A novel 1D polymeric copper(ii) complex of formula {[Cu(l-Arg)2(μ-4,4′-bpy)]Cl2·3H2O∞} was synthesized and characterized using X-ray diffraction, FT-IR, Raman, electron paramagnetic resonance and NIR-vis-UV spectroscopy, and its microbiological properties were analyzed.

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A new unsymmetrical imine with four thiophene rings was synthesized in a one-step reaction, starting from the commercially available and relatively inexpensive reagents.

In this paper, four new aromatic imines containing at least one thiazole-based heterocycle were analyzed in detail by UV–Vis spectroscopy, taking into consideration their chemical structures and interactions with PTB7, a known polymeric electron donor widely used in bulk heterojunction organic solar cells. It is demonstrated that the absorption spectra of the investigated active compositions can be modified not only by changing the chemical structure of imine, but also via formulations with PTB7. For all investigated imines and PTB7:imine compositions, calibration curves were obtained in order to find the optimum concentration in the composition with PTB7 for expansion and optimization of absorption spectra. All imines and PTB7:imine compositions were investigated in 1,2-dichlorobenzene by UV–Vis spectroscopy in various concentrations, monitoring the changes in the π–π* and n–π* transitions. With increasing imine concentrations, we did not observe changes in absorption maxima, while with increasing imine concentrations, a hypochromic effect was observed. Finally, we could conclude that all investigated compositions exhibited wide absorptions of up to 800 nm and isosbestic points in the range of 440–540 nm, confirming changes in the macromolecular organization of the tested compounds. The theoretical calculations of their vibration spectra (FTIR) and LUMO–HOMO levels by Density Functional Theory (DFT) methods are also provided. Finally, IR thermal images were measured for organic devices based on imines and the imine:PTB7 composite.

The main goal of this paper was to show that organic layers prepared for organic solar cells construction can be partially characterized by IR thermographic camera to detect dysfunctionalities of the active layer. Moreover, we used IR thermographic camera to check thermal and electrical behaviour of created simple solar cells to reduce time and cost in global production of solar cells. As model system organic compounds such as PTB7 polymer and small molecule PC71BM as commercial components and newly synthesized imine PV-BLJ-SC11 there were used, to construct simple devices. Full Text: PDF ReferencesK. D. G. I. Jayawardena, L. J. Rozanski, C. A. Mills, M. J. Beliatis, N. A. Nismy, S. R. P. Silva, "Inorganics-in-Organics’: recent developments and outlook for 4G polymer solar cells", Nanoscale, 2013, 5, 8411-8427. CrossRef Y. Lin, X. Zhan, "Oligomer Molecules for Efficient Organic Photovoltaics", Accounts of Chemical Research, 2016, 49, 175-183. CrossRef R. Steim, S. A. Choulis, P. Schilinsky, U. Lemmer, C. J. Brabec, "Formation and impact of hot spots on the performance of organic photovoltaic cells", Applied Physics Letters, 2009, 94, 043304. CrossRef J. Hepp, F. Machui, H. J. Egelhaaf, C. J. Brabec, A. Vetter, "Automatized analysis of IR‐images of photovoltaic modules and its use for quality control of solar cells", Energy Science and Engineering. 2016, 4, 363-371. CrossRef H. Hoppe, J. Bachmann, B. Muhsin, K. H. Drüe, I. Riedel, G. Gobsch, C. Buerhop-Lutz, C. J. Brabec, V. Dyakonov, "Quality control of polymer solar modules by lock-in thermography", Journal of Applied Physics, 2010, 107, 014505. CrossRef J. Bachmann, C. Buerhop-Lutz, C. Deibel, I. Riedel, H. Hoppe, C. J. Brabec, V. Dyakonov, "Organic solar cells characterized by dark lock-in thermography", Solar Energy Materials and Solar Cells, 2010, 94, 642-647. CrossRef A. Różycka, K. A. Bogdanowicz, N. Górska, J. Rysz, M. Marzec, A. Iwan, R. Pich, A. Januszko, "Influence of TiO2 Nanoparticles on Liquid Crystalline, Structural and Electrochemical Properties of (8Z)-N-(4-((Z)-(4-pentylphenylimino)methyl)benzylidene)-4-pentylbenzenamine", Materials, 2019, 12, 1097. CrossRef M. L. Petrus, R. K. M. Bouwer, U. Lafont, S. Athanasopoulos, N. C. Greenham, T. J. Dingemans, "Small-molecule azomethines: organic photovoltaics via Schiff base condensation chemistry", Journal of Materials Chemistry A, 2014, 2, 9474-9477. CrossRef K. A. Bogdanowicz, A. Iwan, "Symmetrical Imines with Trirphenylamine Core and the Method of Obtaining Thereof.", March 11th 2019, patent application P.429044. DirectLink K. P. Korona, T. Korona, D. Rutkowska-Zbik, S. Grankowska-Ciechanowicz, A. Iwan, M. Kamińska, "Polyazomethine as a component of solar cells-theoretical and optical study", Journal of Physics and Chemistry of Solids, 2015, 86, 186-193. CrossRef

The crystal structure was determined for the first time for 4-[(di-p-tolyl-amino)benzylidene]-(5-pyridin-4-yl-[1,3,4]thiadiazol-2-yl)-imine (trans-PPL9) by X-ray diffraction. The imine crystallized in the monoclinic P21/n space group with a = 18.9567(7) Å, b = 6.18597(17) Å, c = 22.5897(7) Å, and β = 114.009(4)°. Intermolecular interactions in the PPL9 crystal were only weak C−H∙∙∙N hydrogen bonds investigated using the Hirshfeld surface. The electronic and geometric structure of the imine were investigated by the density functional theory and the time-dependent density-functional theory. The properties of the imine in neutral and protonated form with camforosulphonic acid (CSA) were investigated using cyclic voltammetry, UV–vis and 1H NMR spectroscopy. Theoretical and experimental studies showed that for the 1:1 molar ratio the protonation occured on nitrogen in pyridine in the PPL9 structure, as an effect of Brönsted acid–base interactions. Thermographic camera was used to defined defects in constructed simple devices with ITO/PPL9 (or PPL9:CSA)/Ag/ITO architecture. In conclusion, a thermally stable imine was synthesized in crystalline form and by CSA doping, a modification of absorption spectra together with reduction of overheating process was observed, suggesting its potential application in optoelectronics.

The aim of presented research is to develop a simple and quick method of spectrophotometric detection for the determination of doxorubicin hydrochloride in blood and plasma. Anthracycline antibiotics are among the most effective antineoplastic agents. However, despite their high efficacy in the treatment of various types of cancer, their administration is limited primarily because they exhibit myocardial toxicity. This may be a limiting factor in the dosage of medications; nevertheless, drugs exhibiting this mechanism of action constitute a very important group of chemotherapeutics. One of the more widely studied antibiotics from the anthracycline group is doxorubicin. It exhibits the highest antineoplastic activity from among a number of derivative compounds. Because of the adverse effects of doxorubicin, especially cardiotoxicity, it is important to maintain control of its concentration in body fluids. The method in the study consists of extraction doxorubicin from the plasma or blood and measurements of the absorbance of light in the visible light range in a DOX solution with respect to a reference sample. The research used blood and plasma samples spiked with doxorubicin to give concentrations in the range of 0.2–10 µg/mL. Obtained LODs were 1.6 µg/mL and 1.2 µg/mL, respectively.

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