.1021/jo051035q

  日期：2005.9.1

  (7) with a dialkyl malonate-BSA-LiOAc system with high enantioselectivities (up to 97% ee). Results indicated that the chiral fluorous palladium catalyst from ligand 4c was easily separated from the reaction mixture by simple solid/liquid separation and could be reused up to five times.

  由（S）-脯氨醇制备带有两个氟马尾的手性氟氨基膦4c，并用高丙二酸二烷基酯-BSA-LiOAc体系应用于钯催化的1,3-二苯-2-丙烯乙酸丙烯酯（7）的钯催化不对称烯丙基烷基化。对映选择性（高达97％ee）。结果表明，通过简单的固/液分离，容易将配体4c的手性氟钯催化剂从反应混合物中分离出来，最多可重复使用5次。
• 6-(biphenyl-ester)-3H-naphtho[2,1-b]pyrans as photochromic dichroic dyes and optical article containing them
  申请人：Aiken Stuart

  公开号：US08436184B2

  公开（公告）日：2013-05-07

  A naphthopyran compound represented by the formula (I) wherein: n1, n2, p, m and q represent an integer; R1, R2 and R4, represent a group selected from halogen, —Ra, —OH, —ORa, —SH, —SRa, —NH2, —NRaRa1, —NRbRc, —CO—Ra, —CO2Ra1, —OC(O)—Rd, —X—(Re)—Y, linear or branched (C1-C18) perfluoroalkyl group, wherein Ra, Ra1, Rb, Rc, X, Y, Re, and Rd are as defined in the description; Z represents a group selected from CO, CS, SO, SO2, CO2, C(O)S, CS2, C(O)NH, C(O)NRa, C(S)NH, C(S)NRa and C═NRa; R3 represents a group selected from halogen, —Ra, linear or branched (C1-18) perfluoroalkyl group —OH, —ORa, —SH, —SRa, —NH2, and —NRaRa1; R6 represents a group selected from —Ra which may be optionally substituted, linear or branched (C1-18) perfluoroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, which may be optionally substituted; R5 represents a group selected from: halogen, —Ra, linear or branched (C1-18) perfluoroalkyl group, —OH, —ORa, —SH, —SRa, —NH2, —NRaRa1, —CO—Ra, —O—C(O)—Ra and —CO2Ra1; or when q is equal to 2, then two R5 together represents further a group —O—(CH2)q1—O— wherein q1 represents an integer comprised from 1 to 3 inclusive.

  一种由化学式（I）表示的萘吡喃化合物，其中：n1、n2、p、m和q代表整数；R1、R2和R4代表从卤素，—Ra，—OH，—ORa，—SH，—SRa，—NH2，—NRaRa1，—NRbRc，—CO—Ra，—CO2Ra1，—OC(O)—Rd，—X—（Re）—Y，线性或支链（C1-C18）全氟烷基基团中选择的基团，其中Ra，Ra1，Rb，Rc，X，Y，Re和Rd如描述中定义；Z代表从CO，CS，SO，SO2，CO2，C(O)S，CS2，C(O)NH，C(O)NRa，C(S)NH，C(S)NRa和C═NRa中选择的基团；R3代表从卤素，—Ra，线性或支链（C1-18）全氟烷基基团，—OH，—ORa，—SH，—SRa，—NH2和—NRaRa1中选择的基团；R6代表从—Ra（可选地取代），线性或支链（C1-18）全氟烷基，环烷基，杂环烷基，芳基和杂芳基中选择的基团，可选地取代；R5代表从：卤素，—Ra，线性或支链（C1-18）全氟烷基基团，—OH，—ORa，—SH，—SRa，—NH2，—NRaRa1，—CO—Ra，—O—C(O)—Ra和—CO2Ra1中选择的基团；或当q等于2时，则两个R5一起进一步表示一个基团—O—（CH2）q1—O—，其中q1代表从1到3（含）的整数。
• 6-(BIPHENYL-ESTER)-3H-NAPHTHO[2,1-B]PYRANS AS PHOTOCHROMIC DICHROIC DYES AND OPTICAL ARTICLE CONTAINING THEM
  申请人：Aiken Stuart

