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1 esigned based on boronic acid-functionalized polythiophene.
2 sion in hexafluoroisopropanol functionalized polythiophene.
3 ated polymers: polyaniline, polypyrrole, and polythiophene.
4 l and electronic properties of the resulting polythiophenes.
5 stituted trans-polyacetylenes, polyynes, and polythiophenes.
6                          The assay relies on polythiophene acetic acid (PTAA) as an optical reporter
7 o cause considerable twists in its oligo- or polythiophene analogues.
8 le coupling polymerization of end-functional polythiophene and AA + BB monomers, is presented.
9 nd molecular weight is examined for a p-type polythiophene and an n-type naphthalene diimide-based po
10  the structural and electronic properties of polythiophene and polyprrrole-based systems have been in
11 monstrate concurrent redox reactions of both polythiophene and viologen in solid-state devices and co
12 ting polymer nanofibers such as polyaniline, polythiophene, and poly(3-hexylthiophene) can be produce
13 operties of excited states in the archetypal polythiophene are investigated via aggregates suspended
14 ing that highly regioregular and crystalline polythiophenes are not required in order to effectively
15 at ethylenedioxy substitution planarizes the polythiophene backbone but the experimentally observed b
16   Solution self-assembly of the regioregular polythiophene-based block copolymer poly(3-hexylthiophen
17   Previous efforts to generate this phase in polythiophene-based block copolymers have failed due to
18           We report the synthesis of a novel polythiophene-based host-guest copolymer incorporating a
19 ortant concept in organic electronics and in polythiophene-based solid-state electrochromic devices t
20                       We examine a family of polythiophenes bearing nitroxide radical groups, showing
21                                Addition of a polythiophene block copolymer with a different corona-fo
22 n) in the observed thermochromic behavior of polythiophene but instead point on the major role of cha
23                             The oxidation of polythiophenes can be controlled with this potent, yet o
24   This work highlights an optimally designed polythiophene-carboxylic acid based CSCP, POET-T2-COOH,
25                                     Pristine polythiophene chains are hydrophobic and are not easily
26 the relaxation mode spectra of locally stiff polythiophene chains.
27                      Upon rebinding, the TNV-polythiophene complex changes the fluorescence intensity
28 ke micelles with a crystalline pi-conjugated polythiophene core with lengths up to ca. 700 nm were su
29 rent synthetic strategies to access cationic polythiophenes (CPTs) via chemical oxidation using iron(
30 ch enables the treatment of relatively large polythiophene dendrimers that serve as two-photon absorb
31 o identify a new conformationally restricted polythiophene derivative for p-type accumulation-mode or
32 thoxy-5'-octylphenyl)thiophene) (POMeOPT), a polythiophene derivative with bulky side chains, can be
33 ]methyl}thiophene-2,5-diyl) (P3MEEMT), a new polythiophene derivative with ethylene glycol-based side
34 tectable conformational change in conjugated polythiophene derivatives from forming single-stranded D
35 rroics consisting of electronically distinct polythiophene derivatives is reported.
36 and electrical properties of a series of six polythiophene derivatives with varying regiochemistry an
37 he solution-state assembly of all-conjugated polythiophene diblock copolymers containing nonpolar (he
38 tion organic solar cells comprising either a polythiophene donor and two fullerene acceptors or two p
39 ene donor and two fullerene acceptors or two polythiophene donors and a fullerene acceptor are shown
40 The device structure is similar to that of a polythiophene field effect transistor, but ethylviologen
41 sion is not affected by the thickness of the polythiophene film and the nature of TNV specific bindin
42 densities exceeding 2.5 x 10(14) cm(-2), the polythiophene film becomes superconducting.
43 ion by electropolymerization of biotinylated polythiophene films on the surface of miniaturized, disp
44                       A series of glycolated polythiophenes for use in organic electrochemical transi
45 per ions and the effect of their addition to polythiophene-fullerene (P3HT-PC(71)BM) OPV devices was
46 ight emitting diode as the light source, and polythiophene: fullerene type bulk-heterojunction device
47 study is to produce a novel ternary chitosan-polythiophene-graphene oxide (CS-PTh-GO) bionanocomposit
48                                 Among these, polythiophenes have been established as a model system t
49                           CPEs with cationic polythiophenes, in both homopolymer and block copolymer
50                     The biosensor utilizes a polythiophene interface containing fused quinone moietie
51                        In this report, a new polythiophene interface is fabricated containing fused q
52 integrate SWNT and a suitably functionalized polythiophene into nanostructured ITO electrodes.
53 substitution of alternative heteroatoms into polythiophenes is a promising strategy for tuning their
54                                  Three novel polythiophene isomers are reported whereby the only diff
55                      The conductivity of the polythiophene layer was reversibly switched between high
56 ally, S has been substituted by Se and Te in polythiophene, leading to polyseleophene and polytelluro
57 necessary for good electronic performance of polythiophene-like systems.
58 get analyte concentration in solution at the polythiophene MIP-film coated electrode did not originat
59 f-flight charge transport of the homopolymer polythiophene (mu(h) ~10(-4) cm(2) V(-1) s(-1)) in the c
60                       Here we show that pure polythiophene nanofibres can have a thermal conductivity
61 necrosis virus (TNV) have been formed within polythiophene nanofilms with an approximate thickness of
62 Nanohybrids consisting of Au nanocluster and polythiophene nanowire assemblies exhibit unique thermal
63    Mixed bilayers, including one formed from polythiophene on top of polypyrrole, have also been cons
64                      However, in the case of polythiophenes, one of the most important classes of con
65 ographic data of PEDOT and other substituted polythiophenes, our work seeks to establish a comprehens
66       Raman spectroscopy revealed reversible polythiophene oxidation to its polaron form accompanied
67        Optical signal generation is based on polythiophene particulates dispersed within the ion-sele
68           Furthermore, the epoxy-substituted polythiophene polymer coated indium tin oxide electrode
69 ker was described by using epoxy-substituted polythiophene polymer modified disposable indium tin oxi
70 active scaffold to engineer soluble BN-doped polythiophene polymers.
71 n thin films of regioregular and regiorandom polythiophene polymers.
72         Stacking (bilayer formation) of pure polythiophene, polypyrrole and their derivatives leads t
73 posite as tracing tag to label DNA probe and polythiophene (PT) as immobilization platform of sensing
74 otosensitizers were screened, and eventually polythiophene PT10 was selected with high singlet oxygen
75  CPs, polyaniline (PANI), polypyrrole (PPy), polythiophene (PTh) and their derivates, including poly(
76 thod and formulation of its nanohybrids with polythiophene (PTh).
77 tice of semicrystalline spin-coated films of polythiophenes (PTs) may be resolved using AFM under amb
78 hiolated mannose (TM)/quinone functionalised polythiophene (QFPT) thin film was modified on EQCM/Au e
79 rovide a redox counter-reaction to accompany polythiophene redox reactions.
80 ting electron donor/acceptor nanocomposites, polythiophene represents the light-harvesting chromophor
81 , synthesis and characterization of a random polythiophene (RP-T50) containing ~50 mol% of thiophene
82                The threshold voltages of our polythiophene-sorted SWNT thin-film transistors can be t
83  cationic-functionalized oligothiophenes and polythiophenes, their properties, and their diverse appl
84 arge transport is demonstrated in an undoped polythiophene thin film, with average mobilities above 3
85 se of Rozen's reagent (HOFCH3 CN) to convert polythiophenes to polymers containing thiophene-1,1-diox
86 nthesis of ionically functionalized branched polythiophenes with either carboxylic acid (anionic, P3T