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1 ive deposition of an electrochromic polymer (polyaniline).
2 -FePc-CH (where VS-PANI is vinyl substituted polyaniline).
3 oligoaniline shell on gold nanoparticles to polyaniline.
4 n/off fluorescence switching, reminiscent of polyaniline.
5 of APSA during electropolymerization of the polyaniline.
6 polymerization of aniline to form conductive polyaniline.
7 H 5, corresponding to the conductive form of polyaniline.
8 een pre-modified with the conductive polymer polyaniline.
9 d chemical properties typical of para-linked polyanilines.
10 s of emeraldine base polyaniline (PANI) and (polyaniline)(0.5)V(2)O(5) x 1.0 H(2)O have been determin
11 ne-step process involving the pyrolysis of a polyaniline aerogel synthesized in the presence of phyti
12 ges in Raman spectra of boronate-substituted polyaniline after addition of glucose are similar to tho
16 onsive nanocapsules consisting of conductive polyaniline and polypyrrole shells were successfully syn
18 nd then discharges continuously by oxidizing polyaniline and reducing Fe(3+) under isothermal heating
19 detection of various small soluble n-mers of polyaniline and silver ion solvent clusters formed from
21 . nafion, polyphenylenediamine, polypyrrole, polyaniline, and polynaphthol using a novel silica-based
22 e oxide/platinum nanoparticles cathode and a polyaniline anode in Fe(2+)/Fe(3+) redox electrolyte via
23 rein the redox energies of Al and conducting polyaniline are exploited to design a battery type senso
25 dispersed active sites are prepared by using polyaniline as a graphene precursor and introducing phen
26 nd this scope by utilizing phytic acid-doped polyaniline as a novel redox-charging polymer support en
27 en proposed for the excellent sensitivity of polyaniline as a pH sensor for detection of H(+) ions re
29 ple electrostatic binding of the antibody to polyaniline as well as a more complex procedure using a
30 own for boronate- and sulfate-functionalized polyanilines as well as for Prussian Blue, a member of t
32 oligomers were produced, and the self-doped polyaniline backbone had a longer conjugation length and
33 he switching of amine functionalities in the polyaniline backbone, converting them to imine forms.
36 performance when compared with conventional polyaniline-based sensors, and this was attributed to th
38 2+) and Mn(2+) on the activity of native and polyaniline chitosan nanocomposites bound Aspergillus or
40 tional changes in the secondary structure of polyaniline chitosan silver nanocomposite bound beta-gal
42 tained by thermal activation of a mixture of polyaniline-coated graphene oxide and ammonium hexafluor
45 was demonstrated that the positively charged polyaniline colloids can be electrophoretically deposite
46 yl acetate) itaconic acid (PANI(PVIA)) doped polyaniline conducting nanobeads (SiO2(LuPc2)PANI(PVIA)-
47 ormed to characterize the interconversion of polyaniline content (from amine to imine) in manno-PANI
49 e screen-printed electrode was modified with polyaniline-decorated sulfur-doped graphitic carbon nitr
51 were first coated with emulsion-polymerized polyaniline/dinonylnaphthalenesulfonic acid (PANI/DNNSA)
54 fluorous surfactant formulation with undoped polyaniline (F-PANI) fabricated to create test lines for
57 voltammogram obtained from the experiment on polyaniline film using Fe(2+)/Fe(3+) in HCl as the redox
59 cal conductivities in excess of 50 S/cm when polyaniline films are exposed to dichloroacetic acid.
60 xploration of the viscoelastic properties of polyaniline films exposed to aqueous perchloric acid has
61 oating small polymer objects with conductive polyaniline films preventing accumulation of static elec
63 C3 N) can be attributed to their inherent 2D polyaniline frameworks, which provide large net positive
65 posited on top of an electrosprayed graphene/polyaniline (G/PANI) modified screen printed carbon elec
69 he as-obtained anisotropic polyvinyl alcohol/polyaniline hydrogel can work as a stretching/compressin
70 e and bendable anisotropic polyvinyl alcohol/polyaniline hydrogel with a complete recovery of 100% st
73 nedioxythiophene):poly(4-styrene sulfonate), polyaniline) in combination with passive fibrotic and el
76 ant E. coli cells in the microenvironment of polyaniline led to a change in its conductivity, which w
81 use of a novel ammonium ion-specific copper-polyaniline nano-composite as transducer for hydrolase-b
82 ess was 4,500 times faster when a self-doped polyaniline nanocomposite was fabricated using in situ p
83 properties of a multiwalled carbon nanotube/polyaniline nanofiber (MWCNT/PAnNF) nanocomposite film o
87 ydrolysis of B-lactams, on the electroactive polyaniline nanofibers, altered the polymeric backbone o
88 iew explores some intriguing applications of polyaniline nanofibers, as well as the advantages and re
91 e tumor-targeting rapamycin/DiR loaded lipid-polyaniline nanoparticle (RDLPNP) for dual-modal imaging
92 Correlating the shape and aggregation of polyaniline nanoparticles with the mode of nucleation, a
