ライフサイエンスコーパス: perylene

1 fluoranthene) to 95.7 +/- 4.1% (benzo[ g,h,i]perylene).

2 ylphenyl linker is attached to the C9-linked perylene).

3 ll-hydrocarbon macrocycle, D(4d)-CDMB-8, and perylene.

4 for naphthalene up to 5.5 x 10(6) M(-1) for perylene.

5 drocarbons including anthracene, pyrene, and perylene.

6 nylenes, hexabenzocoronene, oligoacenes, and perylene.

7 ilities, which is, for instance, the case of perylene.

8 e rearrangements, with slower cyclization to perylene.

9 -catalyzed cyclization of 1,1'-binaphthyl to perylene.

10 Condensation of benzo[ghi]perylene-1,2-dicarboxylic anhydride in the presence of "

11 e phenanthrene and pyrene (22%), followed by perylene (21%) and fluoranthene (16%), but the fingerpri

12 [(N,N'-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2]

13 The dendronized perylene 3,4:9,10-tetracarboxylic acid bisimide (PBI), (

14 The synthesis of perylene 3,4:9,10-tetracarboxylic acid bisimides (PBIs)

15 1,6,7,12-Tetra-(4-tert-butylphenoxy)-perylene-3,4 : 9,10-bis(dicarboximide) (tpPDI) linked to

16 odisperse, C4-symmetric octamer of a guanine-perylene-3,4,9,10-bis(dicarboximide) conjugate (GPDI) wa

17 N-(1-hexylheptyl)-N'-(12-carboxylicdodecyl)perylene-3,4,9,10-tetracarboxyl bisimide was synthesized

18 nthesis starting from commercially available perylene-3,4,9,10-tetracarboxylic bisanhydride.

19 Using perylene-3,4,9,10-tetracarboxylic bisimide (PBI) as the

20 tals of the molecules pentacene (C22H14) and perylene-3,4,9,10-tetracarboxylic dianhydride (C24H8O6),

21 on substrates coated by the organic molecule perylene-3,4,9,10-tetracarboxylic dianhydride.

22 Here, perylene-3,4,9,10-tetracarboxylic diiimide-based near-in

23 ctly different side-chains, N,N'-di(dodecyl)-perylene-3,4,9,10-tetracarboxylic diimide (DD-PTCDI) and

24 c diimide (DD-PTCDI) and N,N'-di(nonyldecyl)-perylene-3,4,9,10-tetracarboxylic diimide (ND-PTCDI).

25 tral perylene diimide (N,N'-bis(butoxypropyl)perylene-3,4,9,10-tetracarboxylic diimide) and cationic

26 in solutions containing N,N-bis(ethylpropyl)perylene-3,4,9,10-tetracarboxylicdiimide (PDI) or tetrac

27 Robust perylene-3,4-dicarboximide (PMI) pi-aggregates provide i

28 4,5,5-tetramethyl-[1,3,2]dioxa borolan-2-yl)-perylene-3,4-dicarboximide.

29 ction of the lowest excited singlet state of perylene-3,4:9,10-bis(dicarboximide) ((1*)PDI) with a st

30 thin films of N,N-bis(2,6-diisopropylphenyl)perylene-3,4:9,10-bis(dicarboximide) (1) and the 1,7-dip

31 an oligo(2,7-fluorene) (FL(n)) bridge, and a perylene-3,4:9,10-bis(dicarboximide) (PDI) acceptor, PTZ

32 nors, 2,7-oligofluorene (FL(n)) bridges, and perylene-3,4:9,10-bis(dicarboximide) (PDI) acceptors was

33 s are derivatives of the strong photooxidant perylene-3,4:9,10-bis(dicarboximide) (PDI) and the molec

34 Each building block is based on perylene-3,4:9,10-bis(dicarboximide) (PDI) chromophores.

35 either one or both imide nitrogen atoms of a perylene-3,4:9,10-bis(dicarboximide) (PDI) electron acce

36 e steric bulk of the 1,7-substituents of the perylene-3,4:9,10-bis(dicarboximide) (PDI) impedes aggre

37 spectra of a N-N'-bis(2,6-diisopropylphenyl)-perylene-3,4:9,10-bis(dicarboximide) (PDI) self-assemble

38 ree covalently linked 1,6,7,12-tetra(phenoxy)perylene-3,4:9,10-bis(dicarboximide) (PDI) units.

