In this report, we present the results of our investigations into the elucidation of the chemical structure of moieties responsible for the blue and green luminescence of CDs derived from the microwave-assisted pyrolysis of citric acid in the presence of urea. The molecular fluorophore that forms during the synthesis of green fluorescing CDs is 4-hydroxy-1H-pyrrolo[3,4-c]pyridine-1,3,6(2H,5H)-trione (HPPT).

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Citric acid was reacted with α,β-diamines, β-amino thiols and β-amino alcohols to produce fluorescent derivatives of 2-pyridone (QY up to ∼79%). The chemical structures of these compounds were confirmed by analyses of 1D, 2D NMR and ESI-MS data.

The possible origin of luminescent properties of biodegradable photoluminescent polyesters (BPLPs) has been revealed by isolation and identification of luminescent agent from the hydrolyzate of BPLP. Elemental analysis, ESI-MS, (1)H, (13)C, 2D HSQC and COSY NMR spectra confirmed the chemical structure as 5-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyridine-3,7-dicarboxylic acid (TPA).

a b s t r a c tGreen metrics is a methodology which allows the greenness of either new or already existing processes to be assessed. This paper is a part of a special issue devoted to green metrics in which this methodology is applied to different processes to assess bio and petrochemical routes. In this work, green metrics were used as a tool to validate and compare the petrochemical and biological processes of isoprene production. The Sumitomo process has been selected for this comparison as it is beneficial because of it using less expensive C 1 components as well as the fact that it has lower investment costs for a single-step process. The production of isoprene through a modified Escherichia coli bacterial process has been selected for comparison with the fossil pathway. The green metrics evaluation was performed for both processes to produce isoprene and to target 50,000 tonnes of isoprene yearly.Although, the calculated costs for the bio-isoprene are slightly higher than the actual market price of its fossil counterpart, the results obtained reveal that the bacteria-based isoprene production is able to substitute the petrochemical process, with material and energy efficiency. This conclusion has also been proved by the increasing number of industrial interest in bioisoprene. The challenge comes from the land use needed for the production of a carbon source which might be solved by the use of waste and residues which are rich in carbohydrates or lignocellulosic biomass which can be converted to simple sugars.

Massive blood loss is responsible for numerous causes of death. Hemorrhage may occur on the battlefield, at home or during surgery. Commercially available biomaterials may be insufficient to deal with excessive bleeding. Therefore novel, highly efficient hemostatic agents must be developed. The aim of the following research was to obtain a new type of biocompatible chitosan-based hemostatic agents with increased hemostatic properties. The biomaterials were obtained in a quick and efficient manner under microwave radiation using l-aspartic and l-glutamic acid as crosslinking agents with no use of acetic acid. Ready products were investigated over their chemical structure by FT-IR method which confirmed a crosslinking process through the formation of amide bonds. Their high porosity above 90% and low density (below 0.08 g/cm3) were confirmed. The aerogels were also studied over their water vapor permeability and antioxidant activity. Prepared biomaterials were biodegradable in the presence of human lysozyme. All of the samples had excellent hemostatic properties in contact with human blood due to the platelet activation confirmed by blood clotting tests. The SEM microphotographs showed the adherence of blood cells to the biomaterials’ surface. Moreover, they were biocompatible with human dermal fibroblasts (HDFs). The biomaterials also had superior antibacterial properties against both Staphylococcus aureus and Escherichia coli. The obtained results showed that proposed chitosan-based hemostatic agents have great potential as a hemostatic product and may be applied under sterile, as well as contaminated conditions, by both medicals and individuals.

Polymerization of two isomeric heterocyclic monomers, 3-methyl-1-vinylpyrazole and 1-allylimidazole, was investigated under pulsed plasma conditions. Large-scale, progressive variations in polymer compositions were observed with sequential changes in the plasma duty cycles employed, all other plasma variables being held constant. In particular, unusually linear polymers (by normal plasma polymerization standards) are achieved at exceptionally low average power inputs, employed when the pulsed plasma technique is operated at low duty cycles. With both monomers, a pronounced increased retention of their aromatic rings is observed in the plasma-synthesized polymers as the duty cycle employed during film formation is reduced. Overall, a higher ring retention is achieved with the imidazole, compared to the pyrazole, reflecting bond energy differences in these two isomers. This study also includes synthesis and spectral characterization of a conventionally prepared linear poly(3-methyl-1-vinylpyrazole) which was employed to assess the degree of ring retention in the plasma polymers. On the basis of the results of this study, it appears that relatively linear polymers of fairly complex molecules are readily synthesized using the low duty cycle pulsed plasma technique. Accordingly, this approach is useful in extending the utility of plasma polymerizations which have heretofore tended to focus on synthesis of unique, relatively highly cross-linked materials. The pulsed technique provides synthesis of these polymers while maintaining the many inherent advantages of the plasma polymerization technique, including particularly the pinhole-free, conformal, and adhesive qualities of these films.

Condensation of salicyaldehyde or its derivatives with various derivatives of ethyl acetate in the presence of piperidine leads to the synthesis of coumarins by a solvent free reaction under microwave irradiation.