Abstract  A new diamine with phthalic diimide moiety, i.e. N,N'-bis(4-amino-2,3,5,6-tetramethylphenyl)phthalene-1,4-dicarboxyimide was synthesized and applied for condensation with 4-(4,4,5,5,6,6,7,7,8,8,9,9,10, 10,11,11,11-heptadecafluoroundecyloxy)benzaldehyde and 4-octadecyloxybenzaldehyde, which resulted in two new azomethine-phthalic diimides (AZ-PDIs). Thermal, optical and electrochemical properties of AZ-PDIs were discussed in relation to their analogous containing instead of five-membered six-membered imide rings (AZ-NDIs) described in our previous work. The phase behavior of AZ-PDIs examined by differential scanning calorimetry (DSC) and polarized optical microscopy (POM) confirms their liquid crystalline properties in wide range of temperatures. AZ-PDIs do not show decomposition below 400 degrees C as was found based on thermogravimetric analyses (TGA). Optical properties of the prepared compounds were investigated by UV-vis and photoluminescence (PL) measurements. Azomethine-phthalic diimides emitted blue light with emission maximum (lambda(em)) at ca. 446-492 nm contrary to azomethine-naphthalene diimides which emitted green light and lambda(em) was at 536 and 540 nm. The obtained compounds are electrochemically active and undergo reversible reduction and oxidation as evidenced by differential pulse voltammetry (DPV). The azomethine-phthalic diimides exhibited low electrochemical band gap ca. 1.68 eV being promising for optoelectronic applications. (c) 2013 Elsevier B.V. All rights reserved.

Abstract  Phenol substituted 1,8-naphthalimide derivatives acting as a donor and an iridium(III) complex which emits orange light acting as an acceptor were synthesized to fabricate a novel white-light-emitting two-component gel. The intermolecular energy transfer between the two components plays a crucial role in providing the tuneable emission in the mixed gels. The emission of white light can be obtained by carefully tuning the ratio of the two components. These gels are ideal constituents for the design of supramolecular light-harvesting materials, which afford a novel approach to displaying information in soft materials with tuneable optical properties. Furthermore, the two-component gel can respond to cysteine with an obvious change in luminescence that is visible to the naked eye.

Abstract  Chemical vapor deposition-grown graphene has been an attractive electrode material for organic electronic devices, such as organic field-effect transistors (OFETs), because it is highly conductive and provides good oxidation and thermal stability properties. However, it still remains a challenge to demonstrate organic complementary circuits using graphene electrodes because of the relatively poor performance of n-type OFETs. Here, we report the development of high-performance organic complementary inverters using graphene as source/drain electrodes and N, N'-ditridecyl-3,4,9,10-perylenetetracarboxylic diimide (PTCDI-C13) and pentacene as n- and p-type organic semiconductors, respectively. Graphene electrodes were n-doped via the formation of NH2-terminated self-assembled monolayers that lowered the work function and the electron injection barrier between the graphene and PTCDI-C13. Thermal annealing improved the molecular packing among PTCDI-C13 groups on the graphene surface, thereby increasing the crystallinity and grain size. The thermally annealed PTCDI-C13 OFETs prepared using n-doped graphene electrodes exhibited a good field-effect mobility of up to 0.43 cm2/(V s), which was comparable to the values obtained from other p-type pentacene OFETs. By integrating p- and n-type OFETs, we successfully fabricated organic complementary inverters that exhibited highly symmetric operation with an excellent voltage gain of up to 124 and good noise margin.

Abstract  We prepared a solution-processed film comprising a drop-casted mixture of melamine-diacetylene and perylene bis(dicarboximide) (PDI). We show that the diacetylene monomers adopt distinct crystalline organization in the presence of the PDI residues. Importantly, the drop-casted diacetylene/PDI film exhibits ultraviolet light-induced conductivity, ascribed to effective transport of charge carriers in the conjugated polymerized network.

