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1  airspace was filled with a water-immiscible fluorocarbon.
2 f various liquids such as mercury, water and fluorocarbon.
3 e presence of the vicinal CF2 groups in this fluorocarbon.
4 s explaining the prevalent hydrophobicity of fluorocarbons.
5 R method for determining the log P values of fluorocarbons.
6 vo using (19)F nanoparticles of two distinct fluorocarbons.
7 nvironmentally detrimental hydro- and chloro-fluorocarbons.
8 ss spectrometry imaging of tissues where the fluorocarbons act as a Teflon-like coating for nanostruc
9 Ps shows a direct correlation between higher fluorocarbon adsorption capacities and increasing pore v
10     Here, we report the first exploration of fluorocarbon adsorption using porous covalent organic po
11 mino acid core, onto which were grafted both fluorocarbon and hydrocarbon chains of different lengths
12                   The incompatibility of the fluorocarbon and hydrocarbon segments causes the LMOGs t
13 iffusivity are significantly faster near the fluorocarbon and the acidic groups lining the water chan
14       A selection of the myriad applications fluorocarbons and their derivatives have found in modern
15 nts for separation of azeotropic mixtures of fluorocarbons and use in eco-friendly fluorocarbon-based
16 ctants that organize at water/organic, water/fluorocarbon, and organic/fluorocarbon liquid interfaces
17      Crystals of MOFF-5 adsorb hydrocarbons, fluorocarbons, and chlorofluorocarbons (CFCs)-the latter
18 everal series of alpha,omega- and beta,beta'-fluorocarbon- and alkyl-substituted and unsubstituted ol
19                                              Fluorocarbons are lipophobic and non-polar molecules tha
20       Mechanisms for photodegradation of the fluorocarbons are proposed, which involve Rydberg excite
21 embranes (PEMs) in fuel cells, consists of a fluorocarbon backbone and acidic groups that, upon hydra
22 itutes, such as produced but not-yet-emitted fluorocarbon banks, remains a significant challenge.
23 n observed in air-stable semiconductors with fluorocarbon barriers.
24 ites provide preferable adsorption sites for fluorocarbon based on favorable C-F ... M(+) interaction
25 res of fluorocarbons and use in eco-friendly fluorocarbon-based adsorption cooling.
26     Full-motion MCE utilizing an intravenous fluorocarbon-based agent and pulse inversion power Doppl
27 sion assessment from a venous injection of a fluorocarbon-based contrast agent.
28 fusion assessment from a venous injection of fluorocarbon-based contrast agent.
29                       The development of new fluorocarbon-based echocardiographic contrast agents suc
30           This behavior is consistent with a fluorocarbon-based O2 barrier mechanism.
31    Here we present a simple formulation of a fluorocarbon-based oxygen carrier embedded in collagen g
32 ive, offering an alternative to the types of fluorocarbon-based structures under scrutiny as perfluor
33  acquired at the resonance frequency of each fluorocarbon by using a three-dimensional fast spin-echo
34 ry images from a patterned polymer sample of fluorocarbon (C(x)F(y)) and poly(aminopropyl siloxane) (
35 re nanodroplets containing condensed gaseous fluorocarbons can be vaporized at clinically relevant ac
36   A growing body of literature suggests that fluorocarbons can direct self-assembly within hydrocarbo
37 n cyclodextrin nanoparticles with ferrocenyl fluorocarbons capable of carrying mRNA and additional sm
38 racterize the global stocks and flows of two fluorocarbon categories, hydrochlorofluorocarbons (HCFCs
39 el CF(b) generally increased with increasing fluorocarbon chain length and were greater for sulfonate
40 demonstrate that all nTs functionalized with fluorocarbon chains at the thiophene termini are n-type
41 ase separation between the aromatic core and fluorocarbon chains.
42 its low ice adhesion strengths comparable to fluorocarbon-coated fibers, with the low ice adhesion a
43 ple preparation steps in small droplets on a fluorocarbon-coated glass slide.
44 n ionization (SALDI) technique, coupled with fluorocarbon coating, to achieve selective segregation o
45 ra work of cavity formation to accommodate a fluorocarbon, compared to a hydrocarbon, is not offset b
46 ient aspects of the nature and reactivity of fluorocarbon compounds are highlighted by comparison wit
47 ibited by 1-F appear to result from specific fluorocarbon conformational rigidity.
48 y is demonstrated through the synthesis of a fluorocarbon dendron containing 243 chemically identical
49 port the adsorption behaviour of a series of fluorocarbon derivatives on a set of microporous and hie
50                             Of the myriad of fluorocarbons described herein, the models which have re
51 racteristics towards CO2 and the refrigerant fluorocarbon dichlorodifluoromethane.