39 hiazine (PTZ), B = p-oligophenylene, and A = perylene-3,4:9,10-bis(dicarboximide) (PDI), by measuring

40 (Z3PN) attached to the 1,7,N,N'-positions of perylene-3,4:9,10-bis(dicarboximide) (PDI).

41 ), B = p-phenylene (Ph(n)), n = 1-4, and A = perylene-3,4:9,10-bis(dicarboximide) (PDI).

42 onse parameters as follows: N,N'-bis(n-octyl)perylene-3,4:9,10-bis(dicarboximide) (PDI-8): mu = 0.32

43 etraphenylporphyrin (ZnTPP) as a donor and a perylene-3,4:9,10-bis(dicarboximide) dimer as the accept

44 -1,8:4,5-bis(dicarboximide) or either of two perylene-3,4:9,10-bis(dicarboximide) electron acceptors

45 talline thin films of 1,6,7,12-tetra(phenoxy)perylene-3,4:9,10-bis(dicarboximide) having either n-oct

46 1,6- and 1,7-bis(n-octylamino)perylene-3,4:9,10-bis(dicarboximide) were synthesized by

47 n arylene imide and bis(imide) dyes, such as perylene-3,4:9,10-bis(dicarboximide)s.

48 ships based on pi-pi stacking in the related perylene-3,4:9,10-bis(dicarboximides) (PDIs) have been w

49 have prepared a large molecule in which four perylene-3,4:9,10-tetracarboxydiimide (PDI) molecules th

50 and 1,1'-ethynyl-bis[N,N'-bis(1-hexylheptyl)-perylene-3,4:9,10-tetracarboxylic diimide] ([PDI]2CC, 2)

51 roups, bis[1-ethynyl-N,N'-bis(1-hexylheptyl)-perylene-3,4:9,10-tetracarboxylic diimide] ([PDICC]2, 1)

52 We report for the first time the use of perylene-3-ylmethanol fluorescent organic nanoparticles

53 al studies revealed that the newly developed perylene-3-ylmethanol nanoparticles exhibit good biocomp

54 In the present system, perylene-3-ylmethanol nanoparticles performed four impor

55 xcited states: the fluorescent S(1) state of perylene, a luminescent doublet ligand-to-metal charge t

56 Excitation at 490 nm, where the perylene absorbs preferentially, results in fluorescence

57 Examples of these new series of perylene analogues were partially oxidized to the corres

58 probes based on larger intercalators, i.e., perylene and coronene, expecting that the larger pi-surf

59 ort of charges through vertically segregated perylene and hexabenzocoronene pi systems.

60 roduce thin films with vertically segregated perylene and hexabenzocoronene, with large interfacial s

61 Isotope-mass balance-calculations of perylene and n-alkanoic acids indicate that ~40% of sedi

62 dual PAHs ranged between 0.13 ng m(-2)d(-1) (Perylene) and 1.96 ng m(-2)d(-1) (Methyl Pyrene), and fo

63 rubrene, 9,10-diphenylanthracene, pyrene, or perylene) and BODIPY were trapped in a toluene and tri-n

64 e, benzo[e]pyrene, benzo[a]pyrene, benzo[ghi]perylene, and benzo[b]chrysene when extracted at the hig

65 ene, anthracene, anthanthrene, fluoranthene, perylene, and benzo[ghi]fluoranthene at ppm levels.

66 ss accumulation rates and isotope records of perylene, and compare them with total organic carbon and

67 nz[a]pyrene, dibenz[a,h]anthracene, benz[ghi]perylene, and indeno[1,2,3-cd]pyrene were used as target

68 m vapor pressure --benzo[a]pyrene, benzo[ghi]perylene, and indeno[1,2,3-cd]pyrene-- the mass in the n

69 e transfer between the hexabenzocoronene and perylene, as well as from effective transport of charges

70 a valuable addition to the family of robust perylene-based chromophores that can be used to develop

71 We have developed a new series of dual-pore perylene-based COFs and demonstrated that their imine bo

72 ghly desirable and will be proposed here for perylene-based materials.

73 ow relaxation processes can be diminished in perylene-based materials.