Abstract  Most polymers employed in organic photovoltaic cells have pi-conjugated backbones Here we investigate the physical and optoelectionic properties of three nonconjugated polymers based on perylene diimides The optical properties. exciton diffusion length, band edge positions, conductivity, and carrier mobility of these polymers are described They are electron-conducting and highly photostable The film structure and optoelectronic properties vary with deposition conditions and annealing procedures One of the polymers has an unusually long exciton diffusion length of 22 nm. The free electron density resulting from n-type charged defects is similar to 3 x 10(15) cm(-3) in one polymer and is even lower in the others Simple bilayer solar cells are limited by their series resistance suggesting that these semiconductor films would benefit from doping

Abstract  Fluorescent monodisperse polystyrene microspheres were prepared by two-stage dispersion polymerization, which successfully covalently labeled microspheres with two dyes without disturbing the final particle size and size distribution. By varying the dye concentrations, microspheres show tuned colors with different fluorescent intensity under a single wavelength excitation. Fluorescence resonance energy transfer (FRET) between two labeled dyes was proved to contribute to the emission of the longer-wavelength dye at a shorter-wavelength excitation. There is no dye leakage for microspheres because of the covalent incorporation of dye molecules. The microsphere matrix provides good protection of dye molecules and blocks the influence of media outside on the fluorescence of microspheres. Single microsphere shows intense fluorescence due to a large number of encapsulated dye molecules. These uniform barcoding fluorescent microspheres have potential application in multiplexed bioanalysis. (c) 2007 Elsevier B.V. All rights reserved.

Abstract  A new class of polyelectrolyte-surfactant (PE-surf) composites having potential applications as thin film organic semiconductors is introduced. These materials are comprised of cationic asymmetrically substituted perylene diimides and oppositely charged poly(acrylate) polyanions. Thin films of the composite materials are prepared by mixing and drop casting aqueous solutions of the two precursors onto appropriate substrates. The resulting materials yield photovoltages of >140 mV for approximately equal to 0.6 W/cm(2) illumination intensities, when incorporated in p-n heterojunction devices. Solution-phase spectra obtained from the PE-surf complexes exhibit excimer-like emission and evidence for formation of weakly coupled aggregates in the ground state. Wide-angle X-ray scattering data show the composite films are locally amorphous, while small-angle X-ray data are consistent with a mixture of polymorphic structures that incorporate planar PE-surf bilayers of 3.9-nm repeat distances. Images obtained by conventional far-field light microscopy and multiphoton-excited fluorescence microscopy (MPEFM) indicate that the films are heterogeneous, incorporating submicrometer sized clusters dispersed among much thinner film regions that also incorporate dye. Polarization-dependent MPEFM studies prove the clusters are semiorganized, yielding order parameters (s and P(4)) of 0.09 and 0.01 for in-plane alignment of the chromophores, consistent with a relatively high degree of disorder.

Abstract  In this study, a solution-processed n-type photo-sensing organic thin film transistor was investigated using polymeric dielectric under different white light illuminations. N, N'-di (2-ethylhexyl)-3,4,9,10-perylene diimide and divinyl tetramethyl disiloxane-bis (benzo-cyclobutene) were used as a soluble active organic semiconductor and as a dielectric material, respectively. Stable amplification was observed in the visible region without gate bias by the device. The electrical characterization results showed that an n-type phototransistor with a saturated electron mobility of 0.6 x 10(-3) cm(2)/V.s and a threshold voltage of 1.8 V was obtained. The charge carrier density of the channel of the device exhibited photo-induced behaviors that strongly affected the electrical properties of the transistor. The photosensitivity and photoresponsivity values of the device were 63.82 and 24 mA/W, respectively. These findings indicate that perylene diimide is a promising material for use on organic based phototransistors. (C) 2014 Elsevier B.V. All rights reserved.

Abstract  Several new 1,8-naphthalimide dyad compounds connected with 1,3,4-oxadiazole at different substitution positions were synthesized, in which there are two compounds to be copolymerized with N-vinyl carbazole to form a single-layer electroluminescence (EL) device film, which consists of electron-transporting unit (oxadiazole), hole-transporting unit (PVK) and emitting unit. The photoemission and electroemission of these dyad compounds are near 540 nm, with a maximum luminance of 350 cd/m(2) and luminous efficiency of 3.02 lm/W at 14 V. (C) 1998 Elsevier Science S.A. All rights reserved.

Abstract  The reduction of the two 3,4,9,10-perylene diimide (PDI) derivatives in the mixture of hydrazine hydrate and N, N-dimethylformamide was investigated by the UV-vis absorption spectra, fluorescence spectra (FL) and electron spin resonance spectroscopy (ESR). The time dependence of the PDI content, as well as the structure of PDI aggregates were also investigated and discussed. Combining the electro-migration behavior of PDI- with the molecular self-assembly properties, the films of two PDI derivatives (PDI-32 and PDI-123) were successfully fabricated via anode electro-deposition (AED). The difference of aggregation state between the two PDI films was studied by UV-vis absorption spectra, XRD and SEM. Based on these, the formation mechanism of PDI films was also deduced.