52 the nearest solvation shell, even though the fluorocarbons do have a stronger electrostatic interacti
53 e efficacy of an oxygenated perflubron-based fluorocarbon emulsion (PFE) was tested for its anti-vaso
54 ethods: A functionalized nanoemulsion with a fluorocarbon-encapsulated radiometal chelate (FERM) was
55    This is particularly true for mixtures of fluorocarbon (FC) and hydrocarbon (HC) surfactants, whic
56 am by immiscible guard segments, typically a fluorocarbon (FC) liquid, of significantly greater imped
57 tes fabricated from vacuum-formed ultra-thin fluorocarbon (FEP) foils.
58                                              Fluorocarbon films were deposited onto zinc selenide (Zn
59 roplets transported through microchannels by fluorocarbon fluids.
60 ution to enhancing protein stability than do fluorocarbon-fluorocarbon interactions between fluorinat
61 computations, comparative experiments with a fluorocarbon-free alpha,omega-dihexylquaterthiophene (DH
62 lications, including C-F bond activation and fluorocarbon functionalization.
63 ero-3-phosphocholine (DPPC) and a synthetic, fluorocarbon-functionalized analogue, 1.
64         The tissue section is stamped onto a fluorocarbon-functionalized pSi chip, which extracts and
65  the basis of the larger surface area of the fluorocarbon group, rather than a unique nature of fluor
66 ocarbon solvents by attachment of a suitable fluorocarbon group.
67 butions to the total interaction energy, and fluorocarbons have a noticeably weaker (by 10-15%) van d
68                    Four double-tailed hybrid fluorocarbon-hydrocarbon (F-H) surfactants with a poly(e
69                   These results suggest that fluorocarbon-hydrocarbon separation, in addition to an i
70 lms show very low solvent sorption, improved fluorocarbon/hydrocarbon selectivity, and excellent tran
71 irements for the remaining 40% of demand are fluorocarbons, hydrochlorofluorocarbons (HCFs), and hydr
72 carbon group, rather than a unique nature of fluorocarbon hydrophobicity.
73  stages while focusing on the role of banked fluorocarbons in global and regional decarbonization eff
74 ide chain, rather than the low solubility of fluorocarbons in hydrocarbon solvents that forms the bas
75 us emulsions, and inverted double emulsions (fluorocarbon-in-LC-in-water, F/LC/W) in response to chan
76 gy can be dynamically switched between LC-in-fluorocarbon-in-water double emulsions (LC/F/W), spheric
77 ic studies on the photolysis of liquid model fluorocarbons, including perfluorobutylethyl ether and p
78        A novel insulation technique based on fluorocarbon insulation layers deposited from pentafluor
79 (C4) configuration with the aid of Cs+...FC (fluorocarbon) interactions more clearly than the exciton
80 spread handling are expected to release this fluorocarbon into terrestrial and aquatic environments,
81           The unusual superhydrophobicity of fluorocarbons is found to be related to their larger siz
82 ion of f-AuNPs results in the release of the fluorocarbon ligands providing a driving force for analy
83 lt from immiscibility of the hydrocarbon and fluorocarbon lipid gel phases.
84 ter/organic, water/fluorocarbon, and organic/fluorocarbon liquid interfaces.
85 xploited by infusing f-AuNPs into tissue via fluorocarbon liquids to facilitate multimodal (molecular
86 s fabricated from immiscible hydrocarbon and fluorocarbon liquids to form responsive micro-lenses tha
87 ive miscibility of hydrocarbon, silicone and fluorocarbon liquids, and is applied to both the microfl
88 ure-sensitive miscibility of hydrocarbon and fluorocarbon liquids.
89  (sigma(EP)) occurs when the dynamics of the fluorocarbon matrix induces contact between different de
90      On the basis of the properties of small fluorocarbon molecules, extensively fluorinated proteins
91                                              Fluorocarbons often have distinct miscibility properties
92 PFPE) segment that confer low IFTs between a fluorocarbon oil (HFE-7700) and water.
93 s droplets that are completely surrounded by fluorocarbon oil and do not come into direct contact wit
94 droplet generation microfluidic device using fluorocarbon oil as the continuous phase.
95 ed by using surfactants that were soluble in fluorocarbon oil but insoluble in aqueous solutions.
96                                              Fluorocarbon oil isolates the droplets and provides solu
97                                              Fluorocarbon oil reinforced triple emulsion drops are pr
98 er improvements are observed upon doping the fluorocarbon oil with myoglobin.
99     In addition, it is demonstrated that the fluorocarbon oil within the emulsion drop acts as an eff
100 pe of a crescent moon are formed; removal of fluorocarbon oil yields amphiphilic particles due to the
101 ace provided by the nanoreactor suspended in fluorocarbon oil.