96 cluding a continuous electrically conductive polyaniline network, binding with the Si surface through
97 n ether (G-quadruplexes), chemical (pH-doped polyaniline), or biocatalytic (glucose oxidase/urease) t
98 idized microRNA (miRNA)-guided deposition of polyaniline (PAn), a highly sensitive impedimetric miRNA
99 roblem, we present an approach to synthesize polyaniline (PAN)-based conductive single enzyme nanocom
100 ce of the Al(2)O(3) NPs is modified by ionic polyaniline (PANDB) rather than the conventional silane
102 ee-dimensional structures of emeraldine base polyaniline (PANI) and (polyaniline)(0.5)V(2)O(5) x 1.0
103 ultrasensitive electrochemical sensor using polyaniline (PANi) and carboxyl functionalized multi-wal
104 horetically deposited nanocomposite films of polyaniline (PANI) and core-shell Ag@AgO nanoparticles (
106 ChE) biosensor was successfully developed on polyaniline (PANI) and multi-walled carbon nanotubes (MW
108 omposite of camphorsulfonic acid (CSA)-doped polyaniline (PANI) and the room-temperature ionic liquid
109 situ polymerized mesoporous silica-supported polyaniline (PANI) by carbonization of the latter, follo
111 of the microtiter reader plates well with a polyaniline (PANI) film sensitive for ascorbic acid is p
113 experimental evidence of proton release from polyaniline (PANI) films subjected to anodic potentials
115 graphene (G), polyvinylpyrrolidone (PVP) and polyaniline (PANI) has been successfully prepared and us
119 ding an alpha-amylase specific antibody to a polyaniline (PANI) layer and controlling device assembly
121 orods (AuMRs), Pd-nanoparticles (PdNPs), and Polyaniline (PANI) nanocomposite-interface was fabricate
122 composed of mesoporous silica (SBA-15) with polyaniline (PANI) nanostructures within its channel por
124 rbon nanotube (S/SWNT) composite coated with polyaniline (PANI) polymer as polysulfide block to achie
125 he AuNPs-AOx conjugate was encapsulated with polyaniline (PANI) synthesized by oxidative polymerizati
126 Tailoring conducting polymers (CPs) such as polyaniline (PANI) to deliver the appropriate morphology
129 We demonstrate this concept by integrating polyaniline (PANI), an electro-optically active polymer,
131 uctures encapsulated with (iii) pH-sensitive polyaniline (PANI), assembled between laser-cut cover la
132 Composed exclusively of organic components, polyaniline (PANi), graphene, and double-walled nanotube
134 ications, in particular the most common CPs, polyaniline (PANI), polypyrrole (PPy), polythiophene (PT
135 measurements are done by potentiometry using polyaniline (PAni)-based working electrodes and silver/s
141 y using an electrochemical growth of bilayer polyaniline/platinum microtubes within the conically sha
142 ofibers (GMnO) and direct electrospinning of polyaniline/polyethylene oxide (PANi/PEO) composite nano
143 es of electronic conducting polymers such as polyaniline, polypyrrole, and poly(3,4-ethylenedioxythio
145 port an advanced processable and nanofibrous polyaniline:polystyrene-sulphonate (nano-PANI:PSS) as a
146 ers of conducting polymer nanofibers such as polyaniline, polythiophene, and poly(3-hexylthiophene) c
150 to a battery type discharge reaction wherein polyaniline redox energy changes from the conducting to
155 mechanism of the resistance decrease is the polyaniline self-doping, i.e., as an alternative to prot
156 ymerization technique was adapted to produce polyaniline sensing layers doped with poly(4-styrenesulf
157 increase in porosity, for example, when the polyaniline shell is swollen using small amounts of DMF
158 introduced (gold triangular nanoprism core)/(polyaniline shell) nanoparticles (GTNPs@PANI) as an OCT
160 he gaps are bridged with conducting polymer (polyaniline) so that one can measure the conductance of
161 des featuring 4-nm underlayers of sulfonated polyaniline (SPAN) covered with a film containing myoglo
166 llustrated by electrophoretically patterning polyaniline thin films onto selected individual micromet
167 xide first oxidizes HRP, which then oxidizes polyaniline, thus resulting in decreased conductivity of
169 Subsequent steps include the oxidation of polyaniline to lower the pH, the delivery of molybdate v
170 for covalent immobilization of human IgG on polyaniline using glutaraldehyde as the cross-linker is
171 of MIP was photochemically grafted over the polyaniline, via N,N'-diethyldithiocarbamic acid benzyl
172 uced grapheme oxide (rGO), vinyl substituted polyaniline (VS-PANI) and lutetium Phthalocyanine (LuPc2
173 a unique tetragonal star-like morphology of polyaniline was applied as a efficient solid phase for s
177 zeolitic imidazolate frameworks and covalent polyaniline), we comparatively diagnose the intrinsic ki
178 le a nitrate-selective redox-electrosorbent (polyaniline) with an electrocatalyst (cobalt oxide) for
179 -graphite particles with electrolyte-swollen polyaniline yields a stable solid-electrolyte interphase
181 , we develop an ultralow temperature aqueous polyaniline| |Zn battery that exhibits a high capacity (