Abstract  We report the interface properties of a perylene-diimide thin film between Au and n-Si substrate fabricated by the spin coating method. The relaxation time (tau) and interface trap density (D (it)) characteristics of the fabricated structure were obtained across various voltage ranges (0.0 V-300 mV) and various frequency ranges (1 kHz-1 MHz). We observed a peak in G (it)/omega versus log (f) plots from 0.0 V to 300 mV. This peak shows the presence of the interface state and its relaxation time. We observed a decrease in values at the same time as an increase in N (ss) values with the increasing applied voltage for the sample. The N (ss) and tau values found to be in the ranges 1.50 x 10(12) eV(-1) cm(-2)-2.83 x 10(12) eV(-1) cm(-2) and 2.83 x 10(-6) s-4.82 x 10(-7) s between 0.0 V and 0.3 V, respectively.

Abstract  We report herein that a mixed layer of the electron-donating copper phthalocyanine (CuPc) and electron-accepting N,N'-ditridecyl perylene diimide (PTCDI-C13) can be an efficient hole injection layer (HIL) for high-performance organic light-emitting diodes (OLEDs). From photophysical, morphological, and structural studies combined with electrical analysis based on the Mott-Schottky model, we conclude that the excellent miscibility between CuPc and PTCDI-C13 enables highly efficient charge transfer, and thus effective p-doping of CuPc, leading to increased hole conductivity of the HIL. As a result, turn-on voltages as low as 2.45 V and greatly improved thermal stabilities as compared to those of OLEDs with conventional CuPc HILs are observed.

Abstract  Two different organic molecules with similar structure, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) and N,N'-dimethyl-3,4,9, 10-perylenetetracarboxylic diimide (DiMe-PTCDI), were used for the modification of Ag Schottky contacts on sulphur passivated GaAs(I 0 0) (S-GaAs). Such diodes were investigated recording in situ current-voltage (I-V) characteristics. As a function of the PTCDA thickness the effective barrier height of Ag/PTCDA/S-GaAs contacts initially increases from 0.59 +/- 0.01 to 0.72 +/- 0.01 eV, and then decreases to 0.54 +/- 0.01 eV, while only a decrease in barrier height from 0.54 +/- 0.01 to 0.45 +/- 0.01 eV is observed for DiMe-PTCDI interlayers. The initial increase and decrease in effective barrier height for PTCDA and DiMe-PTCDI respectively, is correlated with the energy level alignment of the lowest unoccupied molecular orbital (LUMO) with respect to the conduction band minimum (CBM) of S-GaAs at the organic/inorganic semiconductor interface. Whilst there is an additional barrier for electrons at the PTCDA/S-GaAs interface of about 150 meV, i.e. the LUMO lies above CBM, the LUMO is aligned or below CBM in the DiMe-PTCDI case. The results also shine light on the important issue of the transport gap in organic semiconductors for which an estimation can be obtained. (C) 2003 Elsevier Science B.V. All rights reserved.

Abstract  A series of sulfonated poly(p-phenylene-co-aryl ether ketone) (SPP-co-PAEK) membranes are successfully prepared from 2,5-dichloro-3'-sulfobenzophenone and 2,2'-bis[4-(4-chlorobenzoyl)] phenoxyl perfluoropropane through Ni(0)-catalyzed copolymerization for polymer electrolyte membrane fuel cell (PEFC) applications. The obtained SPP-co-PAEKs have fairly high reduced viscosities and give ductile and transparent membranes with good mechanical strength. All the membranes exhibit comparable or even better proton conductivities than that of Nafion 112 in the full hydrate state. In addition, the membranes showed almost isotropic proton conductive behavior with a sigma(perpendicular to)/sigma(parallel to) values in the range of 0.85-0.92. Fuel cell operation using SPP-co-PAEK(3/1) (IEC = 2.0 meq g(-1), thickness of 38 mu m, feed gases: H-2/air) exhibited rather good performances: open circuit voltage of 0.94 V. cell voltage at 1.0 A cm(-2) of 0.61 V. and output at 1.7 A cm(-2) of 0.85W cm(-2) under 90 degrees C and 82/68% relative humidity condition. The results suggested that these SPP-co-PAEK membranes are promising candidates for PEFC applications. (c) 2012 Elsevier B.V. All rights reserved.

