ライフサイエンスコーパス: perfluorinated

1 preparing a receptor in which the arene was perfluorinated.

2 ortho'-phenol groups while the other two are perfluorinated.

3 ereas in the other the two other phenyls are perfluorinated.

4 torical potential of PFAMs as an atmospheric perfluorinated acid (PFCA) source we studied N-ethylperf

5 ters (PAPs) are known to degrade to terminal perfluorinated acids and toxic reactive intermediates th

6 lower concentrations of their corresponding perfluorinated acids prior to oxidation.

7 For all perfluorinated acids, a U-shaped retention profile was o

8 ogel elastomers were prepared by photocuring perfluorinated acrylates and a perfluoropolyether crossl

9 mprises alternating layers of a hydrophobic, perfluorinated acrylic copolymer and hydrophobic surface

10 Three perfluorinated alkane surfactants capped with different

11 Es) are currently in use as replacements for perfluorinated alkanes (PFCs) and poly-ether heat transf

12 s possible sources of the helicity in linear perfluorinated alkanes through analysis of natural bond

13 perfluorinated carboxylic acids (PFCAs) and perfluorinated alkanesulfonates (PFSAs).

14 temporal trends of blood serum levels of 13 perfluorinated alkyl acids (PFAAs) and perfluorooctane s

15 Perfluorinated alkyl acids (PFAAs) are important global

16 Mass balances of ten individual perfluorinated alkyl acids (PFAAs) in two nested pristin

17 ut to assess the potential human exposure to perfluorinated alkyl acids (PFAAs) through the ingestion

18 Eleven perfluorinated alkyl acids (PFAAs) were analyzed in plas

19 In this study, mono-, di-, and triPAPs, perfluorinated alkyl acids (PFAAs), saturated, and unsat

20 ne standard deviation of measured values for perfluorinated alkyl acids (PFAAs).

21 chanisms that control the bioaccumulation of perfluorinated alkyl acids (PFAAs).

22 -Bingel reaction with a malonate bearing two perfluorinated alkyl chains.

23 One focus of the work is isonitriles bearing perfluorinated alkyl groups that enable the ready separa

24 Perfluorinated alkyl iodide initiators also induce a con

25 responding tin salt (I) and reacting it with perfluorinated alkyl or aryl anhydrides.

26 For example, the conductivity induced by perfluorinated alkyl silanes in organic molecular crysta

27 ions remain, further research should include perfluorinated alkyl substances (PFASs) beyond the long-

28 Increasing levels of poly- and perfluorinated alkyl substances (PFASs) have recently be

29 heric versus oceanic transport for poly- and perfluorinated alkyl substances (PFASs) reaching the Arc

30 ke PCBs, polybrominated diphenyl ethers, and perfluorinated alkyl substances and elements, such as ar

31 alkyl-modified (n-octyl and n-octadecyl) and perfluorinated (alkyl and phenyl) silica surfaces.

32 Perfluorinated alkylate substances (PFASs) are widely us

33 Postnatal exposure to perfluorinated alkylate substances (PFASs) is associated

34 Perfluorinated alkylated substances (PFASs) are today co

35 quantitative assessment of concentrations of perfluorinated alkylcarboxylates (PFCAs) and sulfonates

36 anols and the much shorter cutoffs for their perfluorinated analogues.

37 n of the carbon-fluorine bond of a series of perfluorinated and polyfluorinated arenes across the Mg-

38 paradox by implementing a highly hydrophobic perfluorinated anion (perfluorooctanesulfonate, PFOS(-))

39 nt Suzuki-Miyaura cross-coupling reaction of perfluorinated arenes with aryl boronate esters using NH

40 The hydrodefluorination (HDF) of perfluorinated aromatic compounds (hexafluorobenzene, pe

41 ing molecules in the prone position with the perfluorinated aromatic rings located above the siloxane

42 ere an efficient defluorination of poly- and perfluorinated aromatics under oxidative conditions cata

43 ryl azide (AB-dUMP), benzophenone (BP-dUMP), perfluorinated aryl azide (FAB-dUMP) or diazirine (DB-dU

44 he structure [Ru(L(2))L'](2+), where L' is a perfluorinated biphenyl bridge (F(8)bp) connecting 4,4'-

45 n the ruthenium wires, [Ru(L)2L']2+, L' is a perfluorinated biphenyl bridge connecting 4,4'-dimethylb

46 1 is 4,7-dimethylphenanthroline and L1' is a perfluorinated biphenyl bridge connecting a rhenium-liga

47 L is 4,7-dimethylphenanthroline and L' is a perfluorinated biphenyl bridge connecting a rhenium-liga

48 Our results reveal that one single perfluorinated carbon is already enough to induce a dras

49 erivatives to study the effect of one single perfluorinated carbon on the chromatographic behavior an

50 to 43 days and increased with the number of perfluorinated carbons present in the chemical.