  公开号：US20100039688A1

  公开（公告）日：2010-02-18

  A naphthopyran compound represented by the formula (I) wherein: n 1 , n 2 , p, m and q represent an integer; R 1 , R 2 and R 4 , represent a group selected from halogen, —R a , —OH, —OR a , —SH, —SR a , —NH 2 , —NR a R a1 , —NR b R c , —CO—R a , —CO 2 R a1 , —OC(O)—R d , —X—(R e )—Y, linear or branched (C 1 -C 18 ) perfluoroalkyl group, wherein R a , R a1 , R b , R c , X, Y, R e , and R d are as defined in the description; Z represents a group selected from CO, CS, SO, SO 2 , CO 2 , C(O)S, CS 2 , C(O)NH, C(O)NR a , C(S)NH, C(S)NR a and C═NR a ; R 3 represents a group selected from halogen, —R a , linear or branched (C 1-18 ) perfluoroalkyl group —OH, —OR a , —SH, —SR a , —NH 2 , and —NR a R a1 ; R 6 represents a group selected from —R a which may be optionally substituted, linear or branched (C 1-18 ) perfluoroalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, which may be optionally substituted; R 5 represents a group selected from: halogen, —R a , linear or branched (C 1-18 ) perfluoroalkyl group, —OH, —OR a , —SH, —SR a , —NH 2 , —NR a R a1 , —CO—R a , —O—C(O)—R a and —CO 2 R a1 ; or when q is equal to 2, then two R 5 together represents further a group —O—(CH 2 ) q1 —O— wherein q 1 represents an integer comprised from 1 to 3 inclusive.

  一种萘吡喃化合物，其化学式为（I），其中：n1、n2、p、m和q表示整数；R1、R2和R4表示从卤素、—Ra、—OH、—ORa、—SH、—SRa、—NH2、—NRaRa1、—NRbRc、—CO—Ra、—CO2Ra1、—OC(O)—Rd、—X—(Re)—Y、线性或支链（C1-C18）全氟烷基组中选择的一个基团，其中Ra、Ra1、Rb、Rc、X、Y、Re和Rd如描述中所定义；Z表示从CO、CS、SO、SO2、CO2、C(O)S、CS2、C(O)NH、C(O)NRa、C(S)NH、C(S)NRa和C═NRa中选择的一个基团；R3表示从卤素、—Ra、线性或支链（C1-18）全氟烷基组、—OH、—ORa、—SH、—SRa、—NH2和—NRaRa1中选择的一个基团；R6表示从可选择替代的—Ra、线性或支链（C1-18）全氟烷基、环烷基、杂环烷基、芳基和杂芳基中选择的一个基团；R5表示从卤素、—Ra、线性或支链（C1-18）全氟烷基组、—OH、—ORa、—SH、—SRa、—NH2、—NRaRa1、—CO—Ra、—O—C(O)—Ra和—CO2Ra1中选择的一个基团；或者当q等于2时，那么两个R5一起进一步表示一个基团—O—(CH2)q1—O—，其中q1表示从1到3的整数。
• Synthesis of 6-(perfluoroalkyl)salicylates by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-ethoxy-1-(perfluoroalkyl)prop-2-en-1-ones
  作者：Mathias Lubbe、Constantin Mamat、Christine Fischer、Peter Langer

  DOI：10.1016/j.tet.2006.10.062

  日期：2007.1

  6-(Perfluoroalkyl)salicylates were prepared by [3+3] cyclization of 1,3-bis(silyl enol ethers) with 3-ethoxy-1-(perfluoroalkyl)prop-2-en-1-ones.

  通过用3-乙氧基-1-（全氟烷基）丙-2-烯-1-酮对1,3-双（甲硅烷基烯醇醚）进行[3 + 3]环化制备6-（全氟烷基）水杨酸酯。
• Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: F: PerFHalOrg.9, 7.3, page 102 - 124
  作者：

  DOI：——

  日期：——