Abstract  In this study, a novel ratiometric pH probe RNL based on fluorescence resonance energy transfer (FRET) was well developed. It was fabricated by integrating the naphthalimide moiety as an FRET donor with the rhodamine moiety as an FRET acceptor. Meanwhile, 4-(2-aminoethyl)morpholine, which was a lysosome-locating group, was introduced. The sensing mechanism was the integration of PET and FRET processes and the comprehensive effect led to the simultaneous intensity enhancement of naphthalimide and rhodamine along with the pH value decrease. With a pK(a) of 4.82, the fluorescence intensity ratio (I-529/I-580) of the probe changed significantly within the pH range from 4.50 to 5.50. The probe showed excellent selectivity among various metal cations, amino acids and ATP. Moreover, RNL has been successfully applied in HeLa cells, and the results demonstrated that it could be used to detect lysosomal pH changes. The probe could also selectively stain lysosome in HeLa cells. Besides, the probe exhibited low cytotoxicity and satisfactory photostability in living HeLa cells.

Abstract  Two n-type conjugated D-A copolymers with perylene diimide (PDI) as acceptor unit and benzodithiophene (BDT) as donor unit, P(PDI-BDT-Ph) and P(PDI-BDT-Th), were synthesized and applied as electron acceptor in all-polymer solar cells (all-PSCs). P(PDI-BDT-Ph) and P(PDI-BDT-Th) films exhibit similar absorption spectra in the visible region with optical bandgap (E-g) of 1.65 eV and 1.55 eV respectively, and the identical LUMO level of -3.89 eV. The all-PSCs based on P(PDI-BDT-Ph) as acceptor and PTB7-Th as donor demonstrated a power conversion efficiency (PCE) of 4.31% with a short-circuit current density (J(sc)) of 11.94 mA cm(-2), an open-circuit voltage (V-oc) of 0.81 V, and a fill factor (FF) of 44.49%. By contrast, the corresponding all-PSCs with P(PDI-BDT-Th) as acceptor showed a relative lower PCE of 3.58% with a Jsc of 11.36 mA cm(-2), V-oc of 0.79 V, and FF of 40.00%. (C) 2016 Elsevier B.V. All rights reserved.

Abstract  Two star polycations, poly(2-aminoethyl methacrylate) (PAEMA, P1) and poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA, P2), have been synthesized with perylene diimide (PDI) as the central fluorophore. (1)H NMR and (13)C NMR are used to confirm the successful synthesis of a macromolecular initiator. Using ATRP strategy, P1 and P2 are obtained with narrow molecular weight distribution. The star polymers have good fluorescence properties in aqueous solution, which provides fluorescent tracing and imaging during gene delivery. Both P1 and P2 can efficiently condense DNA into stable nanoparticles. Transfection studies demonstrate that P1 and P2 deliver DNA into live cells with higher efficiency and lower cytotoxicity than polyethylenimine (PEI, 25 kDa). P2 shows higher capacity for gene delivery than P1 due to its better buffering and faster rate of cellular internalization.

Abstract  A non-fullerene, all-small-molecule solar cell (NF-SMSC) device uses the blend of a small molecule donor and a small molecule acceptor as the active layer. Aggregation ability is a key factor for this type of solar cell. Herein, we used the alkylthienyl unit to tune the aggregation ability of the diketopyrrolopyrrole (DPP)-based small molecule donors. Replacing two alkoxyl units in BDT-O-DPP with two alkylthienyl units yields BDT-T-DPP, and further introducing another two alkylthienyl units into the backbone produces BDT-T-2T-DPP. With the introduction of alkylthienyl, the backbone becomes twisted. As a result, the ππ-stacking strength, aggregation ability, and crystallite size all obey the sequence of BDT-O-DPP > BDT-T-DPP > BDT-T-2T-DPP. When selected a reported perylene diimide dimer of bis-PDI-T-EG as acceptor, the best NF-SMSC device exhibits a power conversion efficiency of 1.34, 2.01, and 1.62%, respectively, for the BDT-O-DPP, BDT-T-DPP, and BDT-T-2T-DPP based system. The BDT-T-DPP/bis-PDI-T-EG system yields the best efficiency of 2.01% among the three combinations. This is due to the moderate aggregation ability of BDT-T-DPP yields moderate phase size of 30-50 nm, whereas the strong aggregation ability of BDT-O-DPP gives a bigger size of 50-80 nm, and the weak aggregation ability of BDT-T-2T-DPP produces a smaller size of 10-30 nm. The BDT-T-DPP/bis-PDI-T-EG combination exhibits balanced hole/electron mobility of 0.022/0.016 cm(2)/(V s), whereas the BDT-O-DPP/bis-PDI-T-EG and the BDT-T-2T-DPP/bis-PDI-T-EG blend show a hole/electron mobility of 0.0011/0.0057 cm(2)/(V s) and 0.0016/0.11 cm(2)/(V s), respectively.