74 ze a series of HMGA1 inhibitors, including a perylene-based nanoparticle, PDIC-DPC, which effectively

75 N,N'-1H,1H-Perfluorobutyl derivatives of the perylene-based semiconductors were also synthesized and

76 oral feature allows the present D(4d)-CDMB-8 perylene-based system to be used as a time-dependent, co

77 aP), indeno[123-cd]pyrene (IP) and benzo[ghi]perylene (BghiP) were separated and quantified using GC-

78 Supramolecular complexation of perylene bis(diimide) (PDI) dyes with the macrocyclic ho

79 enevinylene) electron donor and a C-terminal perylene bis-imide electron acceptor.

80 6-isomer and other related amino-substituted perylene bis-imide species.

81 The perylene-bis(porphyrin)-phthalocyanine architecture exhi

82 The perylene-bis(porphyrin)-phthalocyanine array absorbs str

83 d coupling of an ethynylperylene to afford a perylene-bis(porphyrin)-phthalocyanine linear array.

84 In addition, azabenz-annulated perylene bisanhydrides (ab-PBA 6 and syn-(ab)2-PBA 19) w

85 sonance energy transfer, FRET) of dyads with perylene biscarboximides is very efficient and achieves

86 Perylene bisimide (PBI) and azo-compounds are fascinatin

87 ssembly of octahedral Fe(II) ions and linear perylene bisimide (PBI) dyes with 2,2'-bipyridine groups

88 enables the synthesis of previously unknown perylene bisimide (PBI) dyes with up to five different s

89 A series of semirigid perylene bisimide (PBI) macrocycles with varied ring siz

90 Herein, we describe a perylene bisimide (PBI) organogelator molecule PBI-4 tha

91 izations of a series of amide-functionalized perylene bisimide (PBI) organogelator molecules bearing

92 are based on 1,4-distyrylbenzene (OPV3) and perylene bisimide (PBI) units.

93 Discovered with a dendronized perylene bisimide (PBI), this mechanism arranges the alk

94 c (Hg(2)(+)) ions that we constructed from a perylene bisimide (PBI)-based organic thin film transist

95 on, we show that the covalent tethering of a perylene bisimide (PBI)-derived supramolecular polymer w

96 chetype organogelator molecule composed of a perylene bisimide aromatic scaffold and two amide substi

97 We show that both homochiral and racemic perylene bisimide compounds, including a mixture of 21 d

98 Perylene bisimide derivatives (PBIs) are known to form o

99 Here, we report the self-assembly of perylene bisimide derivatives in a supramolecular helix

100 , we study the mechanism of self-assembly of perylene bisimide derivatives possessing dipolar carbona

101 nd temperature-dependent fluorescence of the perylene bisimide dye PBI 1 in methylcyclohexane point t

102 c acids with aryl iodides in the presence of perylene bisimide dye to afford 1,2-diketones.

103 as antennae for small amounts of the valued perylene bisimide Lumogen F Red 305 is presented.

104 haracterization, and complexation studies of perylene bisimide macrocycles obtained through bayside c

105 ractive forces, we succeeded in synthesizing perylene bisimide macrocyclic dimer and a concatenated d

106 Perylene bisimide-based materials are good candidates fo

107 regardless of the enantiomeric purity of the perylene bisimide.

108 uch as benzene-1,3,5-tricarboxamides (BTAs), perylenes bisimide (PBI), and phthalocyanines (Pc) beari

109 tetrathiafulvalene and an electron-acceptor perylene-bisimide were self-organized separately obtaini

110 self-assembled supramolecular structures of perylene bisimides (PBIs) are commonly limited to column

111 d living polymerization of properly designed perylene bisimides (PBIs) under precise kinetic control.

112 es in self-assembled nanowires prepared from perylene bisimides with oligopeptide-polymer side chains

113 localized pi bonds, analogous to benzo(g,h,i)perylene (C22H12).

114 de)-linked short wire, (33 ps)(-1) and >99%; perylene-(C9)-linked short wire, (26 ps)(-1) and >99%; b

115 The first highly water-soluble perylene-calix[4]arene hybrid with the calixarene scaffo

116 a phenylene ethynylene dendrimer tethered to perylene) can be enhanced by 15% through iterative phase

117 ments, both 1 and 2 were found to exist in a perylene-centered conformational dynamic equilibrium (De

118 molecular codes, which were dictated by the perylene chirality, ultimately gauged the weak pi-stack

119 transfer events: electron injection from the perylene chromophore into the conduction band of the ITO

120 stability of these alkylamino-functionalized perylene compounds make them a valuable addition to the

121 Not only did perylene concentrations in these sediments increase with

122 0 years previously showed large increases in perylene concentrations.

