ライフサイエンスコーパス: fluorocarbon

1 f various liquids such as mercury, water and fluorocarbon.

2 e presence of the vicinal CF2 groups in this fluorocarbon.

3 airspace was filled with a water-immiscible fluorocarbon.

4 R method for determining the log P values of fluorocarbons.

5 s explaining the prevalent hydrophobicity of fluorocarbons.

6 ss spectrometry imaging of tissues where the fluorocarbons act as a Teflon-like coating for nanostruc

7 The incompatibility of the fluorocarbon and hydrocarbon segments causes the LMOGs t

8 iffusivity are significantly faster near the fluorocarbon and the acidic groups lining the water chan

9 A selection of the myriad applications fluorocarbons and their derivatives have found in modern

10 nts for separation of azeotropic mixtures of fluorocarbons and use in eco-friendly fluorocarbon-based

11 Crystals of MOFF-5 adsorb hydrocarbons, fluorocarbons, and chlorofluorocarbons (CFCs)-the latter

12 everal series of alpha,omega- and beta,beta'-fluorocarbon- and alkyl-substituted and unsubstituted ol

13 Fluorocarbons are lipophobic and non-polar molecules tha

14 Mechanisms for photodegradation of the fluorocarbons are proposed, which involve Rydberg excite

15 embranes (PEMs) in fuel cells, consists of a fluorocarbon backbone and acidic groups that, upon hydra

16 n observed in air-stable semiconductors with fluorocarbon barriers.

17 res of fluorocarbons and use in eco-friendly fluorocarbon-based adsorption cooling.

18 Full-motion MCE utilizing an intravenous fluorocarbon-based agent and pulse inversion power Doppl

19 sion assessment from a venous injection of a fluorocarbon-based contrast agent.

20 fusion assessment from a venous injection of fluorocarbon-based contrast agent.

21 The development of new fluorocarbon-based echocardiographic contrast agents suc

22 This behavior is consistent with a fluorocarbon-based O2 barrier mechanism.

23 Here we present a simple formulation of a fluorocarbon-based oxygen carrier embedded in collagen g

24 ry images from a patterned polymer sample of fluorocarbon (C(x)F(y)) and poly(aminopropyl siloxane) (

25 re nanodroplets containing condensed gaseous fluorocarbons can be vaporized at clinically relevant ac

26 A growing body of literature suggests that fluorocarbons can direct self-assembly within hydrocarbo

27 demonstrate that all nTs functionalized with fluorocarbon chains at the thiophene termini are n-type

28 ase separation between the aromatic core and fluorocarbon chains.

29 n ionization (SALDI) technique, coupled with fluorocarbon coating, to achieve selective segregation o

30 ra work of cavity formation to accommodate a fluorocarbon, compared to a hydrocarbon, is not offset b

31 ient aspects of the nature and reactivity of fluorocarbon compounds are highlighted by comparison wit

32 ibited by 1-F appear to result from specific fluorocarbon conformational rigidity.

33 y is demonstrated through the synthesis of a fluorocarbon dendron containing 243 chemically identical

34 port the adsorption behaviour of a series of fluorocarbon derivatives on a set of microporous and hie

35 racteristics towards CO2 and the refrigerant fluorocarbon dichlorodifluoromethane.

36 the nearest solvation shell, even though the fluorocarbons do have a stronger electrostatic interacti

37 e efficacy of an oxygenated perflubron-based fluorocarbon emulsion (PFE) was tested for its anti-vaso

38 This is particularly true for mixtures of fluorocarbon (FC) and hydrocarbon (HC) surfactants, whic

39 Fluorocarbon films were deposited onto zinc selenide (Zn

40 roplets transported through microchannels by fluorocarbon fluids.

41 ution to enhancing protein stability than do fluorocarbon-fluorocarbon interactions between fluorinat

42 computations, comparative experiments with a fluorocarbon-free alpha,omega-dihexylquaterthiophene (DH

43 lications, including C-F bond activation and fluorocarbon functionalization.

44 ero-3-phosphocholine (DPPC) and a synthetic, fluorocarbon-functionalized analogue, 1.

45 The tissue section is stamped onto a fluorocarbon-functionalized pSi chip, which extracts and

46 the basis of the larger surface area of the fluorocarbon group, rather than a unique nature of fluor

47 ocarbon solvents by attachment of a suitable fluorocarbon group.

48 butions to the total interaction energy, and fluorocarbons have a noticeably weaker (by 10-15%) van d

49 These results suggest that fluorocarbon-hydrocarbon separation, in addition to an i

50 lms show very low solvent sorption, improved fluorocarbon/hydrocarbon selectivity, and excellent tran

51 irements for the remaining 40% of demand are fluorocarbons, hydrochlorofluorocarbons (HCFs), and hydr

52 carbon group, rather than a unique nature of fluorocarbon hydrophobicity.