Abstract  A new D-A (Donor-Accept) type N-(1,2,4-triazolyl)-N'-(2-ethylhexyl) naphthalenediimide (L) was synthesized. AgL(2)PF(6) (1) and AgL(2)NO(3) (2) were obtained through the reactions of L with AgPF(6) and AgNO(3), respectively. All the compounds were fully characterized. Optical, electrochemical properties and electrogenerated chemiluminescence (ECL) were systematically investigated. Those dual fluorescent emissions for L, short wavelength (SW) and long wavelength (LW) emission bands, are rationally explained by the planar intramolecular charge transfer (PICT) model. All the compounds display anodically shift reduction waves with positive reduction potential, compared to its parent compound, Naphthalene bisimide (NBI). It is very interesting that the ECL intensity of the complexes is successfully increased, which is 20 times larger than that of L explaining that the radical anions of the complexes are stabilized by coordinating L with Ag(I) ion. The results provide a new approach to study ECL materials. (C) 2010 Elsevier Ltd. All rights reserved.

Abstract  Charge transport is studied in single-molecule junctions formed with a 1,7-pyrrolidine-substituted 3,4,9,10-perylenetetracarboxylic diimide (PTCDI) molecular block using an electrochemical gate. Compared to an unsubstituted-PTCDI block, spectroscopic and electrochemical measurements indicate a reduction in the highest occupied (HOMO)-lowest unoccupied (LUMO) molecular orbital energy gap associated with the electron donor character of the substituents. The small HOMO-LUMO energy gap allows for switching between electron- and hole-dominated charge transports as a function of gate voltage, thus demonstrating a single-molecule ambipolar field-effect transistor. Both the unsubstituted and substituted molecules display similar n-type behaviors, indicating that they share the same n-type conduction mechanism. However, the substituted-PTCDI block shows a peak in the source-drain current vs gate voltage characteristics for the p-type transport, which is attributed to a two-step incoherent transport via the HOMO of the molecule.

Abstract  Sequential deposition of nanofibrous composites of charged perylene diimide (PDI) dyes and oppositely charged polyelectrolyte (PE) is demonstrated within fluidic devices. The PDIs employed include an amphiphilic, singly charged PDI (C(7)OPDI(+)) and a doubly charged species (TAPDI(2+)). Anionic poly(acrylate) (PA(-), 5100 and 250K MW) is used as the PE. As previously demonstrated [Weitzel, C. R.; Everett, T. A.; Higgins, D. A. Langmuir, 2009, 25, 1188], dip-coated PDI/PE composites form nanofibrous films that exhibit flow-induced alignment due to gravitational draining of the dipping solution. In this study, the potential for producing patterned, flow-aligned PDI/PE composites by deposition using pressure-driven flow within fluidic channels is explored. The influence of flow profile, PE molecular weight (MW) and PDI structure on deposition efficiency, macroscopic and microscopic morphology, and the potential for nanofiber alignment are also investigated. Optical absorbance microscopy and tapping mode AFM data demonstrate that C(7)OPDI(+)/PA(-) deposition is controlled by PDI aggregation, while TAPDI(2+)/PA(-) composites are more dependent upon PE MW. Optical dichroism images show that C(7)OPDI(+)/PA(-) composites form serpentine, partially aligned nanofibers under all conditions explored, while TAPDI(2+)/PA(-) films incorporate more tightly packed nanofibers that form randomly oriented nematic-like domains when high MW PA(-) is employed. In-plane organization in C(7)OPDI(+)/PA(-) films is concluded to result from flow-induced alignment of solution-formed C(7)OPDI(+) aggregates, while the unaligned domains found in TAPDI(2+)/PA(-) films are concluded to form on the substrate surface by the complexation of small TAPDI(2+) aggregates or monomers with PE.

