Synthesis of a Fluorescent Solvatochromic Resin Using Suzuki–Miyaura Cross-Coupling and Its Optical Waveguide Spectra to Measure the Solvent Polarity on the Surface

We have established a novel analytical method for solvent polarity on resin surface by combining the synthesis of fluorescent solvatochromic resin with optical waveguide spectrometry. The fluorescent solvatochromic resin was obtained via Suzuki–Miyaura cross-coupling between 4-iodobenzoic acid immobilized on Wang resin and 5-[4-(N,N-dihexylamino)phenyl]-2-thienylboronic acid N-methyl-iminodiacetic acid (MIDA) ester. The optical waveguide spectrometry studies on the resin showed a strong fluorescent solvatochromism in various organic solvents.

Antioxidant potential and iodine accumulation in tomato (Solanum lycopersicum L.) seedlings as the effect of the application of three different iodobenzoates

Iodine (I) has a beneficial effect on plant growth, development and antioxidant activity. The study aimed to compare iodine uptake after the application of iodobenzoates (2-iodobenzoic acid (2-IBeA), 4-iodobenzoic acid (4-IBeA) and 2,3,5-triiodobenzoic acid (2,3,5-triIBeA)) as well as potassium iodide (KI) to tomato seedlings. One of the main tasks was to evaluate how the tested compounds applied in different concentrations (5, 10, 25 and 50 μM) affect the growth and antioxidative potential of tomato seedlings. Negative effect on growth and development of tomato seedlings was noted for 4-IBeA applied in 10–50 μM I concentrations. The 2,3,5-triIBeA application affected shoot deformation. All tested iodine compounds increased iodine level in leaves and roots of tomato seedlings. Iodine after KI application was accumulated mainly in leaves, while after iodobenzoates treatment in roots of tomato seedlings, which is probably related to their weaker transport to the upper parts of the plant. Tested compounds variously modified the content of ascorbic and dehydroascorbic acids in tomato leaves depending on applied concentration. KI treatment improved ascorbate peroxidase activity, but all iodobenzoates decreased APX and catalase activity in leaves. 4-IBeA (5 μM I) and 2,3,5-triIBeA (25 and 50 μM I) increased guaiacol peroxidase activity in leaves. It can be concluded that mechanisms responsible for plant oxidative metabolism were variously affected by the iodine compounds and its concentration in the nutrient solution.

Iodosalicylates and iodobenzoates supplied to tomato plants affect the antioxidative and sugar metabolism differently than potassium iodide

Iodine is considered as a beneficial element for plants. As compared to the mineral form of iodine, the effect of organoiodine compounds on physiological and biochemical processes in plants is weakly recognized. This study describes the influence of different forms of iodine – mineral as KI and organic as iodosalicylates and iodobenzoates on the antioxidative and sugar metabolism of tomato plants. Plants were treated with KI and with the following organoiodine compounds: 5-iodosalicylic acid (5-ISA), 3,5-diiodosalicylic acid (3,5-diISA), 2-iodobenzoic acid (2-IBeA) and 4-iodobenzoic acid (4-IBeA). The effect of salicylic acid (SA) and benzoic acid (BeA) on plants was also tested. The plants revealed a lower tolerance to 3,5-diISA, 4-IBeA and slightly to BeA as compared to control. Tested compounds did not affect the content of ascorbic (AA) and dehydroascorbic (DHA) acid. All tested compounds, with the exception of 2-IBeA, did not affect the content of phenols, phenylpropanoids and anthocyanins in leaves. Tested compounds variously modified the activity of catalase (CAT), ascorbic peroxidase (APX) and peroxidase (POX) in leaves and roots. The content of soluble sugars in tomato leaves and roots varied depending on the combination, with a noticeable tendency to increase after the application of organoiodine compounds.

Structural analysis of 2-iodobenzamide and 2-iodo-N-phenylbenzamide

The title compounds, 2-iodobenzamide, C7H6INO (I), and 2-iodo-N-phenylbenzamide, C13H10INO (II), were both synthesized from 2-iodobenzoic acid. In the crystal structure of (I), N—H...O and hydrogen bonds form two sets of closed rings, generating dimers and tetramers. These combine with C—I...π(ring) halogen bonds to form sheets of molecules in the bc plane. For (II), N—H...O hydrogen bonds form chains along the a-axis direction, while inversion-related C—I...π(ring) contacts supported by C—H...π(ring) interactions generate sheets of molecules along the ab diagonal.