123 imide dendrimers, including decacyclene- and perylene-containing dendrimer D6, in which two types of

124 five different substituents attached to the perylene core (e.g., compound 15).

125 el dicationic dye with a polycyclic aromatic perylene core and flexible cationic side chains- N,N'-bi

126 ffraction reveals that 1 has a nearly planar perylene core and pi-pi stacks at a 3.5 A interplanar di

127 d 1,7-isomers demonstrating the twist of the perylene core in the solid state.

128 A strategy involving functionalization of perylene core with several polyhedral oligomeric silsesq

129 ical conjugated phenylacetylene branches and perylene cores, one with pi-conjugation from the branche

130 ed scaffolds and unique rectangular shape of perylene cores.

131 ntent was attributed to five PAHs: benzo[ghi]perylene, coronene, indeno[1,2,3-cd]pyrene, benzo[e]pyre

132 The perylene cyclic dimer and its concatenated tetramer were

133 enzo[k]fluoranthene-d12 (BkF-d12), benzo[ghi]perylene-d12 (BghiP-d12), dibenzo[a,i]pyrene-d14 (DaiP-d

134 The perylene derivative 1,7-dibromoperylene-3,4,9,10-tetraca

135 The amino-functionalized perylene derivative, 4,9-diaminoperylene quinone-3,10-di

136 0-perylenetetracarboxylic diimide (PIPER), a perylene derivative, is a very potent and selective G-qu

137 quadruplex-specific cleavage properties of a perylene derivative, perylene-EDTA*Fe(II).

138 rt, we present data concerning the role of a perylene derivative, PIPER, in the assembly of G-quadrup

139 adducts have been transformed into extended perylene derivatives by deoxygenation and aromatization

140 nitro-PMIDE 10 and thus of azabenz-annulated perylene derivatives with unsymmetric peri-substitution

141 ble route for the ortho-functionalization of perylene derivatives.

142 a collection of different azabenz-annulated perylene derivatives.

143 of diketopyrrolopyrrole electron donors and perylene derived bisimide (PDI) electron acceptors forms

144 Unique perylene diastereomeric linear and cyclic dimers were sy

145 Both neutral perylene diimide (N,N'-bis(butoxypropyl)perylene-3,4,9,1

146 We report on hybrids, in which perylene diimide (PDI) amphiphiles are noncovalently imm

147 e describe a simple histidine (H) conjugated perylene diimide (PDI) bolaamphiphile (HPH) as a dual-re

148 shapes of a series of linear and star-shaped perylene diimide (PDI) complexes are evaluated theoretic

149 quadruplex-interactive agents as well as new perylene diimide (PDI) derivatives have been investigate

150 Rigid fused perylene diimide (PDI) dimers bridged with heterocycles

151 lational and orientational diffusion of four perylene diimide (PDI) dyes, having different lengths an

152 copy was used to investigate the dynamics of perylene diimide (PDI) molecules in thin supported polys

153 from the double fusion of an acene with two perylene diimide (PDI) subunits.

154 ncorporates a bay tetrachloro-functionalized perylene diimide (PDI) unit and two triazolium anion-bin

155 ed via ring-fusion between the thiophene and perylene diimide (PDI) units of a PDI-tetramer with a te

156 ucting naphthalene diimide (NDI)-selenophene/perylene diimide (PDI)-selenophene random copolymers, xP

157 onor p-DTS(FBTTh2 )2 with a readily produced perylene diimide acceptor we are able to achieve a power

158 ea that a perfluorooctyl chain attached to a perylene diimide amphiphile can dramatically enhance the

159 yloxy moieties bridged by a quenching-active perylene diimide backbone, the tailor-designed molecule

160 structed to covalently link a dye molecular, perylene diimide derivative (PDI), and an intramolecular

161 rganic thermoelectric materials, self-doping perylene diimide derivatives with modified side chains,

162 the self-assembly of naphthalene diimide and perylene diimide electron acceptors end-capped with two

163 A perylene diimide fluorophore was incorporated into the l

164 n the extended tetracationic cyclophanes and perylene diimide is ultrafast and quantitative, while th

165 The synthesis of a bis(pyridyl)-substituted perylene diimide ligand and its incorporation into a sup

166 The hydrophobic part contains the two perylene diimide moieties, which enable strong pi-pi int

167 ovements of microribbons self-assembled from perylene diimide molecules are reported on various hydro

168 utions on the morphology of self-assembly of perylene diimide molecules has been studied with two der

169 is based on the fusion of electron deficient perylene diimide oligomers with an electron rich alkoxy

170 emble those of lower rylene homologues, e.g. perylene diimide or perylene monoimide.