102 n water, allowing their co-introduction with fluorocarbon oils and minimal leaching.
103                                              Fluorocarbon oils are uniquely suited for many biomedica
104 nsic surface tension between the LCs and the fluorocarbon oils that initially lead to nonspherical, "
105                        In order to interface fluorocarbon oils with biological systems, non-ionic flu
106 prising immiscible liquid crystals (LCs) and fluorocarbon oils.
107 ible chiral nematic liquid crystals (N*) and fluorocarbon oils.
108 aser-emitting aqueous bioreactors (LEABs) in fluorocarbon oils.
109  the type of organic coating (hydrocarbon vs fluorocarbon) on peptide ionization discrimination.
110 ydrophobic cores that are packed with either fluorocarbon or hydrocarbon side chains and compared the
111 -infused oil-repellent surfaces employ toxic fluorocarbons or unstable polar liquids.
112                                              Fluorocarbons, organic molecules with carbon skeletons a
113 icity of fluorinated surfaces arises because fluorocarbons pack less densely on surfaces leading to p
114 active alternative to the use of oxygen-rich fluorocarbon pasting liquids.
115 h low interfacial tension (IFT) to stabilize fluorocarbon phases in aqueous environments (such as oil
116 te to the deposition of polymeric films from fluorocarbon plasmas.
117 ly in the deposition of polymeric films from fluorocarbon plasmas.
118 eable (Dk) RGP lenses (two types of siloxane-fluorocarbon polymer lenses with Dk of 49 and 92).
119    Films cast from stable suspensions of the fluorocarbon polymer Teflon AF 2400 (T(g) approximately
120                                         High fluorocarbon R134a equilibrium capacities and unique ove
121  the first report of adsorption isotherms of fluorocarbon R134a in MOFs.
122 llent sorption capabilities toward water and fluorocarbon R134a.
123 hexanoic acid-and provide direct evidence of fluorocarbon radicals and intermediates.
124  pyrolysis products (i.e., fluoroolefins and fluorocarbon radicals).
125 ormed on ionic liquids for the separation of fluorocarbon refrigerant mixtures.
126 s (HFOs) constitute the newest generation of fluorocarbon refrigerants and foam-blowing agents due to
127 on that has many anthropogenic sources, with fluorocarbon refrigerants being a major one.
128                                              Fluorocarbon refrigerants can be categorized into four g
129                                              Fluorocarbon refrigerants, invented in 1928 by Thomas Mi
130  less environmental impact than conventional fluorocarbon refrigerants.
131                                     Although fluorocarbon releases are expected to decline, the cumul
132 to reduced associative interactions with the fluorocarbon-rich bilayer.
133                                              Fluorocarbon solvents are usually immiscible in organic
134 ch organic molecules are rendered soluble in fluorocarbon solvents by attachment of a suitable fluoro
135 ng element for detecting water droplets in a fluorocarbon stream and quantifying their size and frequ
136 d, in the case of a 6T core, by shifting the fluorocarbon substituents from the terminal to the centr
137 ETs, resulting in air-stable devices for all fluorocarbon-substituted materials, despite generally ha
138 mbined analysis of these data indicates that fluorocarbon-substituted nT molecules strongly interact
139 e-crystal X-ray diffraction data for several fluorocarbon-substituted oligomers are also presented an
140  fundamental roles of the pi-conjugated core fluorocarbon substitution and the unique DFH-4T film mor
141  the most effective CO2-philes are expensive fluorocarbons, such as poly(perfluoroether), the commerc
142 cles the progress made in the field of small fluorocarbon synthesis since their invention in the earl
143 d models of organic glass formers containing fluorocarbon tails of increasing length, corresponding t
144 lly bulk-like, due to the segregation of the fluorocarbon tails to the free surface.
145     We here report the synthesis of Thiele's fluorocarbon (TFC) and its derivatives exhibiting except
146 this framework adsorb hydrocarbons, CFCs and fluorocarbons-the latter two being ozone-depleting subst
147 self-assembled monolayers of hydrocarbon and fluorocarbon thiols.
148 iting the unusual properties associated with fluorocarbons to modulate the physicochemical properties
149  proton MRI, a map of (19)F nuclei from each fluorocarbon was obtained without overlaps or artifacts.
150 n microchannels covered by a lid of a liquid fluorocarbon, was used.
151 ons, indicate that the hydrophobicity of the fluorocarbon, whether the interaction with water is as s
152                                 One oil is a fluorocarbon, while the second is a photocurable monomer
153 Both (19)F nanoparticles formulated with two fluorocarbons with distinct resonance frequencies and a

 
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