53 ide chain, rather than the low solubility of fluorocarbons in hydrocarbon solvents that forms the bas

54 ic studies on the photolysis of liquid model fluorocarbons, including perfluorobutylethyl ether and p

55 A novel insulation technique based on fluorocarbon insulation layers deposited from pentafluor

56 (C4) configuration with the aid of Cs+...FC (fluorocarbon) interactions more clearly than the exciton

57 spread handling are expected to release this fluorocarbon into terrestrial and aquatic environments,

58 The unusual superhydrophobicity of fluorocarbons is found to be related to their larger siz

59 ion of f-AuNPs results in the release of the fluorocarbon ligands providing a driving force for analy

60 lt from immiscibility of the hydrocarbon and fluorocarbon lipid gel phases.

61 xploited by infusing f-AuNPs into tissue via fluorocarbon liquids to facilitate multimodal (molecular

62 s fabricated from immiscible hydrocarbon and fluorocarbon liquids to form responsive micro-lenses tha

63 ive miscibility of hydrocarbon, silicone and fluorocarbon liquids, and is applied to both the microfl

64 (sigma(EP)) occurs when the dynamics of the fluorocarbon matrix induces contact between different de

65 On the basis of the properties of small fluorocarbon molecules, extensively fluorinated proteins

66 Fluorocarbons often have distinct miscibility properties

67 s droplets that are completely surrounded by fluorocarbon oil and do not come into direct contact wit

68 droplet generation microfluidic device using fluorocarbon oil as the continuous phase.

69 ed by using surfactants that were soluble in fluorocarbon oil but insoluble in aqueous solutions.

70 Fluorocarbon oil isolates the droplets and provides solu

71 Fluorocarbon oil reinforced triple emulsion drops are pr

72 er improvements are observed upon doping the fluorocarbon oil with myoglobin.

73 In addition, it is demonstrated that the fluorocarbon oil within the emulsion drop acts as an eff

74 pe of a crescent moon are formed; removal of fluorocarbon oil yields amphiphilic particles due to the

75 the type of organic coating (hydrocarbon vs fluorocarbon) on peptide ionization discrimination.

76 ydrophobic cores that are packed with either fluorocarbon or hydrocarbon side chains and compared the

77 Fluorocarbons, organic molecules with carbon skeletons a

78 icity of fluorinated surfaces arises because fluorocarbons pack less densely on surfaces leading to p

79 active alternative to the use of oxygen-rich fluorocarbon pasting liquids.

80 te to the deposition of polymeric films from fluorocarbon plasmas.

81 ly in the deposition of polymeric films from fluorocarbon plasmas.

82 eable (Dk) RGP lenses (two types of siloxane-fluorocarbon polymer lenses with Dk of 49 and 92).

83 Films cast from stable suspensions of the fluorocarbon polymer Teflon AF 2400 (T(g) approximately

84 the first report of adsorption isotherms of fluorocarbon R134a in MOFs.

85 llent sorption capabilities toward water and fluorocarbon R134a.

86 to reduced associative interactions with the fluorocarbon-rich bilayer.

87 Fluorocarbon solvents are usually immiscible in organic

88 ch organic molecules are rendered soluble in fluorocarbon solvents by attachment of a suitable fluoro

89 ng element for detecting water droplets in a fluorocarbon stream and quantifying their size and frequ

90 d, in the case of a 6T core, by shifting the fluorocarbon substituents from the terminal to the centr

91 ETs, resulting in air-stable devices for all fluorocarbon-substituted materials, despite generally ha

92 mbined analysis of these data indicates that fluorocarbon-substituted nT molecules strongly interact

93 e-crystal X-ray diffraction data for several fluorocarbon-substituted oligomers are also presented an

94 fundamental roles of the pi-conjugated core fluorocarbon substitution and the unique DFH-4T film mor

95 the most effective CO2-philes are expensive fluorocarbons, such as poly(perfluoroether), the commerc

96 this framework adsorb hydrocarbons, CFCs and fluorocarbons-the latter two being ozone-depleting subst

97 self-assembled monolayers of hydrocarbon and fluorocarbon thiols.

98 iting the unusual properties associated with fluorocarbons to modulate the physicochemical properties

99 n microchannels covered by a lid of a liquid fluorocarbon, was used.

100 ons, indicate that the hydrophobicity of the fluorocarbon, whether the interaction with water is as s

101 One oil is a fluorocarbon, while the second is a photocurable monomer