171 tential of extended tetracationic cyclophane/perylene diimide systems as components for artificial ph

172 n with aromatic linkers and a tetraborylated perylene diimide that introduces strain and results in a

173 tion of a boronic acid-appended viologen and perylene diimide was able to perform a complementary imp

174 sed fullerene-based electron acceptor with a perylene diimide-based polymer drastically increases ope

175 s from exciton-like interactions between the perylene-diimide and the helicene moieties.

176 ing the polyhelicene framework with multiple perylene-diimide subunits elicits a significant chiropti

177 We report the synthesis of a new perylene-diimide-based helical nanoribbon, which exhibit

178 Perylene diimides (PDIs) are one of the most highly stud

179 Exploiting perylene diimides (PDIs) as components in cyclic host sy

180 e synthesis of various naphthalic imides and perylene diimides (PDIs) using twin-screw extrusion (TSE

181 rakis(chloride) (ExBox) and three dicationic perylene diimides (PDIs).

182 A number of unsymmetrical perylene diimides containing a solubilizing swallowtail

183 e synthesis of unsymmetrical N-alkyl-N'-aryl perylene diimides is reported that circumvents the need

184 s study explores a new mode of contortion in perylene diimides where the molecule is bent, like a bow

185 of acceptors are characterized: fullerenes, perylene diimides, and PbS and PbSe colloidal nanocrysta

186 aic acceptors, functionalized fullerenes and perylene diimides, are analyzed using a newly developed

187 izing chains by N-9-heptadecanyl-substituted perylene diimides.

188 sing as a case study the interface between a perylene donor and a benzoperylene diimide acceptor, we

189 ric materials with oxygen indicators (pyrene/perylene donor/acceptor pair) display different analytic

190 d strongly conjugated perylenediimide-bridge-perylene dyad (PDIPe) has been investigated in dichlorom

191 The porphyrin-perylene dyad P-PMI displays the most even spectral cove

192 benzocoronene was used in combination with a perylene dye to produce thin films with vertically segre

193 al case, coassembly of protamine sulfate and perylene dye via electrostatic attractions and pi-pi int

194 broad blue-green to yellow absorption of the perylene dyes complements the blue absorption of the por

195 A one-step synthesis of perylene dyes with lateral extension by condensed imidaz

196 Perylene dyes with N-tert-alkyl substituents were prepar

197 of protein/dye aggregates and the release of perylene dyes.

198 MR titration of a parallel G-quadruplex with perylene-EDTA (without metal) indicates that the compoun

199 terize the cleavage reaction with respect to perylene-EDTA*Fe(II) concentration, DNA structural type,

200 leavage properties of a perylene derivative, perylene-EDTA*Fe(II).

201 spectroscopy confirms the selectivity of the perylene-EDTA*metal complex for G-quadruplex DNA.

202 The molecule consists of a perylene electron donor chromophore (D) bound to a pyrom

203 lear picture of the low-lying excitations in perylene emerges, including evidence of an exciton-polar

204 errylene diimide dye to the nanoparticles of perylene-end-capped polyfluorene block copolymers allows

205 h the pyrene-labeled phosphatidylcholine and perylene fluorescence data previously obtained from PLFE

206 lfolobus acidocaldarius have been studied by perylene fluorescence.

207 ansportation of water insoluble fluorophore (perylene) for live cell imaging is explored.

208 I, indeno[1,2,3-c,d]pyrene, and benzo[g,h,i]perylene found at Temple Basin were largely of Australia

209 I) carbene complex, and a dark T(1) state on perylene, from which the upconversion process originates

210 ely benz[a]anthracene approximately benz[ghi]perylene>benzo[b]naphtho[2,3-d]thiophene.