51 To measure the total concentration of perfluorinated carboxylate and sulfonate precursors in a

52 Perfluorinated sulfonates (PFSAs) and perfluorinated carboxylates (PFCAs), as well as selected

53 ate esters (PAPs) are sources of exposure to perfluorinated carboxylates (PFCAs), leading in part to

54 emicals that are potential precursors to the perfluorinated carboxylates and sulfonates are present i

55 y generate significant amounts of additional perfluorinated carboxylates and sulfonates upon remediat

56 The fraction of PFASs consisting of perfluorinated carboxylates and sulfonates was greater i

57 and 28% of total PFASs (i.e., precursors and perfluorinated carboxylates and sulfonates) in groundwat

58 ursors released at the site was converted to perfluorinated carboxylates and sulfonates.

59 These perfluorinated carboxylates form micelles in aqueous sol

60 es hydroxyl radical to oxidize precursors to perfluorinated carboxylates was adapted for these media.

61 eir degradation and subsequent formation, of perfluorinated carboxylic acids (PFCAs) and perfluorinat

62 Eleven perfluorinated carboxylic acids (PFCAs) and three perflu

63 telomer carboxylic acid (FtCA), and C4 to C8 perfluorinated carboxylic acids (PFCAs).

64 ubsequent slow degradation of surface-sorbed perfluorinated carboxylic acids (PFCAs).

65 olyfluorinated compounds were transformed to perfluorinated carboxylic acids, which underwent further

66 ls in nanoliter-volume droplets flowing in a perfluorinated carrier fluid through a microfabricated r

67 tory and field, (2) the relationship between perfluorinated chain length and bioaccumulation, and (3)

68 cursors were transformed to PFCAs of related perfluorinated chain length.

69 try (MS/MS) for measuring trace levels of 18 perfluorinated chemicals (3 perfluorosulfonates, 8 perfl

70 We examined the relation between perfluorinated chemicals (PFCs) and semen quality among

71 Perfluorinated chemicals (PFCs) are emerging environment

72 Perfluorinated chemicals (PFCs) are of concern due to th

73 ee food contact substances (FCSs) containing perfluorinated chemicals from the list of approved FCSs

74 ers collected from locations with historical perfluorinated compound contamination.

75 inhibited transformation of a representative perfluorinated compound, perfluorooctanoic acid.

76 Despite the health risks associated with perfluorinated compounds (PFC) exposure and the detectio

77 be applied to exchange fluorine by oxygen of perfluorinated compounds (PFC).

78 Perfluorinated compounds (PFCs) have been used widely in

79 Perfluorinated compounds (PFCs) have emerged as importan

80 which was similar to the trends observed for perfluorinated compounds (PFCs) in DBS samples.

81 he occurrence of PFOA, PFOS, and eight other perfluorinated compounds (PFCs) in raw water samples fro

82 (PBDEs), hydroxylated PBDEs (OH-PBDEs), and perfluorinated compounds (PFCs) in serum and metals in w

83 complete defluorination and decomposition of perfluorinated compounds (PFCs) which comprise one of th

84 ane sulfonate and perfluorooctanoic acid are perfluorinated compounds (PFCs) widely distributed in th

85 enyls (PCBs), current-use pesticides (CUPs), perfluorinated compounds (PFCs), and polybrominated diph

86 sing demand for the monitoring of industrial perfluorinated compounds (PFCs), the identification of n

87 mones, selenoproteins, clinical markers, and perfluorinated compounds (PFCs), were determined.

88 ational regulation and phase-outs of certain perfluorinated compounds and little is known about their

89 positive associations between measured serum perfluorinated compounds and pregnancy-induced hypertens

90 Although historic perfluorinated compounds are currently under scrutiny an

91 Six classes of perfluorinated compounds are investigated.

92 Perfluorinated compounds are linked to health impacts th

93 nd PFHxA (0.9-9.7 ng/L) were the predominant perfluorinated compounds detected prior to sample treatm

94 g in the reduction or elimination of certain perfluorinated compounds from various products and waste

95 Recently, the unique features of perfluorinated compounds have reached the attention of t

96 industry, are a source of fluorotelomer and perfluorinated compounds to the environment.