Abstract  Multilayer films of oligo(pyrenebutyric acid) (OPB) and N,N'-bis(N,N-dimethylaminopropylaminopropyl)-3,4,9,10-perylenediimide (BDMAPAP-PDI) were successfully fabricated by layer-by-layer deposition. Multilayer growth was monitored by ultraviolet-visible (UV-vis) spectroscopy, fluorescence spectroscopy, ellipsometry, and atomic force microscopy (AFM). It was found that extraction was scarcely observed although both components (OPB and BDMAPAP-PDI) have low molecular weights and both electrostatic interactions and pi-pi stacking contributed to the multilayer deposition. The multilayers exhibit a rapid photocurrent response, and excitations of both OPB and BDMAPAP-PDI can lead to the effective charge dissociation. The incident photon to current conversion efficiency (IPCE) of the composite film with 5 bilayers was measured to be 1.29% at the absorption peak of BDMAPAP-PDI. Fluorescence quenching and photovoltaic conversion studies indicated that strong photoinduced charge transfer interactions occurred at the area of OPB/BDMAPAP-PDI heterojunction in the films, which strongly enhanced the photoresponse of the multilayer films.

Abstract  The properties of N,N'-bis(2-phosphonoethyl)-3,4,9,10-perylenetetracarboxylic diimide (PPDI), a water-soluble perylene dye, have been studied in solution and in thin films. Absorption spectra showed that PPDI exists in the monomeric form in water/ethanol (1:1) and water/dimethyl sulfoxide (DMSO) (3:7) mixtures, but forms dimers in water and higher aggregates in ethanol. The PPDI monomer is highly fluorescent, in contrast to the dimers and aggregates, which are nonfluorescent. The monomer/dimer equilibrium was conveniently followed in a water/ethanol (7:3) mixture by varying the dye concentration. An equilibrium constant of K = 1.25 x 10(5) M(-1) was estimated for the dimerization process in this solvent mixture. The addition of cetyl trimethylammonium bromide (CTAB), a cationic surfactant, to aqueous solutions of PPDI resulted in the dissociation of the dimers, showing that the dye was incorporated into the micellar phase. Self-assembled thin films of PPDI were grown on both silica gel particles and flat surfaces, using zirconium phosphonate chemistry. The growth of multilayered films on flat surfaces was monitored by ellipsometry (silicon substrates) and UV/Vis spectroscopy (quartz slides), and was linear with the number of deposition cycles. No fluorescence was detected from the PPDI films, and the absorption spectra of the films were quite similar to the spectrum of the compound in ethanol, indicating that the dye molecules were stacked in the films. Mixed monolayers containing PPDI and N,N'-bis(2-phosphonoethyl)-1,4,5,8-naphthalenediimide (PNDI) on quartz were also prepared. Monolayers obtained by codeposition from solutions containing both PPDI and PNDI were richer in PPDI, even when the solution contained a large excess of the naphthalene derivative, showing that pi-stacking of PPDI is an important driving force in the formation of the films.

Abstract  A layer-by-layer deposition process has been carried out for two oppositely charged water-soluble perylene diimide dyes without the use of intervening polyelectrolyte layers. The strong pi-pi interactions between the perylene moieties help stabilize the layers and simultaneously diminish the fluorescence quantum yield of the array without strongly affecting the absorption or fluorescence spectra. There is an alternation of fluorescence intensity according to which perylene species is on the outer layer, which is interpreted as the effect of facile energy transfer between the perylenes.

Abstract  A novel perylene diimide (PDI) derivative with typical amphiphilic character, 2, was designed and prepared. The spectroscopic studies on this compound in solution revealed the face-to-face dimeric configuration and effective pi-pi interaction between the two perylene rings. This amphiphilic PDI derivative was fabricated into highly ordered films by Langmuir-Blodgett (LB) technique and fabricated into an organic field effect transistor (OFET), which shows carrier mobility around 0.05 cm(2) V(-1) s(-1) and current modulation of 10(3). This OFET performance is much better than that of monomeric PDI 1 and can be attributed to the unique face-to-face structure of 2, which promotes the interactions between neighboring PDI ring in LB film as indicated by the pi-A isotherms and UV-vis absorption.