211 uted polycyclic aromatics such as pyrene and perylene have been linked via alkyne bridges, as have et

212 Thus, herein we report the synthesis of perylene imide derivatives endowed with a 1,2-diketone f

213 Here, we introduce benzo[ghi]perylene imides as new organic photoredox catalysts for

214 and out-of-plane (R(op)) rotational rates of perylene in PLFE liposomes at various temperatures (20-6

215 a low ionization potential such as benzo[ghi]perylene in the first technique, where the electron for

216 allowing a limit of detection of 0.14 nM for perylene in the presence of 0.1 mM TPTA.

217 The presence of benzo[a]pyrene and perylene in this sample is confirmed, and a peak coeluti

218 For the array containing eight perylenes in benzonitrile, PMI decays approximately 80%

219 Radiocarbon analysis of perylene indicated that 70-85% of perylene observed in t

220 linear array of chromophores consisting of a perylene input unit, a bis(free base porphyrin) transmis

221 A remarkable perylene intensity anomaly was also observed in bilayers

222 ncluding pyrene excimer formation and pyrene-perylene interstrand Forster resonance energy transfer.

223 Perylene is a frequently abundant, and sometimes the onl

224 ansition dipole moment of the electron donor perylene is aligned along the axis of the electric field

225 These findings suggest that perylene is definitely a product of soil-derived fungi,

226 Each perylene is substituted with one or three 4-tert-butylph

227 The restricted rotation of the perylene moieties yields atropisomers that can be separa

228 ift of fluorescence emission for the achiral perylene moiety as a chemical junction of the BCPs* can

229 e spheroidal cavity that can incorporate one perylene molecule.

230 ilt by the supramolecular self-assembly of a perylene monoimide amphiphile.

231 in water and the photocatalytic function of perylene monoimide chromophore amphiphiles with differen

232 ri-guanidine-fused naphthalene monoimide and perylene monoimide chromophores.

233 loped regioselective nitration procedure for perylene monoimide diesters (PMIDE) enables the synthesi

234 longer wavelengths by energy transfer to the perylene monoimide dye.

235 ns (GNRs) with anthraquinone and naphthalene/perylene monoimide units has been achieved through a Suz

236 rylene homologues, e.g. perylene diimide or perylene monoimide.

237 esting arrays containing two, four, or eight perylene-monoimide accessory pigments attached to a zinc

238 t unit consists of a boron-dipyrrin dye or a perylene-monoimide dye (linked either at the N-imide or

239 s per porphyrin in toluene, the photoexcited perylene-monoimide dye (PMI) decays rapidly ( approximat

240 cyclic dimers were synthesized from twisted perylene monomers, revealing that pi-stacking stereoisom

241 ocatalytic systems based on photosensitizing perylene monomimide (PMI) chromophore amphiphiles were f

242 The diimide perylene motif exhibits a dramatic intensity reversal be

243 4,3'- or 4,2'-diarylethyne linker joins the perylene N-imide position and the porphyrin meso-positio

244 yrrin-based long wire, (190 ps)(-1) and 81%; perylene-(N-imide)-linked long wire, (175 ps)(-1) and 86

245 t to output) energy transfer are as follows: perylene-(N-imide)-linked short wire, (33 ps)(-1) and >9

246 d to synthesize OBO-doped tetrabenzo[a,f,j,o]perylenes (namely "bistetracenes") and tetrabenzo[bc,ef,

247 In this work, N-annulated perylene (NP) was used to functionalize the Zn-porphyrin

248 First, we synthesized perylene-nucleoside reagents and incorporated them into

249 nalysis of perylene indicated that 70-85% of perylene observed in the deeper sediments could be expla

250 e report the synthesis of a series of linear perylene oligomers that undergo endothermic singlet fiss

251 tion experiment with the shorter "periacene" perylene, only the bisanthene reacts, and the perylene r

252 he polycyclic compounds are either pyrene or perylene, or a mixture of both.

