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The effect of a coating material containing organic photoluminophore (PL) on the growth and development of mustard Brassica juncea L. plants colonized with beneficial associative bacteria Pseudomonas putida KT2442 and Rhodococcus erythropolis X5 was studied in vitro and in vivo. Plants grown with the use of microbial bacterization in combination with a photoluminophore coating (PLC) had significantly faster growth rates in vitro (2.1 times faster, P. putida; 1.8 times faster, R. erythropolis) than those grown using PLC alone (1.2 times faster). The leaves of plants grown with PLC had higher contents of glucose and fructose (28.4 ± 0.3% more glucose and 60.4 ± 0.3% more fructose accumulated compared to plants grown without PLC). It was found that seed weights and seed number increased 1.9-fold and 1.6-fold, respectively, for plants grown with PLC and colonized with beneficial P. putida KT2442 bacteria. The stimulatory effect of PLC on photosynthetic parameters of Photosystem II (PSII) was observed in colonized plants grown in vitro. For the first time, it was shown that providing plants with a PLC for only 4 weeks may make it possible to support further plant growth without PLC to obtain higher yields in the future. Thus, PLCs that convert shorter-wavelength radiation into red light may induce enhancement of biochemical processes not only in plants but also in microorganisms that supply plants with growth regulators and other active compounds. The results indicate the need for further research to understand the mechanisms of photobiological and photoregulatory systems in the interaction of microbes and plants. [ABSTRACT FROM AUTHOR]

The strategy of incorporating self‐assembled monolayers (SAMs) with anchoring groups is an effective and promising method for interface engineering in perovskite solar cells with metal oxide charge‐transporting layers. However, coating SAM layers in upscaled perovskite solar modules (PSMs) using slot‐die coating is challenging due to the low viscosity and wettability of the solutions. In this study, a triphenylamine‐based polymer poly([{5‐[4‐(diphenylamino)phenyl]‐2‐thienyl}(4‐fluorophenyl)methylene]malononitrile) (pTPA)–TDP, blended with SAM based on 5‐[4‐[4‐(diphenylamino)phenyl]thiophene‐2‐carboxylic acid, is integrated to address these challenges. And, p–i–n‐oriented PSMs on 50 × 50 mm2 substrates (12 sub‐cells) are fabricated with a NiO hole‐transport layer and organic interlayers for surface modification. Wetting angle mapping shows that ununiform regions of the slot‐die‐coated SAM has extreme hydrophobicity, causing absorber thickness fluctuations and macro‐defects at buried interfaces. The blended interlayer at the NiO/perovskite junction homogenizes surface wettability and mitigates lattice strain, enabling the effective use of SAM properties on large surfaces. This improved energy level alignment, enhancing the power conversion efficiency of the modules from 13.98% to 15.83% and stability (ISOS‐L‐2, T80 period) from 500 to 1630 h. In these results, the complex effects of using SAM in slot‐die‐coating technology for large‐scale perovskite photovoltaics are highlighted. [ABSTRACT FROM AUTHOR]

Hitherto unknown complexes of dimethyl cyclopropane-1,1-dicarboxylatewith Lewis acids (Sn, Ti, and Ga chlorides) have been isolated andcharacterized. Their structures, which were previously assumed fromtheoretical considerations, have been confirmed, and the activatingeffect of Lewis acids on the cyclopropane ring has been shown experimentally.A single crystal of the complex with SnCl4has been obtained,and an X-ray diffraction study has been performed. Hitherto unknowncomplexes of donor–acceptor cyclopropanes with GaCl3belonging to a new type and having a 1,2-dipole (ylide) structurehave been obtained and characterized. 1D and 2D NMR spectroscopy on 1H, 13C, 35Cl, 71Ga, and 119Sn nuclei were used to study the structures of the complexes.Furthermore, DOSY diffusion NMR spectroscopy was used to determinethe diffusion coefficient in solution and the molecular masses ofthe complexes. The data obtained enrich the picture of transformationsof donor–acceptor cyclopropanes widely used in organic synthesis.The practical use of the gallium phenylcyclopropanedicarboxylate complexin a synthesis of polysubstituted cyclic structures in one syntheticstage has also been demonstrated. [ABSTRACT FROM AUTHOR]