Soo Young Park 교수

A novel donor-acceptor-donor triad that exhibits fluorescence on-off switching with high contrast ratio (ca. 10(3) ) in response to a mechanical stimulus in the solid state is reported. This system provides a very unique example of high-contrast fluorescence switching that is driven by a mechanical-force-controlled photo-induced electron transfer (eT) in molecular assemblies.

2D organic semiconductor crystals are emerging as a fascinating platform with regard to their applications in organic field-effect transistors (OFETs), attributed to their enhanced charge transport efficiency and their new optoelectronic functions, based on their unique morphological features. Advances in material processing techniques have not only enabled easy fabrication of few-monolayered 2D nanostructures but also facilitated exploration of the interesting properties induced by characterist

An efficient bulk heterojunction all-small-molecule organic solar cell composed of a high-performance small-molecule donor and a self-assembling nonfullerene acceptor is demonstrated. Favorable nanoscale phase separation and enhanced charge carrier generation with transport in this donor–acceptor system assures a maximum power conversion efficiency of 5.4%. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer revie

We report on a molecularly tailored 1:1 donor-acceptor (D-A) charge-transfer (CT) cocrystal that manifests strongly red-shifted CT luminescence characteristics, as well as noteworthy reconfigurable self-assembling behaviors. A loosely packed molecular organization is obtained as a consequence of the noncentrosymmetric chemical structure of molecule A1, which gives rise to considerable free volume and weak intermolecular interactions. The stacking features of the CT complex result in an external

New anthracene-based deep-blue emitting molecular glass, 9-(9-phenylcarbazole-3-yl)-10-(naphthalene-1-yl)anthracene (PCAN), which is asymmetrically functionalized with N-phenylcarbazole and naphthalene, has been designed, synthesized, and characterized. The deep-blue emitting PCAN is efficiently secured for color purity, has high glass transition temperature (Tg = 151 °C), and has excellent solubility (>100 mg mL−1 in toluene), due to its highly tilted asymmetric molecular conformation. Using pr

Abstract The unique and unprecedented electroluminescence behavior of the white‐emitting molecule 3‐(1‐(4‐(4‐(2‐(2‐hydroxyphenyl)‐4,5‐diphenyl‐1H‐imidazol‐1‐yl)phenoxy)phenyl)‐4,5‐diphenyl‐1H‐imidazol‐2‐yl)naphthalen‐2‐ol (W1), fluorescence emission from which is controlled by the excited‐state intramolecular proton transfer (ESIPT) is investigated. W1 is composed of covalently linked blue‐ and yellow‐color emitting ESIPT moieties between which energy transfer is entirely frustrated. It is demon

A new 2:1 donor (D):acceptor (A) mixed-stacked charge-transfer (CT) cocrystal comprising isometrically structured dicyanodistyrylbenzene-based D and A molecules is designed and synthesized. Uniform 2D-type morphology is manifested by the exquisite interplay of intermolecular interactions. In addition to its appealing structural features, unique optoelectronic properties are unveiled. Exceptionally high photoluminescence quantum yield (Φ_F ≈ 60%) is realized by non-negligible oscillator

Supramolecular aggregation of a novel nonfluorescent gelator yields highly luminescent organogels in aprotic organic solvents through intermolecular hydrogen bonding, which is a key motif for both self-assembly and photophysical process control.

Abstract Supramolecular polymers (SPs) have received great attention because of their potential for various practical applications. As part of our search for SPs that are highly fluorescent in aqueous media, we designed a system based on a cucurbit[8]uril (CB[8]) host and a newly designed cyanostilbene guest. Fluorescence quantum yields of ≈0 % in the disassembled monomer state and 91 % in the CB[8]‐induced SP state were obtained. The intriguing photophysical properties of the SP are elucidated

Abstract Highly efficient red–green–blue (RGB) tricolor luminescence switching was demonstrated in a bicomponent solid film consisting of (2 Z ,2′ Z )‐2,2′‐(1,4‐phenylene)bis(3‐(4‐butoxyphenyl)acrylonitrile) (DBDCS) and (2 Z ,2′ Z )‐3,3′‐(2,5‐bis(6‐(9 H ‐carbazol‐9‐yl)hexyloxy)‐1,4‐phenylene)bis(2‐(3,5‐bis(trifluoromethyl)phenyl)acrylonitrile) ( m ‐BHCDCS). Reversible RGB luminescence switching with a high ratiometric color contrast ( λ em =594, 527, 458 nm for red, green, and blue, respectively

Silk fibroin/chitosan blend films were prepared by the solvent casting method. Miscibility between silk fibroin and chitosan was examined by dynamic mechanical thermal analysis. Structural changes of silk fibroin by the addition of chitosan were investigated by IR spectroscopy. The conformational transition of silk fibroin from random coil form to β-sheet structure induced by blending with chitosan resulted in the increase of crystallinity and density of the blend films. The blend film containin

Highly fluorescent molecules harnessing the excited state intramolecular proton transfer (ESIPT) process are promising for a new generation of displays and light sources because they can offer very unique and novel optoelectronic properties which are different from those of conventional fluorescent dyes. To realize innovative ESIPT devices comprising full emission colors over the whole visible region, a molecular design strategy for predictable emission color tuning should be established. Here,

Abstract Multicolor tunable and multistate switchable organogel is reported, which consists of a cyanostilbene organogelator showing aggregation‐induced enhanced emission and a turn‐on type photochromic diarylethene dye. The mixed organogel can be reversibly switched among four different states (blue‐emitting gel, nonemissive sol, green‐emitting gel, and green‐emitting sol) modulated by a combination of orthogonal stimuli of heat and light. It is interestingly noted that this four‐state switchin

Abstract Aiming for highly efficient blue electroluminescence, we have designed and synthesized a novel class of tetraphenylimidazole‐ based excited‐state intramolecular proton‐transfer (ESIPT) molecules with covalently linked charge‐transporting functional groups (carbazole‐ and oxadiazole‐functionalized hydroxyl‐substituted tetraphenylimidazole (HPI), i.e., HPI‐Cbz and HPI‐Oxd, respectively). High T g (ca. 130 °C) amorphous films of HPI‐Cbz and HPI‐Oxd showed intense and ideal blue‐light emiss