253 ctionalized at the N2'-position with pyrene, perylene, or coronene moieties and incorporated these mo

254 to heterogeneous environments for the pyrene/perylene pair and a concomitant quenching of the fluores

255 ransistors (TFTs) based on electron-depleted perylene- (PDI) and naphthalene-dicarboxyimide (NDI) pol

256 -chrysene and dibenz[a,h]anthracene-benz[ghi]perylene peaks coelute under the employed chromatographi

257 For the array containing four perylenes per porphyrin in both nonpolar (toluene) and p

258 le) media and for the array containing eight perylenes per porphyrin in toluene, the photoexcited per

259 It was found that retene (Re) and perylene (Per) are both mainly of natural origin in Zaka

260 silver nanoparticles (AgNP) were loaded onto Perylene (PER) to develop a sensing probe that was chara

261 Using perylene pi-pi stacking weak attractive forces, we succe

262 nding phenylethyne-linked dyads, including a perylene-porphyrin (< or = 0.5 ps) and a porphyrin-phtha

263 uble and stable tetracyano-oligo(N-annulated perylene)quinodimethanes nPer-CN (n = 1-6), with the lon

264 erylene, only the bisanthene reacts, and the perylene remains unchanged.

265 S transformations of 1,6- and/or 1,7-diamino perylenes result in 2-fold annulated nitrogen-containing

266 to give a porphyrin beta,meso annulated with perylene rings (0.7:1 ratio of syn and anti isomers).

267 olecules, including 9,10-diphenylanthracene, perylene, rubrene and TIPS-pentacene, are reported.

268 optical response of thin-film single-crystal perylene samples of distinct polymorphs in transmission

269 Here we investigate whether perylene serves as a source-specific molecular marker of

270 itions (FeCl(3), dichloromethane) occurs for perylene-substituted porphyrins to give a porphyrin beta

271 red light-absorbing photosensitizer to this perylene system, we accomplish the long-wavelength red l

272 transfer between the Fe(III) (2)LMCT and the perylene T(1) excited states, FePer exhibits (2)LMCT lum

273 cteriochlorin), chromophore (boron-dipyrrin, perylene, terrylene), and attachment sites (meso-positio

274 The acceptor block A is a perylene tetracarboxyl diimide (PDI), whereas the donor

275 We used perylene tetracarboxylic acid (PTCA) to functionalize th

276 rong interlayer coupling-MoS(2) and 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA), respective

277 to be true for acenes, phthalocyanines, and perylene tetracarboxylic diimide (PDI)-based molecules.

278 examined the optical properties of gas-phase perylene tetracarboxylic diimide (PTCDI) and its chromop

279 Perylene tetracarboxylic diimide (PTCDI) derivatives sta

280 ue, we measure the conductance histograms of perylene tetracarboxylic diimide (PTCDI) molecules attac

281 ssembled from an electron acceptor molecule, perylene tetracarboxylic diimide (PTCDI), onto which (th

282 organic semiconductor N-N'-dioctyl-3,4,9,10-perylene tetracarboxylic diimide (PTCDI-C8) and a polyme

283 del oligomers containing exactly two or four perylene tetracarboxylic diimide (PTDI) units: linear fo

284 onor-acceptor (D-A) supramolecule comprising perylene tetracarboxylic diimide as the backbone scaffol

285 on transport through single redox molecules, perylene tetracarboxylic diimides, covalently bound to t

286 the short exciton diffusion lengths of alpha-perylene tetracarboxylicdianhydride (PTCDA) are due to u

287 unit, diindeno[4,3,2,1-fghi:4',3',2',1'-opqr]perylene, that is substituted with either triethylsilyl(

288 rapid funneling of energy in a cascade from perylene to bis(porphyrin) to phthalocyanine.

289 In addition to rapid and efficient perylene-to-porphyrin energy transfer, the broad blue-gr

290 high solubility in organic media and facile perylene-to-porphyrin energy transfer, while avoiding ch

291 characterized with and without a fluorescent perylene trap at the core.

292 e higher generation monodendrons without the perylene trap exhibit high molar extinction coefficients

293 When a perylene trap is placed at the core, then the monodendro

294 uent oxidative ring closure reactions of the perylene units and exhibit NIR absorption at 945 nm.

295 chemical species from hydrogen and benzo[ghi]perylene were carried out experimentally in the temperat

296 nd radiocarbon content of pyrogenic PAHs and perylene were determined 20 years after a previous study

297 ne, naphthalene, fluoranthene, and benzo[ghi]perylene) were identified in the leachate and tire sampl

298 ch wire (with the exception of the C9-linked perylene wire) exhibits a visible absorption spectrum th

299 Replacing perylene with pyrene allowed reversal of the direction o

300 The Pictet-Spengler (PS) reaction of 1-amino-perylenes with different aldehydes is used to modify the