We report an experimental study on the current-voltage characteristics of organic solar cells (OSCs) under indoor light illumination. A daylight color light-emitting diode (LED) was used as the indoor light source. We investigated the short circuit current density, open circuit voltage, and fill factor of the OSC under LED irradiation and compared them with those for a crystal silicon solar cell (c-Si-SC), which occupy a large part of the solar cell market. We found that compared with the c-Si-SC, the OSC had higher power conversion efficiency (PCE). We also derived the maximum feasible PCE of an OSC for indoor applications and calculated that a PCE value of 21.3% could be obtained under daylight color LED illumination at approximately 200 lx. From the results of the calculation, it became apparent that the open circuit voltage plays an important role in achieving a high PCE from OSCs, indicating they are promising as electrical energy harvesting module for indoor applications.

Helical structures of oligomers of non-natural β-amino acids are significantly stabilized by intramolecular hydrogen bonding between main-chain amide moieties in many cases, but the structures are generally susceptible to the environment; that is, helices may unfold in protic solvents such as water. For the generation of non-hydrogen-bonded ordered structures of amides (tertiary amides in most cases), control of cis-trans isomerization is crucial, even though there is only a small sterical difference with respect to cis and trans orientations. We have established methods for synthesis of conformationally constrained β-proline mimics, that is, bridgehead-substituted 7-azabicyclo[2.2.1]heptane-2-endo-carboxylic acids. Our crystallographic, 1D- and 2D-NMR, and CD spectroscopic studies in solution revealed that a bridgehead methoxymethyl substituent completely biased the cis-trans equilibrium to the cis-amide structure along the main chain, and helical structures based on the cis-amide linkage were generated independently of the number of residues, from the minimalist dimer through the tetramer, hexamer, and up to the octamer, and irrespective of the solvent (e.g., water, alcohol, halogenated solvents, and cyclohexane). Generality of the control of the amide equilibrium by bridgehead substitution was also examined.

We describe the development of the practical manufacturing of Ensitrelvir, which was discovered as a SARS-CoV-2 antiviral candidate. Scalable synthetic methods of indazole, 1,2,4-triazole and 1,3,5-triazinone structures were established, and convergent couplings of these fragments enabled the development of a concise and efficient scale-up process to Ensitrelvir. In this process, introducing a meta -cresolyl moiety successfully enhanced the stability of intermediates. Compared to the initial route at the early research and development stage, the overall yield of the longest linear sequence (6 steps) was improved by approximately 7-fold. Furthermore, 9 out of the 12 isolated intermediates were crystallized directly from each reaction mixture without any extractive workup (direct isolation). This led to an efficient and environmentally friendly manufacturing process that minimizes waste of organic solvents, reagents, and processing time. This practical process for manufacturing Ensitrelvir should contribute to protection against COVID-19.

The power conversion efficiency (PCE) of organic photovoltaic (OPV) modules with 9.5% (25 cm2) and 8.7% (802 cm2) have been demonstrated. This PCE of the module exceeded our previous world records of 8.5% (25 cm2) and 6.8% (396 cm2) that were listed in the latest Solar Cell Efficiency Tables ver.43 [1]. Both module design and coating/patterning technique were consistently studied for module development. In order to achieve highly efficient modules, we increased the ratio of photo-active area to designated illumination area to 94% without any scribing process and placed insulating layers in order to decrease the leakage current. The meniscus coating method was used for the fabrication of both buffer and photoactive layers. This technique ensures the fabrication of uniform and nanometer order thickness layers with thickness variation less than 3%. Furthermore, the PCE of the OPV under indoor illumination was found to be higher than that of the conventional Si type solar cells. This indicates that OPVs are promising as electrical power supplies for indoor applications. Therefore, we have also developed several prototypes for electronics integrated photovoltaics (EIPV) such as electrical shelf labels and wireless sensors embedded with our OPV modules, which can be operated by indoor lights.

We describe the development of the practical manufacturing of Ensitrelvir, which was discovered as a SARS-CoV-2 antiviral candidate. Scalable synthetic methods of indazole, 1,2,4-triazole and 1,3,5-triazinone structures were established, and convergent couplings of these fragments enabled the development of a concise and efficient scale-up process to Ensitrelvir. In this process, introducing a meta-cresolyl moiety successfully enhanced the stability of intermediates. Compared to the initial route in the medicinal synthetic stage, the overall yield of the longest linear sequence (six steps) was improved by approximately 7-fold. Furthermore, nine out of the twelve isolated intermediates were crystallized directly from each reaction mixture without any extractive work-up (direct isolation). This led to an efficient and environmentally friendly manufacturing process that minimizes waste of organic solvents, reagents, and processing time. This practical process for manufacturing Ensitrelvir should contribute to protection against COVID-19.

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This paper describes a liquid-liquid biphasic flow reaction system that is simple to control. In a liquid-liquid biphasic flow reaction, the slug-flow in the tube reactors generally improves the reaction rate. However, we show that larger tube diameters decreased the reaction rate and the formation of the slug-flow was influenced by the tube diameter, the size of the mixer, and the pump mechanism. These results indicated that technical difficulties with the slug-flow could be an obstacle to scale-up. To resolve this problem, we suggest the use of a Taylor vortex flow reactor to achieve a higher reaction rate than with batch and slugflow systems.