97 ans and the environment to fluorotelomer and perfluorinated compounds, including recalcitrant and tox

98 creased photostability compared to the fully perfluorinated compounds.

99 dren exceeding their total daily intakes for perfluorinated compounds.

100 istent with these expectations, we find that perfluorinated fatty acids are powerful CPP activators i

101 self-assembly in membranes was explored with perfluorinated fatty acids.

102 rom a variety of alkyl, semifluorinated, and perfluorinated halides at 40 degrees C, in low-pressure

103 d peptides, saccharides, dyes, hydrocarbons, perfluorinated hydrocarbons, and even high molecular wei

104 arbon fiber electrodes coated with Nafion, a perfluorinated ion-exchange material.

105 nema, the colon is filled with Fluorinert, a perfluorinated liquid that does not produce a proton MR

106 Perfluorinated long chain alkyl amides aggregate in liqu

107 The corresponding perfluorinated long chain alkyl carboxylates form ion pa

108 of this study was to probe the potential of perfluorinated materials for the analysis and enrichment

109 We have established a method to synthesize perfluorinated meso-phenylporphyrins with one phenyl gro

110 samples of biological origin are tagged with perfluorinated moieties and subsequently enriched by sol

111 erally assumed that the electron withdrawing perfluorinated moieties render these functional groups r

112 of electrostatic interactions also holds for perfluorinated molecular carbon compounds, thus explaini

113 a Pd-catalyzed polycondensation employing a perfluorinated multiphase solvent system.

114 Nanoliter aqueous droplets immersed in perfluorinated oil are created in a microfluidic T-junct

115 es M13 inside droplets of media suspended in perfluorinated oil; a single phage M13 in a droplet yiel

116 erature, and is effective for many different perfluorinated or highly activated aryl monomers.

117 e-4,5-dimethanols (TEFDDOLs), by addition of perfluorinated organolithium reagents or Ruppert's reage

118 Apart from a perfluorinated-phenyl derivative (PA = 233 kcal/mol), th

119 nces investigated were functionalized with a perfluorinated phenylalanine residue to promote anion-pi

120 hesized by selective C-F activation, whereby perfluorinated phenylpyridines were readily complexed.

121 Furthermore, a perfluorinated photocurable monomer serves as a transpar

122 ied on one type of surfactants consisting of perfluorinated polyether and polyethylene glycol (PFPE-P

123 erated octadecene droplets in Fomblin Y 06/6 perfluorinated polyether at capillary numbers up to 0.81

124 naval brass and lubricated with Fomblin RT15 perfluorinated polyether grease in order to ensure compa

125 le components (a polymeric hydrocarbon and a perfluorinated polyether) at a common junction leads to

126 When filled with Nafion perfluorinated resin, the PB-nt membrane demonstrates po

127 Despite the widespread use of perfluorinated solvents with amino and ether groups in a

128 C3 tris-adduct shows excellent solubility in perfluorinated solvents, such as FC-72 and FC-75.

129 sights into solute dynamics can be made with perfluorinated solvents, which interact weakly with solu

130 ew fluorescent molecules that are soluble in perfluorinated solvents.

131 he adsorption properties of molecules on the perfluorinated stationary phase.

132 The perfluorinated stibonium cation [Sb(C6F5)4](+) present i

133 or other minor modifications of traditional perfluorinated structures.

134 en (H(*)) and hydroxyl (HO(*)) radicals with perfluorinated sulfonated ionomer membrane, Nafion 211,

135 Perfluorinated sulfonates (PFSAs) and perfluorinated car

136 uorinated carboxylic acids (PFCAs) and three perfluorinated sulfonic acids (PFSAs) were analyzed by H

137 review, recent progress and developments on perfluorinated sulfonic-acid (PFSA) membranes have been

138 Perfluorinated surfactants are demonstrated to dramatica

139 ilitated by the high surface activity of the perfluorinated surfactants on the fluorinated silicon su

140 pharmaceuticals, pesticides, PAHs, PCBs, and perfluorinated surfactants.